NP-MRD: Showing NP-Card for 2-Prenyl-6alpha-hydroxyphaseollidin (NP0045698)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-03-17 19:35:59 UTC

Updated at

2022-03-17 19:35:59 UTC

NP-MRD ID

NP0045698

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-Prenyl-6alpha-hydroxyphaseollidin

Description

2-Prenyl-6alpha-hydroxyphaseollidin is found in Erythrina crista-galli , Erythrina suberosa, Erythrina suberosa var. glabrescences and Erythrina variegata .

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241212142D          

 30 33  0  0  0  0            999 V2000
   -3.0938    2.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8082    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8082    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0938    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3793    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3793    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648    2.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227    2.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9516   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4786    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4786   -0.4715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -0.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9075   -0.4715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -1.2965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -1.7090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -2.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074   -2.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -2.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648   -0.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359    1.5911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  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
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5 29  1  0  0  0  0
  7  8  1  0  0  0  0
 27  8  1  0  0  0  0
  2  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 15 18  2  0  0  0  0
 17 16  2  0  0  0  0
 17 20  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 16  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 29  1  0  0  0  0
 16 15  1  0  0  0  0
 27 30  1  0  0  0  0
M  END


  Mrv0541 02241212142D          

 30 33  0  0  0  0            999 V2000
   -3.0938    2.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8082    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8082    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0938    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3793    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3793    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648    2.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504    2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227    2.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -0.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9516   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4786    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4786   -0.4715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -0.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9075   -0.4715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -1.2965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -1.7090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1930   -2.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074   -2.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -2.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504    1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648   -0.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6648    0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2359    1.5911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  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
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5 29  1  0  0  0  0
  7  8  1  0  0  0  0
 27  8  1  0  0  0  0
  2  9  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 15 18  2  0  0  0  0
 17 16  2  0  0  0  0
 17 20  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 16  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 29  1  0  0  0  0
 16 15  1  0  0  0  0
 27 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0045698

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC2=C(OCC3(O)C2OC2=C(CC=C(C)C)C(O)=CC=C32)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O5/c1-14(2)5-7-16-11-18-22(12-21(16)27)29-13-25(28)19-9-10-20(26)17(8-6-15(3)4)23(19)30-24(18)25/h5-6,9-12,24,26-28H,7-8,13H2,1-4H3

> <INCHI_KEY>
ZAAKSBRPXNODLV-UHFFFAOYSA-N

> <FORMULA>
C25H28O5

> <MOLECULAR_WEIGHT>
408.4868

> <EXACT_MASS>
408.193674006

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
44.325496104961424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,15-bis(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,10,14-triol

> <ALOGPS_LOGP>
4.40

> <JCHEM_LOGP>
5.1652829570000005

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.50783472150392

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.906110510941799

> <JCHEM_PKA_STRONGEST_BASIC>
-4.098954821549101

> <JCHEM_POLAR_SURFACE_AREA>
79.15

> <JCHEM_REFRACTIVITY>
118.15229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.06e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,15-bis(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,10,14-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -5.775   4.510   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.109   3.740   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.109   2.200   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.775   1.430   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.441   2.200   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.441   3.740   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.108   4.510   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.774   3.740   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.442   4.510   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -8.442   1.430   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.442  -0.110   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.776  -0.880   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.776  -2.420   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.110  -0.110   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.440  -0.110   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.440   1.430   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.893   2.200   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.893  -0.880   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.227  -0.110   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.227   1.430   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.561  -0.880   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.893  -2.420   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.227  -3.190   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.227  -4.730   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.560  -5.500   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.893  -5.500   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.774   2.200   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.108  -0.110   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.108   1.430   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.440   2.970   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6    8                                                       
CONECT    8    7   27                                                       
CONECT    9    2                                                            
CONECT   10    3   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   18   28   16                                                  
CONECT   16   17   27   15                                                  
CONECT   17   16   20                                                       
CONECT   18   15   19   22                                                  
CONECT   19   18   20   21                                                  
CONECT   20   17   19                                                       
CONECT   21   19                                                            
CONECT   22   18   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    8   16   29   30                                             
CONECT   28   15   29                                                       
CONECT   29    5   28   27                                                  
CONECT   30   27                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
2-Prenyl-6a-hydroxyphaseollidin	Generator
2-Prenyl-6α-hydroxyphaseollidin	Generator

Chemical Formula

C₂₅H₂₈O₅

Average Mass

408.4868 Da

Monoisotopic Mass

408.19367 Da

IUPAC Name

4,15-bis(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,10,14-triol

Traditional Name

4,15-bis(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11,13,15-hexaene-5,10,14-triol

CAS Registry Number

104363-19-1

SMILES

CC(C)=CCC1=CC2=C(OCC3(O)C2OC2=C(CC=C(C)C)C(O)=CC=C32)C=C1O

InChI Identifier

InChI=1S/C25H28O5/c1-14(2)5-7-16-11-18-22(12-21(16)27)29-13-25(28)19-9-10-20(26)17(8-6-15(3)4)23(19)30-24(18)25/h5-6,9-12,24,26-28H,7-8,13H2,1-4H3

InChI Key

ZAAKSBRPXNODLV-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, 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
Erythrina crista-galli	Plant	KNApSAcK
Erythrina suberosa	LOTUS Database	35616633
Erythrina suberosa var. glabrescences	Plant	KNApSAcK
Erythrina variegata	Plant	KNApSAcK
Phaseolus lunatus	FooDB	KNAPSACK

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
Benzopyran
1-benzopyran
Coumaran
Benzofuran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Tertiary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Polyol
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Pterocarpans (LMPK12070122 )

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	4.4	ALOGPS
logP	5.17	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.91	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	79.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.15 m³·mol⁻¹	ChemAxon
Polarizability	44.33 Å³	ChemAxon
Number of Rings	4	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

FDB001655

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

44257484

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-Prenyl-6alpha-hydroxyphaseollidin (NP0045698)

MOL for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

3D MOL for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

3D SDF for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

3D-SDF for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

PDB for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

3D PDB for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

SMILES for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

INCHI for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

Structure for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)

3D Structure for NP0045698 (2-Prenyl-6alpha-hydroxyphaseollidin)