NP-MRD: Showing NP-Card for (+)-Genkwadaphnin (NP0076587)

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Record Information

Version

1.0

Created at

2022-04-28 21:46:49 UTC

Updated at

2022-04-28 21:46:49 UTC

NP-MRD ID

NP0076587

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Genkwadaphnin

Description

Genkwadaphnin belongs to the class of organic compounds known as rhamnofolane and daphnane diterpenoids. These are diterpenoids with a structure based on one the rhamnofolane or daphnane skeleton. The rhamnofolane and daphnane skeletons are closely related, being formally derived from casbane by two cyclizations (6,10 and 5,14) followed by cleavage of the 1,15 (daphnane) or 2,15 (rhamnofolane) cyclopropane bonds. (+)-Genkwadaphnin is found in Daphne acutiloba, Daphne genkwa, Daphne oleoides, Daphne oleoides ssp.oleoides and Thymelaea hirsuta. Based on a literature review very few articles have been published on Genkwadaphnin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282223462D          

 44 51  0  0  1  0            999 V2000
    1.8496   -0.5110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6744    0.4528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7211   -0.1603    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5457   -0.1372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3632    1.0068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1261    1.2215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2168    0.4858    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.1357    0.9668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2281    3.4621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 39 44  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282223462D          

 44 51  0  0  1  0            999 V2000
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    1.9170   -1.5767    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1840   -1.9554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4310   -1.6184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2250   -0.8195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3638   -1.3974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3242   -2.2045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2196   -2.4076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6025   -2.8270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368   -1.9798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5292   -3.0853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3571   -1.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8973   -0.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2809   -1.6331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6066   -2.5827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1511   -0.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2183   -1.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0399   -1.4490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3861   -2.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9107   -2.8721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0891   -2.7975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7429   -2.0486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  1  9  1  0  0  0  0
  8 10  1  1  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  7 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
  6 22  1  6  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  4 27  1  1  0  0  0
 27 28  1  1  0  0  0
 26 28  1  0  0  0  0
 26 29  1  6  0  0  0
 29 30  1  0  0  0  0
 25 31  1  6  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 23 35  1  6  0  0  0
 34 36  1  0  0  0  0
 24 37  1  6  0  0  0
  5 38  1  1  0  0  0
  1 38  1  0  0  0  0
  1 39  1  1  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 39 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0076587

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H](OC(=O)C2=CC=CC=C2)[C@@]2(O[C@]3(O[C@@H]2[C@@H]2[C@@H]4O[C@]4(CO)[C@@H](O)[C@@]4(O)[C@@H](C=C(C)C4=O)[C@@]12O3)C1=CC=CC=C1)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C34H34O10/c1-17(2)32-25(40-28(37)20-11-7-5-8-12-20)19(4)33-22-15-18(3)24(36)31(22,39)29(38)30(16-35)26(41-30)23(33)27(32)42-34(43-32,44-33)21-13-9-6-10-14-21/h5-15,19,22-23,25-27,29,35,38-39H,1,16H2,2-4H3/t19-,22-,23+,25-,26+,27-,29-,30+,31-,32+,33+,34-/m1/s1

> <INCHI_KEY>
QKMXESBAFIKRAD-MGAVNPOISA-N

> <FORMULA>
C34H34O10

> <MOLECULAR_WEIGHT>
602.636

> <EXACT_MASS>
602.215197295

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
62.32083645891997

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-(prop-1-en-2-yl)-9,13,15,19-tetraoxahexacyclo[12.4.1.0^{1,11}.0^{2,6}.0^{8,10}.0^{12,16}]nonadec-3-en-17-yl benzoate

> <ALOGPS_LOGP>
2.61

> <JCHEM_LOGP>
3.797364205000002

> <ALOGPS_LOGS>
-3.59

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.327888189954965

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.646350016699493

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1497130859472193

> <JCHEM_POLAR_SURFACE_AREA>
144.28

> <JCHEM_REFRACTIVITY>
153.64259999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.56e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-(prop-1-en-2-yl)-9,13,15,19-tetraoxahexacyclo[12.4.1.0^{1,11}.0^{2,6}.0^{8,10}.0^{12,16}]nonadec-3-en-17-yl benzoate

