NP-MRD: Showing NP-Card for Flavin Mononucleotide (NP0000348)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2005-11-16 15:48:42 UTC

Updated at

2021-06-29 00:47:06 UTC

NP-MRD ID

NP0000348

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Flavin Mononucleotide

Description

Flavin mononucleotide (FMN), or riboflavin-5′-phosphate, is a biomolecule produced from riboflavin (vitamin B2) by the enzyme riboflavin kinase and functions as the prosthetic group of various oxidoreductases, including NADH dehydrogenase, as well as cofactor in biological blue-light photo receptors. During the catalytic cycle, a reversible interconversion of the oxidized (FMN), semiquinone (FMNH), and reduced (FMNH2) forms occurs in the various oxidoreductases. FMN is a stronger oxidizing agent than NAD and is particularly useful because it can take part in both one- and two-electron transfers. In its role as blue-light photo receptor, (oxidized) FMN stands out from the 'conventional' photo receptors as the signaling state and not an E/Z isomerization. It is the principal form in which riboflavin is found in cells and tissues. It requires more energy to produce, but is more soluble than riboflavin. Flavin mononucleotide belongs to the class of organic compounds known as flavin nucleotides. These are nucleotides containing a flavin moiety. Flavin is a compound that contains the tricyclic isoalloxazine ring system, which bears 2 oxo groups at the 2- and 4-positions. Flavin mononucleotide exists in all living species, ranging from bacteria to humans. Within humans, flavin mononucleotide participates in a number of enzymatic reactions. In particular, formic acid and flavin mononucleotide can be biosynthesized from FMNH2; which is catalyzed by the enzyme lanosterol 14-alpha demethylase. In addition, formic acid and flavin mononucleotide can be biosynthesized from FMNH2 through the action of the enzyme lanosterol 14-alpha demethylase. In humans, flavin mononucleotide is involved in bloch pathway (cholesterol biosynthesis). Outside of the human body, flavin mononucleotide has been detected, but not quantified in several different foods, such as mandarin orange (clementine, tangerine), horseradish tree, black elderberries, angelica, and ostrich ferns.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


     RDKit          2D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -6.6140   -0.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1140   -0.4683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3622   -1.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8622   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105   -3.0623    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6105   -3.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1413   -4.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6069   -5.6583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6413   -4.3562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3895   -3.0562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8786   -3.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6378   -1.7581    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378   -1.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6140   -0.4622    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    0.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8825    2.1379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4176    2.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1825    1.3897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4343    0.0897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307    2.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    3.9898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2308    1.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5309    1.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5329   -0.3067    0.0000 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.0329   -0.3046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0329   -0.3087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349   -1.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1140   -0.4642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8658    0.8338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3658    0.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1175    2.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7989    1.0182    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6120   -1.9703    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1140   -0.4724    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1105   -3.0664    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3931   -5.6542    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1658    1.5861    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7084    0.2849    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4666    3.5195    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4196    4.3862    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3817    0.4886    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778   -0.9879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    3.5909    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9272    5.2879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6466    0.5600    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9790    3.2416    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2847   -1.6088    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3382   -2.7111    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1175    2.1339    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8195    2.8815    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4975    1.5418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8693    3.4278    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 24 23  1  1
 24 25  2  0
 24 26  1  0
 24 27  1  0
 14 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 28  4  2  0
 13  6  1  0
  1 32  1  6
  1 33  1  0
  1 34  1  0
  3 35  1  0
  9 36  1  0
 15 37  1  1
 15 38  1  0
 16 39  1  1
 17 40  1  0
 18 41  1  6
 19 42  1  0
 20 43  1  1
 21 44  1  0
 22 45  1  6
 22 46  1  0
 26 47  1  0
 27 48  1  0
 29 49  1  0
 31 50  1  1
 31 51  1  0
 31 52  1  0
M  END

HMDB0001520
     RDKit          3D
Flavin mononucleotide
 52 54  0  0  0  0  0  0  0  0999 V2000
   -5.4563    2.6957   -0.3846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3858    1.6916   -0.1441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6669    0.3758   -0.3325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6868   -0.5882   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0236   -1.8768   -0.3205 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1064   -2.8153   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597   -4.1718   -0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -4.5088   -0.6781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3716   -5.0558   -0.0842 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1546   -4.6451    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2941   -5.5687    0.4951 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8471   -3.3518    0.5092 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7774   -2.4147    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.1177    0.5121 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.7790    0.9388 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -0.5223   -0.2408 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9128   -1.6317   -1.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1656   -0.0831    0.3037 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9084    1.0546    1.1030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1006    0.3492   -0.7835 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3921   -0.7522   -1.6146 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4109    0.7435   -0.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3653    1.0980   -1.0927 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8139    1.5327   -0.3524 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4267    0.2968    0.2491 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5675    2.6361    0.9051 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8705    2.1637   -1.4855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4049   -0.2053    0.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1347    1.1267    0.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1251    2.0568    0.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644    3.5168    0.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0686    3.6677   -0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1298    2.2999   -1.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0600    2.7523    0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6613    0.0912   -0.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -6.0909   -0.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3387   -1.6616    1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0660    0.0342    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4524    0.3159   -0.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5799   -2.2889   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6287   -0.8770    0.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2339    1.6355    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7088    1.1625   -1.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8152   -1.4547   -1.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    1.5609    0.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8011   -0.1441    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    3.1105    0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6202    1.5601   -1.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1629    1.4610    0.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    3.6541    1.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8308    4.0424   -0.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7007    3.9192    1.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 14 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 28  4  2  0
 13  6  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  9 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  6
 17 40  1  0
 18 41  1  1
 19 42  1  0
 20 43  1  6
 21 44  1  0
 22 45  1  0
 22 46  1  0
 26 47  1  0
 27 48  1  0
 29 49  1  0
 31 50  1  0
 31 51  1  0
 31 52  1  0
M  END


