NP-MRD: Showing NP-Card for 4-Hydroxycordoin (NP0054762)

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Record Information

Version

2.0

Created at

2022-04-28 01:00:42 UTC

Updated at

2022-04-28 01:00:42 UTC

NP-MRD ID

NP0054762

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-Hydroxycordoin

Description

4-Hydroxycordoin belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, 4-hydroxycordoin is considered to be a flavonoid. 4-Hydroxycordoin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 4-Hydroxycordoin is found in Lonchocarpus neuroscapha and Millettia ferruginea . 4-Hydroxycordoin was first documented in 2011 (PMID: 21353508). Based on a literature review very few articles have been published on 4-hydroxycordoin (PMID: 21158427).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -6.9830   -1.4564    0.0169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3196   -0.1341    0.1708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9287    0.9501    1.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1545    0.0961   -0.4577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5628   -0.9672   -1.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3054   -1.4096   -0.9147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1208   -0.7341   -0.8822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9825   -1.4016   -0.4406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2315   -0.7570   -0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3912    0.5489   -0.7718 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6589    1.2354   -0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494    2.4498   -1.0901 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8446    0.5157   -0.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0313    1.1062   -0.2023 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2533    0.4629    0.2493 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4424    1.1760    0.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6429    0.6453    0.6806 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6949   -0.6657    1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8675   -1.2498    1.5254 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5326   -1.4055    1.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3301   -0.8351    0.6721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355    1.2070   -1.2085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6641    2.5188   -1.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9756    0.5664   -1.2612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2704   -1.6407   -1.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3385   -2.2690    0.4035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9198   -1.4564    0.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0396    0.8889    0.9748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6690    0.7901    2.1018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5372    1.9263    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7043    1.0564   -0.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2609   -1.8553   -1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5467   -0.6282   -2.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -2.4318   -0.1435 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0593   -1.3657   -0.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8354   -0.5112    0.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0607    2.1382   -0.5199 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4300    2.2033   -0.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5660    1.1993    0.6956 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7465   -0.7497    1.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5905   -2.4322    1.4307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4804   -1.4637    0.6956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4687    3.0310   -1.9304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8428    1.1080   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 10 22  1  0
 22 23  1  0
 22 24  2  0
 24  7  1  0
 21 15  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  8 34  1  0
  9 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 17 39  1  0
 19 40  1  0
 20 41  1  0
 21 42  1  0
 23 43  1  0
 24 44  1  0
M  END


  Mrv1652304282203002D          

 24 25  0  0  0  0            999 V2000
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    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   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   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
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  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
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054762

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCOC1=CC=C(C(=O)\C=C\C2=CC=C(O)C=C2)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O4/c1-14(2)11-12-24-17-8-9-18(20(23)13-17)19(22)10-5-15-3-6-16(21)7-4-15/h3-11,13,21,23H,12H2,1-2H3/b10-5+

> <INCHI_KEY>
SFXYAAFUXNWNQF-BJMVGYQFSA-N

> <FORMULA>
C20H20O4

> <MOLECULAR_WEIGHT>
324.376

> <EXACT_MASS>
324.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
36.309017842504694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-1-{2-hydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
4.28

> <JCHEM_LOGP>
5.136769489666667

> <ALOGPS_LOGS>
-4.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.0404476826593

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.089377177260487

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8826558380288745

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
96.4202

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.92e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxycordoin

> <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       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.335 -12.320   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5                                                            
CONECT    8    2    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2E)-1-(2-Hydroxy-4-((3-methylbut-2-enyl)oxy)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one	MeSH

Chemical Formula

C₂₀H₂₀O₄

Average Mass

324.3760 Da

Monoisotopic Mass

324.13616 Da

IUPAC Name

(2E)-1-{2-hydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one

Traditional Name

4-hydroxycordoin

CAS Registry Number

Not Available

SMILES

CC(C)=CCOC1=CC=C(C(=O)\C=C\C2=CC=C(O)C=C2)C(O)=C1

InChI Identifier

InChI=1S/C20H20O4/c1-14(2)11-12-24-17-8-9-18(20(23)13-17)19(22)10-5-15-3-6-16(21)7-4-15/h3-11,13,21,23H,12H2,1-2H3/b10-5+

InChI Key

SFXYAAFUXNWNQF-BJMVGYQFSA-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
Lonchocarpus neuroscapha	Plant	KNApSAcK
Millettia ferruginea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxychalcones

Alternative Parents

Substituents

2'-hydroxychalcone
Cinnamylphenol
Hydroxycinnamic acid or derivatives
Phenoxy compound
Benzoyl
Phenol ether
Aryl ketone
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Acryloyl-group
Enone
Vinylogous acid
Alpha,beta-unsaturated ketone
Ketone
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

aromatic ether (CHEBI:70080 )
polyphenol (CHEBI:70080 )
chalcones (CHEBI:70080 )
Chalcones and dihydrochalcones (LMPK12120044 )

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	4.28	ALOGPS
logP	5.14	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	7.09	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	96.42 m³·mol⁻¹	ChemAxon
Polarizability	36.31 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00007067

Chemspider ID

4732316

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5879763

PDB ID

Not Available

ChEBI ID

70080

Good Scents ID

Not Available

References

General References

Messier C, Epifano F, Genovese S, Grenier D: Inhibition of Candida albicans biofilm formation and yeast-hyphal transition by 4-hydroxycordoin. Phytomedicine. 2011 Mar 15;18(5):380-3. doi: 10.1016/j.phymed.2011.01.013. Epub 2011 Feb 25. [PubMed:21353508 ]
Feldman M, Tanabe S, Epifano F, Genovese S, Curini M, Grenier D: Antibacterial and anti-inflammatory activities of 4-hydroxycordoin: potential therapeutic benefits. J Nat Prod. 2011 Jan 28;74(1):26-31. doi: 10.1021/np100547b. Epub 2010 Dec 15. [PubMed:21158427 ]

Showing NP-Card for 4-Hydroxycordoin (NP0054762)

MOL for NP0054762 (4-Hydroxycordoin)

3D MOL for NP0054762 (4-Hydroxycordoin)

3D SDF for NP0054762 (4-Hydroxycordoin)

3D-SDF for NP0054762 (4-Hydroxycordoin)

PDB for NP0054762 (4-Hydroxycordoin)

3D PDB for NP0054762 (4-Hydroxycordoin)

SMILES for NP0054762 (4-Hydroxycordoin)

INCHI for NP0054762 (4-Hydroxycordoin)

Structure for NP0054762 (4-Hydroxycordoin)

3D Structure for NP0054762 (4-Hydroxycordoin)