NP-MRD: Showing NP-Card for mucroquinone (NP0330509)

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Record Information

Version

1.0

Created at

2022-09-12 15:56:02 UTC

Updated at

2022-09-12 15:56:02 UTC

NP-MRD ID

NP0330509

Secondary Accession Numbers

None

Natural Product Identification

Common Name

mucroquinone

Description

Mucroquinone belongs to the class of organic compounds known as isoflavanquinones. These are isoflavans where the phenyl group carries two C=O groups at position 1 and 4, respectively. Thus, mucroquinone is considered to be a flavonoid. Based on a literature review very few articles have been published on Mucroquinone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    6.4989    0.8944   -0.4366 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9165   -0.3458   -0.0923 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5347   -0.4997   -0.0381 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7479    0.5480    0.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2761    0.4255    0.2005 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6161    1.4827    0.3704 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6718   -0.8928    0.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1925   -1.0124    0.1277 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4108   -0.2637   -1.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8188   -0.4309   -1.0195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4514   -0.2181    0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7860   -0.2493    1.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437   -0.0329    2.5980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8106    0.2201    2.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5062    0.2574    1.3783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8817    0.5128    1.3605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8097    0.0351    0.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5458    0.0816   -0.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6911    1.3001   -1.6541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3245   -0.5185    1.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4521   -1.9685   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9015   -1.8178   -0.1722 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6042   -2.8290   -0.3386 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2148    1.7117    0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5976    0.8088   -0.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1775    1.2420   -1.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845    1.5173    0.2377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1286   -2.0733    0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -0.6687   -1.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2185    0.8159   -0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9231   -0.0572    3.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3477    0.3926    3.4980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3506    0.5310    0.4679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9250    2.1549   -0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5052    1.2439   -2.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7736    1.5887   -2.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1671    0.3816    1.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1145   -1.3257    2.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9916   -2.9420   -0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7 21  2  0
 21 22  1  0
 22 23  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 20  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 22  3  1  0
 20  8  1  0
 17 11  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
 21 39  1  0
  8 28  1  6
  9 29  1  0
  9 30  1  0
 20 37  1  0
 20 38  1  0
 13 31  1  0
 14 32  1  0
 16 33  1  0
 19 34  1  0
 19 35  1  0
 19 36  1  0
M  END


  Mrv1652309122217562D          

 23 25  0  0  1  0            999 V2000
   -4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 20  1  0  0  0  0
  8 20  1  0  0  0  0
  7 21  2  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0330509

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=O)C(=CC1=O)[C@@H]1COC2=C(C1)C=CC(O)=C2OC

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c1-21-15-7-13(19)11(6-14(15)20)10-5-9-3-4-12(18)17(22-2)16(9)23-8-10/h3-4,6-7,10,18H,5,8H2,1-2H3/t10-/m0/s1

> <INCHI_KEY>
BCRMQBPKTAFKBY-JTQLQIEISA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.309

> <EXACT_MASS>
316.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.69305477088762

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(3R)-7-hydroxy-8-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]-5-methoxycyclohexa-2,5-diene-1,4-dione

> <JCHEM_LOGP>
1.8647387366666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.430138528861022

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.34314247836886

> <JCHEM_PKA_STRONGEST_BASIC>
-4.463094280542458

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
84.44779999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
mucroquinone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -6.668  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   21                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   12    8                                                       
CONECT   21    7   22                                                       
CONECT   22   21    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆O₆

Average Mass

316.3090 Da

Monoisotopic Mass

316.09469 Da

IUPAC Name

2-[(3R)-7-hydroxy-8-methoxy-3,4-dihydro-2H-1-benzopyran-3-yl]-5-methoxycyclohexa-2,5-diene-1,4-dione

Traditional Name

mucroquinone

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C(=CC1=O)[C@@H]1COC2=C(C1)C=CC(O)=C2OC

InChI Identifier

InChI=1S/C17H16O6/c1-21-15-7-13(19)11(6-14(15)20)10-5-9-3-4-12(18)17(22-2)16(9)23-8-10/h3-4,6-7,10,18H,5,8H2,1-2H3/t10-/m0/s1

InChI Key

BCRMQBPKTAFKBY-JTQLQIEISA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavanquinones. These are isoflavans where the phenyl group carries two C=O groups at position 1 and 4, respectively.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavanquinones

Direct Parent

Isoflavanquinones

Alternative Parents

Substituents

Isoflavanquinone
Isoflavanol
Isoflavan
Chromane
Benzopyran
1-benzopyran
Anisole
Quinone
P-benzoquinone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous ester
Cyclic ketone
Ketone
Oxacycle
Ether
Organoheterocyclic compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Isoflavans (LMPK12080053 )

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	1.86	ChemAxon
pKa (Strongest Acidic)	10.34	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	84.45 m³·mol⁻¹	ChemAxon
Polarizability	31.69 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

C00009743

Chemspider ID

24843087

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44257519

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for mucroquinone (NP0330509)

MOL for NP0330509 (mucroquinone)

3D MOL for NP0330509 (mucroquinone)

3D SDF for NP0330509 (mucroquinone)

3D-SDF for NP0330509 (mucroquinone)

PDB for NP0330509 (mucroquinone)

3D PDB for NP0330509 (mucroquinone)

SMILES for NP0330509 (mucroquinone)

INCHI for NP0330509 (mucroquinone)

Structure for NP0330509 (mucroquinone)

3D Structure for NP0330509 (mucroquinone)