     RDKit          2D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -6.6140   -0.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1140   -0.4683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3622   -1.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8622   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1105   -3.0623    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6105   -3.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1413   -4.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6069   -5.6583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6413   -4.3562    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3895   -3.0562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8786   -3.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6378   -1.7581    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378   -1.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6140   -0.4622    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1342    0.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8825    2.1379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4176    2.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1825    1.3897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4343    0.0897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307    2.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6790    3.9898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2308    1.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5309    1.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5329   -0.3067    0.0000 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.0329   -0.3046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0329   -0.3087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5349   -1.8067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1140   -0.4642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8658    0.8338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3658    0.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1175    2.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7989    1.0182    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6120   -1.9703    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1140   -0.4724    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1105   -3.0664    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3931   -5.6542    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1658    1.5861    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7084    0.2849    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4666    3.5195    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4196    4.3862    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3817    0.4886    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778   -0.9879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7316    3.5909    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9272    5.2879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6466    0.5600    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9790    3.2416    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2847   -1.6088    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3382   -2.7111    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1175    2.1339    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8195    2.8815    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4975    1.5418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8693    3.4278    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 24 23  1  1
 24 25  2  0
 24 26  1  0
 24 27  1  0
 14 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 28  4  2  0
 13  6  1  0
  1 32  1  6
  1 33  1  0
  1 34  1  0
  3 35  1  0
  9 36  1  0
 15 37  1  1
 15 38  1  0
 16 39  1  1
 17 40  1  0
 18 41  1  6
 19 42  1  0
 20 43  1  1
 21 44  1  0
 22 45  1  6
 22 46  1  0
 26 47  1  0
 27 48  1  0
 29 49  1  0
 31 50  1  1
 31 51  1  0
 31 52  1  0
M  END
> <DATABASE_ID>
NP0000348

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)COP(O)(O)=O)C1=NC(=O)NC(=O)C1=N2

> <INCHI_IDENTIFIER>
InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1

> <INCHI_KEY>
FVTCRASFADXXNN-SCRDCRAPSA-N

> <FORMULA>
C17H21N4O9P

> <MOLECULAR_WEIGHT>
456.3438

> <EXACT_MASS>
456.104614802

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.18863753153134

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4S)-5-{7,8-dimethyl-2,4-dioxo-2H,3H,4H,10H-benzo[g]pteridin-10-yl}-2,3,4-trihydroxypentyl]oxy}phosphonic acid

> <ALOGPS_LOGP>
-0.78

> <JCHEM_LOGP>
-1.0401062913333337

> <ALOGPS_LOGS>
-2.83

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
5.861669782552471

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.4921020390081319

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6107860700389316

> <JCHEM_POLAR_SURFACE_AREA>
201.57999999999998

> <JCHEM_REFRACTIVITY>
107.14129999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.68e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
riboflavin 5'-phosphate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001520
     RDKit          3D
Flavin mononucleotide
 52 54  0  0  0  0  0  0  0  0999 V2000
   -5.4563    2.6957   -0.3846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3858    1.6916   -0.1441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6669    0.3758   -0.3325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6868   -0.5882   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0236   -1.8768   -0.3205 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1064   -2.8153   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597   -4.1718   -0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -4.5088   -0.6781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3716   -5.0558   -0.0842 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1546   -4.6451    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2941   -5.5687    0.4951 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8471   -3.3518    0.5092 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7774   -2.4147    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.1177    0.5121 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.7790    0.9388 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -0.5223   -0.2408 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9128   -1.6317   -1.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1656   -0.0831    0.3037 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9084    1.0546    1.1030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1006    0.3492   -0.7835 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3921   -0.7522   -1.6146 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4109    0.7435   -0.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3653    1.0980   -1.0927 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8139    1.5327   -0.3524 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4267    0.2968    0.2491 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5675    2.6361    0.9051 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8705    2.1637   -1.4855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4049   -0.2053    0.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1347    1.1267    0.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1251    2.0568    0.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644    3.5168    0.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0686    3.6677   -0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1298    2.2999   -1.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0600    2.7523    0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6613    0.0912   -0.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -6.0909   -0.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3387   -1.6616    1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0660    0.0342    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4524    0.3159   -0.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5799   -2.2889   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6287   -0.8770    0.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2339    1.6355    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7088    1.1625   -1.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8152   -1.4547   -1.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    1.5609    0.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8011   -0.1441    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    3.1105    0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6202    1.5601   -1.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1629    1.4610    0.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    3.6541    1.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8308    4.0424   -0.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7007    3.9192    1.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 14 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 28  4  2  0
 13  6  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  9 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  6
 17 40  1  0
 18 41  1  1
 19 42  1  0
 20 43  1  6
 21 44  1  0
 22 45  1  0
 22 46  1  0
 26 47  1  0
 27 48  1  0
 29 49  1  0
 31 50  1  0
 31 51  1  0
 31 52  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0      -9.336   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -4.001  -2.310   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      -4.001  -6.930   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      -6.668  -3.850   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   25  P   UNK     0       5.335  -1.540   0.000  0.00  0.00           P+0
HETATM   26  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       6.105  -2.874   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.565  -0.206   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.334  -3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -1.334  -3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7                                                            
CONECT    9    5   10   19                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   10   18                                                  
CONECT   18   17    4                                                       
CONECT   19    9   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   22   30                                                  
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25                                                            
CONECT   29   22                                                            
CONECT   30   21                                                            
CONECT   31   20                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

