NP-MRD: Showing NP-Card for (+)-medicarpin (NP0307626)

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Record Information

Version

2.0

Created at

2022-09-11 00:52:53 UTC

Updated at

2022-09-11 00:52:53 UTC

NP-MRD ID

NP0307626

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-medicarpin

Description

(+)-Medicarpin belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. (+)-medicarpin is found in Arachis hypogaea, Caragana tibetica, Centrolobium sclerophyllum, Dalbergia decipularis, Dalbergia frutescens, Dalbergia nitidula, Dalbergia odorifera, Dalbergia riparia, Dalbergia sissoo, Dalbergia volubilis, Dalea versicolor, Gliricidia sepium, Hedysarum polybotrys, Maackia amurensis, Machaerium acutifolium, Machaerium aristulatum, Ononis vaginalis, Platymiscium floribundum, Psorothamnus spinosus, Sophora flavescens, Styphnolobium japonicum and Zollernia paraensis. (+)-medicarpin was first documented in 2021 (PMID: 35649147). Based on a literature review a small amount of articles have been published on (+)-medicarpin (PMID: 35974307) (PMID: 35959633) (PMID: 35874019) (PMID: 35381781).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
    5.9262   -0.1110   -1.3342 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6825   -0.3056   -1.9777 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5352   -0.1725   -1.2117 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928    0.1380    0.1286 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951    0.2816    0.9321 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454    0.1079    0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1294   -0.2042   -0.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2626   -0.3408   -1.7363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2357   -0.3317   -1.2874 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8618   -0.7373   -0.0684 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3078   -0.5457   -0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1650   -1.5907   -0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5475   -1.4221   -0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0509   -0.1696   -0.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4129    0.0402   -0.1227 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1937    0.8720    0.1338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8183    0.7077    0.1530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9463    1.7567    0.4022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5996    1.5988    0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1520    0.1793    0.9041 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9505    0.8716   -0.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0394   -0.8831   -0.5294 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7782   -0.1463   -2.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5825    0.2802    0.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5362    0.5256    1.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2093   -0.5864   -2.7953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5484   -1.7671    0.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8136   -2.6100   -0.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2215   -2.2684   -0.5513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8622    0.9120    0.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5453    1.8906    0.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    2.0366    1.8385 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0697    2.2137    0.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2126   -0.2201    1.9368 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  2  0
  6 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
  8  3  1  0
  7  6  1  0
 10 20  1  0
 11 17  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  5 25  1  0
 20 34  1  1
 19 32  1  0
 19 33  1  0
 16 31  1  0
 15 30  1  0
 13 29  1  0
 12 28  1  0
 10 27  1  1
  8 26  1  0
M  END


  Mrv1652309112202522D          

 20 23  0  0  1  0            999 V2000
   -1.2387   -2.9005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5447   -2.4545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1886   -2.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2278   -3.6566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9611   -4.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6551   -3.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6159   -2.7647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8826   -2.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3875   -2.4727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9036   -3.1164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7273   -3.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1799   -2.4738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0036   -2.5209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3746   -3.2578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1982   -3.3049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9219   -3.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0983   -3.9004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456   -4.5901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8220   -4.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4510   -3.8061    0.0000 C   0  0  2  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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  7  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20  6  1  6  0  0  0
 10 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0307626

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2[C@H]3COC4=CC(O)=CC=C4[C@H]3OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H14O4/c1-18-10-3-5-11-13-8-19-14-6-9(17)2-4-12(14)16(13)20-15(11)7-10/h2-7,13,16-17H,8H2,1H3/t13-,16-/m1/s1

> <INCHI_KEY>
NSRJSISNDPOJOP-CZUORRHYSA-N

> <FORMULA>
C16H14O4

> <MOLECULAR_WEIGHT>
270.284

> <EXACT_MASS>
270.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
28.24476429153424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,10S)-14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11,13,15-hexaen-5-ol

> <JCHEM_LOGP>
2.509223396333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.420754148461814

> <JCHEM_PKA_STRONGEST_BASIC>
-4.392070210867522

> <JCHEM_POLAR_SURFACE_AREA>
47.92

> <JCHEM_REFRACTIVITY>
73.0611

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,10S)-14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11,13,15-hexaen-5-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.312  -5.414   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.017  -4.582   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.352  -5.287   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.425  -6.826   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.794  -7.531   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.090  -6.699   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.016  -5.161   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.648  -4.455   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.457  -4.616   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.420  -5.817   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.958  -5.905   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.803  -4.618   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.340  -4.706   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.033  -6.081   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.570  -6.169   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.188  -7.369   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.650  -7.281   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.805  -8.568   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.268  -8.480   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.575  -7.105   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    3                                                       
CONECT    9    7   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    6   10                                                  
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Value	Source
3-Hydroxy-9-methoxypterocarpan	ChEBI
Medicarpin	ChEBI

Chemical Formula

C₁₆H₁₄O₄

Average Mass

270.2840 Da

Monoisotopic Mass

270.08921 Da

IUPAC Name

(1S,10S)-14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11,13,15-hexaen-5-ol

