NP-MRD: Showing NP-Card for Vittacarboline (NP0025773)

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Record Information

Version

1.0

Created at

2021-06-19 17:48:25 UTC

Updated at

2021-06-29 23:50:55 UTC

NP-MRD ID

NP0025773

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Vittacarboline

Provided By

JEOL Database JEOL Logo

Description

Vittacarboline is found in Hippeastrum vittatum. It was first documented in 2001 (Youssef, D. T. A.). Based on a literature review very few articles have been published on 9-[(5-methylfuran-2-yl)methyl]-9H-pyrido[3,4-b]indole.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119483D          

 34 37  0  0  0  0            999 V2000
   -3.1974   -0.3269   -3.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    0.3014   -2.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    1.6085   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942    1.5583   -1.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4340    0.2215   -1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -0.5098   -0.8055 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5280   -0.0845    0.5903 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.8038    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880    1.5341    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    2.3660    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8837    2.4705    2.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    1.7434    3.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0597    0.8969    2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689    0.0464    2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8510   -0.2677    3.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.1552    3.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073   -1.7234    2.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -1.4232    1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872   -0.5464    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -0.5471   -2.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.9605   -4.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8509   -0.9468   -3.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    0.4300   -4.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    2.4894   -3.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1594    2.3937   -1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.3427   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -1.5917   -0.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7598    1.4687   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511    2.9396    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4606    3.1224    3.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.8331    4.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6541    0.1597    4.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -1.4415    4.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530   -1.8906    0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
  2 20  1  0  0  0  0
 15 16  1  0  0  0  0
 20  5  1  0  0  0  0
 16 17  2  0  0  0  0
  5  4  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19  7  1  0  0  0  0
  7  8  1  0  0  0  0
 13  8  1  0  0  0  0
 13 14  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4  3  1  0  0  0  0
 10 11  2  0  0  0  0
 19 14  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3  2  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  4 25  1  0  0  0  0
  3 24  1  0  0  0  0
 15 32  1  0  0  0  0
 16 33  1  0  0  0  0
 18 34  1  0  0  0  0
  9 28  1  0  0  0  0
 10 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
  6 26  1  0  0  0  0
  6 27  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
M  END

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
   -3.1974   -0.3269   -3.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    0.3014   -2.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    1.6085   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942    1.5583   -1.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4340    0.2215   -1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -0.5098   -0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -0.0845    0.5903 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.8038    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880    1.5341    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    2.3660    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8837    2.4705    2.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    1.7434    3.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0597    0.8969    2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689    0.0464    2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8510   -0.2677    3.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.1552    3.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073   -1.7234    2.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -1.4232    1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872   -0.5464    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -0.5471   -2.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.9605   -4.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8509   -0.9468   -3.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    0.4300   -4.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    2.4894   -3.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1594    2.3937   -1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.3427   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -1.5917   -0.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7598    1.4687   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511    2.9396    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4606    3.1224    3.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.8331    4.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6541    0.1597    4.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -1.4415    4.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530   -1.8906    0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
  2 20  1  0
 15 16  1  0
 20  5  1  0
 16 17  2  0
  5  4  2  0
 17 18  1  0
 18 19  2  0
 19  7  1  0
  7  8  1  0
 13  8  1  0
 13 14  1  0
  8  9  2  0
  9 10  1  0
  4  3  1  0
 10 11  2  0
 19 14  1  0
 11 12  1  0
 12 13  2  0
  3  2  2  0
  7  6  1  0
  6  5  1  0
 14 15  2  0
  2  1  1  0
  4 25  1  0
  3 24  1  0
 15 32  1  0
 16 33  1  0
 18 34  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
  6 26  1  0
  6 27  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
M  END


  Mrv1652306192119483D          

 34 37  0  0  0  0            999 V2000
   -3.1974   -0.3269   -3.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    0.3014   -2.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    1.6085   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942    1.5583   -1.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4340    0.2215   -1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -0.5098   -0.8055 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5280   -0.0845    0.5903 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.8038    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880    1.5341    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    2.3660    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8837    2.4705    2.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    1.7434    3.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0597    0.8969    2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689    0.0464    2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8510   -0.2677    3.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.1552    3.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073   -1.7234    2.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -1.4232    1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872   -0.5464    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -0.5471   -2.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.9605   -4.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8509   -0.9468   -3.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    0.4300   -4.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    2.4894   -3.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1594    2.3937   -1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.3427   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -1.5917   -0.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7598    1.4687   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511    2.9396    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4606    3.1224    3.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.8331    4.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6541    0.1597    4.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -1.4415    4.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530   -1.8906    0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
  2 20  1  0  0  0  0
 15 16  1  0  0  0  0
 20  5  1  0  0  0  0
 16 17  2  0  0  0  0
  5  4  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19  7  1  0  0  0  0
  7  8  1  0  0  0  0
 13  8  1  0  0  0  0
 13 14  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4  3  1  0  0  0  0
 10 11  2  0  0  0  0
 19 14  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3  2  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
 14 15  2  0  0  0  0
  2  1  1  0  0  0  0
  4 25  1  0  0  0  0
  3 24  1  0  0  0  0
 15 32  1  0  0  0  0
 16 33  1  0  0  0  0
 18 34  1  0  0  0  0
  9 28  1  0  0  0  0
 10 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
  6 26  1  0  0  0  0
  6 27  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025773

