NP-MRD: Showing NP-Card for (2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one (NP0236533)

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Record Information

Version

2.0

Created at

2022-09-06 19:27:20 UTC

Updated at

2022-09-06 19:27:20 UTC

NP-MRD ID

NP0236533

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one

Description

ZINC14692687 belongs to the class of organic compounds known as isoflavanols. These are polycyclic compounds containing a hydroxylated isoflavan skeleton. Based on a literature review very few articles have been published on ZINC14692687.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062221272D          

 25 29  0  0  1  0            999 V2000
    6.3865    2.6770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1427    1.8888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3383    1.7059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7776    2.3111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9732    2.1282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4125    2.7334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7294    1.3400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2900    0.7348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0462   -0.0534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.2363    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9980   -1.0245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6811    0.3689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2416   -0.3293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5434    0.1102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7190    0.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3341    0.8714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7736    1.5696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980    1.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9829    0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2454    2.2033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5206    1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4657    1.0736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9249    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3642    1.7623    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  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 13 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 13 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 39 43  0  0  0  0  0  0  0  0999 V2000
    6.6502    0.4440    0.5117 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7039   -0.5802    0.6480 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3529   -0.2966    0.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9553    0.9949    0.0880 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    1.2656   -0.1212 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2628    2.5566   -0.4627 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6489    0.2845    0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0403   -1.0007    0.3457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3783   -1.2485    0.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0891   -2.0258    0.4817 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2284   -1.6102    0.7966 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1106   -2.6678    0.8521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -0.5435   -0.1574 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1612   -0.9927   -1.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5119   -0.6028   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8800   -0.4929   -1.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8022    0.0171   -0.5364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3659    0.4298    0.7003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0372    0.3261    1.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1157   -0.1900    0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4963    0.8936    1.3766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4807    1.2024    0.4118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1930    0.2309   -0.6105 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2405    0.5525   -0.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1386    1.7171   -0.4498 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5365    0.9348   -0.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5299    1.2019    1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6866    0.0529    0.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7291    1.7440   -0.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9486    3.2789   -0.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6735   -2.2720    0.8220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1880   -1.1478    1.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1005   -3.1298    1.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0062   -2.0660   -1.7245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8287   -0.3542   -2.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1716   -0.8295   -2.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7138    0.6636    2.0202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2887    2.2277    0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5018    1.0319    0.7624 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  1  0
  5  7  2  0
  7 24  1  0
 24 25  2  0
 13 24  1  6
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 21  1  0
 21 22  1  0
 22 23  1  0
 18 19  1  0
 19 20  2  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
  9  3  1  0
  8  7  1  0
 20 13  1  0
 20 15  1  0
 23 17  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
 14 34  1  0
 14 35  1  0
 16 36  1  0
 22 38  1  0
 22 39  1  0
 19 37  1  0
 11 32  1  1
 12 33  1  0
  9 31  1  0
M  END


  Mrv1652309062221272D          

 25 29  0  0  1  0            999 V2000
    6.3865    2.6770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1427    1.8888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3383    1.7059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7776    2.3111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9732    2.1282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4125    2.7334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7294    1.3400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2900    0.7348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0945    0.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0462   -0.0534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -0.2363    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9980   -1.0245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6811    0.3689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2416   -0.3293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5434    0.1102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7190    0.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3341    0.8714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7736    1.5696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980    1.5381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9829    0.8084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2454    2.2033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5206    1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4657    1.0736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9249    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3642    1.7623    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  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 13 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 13 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0236533

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)[C@@]3(CC4=CC5=C(OCO5)C=C34)[C@@H](O)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O7/c1-22-9-3-11(19)15-14(4-9)25-17(21)18(16(15)20)6-8-2-12-13(5-10(8)18)24-7-23-12/h2-5,17,19,21H,6-7H2,1H3/t17-,18-/m0/s1

> <INCHI_KEY>
HQNATRVFSYNBMS-ROUUACIJSA-N

> <FORMULA>
C18H14O7

> <MOLECULAR_WEIGHT>
342.303

> <EXACT_MASS>
342.073952791

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.97224207857501

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R)-2,5-dihydroxy-7-methoxy-2,4-dihydro-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0^{3,6}]undecane]-1'(8'),2',6'-trien-4-one

> <JCHEM_LOGP>
2.5972681413333336

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.44388234365331

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.605307551399907

> <JCHEM_PKA_STRONGEST_BASIC>
-4.365035158713188

> <JCHEM_POLAR_SURFACE_AREA>
94.45000000000002

> <JCHEM_REFRACTIVITY>
84.1137

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R)-2,5-dihydroxy-7-methoxy-2H-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0^{3,6}]undecane]-1'(8'),2',6'-trien-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      11.922   4.997   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.466   3.526   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.965   3.184   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.918   4.314   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.417   3.973   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.370   5.102   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.961   2.501   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.008   1.372   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.510   1.713   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.553  -0.100   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.051  -0.441   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.596  -1.912   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.005   0.689   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.184  -0.615   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.881   0.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.342   0.264   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.624   1.627   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.444   2.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.983   2.871   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.701   1.509   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.458   4.113   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.972   3.541   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.869   2.004   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.460   2.160   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.413   3.290   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   24                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3                                                       
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   20   24                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15   13                                                  
CONECT   21   18   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17                                                       
CONECT   24   13    7   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄O₇

Average Mass

342.3030 Da

Monoisotopic Mass

342.07395 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)[C@@]3(CC4=CC5=C(OCO5)C=C34)[C@@H](O)OC2=C1

InChI Identifier

InChI=1S/C18H14O7/c1-22-9-3-11(19)15-14(4-9)25-17(21)18(16(15)20)6-8-2-12-13(5-10(8)18)24-7-23-12/h2-5,17,19,21H,6-7H2,1H3/t17-,18-/m0/s1

InChI Key

HQNATRVFSYNBMS-ROUUACIJSA-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 isoflavanols. These are polycyclic compounds containing a hydroxylated isoflavan skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavans

Direct Parent

Isoflavanols

Alternative Parents

Substituents

2-hydroxyisoflavanone
Isoflavanol
Isoflavanone
Chromone
Chromane
Benzopyran
1-benzopyran
Benzodioxole
Anisole
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Hemiacetal
Ketone
Ether
Organoheterocyclic compound
Oxacycle
Acetal
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

92468742

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one (NP0236533)

MOL for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

3D MOL for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

3D SDF for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

3D-SDF for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

PDB for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

3D PDB for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

SMILES for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

INCHI for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

Structure for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)

3D Structure for NP0236533 ((2s,3r)-2,5-dihydroxy-7-methoxy-2h-9',11'-dioxaspiro[1-benzopyran-3,4'-tricyclo[6.3.0.0³,⁶]undecane]-1'(8'),2',6'-trien-4-one)