COMPND    HMDB0001520
HETATM    1  C1  UNL     1      -5.456   2.696  -0.385  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.386   1.692  -0.144  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.667   0.376  -0.332  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.687  -0.588  -0.116  1.00  0.00           C  
HETATM    5  N1  UNL     1      -4.024  -1.877  -0.321  1.00  0.00           N  
HETATM    6  C5  UNL     1      -3.106  -2.815  -0.122  1.00  0.00           C  
HETATM    7  C6  UNL     1      -3.360  -4.172  -0.308  1.00  0.00           C  
HETATM    8  O1  UNL     1      -4.507  -4.509  -0.678  1.00  0.00           O  
HETATM    9  N2  UNL     1      -2.372  -5.056  -0.084  1.00  0.00           N  
HETATM   10  C7  UNL     1      -1.155  -4.645   0.313  1.00  0.00           C  
HETATM   11  O2  UNL     1      -0.294  -5.569   0.495  1.00  0.00           O  
HETATM   12  N3  UNL     1      -0.847  -3.352   0.509  1.00  0.00           N  
HETATM   13  C8  UNL     1      -1.777  -2.415   0.307  1.00  0.00           C  
HETATM   14  N4  UNL     1      -1.442  -1.118   0.512  1.00  0.00           N  
HETATM   15  C9  UNL     1      -0.103  -0.779   0.939  1.00  0.00           C  
HETATM   16  C10 UNL     1       0.818  -0.522  -0.241  1.00  0.00           C  
HETATM   17  O3  UNL     1       0.913  -1.632  -1.046  1.00  0.00           O  
HETATM   18  C11 UNL     1       2.166  -0.083   0.304  1.00  0.00           C  
HETATM   19  O4  UNL     1       1.908   1.055   1.103  1.00  0.00           O  
HETATM   20  C12 UNL     1       3.101   0.349  -0.784  1.00  0.00           C  
HETATM   21  O5  UNL     1       3.392  -0.752  -1.615  1.00  0.00           O  
HETATM   22  C13 UNL     1       4.411   0.744  -0.137  1.00  0.00           C  
HETATM   23  O6  UNL     1       5.365   1.098  -1.093  1.00  0.00           O  
HETATM   24  P1  UNL     1       6.814   1.533  -0.352  1.00  0.00           P  
HETATM   25  O7  UNL     1       7.427   0.297   0.249  1.00  0.00           O  
HETATM   26  O8  UNL     1       6.568   2.636   0.905  1.00  0.00           O  
HETATM   27  O9  UNL     1       7.871   2.164  -1.486  1.00  0.00           O  
HETATM   28  C14 UNL     1      -2.405  -0.205   0.298  1.00  0.00           C  
HETATM   29  C15 UNL     1      -2.135   1.127   0.484  1.00  0.00           C  
HETATM   30  C16 UNL     1      -3.125   2.057   0.262  1.00  0.00           C  
HETATM   31  C17 UNL     1      -2.864   3.517   0.456  1.00  0.00           C  
HETATM   32  H1  UNL     1      -5.069   3.668  -0.708  1.00  0.00           H  
HETATM   33  H2  UNL     1      -6.130   2.300  -1.200  1.00  0.00           H  
HETATM   34  H3  UNL     1      -6.060   2.752   0.553  1.00  0.00           H  
HETATM   35  H4  UNL     1      -5.661   0.091  -0.652  1.00  0.00           H  
HETATM   36  H5  UNL     1      -2.569  -6.091  -0.227  1.00  0.00           H  
HETATM   37  H6  UNL     1       0.339  -1.662   1.499  1.00  0.00           H  
HETATM   38  H7  UNL     1      -0.066   0.034   1.686  1.00  0.00           H  
HETATM   39  H8  UNL     1       0.452   0.316  -0.868  1.00  0.00           H  
HETATM   40  H9  UNL     1       1.580  -2.289  -0.787  1.00  0.00           H  
HETATM   41  H10 UNL     1       2.629  -0.877   0.891  1.00  0.00           H  
HETATM   42  H11 UNL     1       1.234   1.636   0.674  1.00  0.00           H  
HETATM   43  H12 UNL     1       2.709   1.163  -1.406  1.00  0.00           H  
HETATM   44  H13 UNL     1       3.815  -1.455  -1.053  1.00  0.00           H  
HETATM   45  H14 UNL     1       4.236   1.561   0.603  1.00  0.00           H  
HETATM   46  H15 UNL     1       4.801  -0.144   0.395  1.00  0.00           H  
HETATM   47  H16 UNL     1       5.710   3.111   0.830  1.00  0.00           H  
HETATM   48  H17 UNL     1       8.620   1.560  -1.648  1.00  0.00           H  
HETATM   49  H18 UNL     1      -1.163   1.461   0.799  1.00  0.00           H  
HETATM   50  H19 UNL     1      -1.917   3.654   1.019  1.00  0.00           H  
HETATM   51  H20 UNL     1      -2.831   4.042  -0.522  1.00  0.00           H  
HETATM   52  H21 UNL     1      -3.701   3.919   1.059  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    3   30
CONECT    3    4   35
CONECT    4    5   28   28
CONECT    5    6    6
CONECT    6    7   13
CONECT    7    8    8    9
CONECT    9   10   36
CONECT   10   11   11   12
CONECT   12   13   13
CONECT   13   14
CONECT   14   15   28
CONECT   15   16   37   38
CONECT   16   17   18   39
CONECT   17   40
CONECT   18   19   20   41
CONECT   19   42
CONECT   20   21   22   43
CONECT   21   44
CONECT   22   23   45   46
CONECT   23   24
CONECT   24   25   25   26   27
CONECT   26   47
CONECT   27   48
CONECT   28   29
CONECT   29   30   30   49
CONECT   30   31
CONECT   31   50   51   52
END

HMDB0001520
     RDKit          3D
Flavin mononucleotide
 52 54  0  0  0  0  0  0  0  0999 V2000
   -5.4563    2.6957   -0.3846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3858    1.6916   -0.1441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6669    0.3758   -0.3325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6868   -0.5882   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0236   -1.8768   -0.3205 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1064   -2.8153   -0.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3597   -4.1718   -0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072   -4.5088   -0.6781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3716   -5.0558   -0.0842 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1546   -4.6451    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2941   -5.5687    0.4951 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8471   -3.3518    0.5092 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7774   -2.4147    0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.1177    0.5121 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.7790    0.9388 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -0.5223   -0.2408 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9128   -1.6317   -1.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1656   -0.0831    0.3037 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9084    1.0546    1.1030 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1006    0.3492   -0.7835 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3921   -0.7522   -1.6146 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4109    0.7435   -0.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3653    1.0980   -1.0927 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8139    1.5327   -0.3524 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4267    0.2968    0.2491 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5675    2.6361    0.9051 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8705    2.1637   -1.4855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4049   -0.2053    0.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1347    1.1267    0.4844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1251    2.0568    0.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8644    3.5168    0.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0686    3.6677   -0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1298    2.2999   -1.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0600    2.7523    0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6613    0.0912   -0.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -6.0909   -0.2268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3387   -1.6616    1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0660    0.0342    1.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4524    0.3159   -0.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5799   -2.2889   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6287   -0.8770    0.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2339    1.6355    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7088    1.1625   -1.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8152   -1.4547   -1.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2358    1.5609    0.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8011   -0.1441    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7103    3.1105    0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6202    1.5601   -1.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1629    1.4610    0.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    3.6541    1.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8308    4.0424   -0.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7007    3.9192    1.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 14 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 28  4  2  0
 13  6  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  9 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  6
 17 40  1  0
 18 41  1  1
 19 42  1  0
 20 43  1  6
 21 44  1  0
 22 45  1  0
 22 46  1  0
 26 47  1  0
 27 48  1  0
 29 49  1  0
 31 50  1  0
 31 51  1  0
 31 52  1  0
M  END