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C(OC(=C1[H])C([H])([H])N1C2=C([H])N=C([H])C([H])=C2C2=C([H])C([H])=C([H])C([H])=C12)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H14N2O/c1-12-6-7-13(20-12)11-19-16-5-3-2-4-14(16)15-8-9-18-10-17(15)19/h2-10H,11H2,1H3

> <INCHI_KEY>
UANUGMASRPSVFK-UHFFFAOYSA-N

> <FORMULA>
C17H14N2O

> <MOLECULAR_WEIGHT>
262.312

> <EXACT_MASS>
262.110613079

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
29.191636747060958

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-[(5-methylfuran-2-yl)methyl]-9H-pyrido[3,4-b]indole

> <ALOGPS_LOGP>
3.66

> <JCHEM_LOGP>
3.081170412333333

> <ALOGPS_LOGS>
-3.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
5.209126623700691

> <JCHEM_POLAR_SURFACE_AREA>
30.96

> <JCHEM_REFRACTIVITY>
78.36520000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.98e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-[(5-methylfuran-2-yl)methyl]pyrido[3,4-b]indole

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
   -3.1974   -0.3269   -3.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    0.3014   -2.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    1.6085   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942    1.5583   -1.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4340    0.2215   -1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -0.5098   -0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -0.0845    0.5903 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.8038    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880    1.5341    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    2.3660    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8837    2.4705    2.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    1.7434    3.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0597    0.8969    2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689    0.0464    2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8510   -0.2677    3.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.1552    3.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073   -1.7234    2.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -1.4232    1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872   -0.5464    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -0.5471   -2.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.9605   -4.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8509   -0.9468   -3.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    0.4300   -4.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    2.4894   -3.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1594    2.3937   -1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.3427   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -1.5917   -0.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7598    1.4687   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511    2.9396    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4606    3.1224    3.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.8331    4.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6541    0.1597    4.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -1.4415    4.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530   -1.8906    0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
  2 20  1  0
 15 16  1  0
 20  5  1  0
 16 17  2  0
  5  4  2  0
 17 18  1  0
 18 19  2  0
 19  7  1  0
  7  8  1  0
 13  8  1  0
 13 14  1  0
  8  9  2  0
  9 10  1  0
  4  3  1  0
 10 11  2  0
 19 14  1  0
 11 12  1  0
 12 13  2  0
  3  2  2  0
  7  6  1  0
  6  5  1  0
 14 15  2  0
  2  1  1  0
  4 25  1  0
  3 24  1  0
 15 32  1  0
 16 33  1  0
 18 34  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
  6 26  1  0
  6 27  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.197  -0.327  -3.809  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.146   0.301  -2.985  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.801   1.609  -2.721  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.694   1.558  -1.840  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.434   0.222  -1.616  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.570  -0.510  -0.806  0.00  0.00           C+0
HETATM    7  N   UNK     0       0.528  -0.085   0.590  0.00  0.00           N+0
HETATM    8  C   UNK     0       1.412   0.804   1.176  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.488   1.534   0.641  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.215   2.366   1.498  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.884   2.470   2.844  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.811   1.743   3.369  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.060   0.897   2.525  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.069   0.046   2.739  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.851  -0.268   3.861  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.896  -1.155   3.663  0.00  0.00           C+0
HETATM   17  N   UNK     0      -2.207  -1.723   2.480  0.00  0.00           N+0
HETATM   18  C   UNK     0      -1.463  -1.423   1.392  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.387  -0.546   1.518  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.314  -0.547  -2.320  0.00  0.00           O+0
HETATM   21  H   UNK     0      -2.751  -0.961  -4.581  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.851  -0.947  -3.188  0.00  0.00           H+0
HETATM   23  H   UNK     0      -3.814   0.430  -4.303  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.292   2.489  -3.111  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.159   2.394  -1.409  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.578  -0.343  -1.196  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.396  -1.592  -0.824  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.760   1.469  -0.408  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.051   2.940   1.105  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.461   3.122   3.496  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.558   1.833   4.421  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.654   0.160   4.836  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.540  -1.442   4.491  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.753  -1.891   0.458  0.00  0.00           H+0
CONECT    1    2   21   22   23                                             
CONECT    2   20    3    1                                                  
CONECT    3    4    2   24                                                  
CONECT    4    5    3   25                                                  
CONECT    5   20    4    6                                                  
CONECT    6    7    5   26   27                                             
CONECT    7   19    8    6                                                  
CONECT    8    7   13    9                                                  
CONECT    9    8   10   28                                                  
CONECT   10    9   11   29                                                  
CONECT   11   10   12   30                                                  
CONECT   12   11   13   31                                                  
CONECT   13    8   14   12                                                  
CONECT   14   13   19   15                                                  
CONECT   15   16   14   32                                                  
CONECT   16   15   17   33                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   34                                                  
CONECT   19   18    7   14                                                  
CONECT   20    2    5                                                       
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    3                                                            
CONECT   25    4                                                            
CONECT   26    6                                                            
CONECT   27    6                                                            
CONECT   28    9                                                            
CONECT   29   10                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   15                                                            
CONECT   33   16                                                            
CONECT   34   18                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