Traditional Name

(1S,10S)-14-methoxy-8,17-dioxatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11,13,15-hexaen-5-ol

CAS Registry Number

Not Available

SMILES

COC1=CC=C2[C@H]3COC4=CC(O)=CC=C4[C@H]3OC2=C1

InChI Identifier

InChI=1S/C16H14O4/c1-18-10-3-5-11-13-8-19-14-6-9(17)2-4-12(14)16(13)20-15(11)7-10/h2-7,13,16-17H,8H2,1H3/t13-,16-/m1/s1

InChI Key

NSRJSISNDPOJOP-CZUORRHYSA-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
Arachis hypogaea	LOTUS Database	35616633
Caragana tibetica	LOTUS Database	35616633
Centrolobium sclerophyllum	LOTUS Database	35616633
Dalbergia decipularis	LOTUS Database	35616633
Dalbergia frutescens	LOTUS Database	35616633
Dalbergia nitidula	LOTUS Database	35616633
Dalbergia odorifera	LOTUS Database	35616633
Dalbergia riparia	LOTUS Database	35616633
Dalbergia sissoo	LOTUS Database	35616633
Dalbergia volubilis	LOTUS Database	35616633
Dalea versicolor	LOTUS Database	35616633
Gliricidia sepium	LOTUS Database	35616633
Hedysarum polybotrys	LOTUS Database	35616633
Maackia amurensis	LOTUS Database	35616633
Machaerium acutifolium	LOTUS Database	35616633
Machaerium aristulatum	LOTUS Database	35616633
Ononis vaginalis	LOTUS Database	35616633
Platymiscium floribundum	LOTUS Database	35616633
Psorothamnus spinosus	LOTUS Database	35616633
Sophora flavescens	LOTUS Database	35616633
Styphnolobium japonicum	LOTUS Database	35616633
Zollernia paraensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Furanoisoflavonoids

Direct Parent

Pterocarpans

Alternative Parents

Substituents

Pterocarpan
Isoflavanol
Isoflavan
Chromane
1-benzopyran
Benzopyran
Coumaran
Benzofuran
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

medicarpin (CHEBI:6714 )
Pterocarpanes (C01729 )

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	2.51	ChemAxon
pKa (Strongest Acidic)	9.42	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.92 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	73.06 m³·mol⁻¹	ChemAxon
Polarizability	28.24 Å³	ChemAxon
Number of Rings	4	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

65860

KEGG Compound ID

C01729

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73067

PDB ID

Not Available

ChEBI ID

6714

Good Scents ID

Not Available

References

General References

Xia X, Gong R, Zhang C: Integrative analysis of transcriptome and metabolome reveals flavonoid biosynthesis regulation in Rhododendron pulchrum petals. BMC Plant Biol. 2022 Aug 16;22(1):401. doi: 10.1186/s12870-022-03762-y. [PubMed:35974307 ]
Sharma K, Awasthi P, Prakash R, Khanka S, Bajpai R, Sahasrabuddhe AA, Goel A, Singh D: Maintenance of increased bone mass after PTH withdrawal by sequential medicarpin treatment via augmentation of cAMP-PKA pathway. J Cell Biochem. 2022 Aug 12. doi: 10.1002/jcb.30313. [PubMed:35959633 ]
Alvarez-Rivera G, Sanz A, Cifuentes A, Ibanez E, Paape T, Lucas MM, Pueyo JJ: Flavonoid Accumulation Varies in Medicago truncatula in Response to Mercury Stress. Front Plant Sci. 2022 Jul 7;13:933209. doi: 10.3389/fpls.2022.933209. eCollection 2022. [PubMed:35874019 ]
Chern CM, Lu CK, Liou KT, Wang YH, Tsai KC, Chang CL, Chang CC, Shen YC: Medicarpin isolated from Radix Hedysari ameliorates brain injury in a murine model of cerebral ischemia. J Food Drug Anal. 2021 Dec 15;29(4):581-605. doi: 10.38212/2224-6614.3377. [PubMed:35649147 ]
Yigin AK, Donmez H, Hitit M, Seven S, Eser N, Kurar E, Seven M: The effect of medicarpin on PTEN/AKT signal pathway in head and neck squamous cell carcinoma. J Cancer Res Ther. 2022 Jan-Mar;18(1):180-184. doi: 10.4103/jcrt.jcrt_641_21. [PubMed:35381781 ]
LOTUS database [Link]

Showing NP-Card for (+)-medicarpin (NP0307626)

MOL for NP0307626 ((+)-medicarpin)

3D MOL for NP0307626 ((+)-medicarpin)

3D SDF for NP0307626 ((+)-medicarpin)

3D-SDF for NP0307626 ((+)-medicarpin)

PDB for NP0307626 ((+)-medicarpin)

3D PDB for NP0307626 ((+)-medicarpin)

SMILES for NP0307626 ((+)-medicarpin)

INCHI for NP0307626 ((+)-medicarpin)

Structure for NP0307626 ((+)-medicarpin)

3D Structure for NP0307626 ((+)-medicarpin)