View in JSmol

Synonyms

Value	Source
Riboflavin 5'-(dihydrogen phosphate)	ChEBI
Riboflavin 5'-monophosphate	ChEBI
Riboflavin 5'-phosphate	ChEBI
Riboflavin monophosphate	ChEBI
Riboflavin-5-phosphate	ChEBI
Riboflavine dihydrogen phosphate	ChEBI
Riboflavin 5'-(dihydrogen phosphoric acid)	Generator
Riboflavin 5'-monophosphoric acid	Generator
Riboflavin 5'-phosphoric acid	Generator
Riboflavin monophosphoric acid	Generator
Riboflavin-5-phosphoric acid	Generator
Riboflavine dihydrogen phosphoric acid	Generator
Flanin	HMDB
Flavine mononucleotide	HMDB
Flavol	HMDB
FMN	HMDB
Riboflavin	HMDB
Riboflavin mononucleotide	HMDB
Riboflavin phosphate	HMDB
Riboflavin-5'-phosphate na	HMDB
Riboflavine 5'-monophosphate	HMDB
Riboflavine 5'-phosphate	HMDB
Riboflavine monophosphate	HMDB
Riboflavine phosphate	HMDB
Riboflavine-5'-phosphate	HMDB
Vitamin b2 phosphate	HMDB
5'-monoPhosphate, riboflavin	HMDB
5'-Phosphate, riboflavin	HMDB
Flavin mononucleotide sodium salt	HMDB
Mononucleotide, riboflavin	HMDB
Flavin mononucleotide monosodium salt	HMDB
Flavin mononucleotide monosodium salt, dihydrate	HMDB
Phosphate, sodium riboflavin	HMDB
Riboflavin 5' phosphate	HMDB
Riboflavin phosphate, sodium	HMDB
Mononucleotide, flavin	HMDB
Riboflavin 5' monophosphate	HMDB
Flavin mononucleotide disodium salt	HMDB
Sodium riboflavin phosphate	HMDB

Chemical Formula

C₁₇H₂₁N₄O₉P

Average Mass

456.3438 Da

Monoisotopic Mass

456.10461 Da

IUPAC Name

{[(2R,3S,4S)-5-{7,8-dimethyl-2,4-dioxo-2H,3H,4H,10H-benzo[g]pteridin-10-yl}-2,3,4-trihydroxypentyl]oxy}phosphonic acid

Traditional Name

riboflavin 5'-phosphate

CAS Registry Number

146-17-8

SMILES

CC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)COP(O)(O)=O)C1=NC(=O)NC(=O)C1=N2