RDKit          3D

34 37  0  0  0  0  0  0  0  0999 V2000
   -3.1974   -0.3269   -3.8089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461    0.3014   -2.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8008    1.6085   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6942    1.5583   -1.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4340    0.2215   -1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -0.5098   -0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5280   -0.0845    0.5903 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.8038    1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4880    1.5341    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2147    2.3660    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8837    2.4705    2.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8109    1.7434    3.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0597    0.8969    2.5251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689    0.0464    2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8510   -0.2677    3.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -1.1552    3.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073   -1.7234    2.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -1.4232    1.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872   -0.5464    1.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3144   -0.5471   -2.3202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.9605   -4.5813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8509   -0.9468   -3.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8142    0.4300   -4.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    2.4894   -3.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1594    2.3937   -1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5776   -0.3427   -1.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3961   -1.5917   -0.8236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7598    1.4687   -0.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511    2.9396    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4606    3.1224    3.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5576    1.8331    4.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6541    0.1597    4.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5400   -1.4415    4.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7530   -1.8906    0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
  2 20  1  0
 15 16  1  0
 20  5  1  0
 16 17  2  0
  5  4  2  0
 17 18  1  0
 18 19  2  0
 19  7  1  0
  7  8  1  0
 13  8  1  0
 13 14  1  0
  8  9  2  0
  9 10  1  0
  4  3  1  0
 10 11  2  0
 19 14  1  0
 11 12  1  0
 12 13  2  0
  3  2  2  0
  7  6  1  0
  6  5  1  0
 14 15  2  0
  2  1  1  0
  4 25  1  0
  3 24  1  0
 15 32  1  0
 16 33  1  0
 18 34  1  0
  9 28  1  0
 10 29  1  0
 11 30  1  0
 12 31  1  0
  6 26  1  0
  6 27  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄N₂O

Average Mass

262.3120 Da

Monoisotopic Mass

262.11061 Da

IUPAC Name

9-[(5-methylfuran-2-yl)methyl]-9H-pyrido[3,4-b]indole

Traditional Name

9-[(5-methylfuran-2-yl)methyl]pyrido[3,4-b]indole

CAS Registry Number

Not Available

SMILES

[H]C1=C(OC(=C1[H])C([H])([H])N1C2=C([H])N=C([H])C([H])=C2C2=C([H])C([H])=C([H])C([H])=C12)C([H])([H])[H]

InChI Identifier

InChI=1S/C17H14N2O/c1-12-6-7-13(20-12)11-19-16-5-3-2-4-14(16)15-8-9-18-10-17(15)19/h2-10H,11H2,1H3

InChI Key

UANUGMASRPSVFK-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Hippeastrum vittatum	JEOL database	Youssef, D. T. A. J. Nat. Prod. 64, 839 (2001)
Hippeastrum vittatum Herbert	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as beta carbolines. These are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
N-alkylindole
Indole
Pyridine
Substituted pyrrole
Benzenoid
Furan
Pyrrole
Heteroaromatic compound
Oxacycle
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.66	ALOGPS
logP	3.08	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Basic)	5.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	30.96 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	78.37 m³·mol⁻¹	ChemAxon
Polarizability	29.19 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00027030

Chemspider ID

9982148

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11807483

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Youssef, D. T. A. (2001). Youssef, D. T. A. J. Nat. Prod. 64, 839 (2001). J. Nat. Prod..

Showing NP-Card for Vittacarboline (NP0025773)

MOL for NP0025773 (Vittacarboline)

3D MOL for NP0025773 (Vittacarboline)

3D SDF for NP0025773 (Vittacarboline)

3D-SDF for NP0025773 (Vittacarboline)

PDB for NP0025773 (Vittacarboline)

3D PDB for NP0025773 (Vittacarboline)

SMILES for NP0025773 (Vittacarboline)

INCHI for NP0025773 (Vittacarboline)

Structure for NP0025773 (Vittacarboline)

3D Structure for NP0025773 (Vittacarboline)