NP-MRD: Showing NP-Card for α catechin (NP0201954)

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Record Information

Version

1.0

Created at

2022-09-04 21:04:54 UTC

Updated at

2022-09-04 21:04:54 UTC

NP-MRD ID

NP0201954

Secondary Accession Numbers

None

Natural Product Identification

Common Name

α catechin

Description

(-)-Catechin, also known as catechin L-form, belongs to the class of organic compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-Tiol. α catechin is found in Acanthophora spicifera, Arbutus unedo, Bauhinia racemosa, Begonia nantoensis, Berchemia racemosa, Betula papyrifera, Betula pendula, Chamaebatia foliolosa, Cinnamomum kotoense, Crateva religiosa, Cynomorium songaricum, Hedysarum theinum, Loranthus kaoi, Nelumbo nucifera, Persicaria hydropiper, Persicaria lapathifolia, Pinus sylvestris, Podocarpus macrophyllus, Dasiphora fruticosa, Pseudocedrela kotschyi, Rosa transmorrisonensis, Smilax corbularia, Ulmus davidiana and Ziziphus jujuba. The (-)-enantiomer of catechin (-)-Catechin is an extremely weak basic (essentially neutral) compound (based on its pKa) (-)-Catechin is a potentially toxic compound.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
    3.9536    2.7050    2.0833 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3788    1.6026    1.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1098    0.8641    0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5437   -0.2230   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2985   -0.9376   -1.0030 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2427   -0.6161    0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120    0.1236    1.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771    1.2173    1.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2058   -0.2764    1.2673 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5168   -1.1739    0.4669 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8614   -0.6059    0.1889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9565   -1.4294    0.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2033   -0.8706    0.0415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3211    0.4535   -0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5934    0.9692   -0.5823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1979    1.2594   -0.4368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3405    2.5887   -0.8072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9730    0.7055   -0.1738 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1828   -1.3732   -0.8601 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4628   -2.2872   -1.6539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6164   -1.7879   -0.5515 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8318    3.5941    1.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1341    1.1787    0.3504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2565   -0.7101   -1.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5040    1.7849    2.3800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6000   -2.1906    0.9314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9147   -2.4621    0.5892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0827   -1.5128    0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7050    1.9299   -0.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5152    3.1488   -0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    1.3424   -0.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2500   -0.3633   -1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4770   -1.9551   -2.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1677   -2.0977   -1.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5387   -2.5948    0.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  1  0
 21  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2  8  1  0
  8  7  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 18  2  0
 18 16  1  0
 16 17  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  2  0
 10 19  1  0
 12 11  1  0
  7  6  1  0
 20 33  1  0
 19 32  1  6
 21 34  1  0
 21 35  1  0
  5 24  1  0
  3 23  1  0
  1 22  1  0
  8 25  1  0
 10 26  1  1
 18 31  1  0
 17 30  1  0
 15 29  1  0
 13 28  1  0
 12 27  1  0
M  END


  Mrv1652307201900052D          

 21 23  0  0  0  0            999 V2000
   -2.8635   -0.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8647   -1.1162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1499   -1.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1518    0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4367   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4333   -1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7182   -1.5226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0019   -1.1078    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0053   -0.2795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7250    0.1338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7076    0.1349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4221   -0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1347    0.1362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1326    0.9620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4120    1.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7024    0.9557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8500   -0.2740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8449    1.3774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7134   -1.5184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1494   -2.3539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5779    0.1231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  1 21  1  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3 20  1  0  0  0  0
  3  6  2  0  0  0  0
  5  4  2  0  0  0  0
  5 10  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8 19  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  1  0  0  0
 16 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 17  1  0  0  0  0
 13 14  2  0  0  0  0
 14 18  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0201954

> <DATABASE_NAME>
NP-MRD

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

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

> <INCHI_KEY>
PFTAWBLQPZVEMU-HIFRSBDPSA-N

> <FORMULA>
C15H14O6

> <MOLECULAR_WEIGHT>
290.2681

> <EXACT_MASS>
290.07903818

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
28.301206055287867

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
1.02

> <JCHEM_LOGP>
1.795107015333333

> <ALOGPS_LOGS>
-2.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.624022697297178

