NP-MRD: Showing NP-Card for (2R,3R)-3,5,7,3',5'-Pentahydroxyflavan (NP0056083)

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Record Information

Version

2.0

Created at

2022-04-28 01:58:05 UTC

Updated at

2022-04-28 01:58:05 UTC

NP-MRD ID

NP0056083

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2R,3R)-3,5,7,3',5'-Pentahydroxyflavan

Description

(2R,3r)-3,5,7,3',5'-pentahydroxyflavan belongs to the class of organic compounds known as flavan-3-ols. These are flavans that bear and hydroxyl group at position 3 (B ring), but not at position 4. Thus, (2R,3R)-3,5,7,3',5'-pentahydroxyflavan is considered to be a flavonoid. (2R,3R)-3,5,7,3',5'-Pentahydroxyflavan is found in Humboldtia laurifolia. (2R,3R)-3,5,7,3',5'-Pentahydroxyflavan was first documented in 2012 (PMID: 23252270). Based on a literature review very few articles have been published on (2r,3r)-3,5,7,3',5'-pentahydroxyflavan.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
    5.0993   -1.4253   -1.0056 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1486   -0.4633   -0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4914    0.8751   -0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5456    1.8215   -0.3866 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8642    3.1855   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2877    1.4280   -0.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9069    0.0850    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5353   -0.1899    0.4475 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3236    0.7082   -0.2539 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6871    0.4415   -0.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5382    1.3807   -0.7319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8964    1.1442   -0.6846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7453    2.0947   -1.2311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3799   -0.0115   -0.1057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5518   -0.9709    0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0298   -2.1358    1.0284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1843   -0.7128    0.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2662   -1.7112    0.9618 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0534   -1.5727    0.1850 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2869   -1.6962   -1.1620 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8576   -0.8422   -0.2929 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7244   -1.8424   -0.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4883    1.1781   -1.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7296    3.7264   -1.2620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754    2.2237    0.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4490    0.0155    1.5377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1329    2.2774   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0768    2.8320   -0.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4522   -0.2075   -0.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -2.2587    1.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0098   -1.3617    2.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6403   -2.7370    0.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7461   -2.3746    0.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1523   -1.0224   -1.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5816   -1.8814   -0.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7 21  2  0
 21  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  8 19  1  0
  6  7  1  0
 10 17  1  0
 20 34  1  0
 19 33  1  1
 18 31  1  0
 18 32  1  0
 16 30  1  0
 14 29  1  0
 13 28  1  0
 11 27  1  0
  8 26  1  1
 21 35  1  0
  1 22  1  0
  3 23  1  0
  5 24  1  0
  6 25  1  0
M  END


  Mrv1652304282203582D          

 21 23  0  0  1  0            999 V2000
   -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
    0.7145   -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
    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  1  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
    1.4289   -1.6500    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
    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
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   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
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  9 11  1  6  0  0  0
  8 12  1  6  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 16 18  1  0  0  0  0
 14 19  1  0  0  0  0
  3 20  1  0  0  0  0
  1 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0056083

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1CC2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O6/c16-8-1-7(2-9(17)3-8)15-13(20)6-11-12(19)4-10(18)5-14(11)21-15/h1-5,13,15-20H,6H2/t13-,15-/m1/s1

> <INCHI_KEY>
MKXNQWPXEHIMRX-UKRRQHHQSA-N

> <FORMULA>
C15H14O6

> <MOLECULAR_WEIGHT>
290.271

> <EXACT_MASS>
290.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
28.158990247813364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R)-2-(3,5-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <ALOGPS_LOGP>
0.88

> <JCHEM_LOGP>
1.795107015333333

> <ALOGPS_LOGS>
-2.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.553577392540136

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.92366756128485

> <JCHEM_PKA_STRONGEST_BASIC>
-3.303651735682677

> <JCHEM_POLAR_SURFACE_AREA>
110.38000000000001

> <JCHEM_REFRACTIVITY>
73.99969999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.31e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-2-(3,5-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   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       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1    2    6   21                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9                                                            
CONECT   12    8   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16   12                                                       
CONECT   18   16                                                            
CONECT   19   14                                                            
CONECT   20    3                                                            
CONECT   21    1                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₆

Average Mass

290.2710 Da

Monoisotopic Mass

290.07904 Da

IUPAC Name

(2R,3R)-2-(3,5-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

Traditional Name

(2R,3R)-2-(3,5-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

CAS Registry Number

Not Available

SMILES

O[C@@H]1CC2=C(O)C=C(O)C=C2O[C@@H]1C1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C15H14O6/c16-8-1-7(2-9(17)3-8)15-13(20)6-11-12(19)4-10(18)5-14(11)21-15/h1-5,13,15-20H,6H2/t13-,15-/m1/s1

InChI Key

MKXNQWPXEHIMRX-UKRRQHHQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Humboldtia laurifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavan-3-ols. These are flavans that bear and hydroxyl group at position 3 (B ring), but not at position 4.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Flavan-3-ols

Alternative Parents

Substituents

3'-hydroxyflavonoid
3-hydroxyflavonoid
Flavan-3-ol
7-hydroxyflavonoid
Hydroxyflavonoid
5-hydroxyflavonoid
Benzopyran
Chromane
1-benzopyran
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Ether
Polyol
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Alcohol
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavans, Flavanols and Leucoanthocyanidins (LMPK12020024 )

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	0.88	ALOGPS
logP	1.8	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	110.38 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	74 m³·mol⁻¹	ChemAxon
Polarizability	28.16 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

C00008828

Chemspider ID

24842506

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44257055

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xie FG, Li CJ, Yang JZ, Luo YM, Zhang DM: [Study on chemical constituents from the root bark of Tripterygium hypoglaucum]. Zhong Yao Cai. 2012 Jul;35(7):1083-7. [PubMed:23252270 ]

Showing NP-Card for (2R,3R)-3,5,7,3',5'-Pentahydroxyflavan (NP0056083)

MOL for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

3D MOL for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

3D SDF for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

3D-SDF for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

PDB for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

3D PDB for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

SMILES for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

INCHI for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

Structure for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)

3D Structure for NP0056083 ((2R,3R)-3,5,7,3',5'-Pentahydroxyflavan)