NP-MRD: Showing NP-Card for (-)-(Z)-Volkendousin (NP0075958)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 21:09:24 UTC

Updated at

2022-04-28 21:09:25 UTC

NP-MRD ID

NP0075958

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-(Z)-Volkendousin

Description

(Z)-Volkendousin belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. (-)-(Z)-Volkendousin is found in Aglaia mariannensis, Ekebergia capensis and Melia volkensii. Based on a literature review very few articles have been published on (Z)-Volkendousin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    6.1672    0.0112   -0.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    0.5379   -0.2629 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7454   -0.2523   -0.1158 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7976   -1.7065   -0.1402 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8127   -2.4407   -0.1931 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3874   -2.2446   -0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6159   -1.0536   -0.5013 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2023   -0.9597    0.0058 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5943   -2.1521   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0487   -1.8692   -0.3084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5903   -0.6732   -0.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0839   -0.6100   -0.0678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4797   -0.8401    1.2588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6220    0.6817   -0.5831 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8979    0.8721   -0.0233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7780    1.8692   -0.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3698    1.6870   -0.7606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7479    0.5409    0.0204 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6590    0.9735    1.4744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3962    0.2790   -0.5950 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4319    1.4987   -0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9032    1.3253   -0.6904 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3580    0.1230    0.0975 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0448    0.3400    1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2380   -0.5318   -1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8938    0.8217   -0.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3934   -0.7362    0.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6364    1.6249   -0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1318   -2.6455    0.8874 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3494   -3.0070   -0.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5740   -0.9279   -1.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2327   -0.9319    1.1063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3057   -2.5487   -1.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3803   -2.9671    0.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7517   -2.7310   -0.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5387   -1.4315   -0.6676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4809   -1.8316    1.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7809    0.6244   -1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4107    0.0263   -0.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8163    2.1506    0.8059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2036    2.7395   -0.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8103    2.6098   -0.6003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4247    1.3578   -1.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039    0.3495    2.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6785    0.8866    1.9574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3485    2.0309    1.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6113    0.0231   -1.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    2.1446   -1.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438    2.1737    0.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1775    1.2530   -1.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4141    2.2308   -0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9744    0.8314    1.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9545   -0.5959    2.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2429    1.0700    1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
 23  3  1  0
 23  7  1  0
 20  8  1  0
 18 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  6
  8 32  1  1
  9 33  1  0
  9 34  1  0
 10 35  1  0
 12 36  1  6
 13 37  1  0
 14 38  1  6
 15 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 17 43  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  6
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
M  END


  Mrv1652304282223092D          

 24 27  0  0  1  0            999 V2000
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2424   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1996    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  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  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  1  0  0  0
  8 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 14 22  1  1  0  0  0
  3 23  1  1  0  0  0
  2 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0075958

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C1/C(=O)C[C@H]2[C@@H]3CC=C4[C@@H](O)[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O3/c1-4-13-18(23)11-16-12-5-6-15-19(24)17(22)8-10-21(15,3)14(12)7-9-20(13,16)2/h4,6,12,14,16-17,19,22,24H,5,7-11H2,1-3H3/b13-4+/t12-,14+,16+,17+,19-,20-,21-/m1/s1

> <INCHI_KEY>
QAKWWXLYSGFAQN-DPTUMOBZSA-N

> <FORMULA>
C21H30O3

> <MOLECULAR_WEIGHT>
330.468

> <EXACT_MASS>
330.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.4242365986481

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,5S,6R,10R,11S,14Z,15S)-14-ethylidene-5,6-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-13-one

> <ALOGPS_LOGP>
3.34

> <JCHEM_LOGP>
2.7687171883333335

> <ALOGPS_LOGS>
-3.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.091524169946556

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.500174139443896

> <JCHEM_PKA_STRONGEST_BASIC>
-3.174743836620121

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
95.86599999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.02e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,6R,10R,11S,14Z,15S)-14-ethylidene-5,6-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-13-one

> <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      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.047   1.738   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.978  -1.480   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.452  -1.269   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.791  -1.700   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.573   3.667   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      13.558   1.312   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3   24                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   15                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9    1                                                       
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19   22                                             
CONECT   15   14    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   14   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   14                                                            
CONECT   23    3                                                            
CONECT   24    2                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₃

Average Mass

330.4680 Da

Monoisotopic Mass

330.21949 Da

IUPAC Name

(1S,2R,5S,6R,10R,11S,14Z,15S)-14-ethylidene-5,6-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-13-one

Traditional Name

(1S,2R,5S,6R,10R,11S,14Z,15S)-14-ethylidene-5,6-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-13-one

CAS Registry Number

Not Available

SMILES

C\C=C1/C(=O)C[C@H]2[C@@H]3CC=C4[C@@H](O)[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C21H30O3/c1-4-13-18(23)11-16-12-5-6-15-19(24)17(22)8-10-21(15,3)14(12)7-9-20(13,16)2/h4,6,12,14,16-17,19,22,24H,5,7-11H2,1-3H3/b13-4+/t12-,14+,16+,17+,19-,20-,21-/m1/s1

InChI Key

QAKWWXLYSGFAQN-DPTUMOBZSA-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
Aglaia mariannensis	LOTUS Database	35616633
Ekebergia capensis	Plant	KNApSAcK
Melia volkensii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Androstane steroids

Direct Parent

Androgens and derivatives

Alternative Parents

Substituents

Androgen-skeleton
3-hydroxy-delta-5-steroid
3-hydroxysteroid
4-hydroxysteroid
Hydroxysteroid
16-oxosteroid
Oxosteroid
3-beta-hydroxy-delta-5-steroid
3-beta-hydroxysteroid
Delta-5-steroid
Cyclic alcohol
Ketone
1,2-diol
Secondary alcohol
Cyclic ketone
Organooxygen compound
Alcohol
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.34	ALOGPS
logP	2.77	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	13.5	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	95.87 m³·mol⁻¹	ChemAxon
Polarizability	38.42 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

C00038107

Chemspider ID

9029213

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10853920

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-(Z)-Volkendousin (NP0075958)

MOL for NP0075958 ((-)-(Z)-Volkendousin)

3D MOL for NP0075958 ((-)-(Z)-Volkendousin)

3D SDF for NP0075958 ((-)-(Z)-Volkendousin)

3D-SDF for NP0075958 ((-)-(Z)-Volkendousin)

PDB for NP0075958 ((-)-(Z)-Volkendousin)

3D PDB for NP0075958 ((-)-(Z)-Volkendousin)

SMILES for NP0075958 ((-)-(Z)-Volkendousin)

INCHI for NP0075958 ((-)-(Z)-Volkendousin)

Structure for NP0075958 ((-)-(Z)-Volkendousin)

3D Structure for NP0075958 ((-)-(Z)-Volkendousin)