> <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       3.453  -0.954   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.125   0.845   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.898   0.949   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.346  -0.299   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.885  -0.256   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.545   1.879   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.969   2.280   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.138   0.907   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.762  -0.547   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.853   1.805   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.048   3.381   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.494   1.871   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.729   3.814   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.674   5.001   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.165   4.691   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.159   6.463   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.136   7.614   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.622   9.075   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.130   9.386   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.153   8.234   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.668   6.773   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.374   3.072   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.879  -1.433   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.578  -2.943   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.210  -3.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.805  -3.021   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.420  -1.530   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.679  -2.608   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.605  -4.115   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.277  -4.494   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.125  -5.277   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.922  -3.696   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.721  -5.759   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.267  -2.608   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.408  -1.252   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.991  -3.048   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.999  -4.821   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       2.149  -1.754   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.141  -2.565   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.675  -2.705   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.321  -4.103   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.433  -5.361   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.900  -5.222   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.253  -3.824   0.000  0.00  0.00           C+0
CONECT    1    2    9   38   39                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   27                                                  
CONECT    5    4    6   23   38                                             
CONECT    6    5    7   22                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    3    9   10                                             
CONECT    9    8    1                                                       
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    7   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22    6                                                            
CONECT   23    5   24   35                                                  
CONECT   24   23   25   32   37                                             
CONECT   25   24   26   31                                                  
CONECT   26   25   27   28   29                                             
CONECT   27   26    4   28                                                  
CONECT   28   27   26                                                       
CONECT   29   26   30                                                       
CONECT   30   29                                                            
CONECT   31   25                                                            
CONECT   32   24   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34   23                                                       
CONECT   36   34                                                            
CONECT   37   24                                                            
CONECT   38    5    1                                                       
CONECT   39    1   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   39                                                       
MASTER        0    0    0    0    0    0    0    0   44    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₄O₁₀

Average Mass

602.6360 Da

Monoisotopic Mass

602.21520 Da

IUPAC Name

(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-(prop-1-en-2-yl)-9,13,15,19-tetraoxahexacyclo[12.4.1.0^{1,11}.0^{2,6}.0^{8,10}.0^{12,16}]nonadec-3-en-17-yl benzoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H](OC(=O)C2=CC=CC=C2)[C@@]2(O[C@]3(O[C@@H]2[C@@H]2[C@@H]4O[C@]4(CO)[C@@H](O)[C@@]4(O)[C@@H](C=C(C)C4=O)[C@@]12O3)C1=CC=CC=C1)C(C)=C

InChI Identifier

InChI=1S/C34H34O10/c1-17(2)32-25(40-28(37)20-11-7-5-8-12-20)19(4)33-22-15-18(3)24(36)31(22,39)29(38)30(16-35)26(41-30)23(33)27(32)42-34(43-32,44-33)21-13-9-6-10-14-21/h5-15,19,22-23,25-27,29,35,38-39H,1,16H2,2-4H3/t19-,22-,23+,25-,26+,27-,29-,30+,31-,32+,33+,34-/m1/s1

InChI Key

QKMXESBAFIKRAD-MGAVNPOISA-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
Daphne acutiloba	LOTUS Database	35616633
Daphne genkwa	LOTUS Database	35616633
Daphne oleoides	LOTUS Database	35616633
Daphne oleoides ssp.oleoides	Plant	KNApSAcK
Thymelaea hirsuta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rhamnofolane and daphnane diterpenoids. These are diterpenoids with a structure based on one the rhamnofolane or daphnane skeleton. The rhamnofolane and daphnane skeletons are closely related, being formally derived from casbane by two cyclizations (6,10 and 5,14) followed by cleavage of the 1,15 (daphnane) or 2,15 (rhamnofolane) cyclopropane bonds.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Rhamnofolane and daphnane diterpenoids

Alternative Parents

Substituents

Daphnane diterpenoid
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Carboxylic acid orthoester
Ortho ester
1,3-dioxepane
Dioxepane
Meta-dioxane
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Meta-dioxolane
Secondary alcohol
Carboxylic acid ester
Orthocarboxylic acid derivative
Ketone
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxirane
Ether
Primary alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organooxygen compound
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	2.61	ALOGPS
logP	3.8	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	11.65	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	144.28 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	153.64 m³·mol⁻¹	ChemAxon
Polarizability	62.32 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00039258

Chemspider ID

30811986

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73351913

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Genkwadaphnin (NP0076587)

MOL for NP0076587 ((+)-Genkwadaphnin)

3D MOL for NP0076587 ((+)-Genkwadaphnin)

3D SDF for NP0076587 ((+)-Genkwadaphnin)

3D-SDF for NP0076587 ((+)-Genkwadaphnin)

PDB for NP0076587 ((+)-Genkwadaphnin)

3D PDB for NP0076587 ((+)-Genkwadaphnin)

SMILES for NP0076587 ((+)-Genkwadaphnin)

INCHI for NP0076587 ((+)-Genkwadaphnin)

Structure for NP0076587 ((+)-Genkwadaphnin)

3D Structure for NP0076587 ((+)-Genkwadaphnin)