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.004573813837975

> <JCHEM_PKA_STRONGEST_BASIC>
-3.289719332242856

> <JCHEM_POLAR_SURFACE_AREA>
110.38000000000001

> <JCHEM_REFRACTIVITY>
73.99970000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.45e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
α catechin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-JUL-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUL-19         0                                  
HETATM    1  C   UNK     0      -5.345  -0.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.347  -2.084   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.013  -2.854   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.017   0.231   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.682  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.675  -2.079   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.341  -2.842   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.004  -2.068   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.010  -0.522   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.353   0.250   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.321   0.252   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.655  -0.518   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.985   0.254   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.981   1.796   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.636   2.561   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.311   1.784   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.320  -0.511   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       5.310   2.571   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.332  -2.834   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.012  -4.394   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -6.679   0.230   0.000  0.00  0.00           O+0
CONECT    1    4   21    2                                                  
CONECT    2    1    3                                                       
CONECT    3    2   20    6                                                  
CONECT    4    1    5                                                       
CONECT    5    4   10    6                                                  
CONECT    6    3    5    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7   19    9                                                  
CONECT    9    8   10   11                                                  
CONECT   10    5    9                                                       
CONECT   11    9   16   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   17   14                                                  
CONECT   14   13   18   15                                                  
CONECT   15   14   16                                                       
CONECT   16   11   15                                                       
CONECT   17   13                                                            
CONECT   18   14                                                            
CONECT   19    8                                                            
CONECT   20    3                                                            
CONECT   21    1                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
(2S,3R)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-1H-benzopyran-3,5,7-triol	ChEBI
Catechin L-form	ChEBI

Chemical Formula

C₁₅H₁₄O₆

Average Mass

290.2681 Da

Monoisotopic Mass

290.07904 Da

IUPAC Name

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

Traditional Name

α catechin

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

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

InChI Key

PFTAWBLQPZVEMU-HIFRSBDPSA-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
Acanthophora spicifera	LOTUS Database	35616633
Arbutus unedo	LOTUS Database	35616633
Bauhinia racemosa	LOTUS Database	35616633
Begonia nantoensis	LOTUS Database	35616633
Berchemia racemosa	LOTUS Database	35616633
Betula papyrifera	LOTUS Database	35616633
Betula pendula	LOTUS Database	35616633
Chamaebatia foliolosa	LOTUS Database	35616633
Cinnamomum kotoense	LOTUS Database	35616633
Crateva religiosa	LOTUS Database	35616633
Cynomorium songaricum	LOTUS Database	35616633
Hedysarum theinum	LOTUS Database	35616633
Loranthus kaoi	LOTUS Database	35616633
Nelumbo nucifera	LOTUS Database	35616633
Persicaria hydropiper	LOTUS Database	35616633
Persicaria lapathifolia	LOTUS Database	35616633
Pinus sylvestris	LOTUS Database	35616633
Podocarpus macrophyllus	LOTUS Database	35616633
Potentilla fruticosa	LOTUS Database	35616633
Pseudocedrela kotschyi	LOTUS Database	35616633
Rosa transmorrisonensis	LOTUS Database	35616633
Smilax corbularia	LOTUS Database	35616633
Ulmus davidiana	LOTUS Database	35616633
Ziziphus jujuba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as catechins. Catechins are compounds containing a catechin moiety, which is a 3,4-dihydro-2-chromene-3,5.7-Tiol.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

Catechins

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

catechin (CHEBI:33992 )
Flavan 3-ols (C14079 )

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	1.02	ALOGPS
logP	1.8	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9	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	28.3 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

HMDB0037953

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00008808

Chemspider ID

Not Available

KEGG Compound ID

C14079

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73160

PDB ID

Not Available

ChEBI ID

33992

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for α catechin (NP0201954)

MOL for NP0201954 (α catechin)

3D MOL for NP0201954 (α catechin)

3D SDF for NP0201954 (α catechin)

3D-SDF for NP0201954 (α catechin)

PDB for NP0201954 (α catechin)

3D PDB for NP0201954 (α catechin)

SMILES for NP0201954 (α catechin)

INCHI for NP0201954 (α catechin)

Structure for NP0201954 (α catechin)

3D Structure for NP0201954 (α catechin)