InChI Identifier

InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1

InChI Key

FVTCRASFADXXNN-SCRDCRAPSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, H₂O, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Abelmoschus esculentus	FooDB	FooDB
Actinidia chinensis	FooDB	FooDB
Agaricus bisporus	FooDB	FooDB
Agave	FooDB	FooDB
Allium ampeloprasum	FooDB	FooDB
Allium ascalonicum	FooDB	FooDB
Allium cepa	FooDB	FooDB
Allium cepa L.	FooDB	FooDB
Allium fistulosum	FooDB	FooDB
Allium sativum	FooDB	FooDB
Allium schoenoprasum	FooDB	FooDB
Allium tuberosum	FooDB	FooDB
Aloysia triphylla	FooDB	FooDB
Amaranthus	FooDB	FooDB
Amelanchier alnifolia	FooDB	FooDB
Anacardium occidentale	FooDB	FooDB
Ananas comosus	FooDB	FooDB
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anethum graveolens	FooDB	FooDB
Angelica keiskei	FooDB	FooDB
Annona cherimola	FooDB	FooDB
Annona muricata	FooDB	FooDB
Annona reticulata	FooDB	FooDB
Annona squamosa	FooDB	FooDB
Anser anser	FooDB	FooDB
Anthriscus cerefolium	FooDB	FooDB
Apium graveolens	FooDB	FooDB
Apium graveolens var. dulce	FooDB	FooDB
Apium graveolens var. rapaceum	FooDB	FooDB
Apium graveolens var. secalinum	FooDB	FooDB
Arabidopsis thaliana	LOTUS Database	35616633
Arachis hypogaea	FooDB	FooDB
Arctium lappa	FooDB	FooDB
Armoracia rusticana	FooDB	FooDB
Artemisia dracunculus	FooDB	FooDB
Artemisia vulgaris	FooDB	FooDB
Artocarpus altilis	FooDB	FooDB
Artocarpus heterophyllus	FooDB	FooDB
Asparagus officinalis	FooDB	FooDB
Attalea speciosa	FooDB	FooDB
Auricularia auricula-judae	FooDB	FooDB
Auricularia polytricha	FooDB	FooDB
Avena sativa L.	FooDB	FooDB
Averrhoa carambola	FooDB	FooDB
Basella alba	FooDB	FooDB
Benincasa hispida	FooDB	FooDB
Bertholletia excelsa	FooDB	FooDB
Beta vulgaris	FooDB	FooDB
Beta vulgaris ssp. cicla	FooDB	FooDB
Bison bison	FooDB	FooDB
Borago officinalis	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Brassica alboglabra	FooDB	FooDB
Brassica juncea	FooDB	FooDB
Brassica napus	FooDB	FooDB
Brassica napus var. napus	FooDB	FooDB
Brassica oleracea	FooDB	FooDB
Brassica oleracea var. botrytis	FooDB	FooDB
Brassica oleracea var. capitata	FooDB	FooDB
Brassica oleracea var. gemmifera	FooDB	FooDB
Brassica oleracea var. gongylodes	FooDB	FooDB
Brassica oleracea var. italica	FooDB	FooDB
Brassica oleracea var. sabauda	FooDB	FooDB
Brassica oleracea var. viridis	FooDB	FooDB
Brassica rapa	FooDB	FooDB
Brassica rapa ssp. chinensis	FooDB	FooDB
Brassica rapa var. pekinensis	FooDB	FooDB
Brassica rapa var. rapa	FooDB	FooDB
Brassica ruvo	FooDB	FooDB
Brosimum alicastrum	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Byrsonima crassifolia	FooDB	FooDB
Cajanus cajan	FooDB	FooDB
Canarium ovatum	FooDB	FooDB
Cannabis sativa	CannabisDB	Not Available
Cantharellus cibarius	FooDB	FooDB
Capparis spinosa	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Capsicum annuum	FooDB	FooDB
Capsicum annuum L.	FooDB	FooDB
Capsicum annuum var. annuum	FooDB	FooDB
Capsicum chinense	FooDB	FooDB
Capsicum pubescens	FooDB	FooDB
Carica papaya L.	FooDB	FooDB
Carissa macrocarpa	FooDB	FooDB
Carthamus tinctorius	FooDB	FooDB
Carum carvi	FooDB	FooDB
Carya	FooDB	FooDB
Carya illinoinensis	FooDB	FooDB
Castanea	FooDB	FooDB
Castanea crenata	FooDB	FooDB
Castanea mollissima	FooDB	FooDB
Castanea sativa	FooDB	FooDB
Ceratonia siliqua	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Chamaemelum nobile	FooDB	FooDB
Chamerion angustifolium	FooDB	FooDB
Chenopodium album	FooDB	FooDB
Chenopodium quinoa	FooDB	FooDB
Chrysanthemum coronarium	FooDB	FooDB
Cicer arietinum	FooDB	FooDB
Cichorium endivia	FooDB	FooDB
Cichorium intybus	FooDB	FooDB
Cinnamomum	FooDB	FooDB
Cinnamomum aromaticum	FooDB	FooDB
Cinnamomum verum	FooDB	FooDB
Cirsium	FooDB	FooDB
Citrullus lanatus	FooDB	FooDB
Citrus ×limon (L.) Burm. f. (pro sp.)	FooDB	FooDB
Citrus aurantiifolia	FooDB	FooDB
Citrus latifolia	FooDB	FooDB
Citrus limon	FooDB	FooDB
Citrus maxima	FooDB	FooDB
Citrus paradisi	FooDB	FooDB
Citrus reticulata	FooDB	FooDB
Citrus X sinensis (L.) Osbeck (pro. sp.)	FooDB	FooDB
Cocos nucifera	FooDB	FooDB
Coffea arabica L.	FooDB	FooDB
Coffea canephora	FooDB	FooDB
Colocasia esculenta	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Corchorus olitorius	FooDB	FooDB
Coriandrum sativum L.	FooDB	FooDB
Corylus	FooDB	FooDB
Corylus avellana	FooDB	FooDB
Crateva religiosa	FooDB	FooDB
Crocus sativus	FooDB	FooDB
Cucumis melo	FooDB	FooDB
Cucumis metuliferus	FooDB	FooDB
