NP-MRD: Showing NP-Card for (1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate (NP0251785)

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Record Information

Version

2.0

Created at

2022-09-07 15:05:00 UTC

Updated at

2022-09-07 15:05:00 UTC

NP-MRD ID

NP0251785

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate

Description

(1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-4-yl acetate belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. (1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate is found in Commiphora kua. Based on a literature review very few articles have been published on (1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-4-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072217052D          

 35 39  0  0  1  0            999 V2000
    1.7380   -3.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4577   -3.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6456   -2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9895   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092   -1.6009    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8971   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1953   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1486   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4352    0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.7255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608   -0.1943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4926    0.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850   -0.4847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0532   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3335   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020   -1.3791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0083   -2.0304    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.8256   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492   -2.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4728   -2.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3446   -3.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7313   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971   -0.6299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5214   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 15 32  1  0  0  0  0
 19 32  1  0  0  0  0
 32 33  1  1  0  0  0
 16 34  1  6  0  0  0
 35 34  1  6  0  0  0
  5 35  1  0  0  0  0
 12 35  1  0  0  0  0
 16 35  1  0  0  0  0
M  END

     RDKit          3D

 87 91  0  0  0  0  0  0  0  0999 V2000
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   -5.1990    1.7753    2.6426 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 38  1  0
M  END


  Mrv1652309072217052D          

 35 39  0  0  1  0            999 V2000
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    4.1456   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020   -1.3791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0083   -2.0304    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6974   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492   -2.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6555   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4728   -2.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3446   -3.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7313   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971   -0.6299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5214   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 15 32  1  0  0  0  0
 19 32  1  0  0  0  0
 32 33  1  1  0  0  0
 16 34  1  6  0  0  0
 35 34  1  6  0  0  0
  5 35  1  0  0  0  0
 12 35  1  0  0  0  0
 16 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251785

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CCC=C(C)C)[C@H]1CC[C@@]2(C)[C@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)[C@H](C[C@H](O)C4(C)C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H52O3/c1-20(2)10-9-11-21(3)23-14-15-30(8)25-13-12-24-28(5,6)26(34)18-27(35-22(4)33)32(24)19-31(25,32)17-16-29(23,30)7/h10,21,23-27,34H,9,11-19H2,1-8H3/t21-,23+,24-,25+,26-,27-,29+,30-,31-,32+/m0/s1

> <INCHI_KEY>
VIASXDQRTRRXGB-RQQHSQMFSA-N

> <FORMULA>
C32H52O3

> <MOLECULAR_WEIGHT>
484.765

> <EXACT_MASS>
484.391645534

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
58.89923663538504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-4-yl acetate

> <JCHEM_LOGP>
6.685182716666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.624387059819345

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9630931000350165

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
142.65659999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       3.244  -7.062   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.721  -5.614   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.205  -5.343   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.714  -4.437   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.191  -2.988   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.675  -2.717   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.151  -1.269   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.365  -0.998   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.144  -0.092   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.812   0.682   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.674   1.354   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.660  -0.363   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.653   0.815   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.169   0.544   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.692  -0.905   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.699  -2.082   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.222  -3.531   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.738  -3.802   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.731  -2.624   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.403  -4.010   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.270  -2.574   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.216  -3.790   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.635  -5.217   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.741  -3.579   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.686  -4.795   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.212  -4.585   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.157  -5.800   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.683  -5.590   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      15.577  -7.227   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.698  -1.095   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.424  -0.231   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.208  -1.176   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.839   0.319   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.707  -3.259   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.183  -1.811   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   35                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   32                                                  
CONECT   16   15   17   34   35                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   32                                             
CONECT   20   19                                                            
CONECT   21   19   22   30                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   21   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   15   19   33                                             
CONECT   33   32                                                            
CONECT   34   16   35                                                       
CONECT   35   34    5   12   16                                             
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-Hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0,.0,.0,]octadecan-4-yl acetic acid	Generator

Chemical Formula

C₃₂H₅₂O₃

Average Mass

484.7650 Da

Monoisotopic Mass

484.39165 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H](CCC=C(C)C)[C@H]1CC[C@@]2(C)[C@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)[C@H](C[C@H](O)C4(C)C)OC(C)=O

InChI Identifier

InChI=1S/C32H52O3/c1-20(2)10-9-11-21(3)23-14-15-30(8)25-13-12-24-28(5,6)26(34)18-27(35-22(4)33)32(24)19-31(25,32)17-16-29(23,30)7/h10,21,23-27,34H,9,11-19H2,1-8H3/t21-,23+,24-,25+,26-,27-,29+,30-,31-,32+/m0/s1

InChI Key

VIASXDQRTRRXGB-RQQHSQMFSA-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
Commiphora kua	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
Steroid ester
3-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
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

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

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

162950425

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate (NP0251785)

MOL for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

3D MOL for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

3D SDF for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

3D-SDF for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

PDB for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

3D PDB for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

SMILES for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

INCHI for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

Structure for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)

3D Structure for NP0251785 ((1s,3s,4s,6s,8s,11r,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2s)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-4-yl acetate)