NP-MRD: Showing NP-Card for 2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol (NP0200917)

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Record Information

Version

2.0

Created at

2022-09-04 19:51:50 UTC

Updated at

2022-09-04 19:51:51 UTC

NP-MRD ID

NP0200917

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol

Description

2-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol belongs to the class of organic compounds known as leucoanthocyanidins. These are flavonoids consisting of a flavan (3,4-dihydro-2-phenyl-2H-1-benzopyran) moiety that carries two hydroxy groups at the C3- and C4-positions. 2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol is found in Senegalia galpinii and Acacia sparsiflora. 2-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
    5.3818    1.6061   -0.1054 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2043    0.9186   -0.2317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7893    0.0926    0.7927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6042   -0.6143    0.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8613   -0.4699   -0.4456 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5884   -1.1756   -0.6437 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4064   -0.3272   -1.1943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5364    0.0936   -0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8042   -0.2652    0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9252    0.1418    1.4005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8217    0.9524    0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850    1.3307   -0.5954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4807    2.1476   -1.3042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4352    0.9046   -1.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1533    1.2576   -2.5558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8366   -1.1195    1.4383 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1672   -0.3744    2.3698 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0311   -1.9164    0.4995 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8515   -2.8851   -0.0572 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2529    0.3613   -1.5071 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4336    1.0576   -1.3931 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9470    1.5152    0.7261 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3760   -0.0335    1.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2583   -1.2712    1.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -1.9315   -1.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1220   -0.1504    2.4287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7403    1.3100    1.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3255    2.4710   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8310    1.8517   -3.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.8834    2.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898   -0.8725    3.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7199   -2.5129    1.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3463   -2.3954   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6574    0.4645   -2.3967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8254    1.7212   -2.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14  8  2  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 21  1  0
 21 20  2  0
  6 18  1  0
 20  5  1  0
  8  9  1  0
 19 33  1  0
 18 32  1  1
 16 30  1  1
 17 31  1  0
 10 26  1  0
 11 27  1  0
 13 28  1  0
 15 29  1  0
  6 25  1  6
  4 24  1  0
  3 23  1  0
  1 22  1  0
 21 35  1  0
 20 34  1  0
M  END


  Mrv1533004161516562D          

 21 23  0  0  0  0            999 V2000
    0.0000    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
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   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 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   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   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   -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
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   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
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    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
   -0.7145   -1.2375    0.0000 C   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  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  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
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200917

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1C(O)C2=CC=C(O)C(O)=C2OC1C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O6/c16-8-3-1-7(2-4-8)14-13(20)11(18)9-5-6-10(17)12(19)15(9)21-14/h1-6,11,13-14,16-20H

> <INCHI_KEY>
JSZRJOLRIBESNT-UHFFFAOYSA-N

> <FORMULA>
C15H14O6

> <MOLECULAR_WEIGHT>
290.271

> <EXACT_MASS>
290.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
28.531838276199284

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

> <ALOGPS_LOGP>
0.65

> <JCHEM_LOGP>
1.1796761899999997

> <ALOGPS_LOGS>
-2.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.75616493073068

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.15395521858841

> <JCHEM_PKA_STRONGEST_BASIC>
-3.614593773129867

> <JCHEM_POLAR_SURFACE_AREA>
110.38000000000001

> <JCHEM_REFRACTIVITY>
73.22630000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.76e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

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

2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

Traditional Name

2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

CAS Registry Number

Not Available

SMILES

OC1C(O)C2=CC=C(O)C(O)=C2OC1C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C15H14O6/c16-8-3-1-7(2-4-8)14-13(20)11(18)9-5-6-10(17)12(19)15(9)21-14/h1-6,11,13-14,16-20H

InChI Key

JSZRJOLRIBESNT-UHFFFAOYSA-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
Acacia galpinii	LOTUS Database	35616633
Acacia sparsiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as leucoanthocyanidins. These are flavonoids consisting of a flavan (3,4-dihydro-2-phenyl-2H-1-benzopyran) moiety that carries two hydroxy groups at the C3- and C4-positions.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Leucoanthocyanidins

Alternative Parents

Substituents

Leucoanthocyanidin-skeleton
3-hydroxyflavonoid
4'-hydroxyflavonoid
4-hydroxyflavonoid
7-hydroxyflavonoid
8-hydroxyflavonoid
Hydroxyflavonoid
Chromane
Benzopyran
1-benzopyran
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
1,2-diol
Secondary alcohol
Organoheterocyclic compound
Ether
Polyol
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Alcohol
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	0.65	ALOGPS
logP	1.18	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.15	ChemAxon
pKa (Strongest Basic)	-3.6	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	73.23 m³·mol⁻¹	ChemAxon
Polarizability	28.53 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

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

5317352

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol (NP0200917)

MOL for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D MOL for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D SDF for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D-SDF for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

PDB for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D PDB for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

SMILES for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

INCHI for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

Structure for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D Structure for NP0200917 (2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)