Cucumis sativus L.	FooDB	FooDB
Cucurbita	FooDB	FooDB
Cucurbita maxima	FooDB	FooDB
Cucurbita moschata	FooDB	FooDB
Cuminum cyminum	FooDB	FooDB
Curcuma longa	FooDB	FooDB
Cydonia oblonga	FooDB	FooDB
Cymbopogon citratus	FooDB	FooDB
Cynara cardunculus	FooDB	FooDB
Cynara scolymus	FooDB	FooDB
Daucus carota	FooDB	FooDB
Daucus carota ssp. sativus	FooDB	FooDB
Dimocarpus longan	FooDB	FooDB
Dioscorea	FooDB	FooDB
Dioscorea pentaphylla	FooDB	FooDB
Diospyros	FooDB	FooDB
Diospyros kaki	FooDB	FooDB
Diospyros virginiana	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Durio zibethinus	FooDB	FooDB
Dysphania ambrosioides	FooDB	FooDB
Elaeis	FooDB	FooDB
Eleocharis dulcis	FooDB	FooDB
Elettaria cardamomum	FooDB	FooDB
Empetrum nigrum	FooDB	FooDB
Equus caballus	FooDB	FooDB
Eragrostis tef	FooDB	FooDB
Eriobotrya japonica	FooDB	FooDB
Eruca vesicaria subsp. Sativa	FooDB	FooDB
Escherichia coli	Bacteria	KNApSAcK
Eugenia javanica	FooDB	FooDB
Eugenia uniflora	FooDB	FooDB
Eutrema japonicum	FooDB	FooDB
Fagopyrum esculentum	FooDB	FooDB
Fagopyrum tataricum	FooDB	FooDB
Fagus	FooDB	FooDB
Feijoa sellowiana	FooDB	FooDB
Ficus carica	FooDB	FooDB
Flammulina velutipes	FooDB	FooDB
Foeniculum vulgare	FooDB	FooDB
Fragaria x ananassa	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Garcinia mangostana	FooDB	FooDB
Gaylussacia baccata	FooDB	FooDB
Ginkgo biloba	FooDB	FooDB
Glycine max	FooDB	FooDB
Gossypium	FooDB	FooDB
Grifola frondosa	FooDB	FooDB
Hedysarum alpinum	FooDB	FooDB
Helianthus annuus L.	FooDB	FooDB
Helianthus tuberosus	FooDB	FooDB
Hibiscus sabbariffa	FooDB	FooDB
Hippophae rhamnoides	FooDB	FooDB
Hordeum vulgare	FooDB	FooDB
Hyssopus officinalis L.	FooDB	FooDB
Illicium verum	FooDB	FooDB
Ipomoea aquatica	FooDB	FooDB
Ipomoea batatas	FooDB	FooDB
Juglans	FooDB	FooDB
Juglans ailanthifolia	FooDB	FooDB
Juglans cinerea	FooDB	FooDB
Juglans nigra L.	FooDB	FooDB
Juglans regia	FooDB	FooDB
Lablab purpureus	FooDB	FooDB
Lactuca sativa	FooDB	FooDB
Lagenaria siceraria	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Lathyrus sativus	FooDB	FooDB
Laurus nobilis L.	FooDB	FooDB
Lens culinaris	FooDB	FooDB
Lentinus edodes	FooDB	FooDB
Lepidium sativum	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Levisticum officinale	FooDB	FooDB
Linum usitatissimum	FooDB	FooDB
Litchi chinensis	FooDB	FooDB
Luffa aegyptiaca	FooDB	FooDB
Lupinus	FooDB	FooDB
Lupinus albus	FooDB	FooDB
Macadamia	FooDB	FooDB
Macadamia tetraphylla	FooDB	FooDB
Malpighia emarginata	FooDB	FooDB
Malus	FooDB	FooDB
Malus pumila	FooDB	FooDB
Mammea americana	FooDB	FooDB
Mangifera indica	FooDB	FooDB
Manihot esculenta	FooDB	FooDB
Manilkara zapota	FooDB	FooDB
Maranta arundinacea	FooDB	FooDB
Matricaria recutita	FooDB	FooDB
Matteuccia struthiopteris	FooDB	FooDB
Medicago sativa	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Melissa officinalis L.	FooDB	FooDB
Mentha	FooDB	FooDB
Mentha aquatica	FooDB	FooDB
Mentha arvensis	FooDB	FooDB
Mentha spicata	FooDB	FooDB
Mentha x piperita	FooDB	FooDB
Mespilus germanica	FooDB	FooDB
Metroxylon sagu	FooDB	FooDB
Momordica charantia	FooDB	FooDB
Morchellaceae	FooDB	FooDB
Morella rubra	FooDB	FooDB
Moringa oleifera	FooDB	FooDB
Morus	FooDB	FooDB
Morus nigra	FooDB	FooDB
Mus musculus	LOTUS Database	35616633
Musa acuminata	FooDB	FooDB
Musa x paradisiaca	FooDB	FooDB
Myrica	FooDB	FooDB
Myristica fragrans	FooDB	FooDB
Nelumbo	FooDB	FooDB
Nelumbo nucifera	FooDB	FooDB
Nephelium lappaceum	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Nuphar lutea	FooDB	FooDB
Ocimum basilicum	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oenothera biennis	FooDB	FooDB
Olea europaea	FooDB	FooDB
Opuntia	FooDB	FooDB
Opuntia cochenillifera	FooDB	FooDB
Opuntia macrorhiza	FooDB	FooDB
Origanum majorana	FooDB	FooDB
Origanum onites	FooDB	FooDB
Origanum vulgare	FooDB	FooDB
Origanum X majoricum	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Oryza rufipogon	FooDB	FooDB
Oryza sativa	FooDB	FooDB
Ovis aries	FooDB	FooDB
Pachyrhizus erosus	FooDB	FooDB
Panax ginseng	FooDB	FooDB
Pangium edule	FooDB	FooDB
Panicum miliaceum	FooDB	FooDB
Passiflora edulis	FooDB	FooDB
Pastinaca sativa	FooDB	FooDB
Pediomelum esculentum	FooDB	FooDB
Perideridia oregana	FooDB	FooDB
Persea americana	FooDB	FooDB
Petasites japonicus	FooDB	FooDB
Petroselinum crispum	FooDB	FooDB
Phaseolus coccineus	FooDB	FooDB
Phaseolus lunatus	FooDB	FooDB
Phaseolus vulgaris	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Phoenix dactylifera	FooDB	FooDB
