NP-MRD: Showing NP-Card for (2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one (NP0149649)

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Record Information

Version

2.0

Created at

2022-09-02 05:33:50 UTC

Updated at

2022-09-02 05:33:50 UTC

NP-MRD ID

NP0149649

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

Description

(2R,3R)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. (2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one is found in Uvaria dulcis. Based on a literature review very few articles have been published on (2R,3R)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    4.7451   -2.3466   -0.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3755   -2.5363   -0.4690 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683   -1.4481   -0.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1291   -0.1920   -0.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3295    0.9055    0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8088    2.1973    0.1500 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1525    2.5538   -0.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9790    0.7103    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4368   -0.5598    0.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2200   -1.6689    0.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6305   -2.9118   -0.0069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9096   -0.6823    0.5179 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8151    0.3343    0.8080 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1364   -0.0854    0.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5488   -1.3880    0.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7604   -1.7801   -0.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5584   -0.9048   -0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1114    0.3859   -0.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8891    0.8177   -0.4784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614    1.6589    0.2927 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0230    2.7226    0.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0807    1.8223    0.6090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5561    2.8726    1.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9323   -1.8185   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2558   -3.3511   -0.6923 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2052   -1.7762    0.1558 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1840   -0.0400   -0.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8001    1.7912    0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3882    3.5182    0.4670 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4201    2.6282   -1.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950   -3.7708   -0.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9275    0.3647    1.9269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9135   -2.0748    1.0216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1128   -2.8016    0.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5009   -1.2343   -1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7012    1.1147   -1.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5396    1.8136   -0.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5002    1.6755   -0.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9833    3.4840    0.2734 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
  6  7  1  0
  5  8  2  0
  8 22  1  0
 22 23  2  0
 22 20  1  0
 20 21  1  0
 20 13  1  0
 13 12  1  0
 12  9  1  0
  9 10  2  0
 10 11  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 10  3  1  0
 19 14  1  0
  9  8  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
 20 38  1  6
 21 39  1  0
 13 32  1  1
 11 31  1  0
 15 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  0
 19 37  1  0
M  END


  Mrv1652309022207332D          

 23 25  0  0  1  0            999 V2000
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -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
    0.7145   -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
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -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  1  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
  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
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0149649

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(=O)[C@H](O)[C@H](OC2=C1O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c1-21-10-8-11(22-2)13(18)17-12(10)14(19)15(20)16(23-17)9-6-4-3-5-7-9/h3-8,15-16,18,20H,1-2H3/t15-,16+/m0/s1

> <INCHI_KEY>
JJZWXZHIIUVDTN-JKSUJKDBSA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.309

> <EXACT_MASS>
316.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.412137086049576

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
1.7617377016666667

> <ALOGPS_LOGS>
-2.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.163459945561383

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.255579902282536

> <JCHEM_PKA_STRONGEST_BASIC>
-4.050550469047683

> <JCHEM_POLAR_SURFACE_AREA>
85.22

> <JCHEM_REFRACTIVITY>
81.5926

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.17e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   22                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    3   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   20                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   13   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    8   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

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(=O)[C@H](O)[C@H](OC2=C1O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C17H16O6/c1-21-10-8-11(22-2)13(18)17-12(10)14(19)15(20)16(23-17)9-6-4-3-5-7-9/h3-8,15-16,18,20H,1-2H3/t15-,16+/m0/s1

InChI Key

JJZWXZHIIUVDTN-JKSUJKDBSA-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

Species Name	Source	Reference
Uvaria dulcis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
3-hydroxyflavonoid
8-hydroxyflavonoid
Hydroxyflavonoid
Flavanonol
Flavanone
Flavan
Chromone
1-benzopyran
Chromane
Benzopyran
Aryl alkyl ketone
Aryl ketone
Anisole
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
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	2.22	ALOGPS
logS	-2.8	ALOGPS

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

163029868

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one (NP0149649)

MOL for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D MOL for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D SDF for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D-SDF for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

PDB for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D PDB for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

SMILES for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

INCHI for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

Structure for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)

3D Structure for NP0149649 ((2r,3r)-3,8-dihydroxy-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one)