Photinia melanocarpa	FooDB	FooDB
Phyllostachys edulis	FooDB	FooDB
Physalis	FooDB	FooDB
Physalis philadelphica var. immaculata	FooDB	FooDB
Phytolacca americana	FooDB	FooDB
Pimenta dioica	FooDB	FooDB
Pimpinella anisum	FooDB	FooDB
Pinus	FooDB	FooDB
Pinus edulis	FooDB	FooDB
Piper nigrum L.	FooDB	FooDB
Pistacia vera	FooDB	FooDB
Pisum sativum	FooDB	FooDB
Pleurotus ostreatus	FooDB	FooDB
Polygonum alpinum	FooDB	FooDB
Portulaca oleracea	FooDB	FooDB
Pouteria sapota	FooDB	FooDB
Prunus armeniaca	FooDB	FooDB
Prunus avium	FooDB	FooDB
Prunus avium L.	FooDB	FooDB
Prunus cerasus	FooDB	FooDB
Prunus domestica	FooDB	FooDB
Prunus dulcis	FooDB	FooDB
Prunus persica	FooDB	FooDB
Prunus persica var. nucipersica	FooDB	FooDB
Prunus persica var. persica	FooDB	FooDB
Prunus tomentosa	FooDB	FooDB
Prunus virginiana	FooDB	FooDB
Psidium cattleianum	FooDB	FooDB
Psidium guajava	FooDB	FooDB
Psophocarpus tetragonolobus	FooDB	FooDB
Punica granatum	FooDB	FooDB
Pyrus communis	FooDB	FooDB
Pyrus pyrifolia	FooDB	FooDB
Quercus	FooDB	FooDB
Raphanus sativus	FooDB	FooDB
Raphanus sativus var. longipinnatus	FooDB	FooDB
Raphanus sativus var. sativus	FooDB	FooDB
Rheum rhabarbarum	FooDB	FooDB
Ribes aureum	FooDB	FooDB
Ribes glandulosum	FooDB	FooDB
Ribes nigrum	FooDB	FooDB
Ribes rubrum	FooDB	FooDB
Ribes uva-crispa	FooDB	FooDB
Rosa	FooDB	FooDB
Rubus arcticus	FooDB	FooDB
Rubus chamaemorus	FooDB	FooDB
Rubus idaeus	FooDB	FooDB
Rubus occidentalis	FooDB	FooDB
Rubus spectabilis	FooDB	FooDB
Rumex	FooDB	FooDB
Rumex acetosa	FooDB	FooDB
Rumex articus	FooDB	FooDB
Sagittaria latifolia	FooDB	FooDB
Salix pulchra	FooDB	FooDB
Salvia elegans	FooDB	FooDB
Salvia hispanica	FooDB	FooDB
Salvia officinalis	FooDB	FooDB
Salvia rosmarinus	FooDB	FooDB
Sambucus nigra	FooDB	FooDB
Sambucus nigra L.	FooDB	FooDB
Satureja hortensis L.	FooDB	FooDB
Satureja montana	FooDB	FooDB
Scorzonera hispanica	FooDB	FooDB
Secale cereale	FooDB	FooDB
Sechium edule	FooDB	FooDB
Sesamum indicum	FooDB	FooDB
Sesbania bispinosa	FooDB	FooDB
Sinapis alba	FooDB	FooDB
Sisymbrium	FooDB	FooDB
Solanum lycopersicum	FooDB	FooDB
Solanum lycopersicum var. cerasiforme	FooDB	FooDB
Solanum lycopersicum var. lycopersicum	FooDB	FooDB
Solanum melongena	FooDB	FooDB
Solanum quitoense	FooDB	FooDB
Solanum tuberosum	FooDB	FooDB
Sorbus aucuparia	FooDB	FooDB
Sorghum bicolor	FooDB	FooDB
Spinacia oleracea	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB
Syzygium aromaticum	FooDB	FooDB
Syzygium cumini	FooDB	FooDB
Syzygium jambos	FooDB	FooDB
Tamarindus indica	FooDB	FooDB
Taraxacum officinale	FooDB	FooDB
Tetragonia tetragonioides	FooDB	FooDB
Thalassiosira pseudonana	LOTUS Database	35616633
Thelesperma	FooDB	FooDB
Thymus pulegioides	FooDB	FooDB
Thymus vulgaris	FooDB	FooDB
Tilia cordata	FooDB	FooDB
Tilia L.	FooDB	FooDB
Tragopogon porrifolius	FooDB	FooDB
Trigonella foenum-graecum	FooDB	FooDB
Triticum	FooDB	FooDB
Triticum aestivum	FooDB	FooDB
Triticum durum	FooDB	FooDB
Triticum spelta	FooDB	FooDB
Triticum turanicum	FooDB	FooDB
Typha angustifolia	FooDB	FooDB
Vaccinium	FooDB	FooDB
Vaccinium angustifolium	FooDB	FooDB
Vaccinium angustifolium X Vaccinium corymbosum	FooDB	FooDB
Vaccinium arboreum	FooDB	FooDB
Vaccinium corymbosum	FooDB	FooDB
Vaccinium deliciosum	FooDB	FooDB
Vaccinium elliottii	FooDB	FooDB
Vaccinium macrocarpon	FooDB	FooDB
Vaccinium myrtilloides	FooDB	FooDB
Vaccinium myrtillus	FooDB	FooDB
Vaccinium ovalifolium	FooDB	FooDB
Vaccinium ovatum	FooDB	FooDB
Vaccinium oxycoccos	FooDB	FooDB
Vaccinium parvifolium	FooDB	FooDB
Vaccinium reticulatum	FooDB	FooDB
Vaccinium stamineum	FooDB	FooDB
Vaccinium uliginosum	FooDB	FooDB
Vaccinium vitis-idaea	FooDB	FooDB
Valerianella locusta	FooDB	FooDB
Vanilla	FooDB	FooDB
Verbena officinalis	FooDB	FooDB
Viburnum edule	FooDB	FooDB
Vicia faba	FooDB	FooDB
Vigna aconitifolia	FooDB	FooDB
Vigna angularis	FooDB	FooDB
Vigna mungo	FooDB	FooDB
Vigna radiata	FooDB	FooDB
Vigna umbellata	FooDB	FooDB
Vigna unguiculata	FooDB	FooDB
Vigna unguiculata ssp. cylindrica	FooDB	FooDB
Vigna unguiculata ssp. unguiculata	FooDB	FooDB
Vigna unguiculata var. sesquipedalis	FooDB	FooDB
Vitis	FooDB	FooDB
Vitis aestivalis	FooDB	FooDB
Vitis labrusca	FooDB	FooDB
Vitis rotundifolia	FooDB	FooDB
Vitis vinifera L.	FooDB	FooDB
Xanthosoma sagittifolium	FooDB	FooDB
Zea mays L.	FooDB	FooDB
Zingiber officinale	FooDB	FooDB
Zizania	FooDB	FooDB
Zizania aquatica	FooDB	FooDB
Ziziphus zizyphus	FooDB	FooDB

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavin nucleotides. These are nucleotides containing a flavin moiety. Flavin is a compound that contains the tricyclic isoalloxazine ring system, which bears 2 oxo groups at the 2- and 4-positions.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Flavin nucleotides

Sub Class

Not Available

Direct Parent

Flavin nucleotides

Alternative Parents

Substituents

Flavin nucleotide
Flavin
Isoalloxazine
Diazanaphthalene
Pteridine
Quinoxaline
Monoalkyl phosphate
Pyrimidone
Pyrazine
Organic phosphoric acid derivative
Phosphoric acid ester
Benzenoid
Alkyl phosphate
Pyrimidine
Heteroaromatic compound
Vinylogous amide
Secondary alcohol
Lactam
Azacycle
Polyol
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

flavin mononucleotide (CHEBI:17621 )

Physical Properties

State

Solid

Experimental Properties

Property	Value	Reference
Melting Point	290 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	92 mg/mL	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.67 g/L	ALOGPS
logP	-0.78	ALOGPS
logP	-1	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	1.49	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	201.58 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.14 m³·mol⁻¹	ChemAxon
Polarizability	42.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0001520

DrugBank ID

DB03247

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

Flavin_mononucleotide

METLIN ID

6295

PubChem Compound

643976

PDB ID

Not Available

ChEBI ID

17621

Good Scents ID

rw1610921

References

General References

Mathew JL, Kabi BC, Rath B: Anti-oxidant vitamins and steroid responsive nephrotic syndrome in Indian children. J Paediatr Child Health. 2002 Oct;38(5):450-37. [PubMed:12354259 ]
Booth CK, Clark T, Fenn A: Folic acid, riboflavin, thiamine, and vitamin B-6 status of a group of first-time blood donors. Am J Clin Nutr. 1998 Nov;68(5):1075-80. [PubMed:9808225 ]
Mikalunas V, Fitzgerald K, Rubin H, McCarthy R, Craig RM: Abnormal vitamin levels in patients receiving home total parenteral nutrition. J Clin Gastroenterol. 2001 Nov-Dec;33(5):393-6. [PubMed:11606856 ]
Baeckert PA, Greene HL, Fritz I, Oelberg DG, Adcock EW: Vitamin concentrations in very low birth weight infants given vitamins intravenously in a lipid emulsion: measurement of vitamins A, D, and E and riboflavin. J Pediatr. 1988 Dec;113(6):1057-65. [PubMed:3142982 ]
Bamji MS, Bhaskaram P, Jacob CM: Urinary riboflavin excretion and erythrocyte glutathione reductase activity in preschool children suffering from upper respiratory infections and measles. Ann Nutr Metab. 1987;31(3):191-6. [PubMed:3592624 ]
Ajayi OA: Bioavailability of riboflavin from fortified palm juice. Plant Foods Hum Nutr. 1989 Dec;39(4):375-80. [PubMed:2631092 ]
Brun TA, Chen J, Campbell TC, Boreham J, Feng Z, Parpia B, Shen TF, Li M: Urinary riboflavin excretion after a load test in rural China as a measure of possible riboflavin deficiency. Eur J Clin Nutr. 1990 Mar;44(3):195-206. [PubMed:2369885 ]
Rao PN, Levine E, Myers MO, Prakash V, Watson J, Stolier A, Kopicko JJ, Kissinger P, Raj SG, Raj MH: Elevation of serum riboflavin carrier protein in breast cancer. Cancer Epidemiol Biomarkers Prev. 1999 Nov;8(11):985-90. [PubMed:10566553 ]
Zhou X, Huang C, Hong J, Yao S: [Nested case-control study on riboflavin levels in blood and urine and the risk of lung cancer]. Wei Sheng Yan Jiu. 2003 Nov;32(6):597-8, 601. [PubMed:14963913 ]
Thurnham DI, Zheng SF, Munoz N, Crespi M, Grassi A, Hambidge KM, Chai TF: Comparison of riboflavin, vitamin A, and zinc status of Chinese populations at high and low risk for esophageal cancer. Nutr Cancer. 1985;7(3):131-43. [PubMed:3878498 ]
Bates CJ, Prentice AM, Paul AA, Prentice A, Sutcliffe BA, Whitehead RG: Riboflavin status in infants born in rural Gambia, and the effect of a weaning food supplement. Trans R Soc Trop Med Hyg. 1982;76(2):253-8. [PubMed:7101408 ]
Edelbroek PM, Linssen AC, Zitman FG, Rooymans HG, de Wolff FA: Analgesic and antidepressive effects of low-dose amitriptyline in relation to its metabolism in patients with chronic pain. Clin Pharmacol Ther. 1986 Feb;39(2):156-62. [PubMed:3510800 ]
Ahmed F, Khan MR, Akhtaruzzaman M, Karim R, Marks GC, Banu CP, Nahar B, Williams G: Efficacy of twice-weekly multiple micronutrient supplementation for improving the hemoglobin and micronutrient status of anemic adolescent schoolgirls in Bangladesh. Am J Clin Nutr. 2005 Oct;82(4):829-35. [PubMed:16210713 ]
Buzina R, Grgic Z, Jusic M, Sapunar J, Milanovic N, Brubacher G: Nutritional status and physical working capacity. Hum Nutr Clin Nutr. 1982;36(6):429-38. [PubMed:7161138 ]
Ortega RM, Quintas ME, Martinez RM, Andres P, Lopez-Sobaler AM, Requejo AM: Riboflavin levels in maternal milk: the influence of vitamin B2 status during the third trimester of pregnancy. J Am Coll Nutr. 1999 Aug;18(4):324-9. [PubMed:12038475 ]
Lartey A, Manu A, Brown KH, Dewey KG: Predictors of micronutrient status among six- to twelve-month-old breast-fed Ghanaian infants. J Nutr. 2000 Feb;130(2):199-207. [PubMed:10720170 ]
Blajchman MA, Goldman M, Baeza F: Improving the bacteriological safety of platelet transfusions. Transfus Med Rev. 2004 Jan;18(1):11-24. [PubMed:14689374 ]
Cikot RJ, Steegers-Theunissen RP, Thomas CM, de Boo TM, Merkus HM, Steegers EA: Longitudinal vitamin and homocysteine levels in normal pregnancy. Br J Nutr. 2001 Jan;85(1):49-58. [PubMed:11227033 ]
Hardwick CC, Herivel TR, Hernandez SC, Ruane PH, Goodrich RP: Separation, identification and quantification of riboflavin and its photoproducts in blood products using high-performance liquid chromatography with fluorescence detection: a method to support pathogen reduction technology. Photochem Photobiol. 2004 Nov-Dec;80(3):609-15. [PubMed:15382964 ]
Schorah CJ, Wild J, Hartley R, Sheppard S, Smithells RW: The effect of periconceptional supplementation on blood vitamin concentrations in women at recurrence risk for neural tube defect. Br J Nutr. 1983 Mar;49(2):203-11. [PubMed:6830748 ]

Showing NP-Card for Flavin Mononucleotide (NP0000348)

MOL for NP0000348 (Flavin Mononucleotide)

3D MOL for NP0000348 (Flavin Mononucleotide)

3D SDF for NP0000348 (Flavin Mononucleotide)

3D-SDF for NP0000348 (Flavin Mononucleotide)

PDB for NP0000348 (Flavin Mononucleotide)

3D PDB for NP0000348 (Flavin Mononucleotide)

SMILES for NP0000348 (Flavin Mononucleotide)

INCHI for NP0000348 (Flavin Mononucleotide)

Structure for NP0000348 (Flavin Mononucleotide)

3D Structure for NP0000348 (Flavin Mononucleotide)