NP-MRD: Showing NP-Card for (3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate (NP0292351)

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Record Information

Version

2.0

Created at

2022-09-09 23:50:14 UTC

Updated at

2022-09-09 23:50:14 UTC

NP-MRD ID

NP0292351

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate

Description

6Alpha,16beta-diacetoxy-hopan-22-ol belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30). Thus, 6alpha,16beta-diacetoxy-hopan-22-ol is considered to be a hopanoid. (3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate is found in Physcia aipolia. Based on a literature review very few articles have been published on 6alpha,16beta-diacetoxy-hopan-22-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102201502D          

 39 43  0  0  1  0            999 V2000
    1.0200   -7.9134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4433   -7.2053    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
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
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 21 18  1  6  0  0  0
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 39 34  1  1  0  0  0
  5 39  1  0  0  0  0
 30 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102201502D          

 39 43  0  0  1  0            999 V2000
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    2.2900   -5.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7133   -5.0809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1149   -5.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3117   -4.3603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7350   -3.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5599   -3.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -4.3853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7864   -4.3979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3848   -3.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2097   -3.6898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0346   -3.7023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4362   -4.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0129   -5.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8573   -5.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7838   -5.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1880   -5.1186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7647   -5.8267    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1663   -6.5473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7430   -7.2554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1445   -7.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9181   -7.2429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9398   -5.8141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -5.0935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6119   -5.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4868   -4.3477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8338   -3.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9442   -3.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1855   -4.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2592   -4.8720    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3622   -5.4147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9836   -5.9573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9048   -4.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1804   -6.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0635   -5.0558    0.0000 C   0  0  2  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  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  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
 18 20  1  0  0  0  0
 21 18  1  6  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 12 28  1  0  0  0  0
  7 28  1  0  0  0  0
 28 29  1  6  0  0  0
  9 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 38  1  0  0  0  0
 39 34  1  1  0  0  0
  5 39  1  0  0  0  0
 30 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292351

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@]2(C)[C@H](CC[C@@H]3[C@@]4(C)CCCC(C)(C)[C@@H]4[C@H](C[C@@]23C)OC(C)=O)[C@@]2(C)CC[C@@H]([C@H]12)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C34H56O5/c1-20(35)38-23-18-33(9)25(31(7)17-14-22(27(23)31)30(5,6)37)12-13-26-32(8)16-11-15-29(3,4)28(32)24(39-21(2)36)19-34(26,33)10/h22-28,37H,11-19H2,1-10H3/t22-,23-,24-,25+,26+,27+,28-,31+,32+,33+,34+/m0/s1

> <INCHI_KEY>
RPKCITIBMZPVBD-VQAWAFHESA-N

> <FORMULA>
C34H56O5

> <MOLECULAR_WEIGHT>
544.817

> <EXACT_MASS>
544.412774903

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
64.91758702392104

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4S,5S,6S,9R,10R,13R,14R,19S,20S)-20-(acetyloxy)-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-4-yl acetate

> <JCHEM_LOGP>
5.898063630666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.054622455864358

> <JCHEM_PKA_STRONGEST_BASIC>
-2.77490813780493

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
152.86240000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4S,5S,6S,9R,10R,13R,14R,19S,20S)-20-(acetyloxy)-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       1.904 -14.772   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.694 -13.450   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.234 -13.473   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.945 -12.105   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.735 -10.783   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.275 -10.806   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.065  -9.484   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.814 -10.830   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.315  -8.139   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.105  -6.817   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.645  -6.841   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.395  -8.186   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.935  -8.209   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.185  -6.864   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.725  -6.888   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.265  -6.911   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.644 -12.222   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.854 -13.544   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.603 -14.889   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.314 -13.520   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.775  -8.116   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.423  -6.719   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.762  -6.956   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.346  -7.561   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.484  -9.094   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.676 -10.107   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.836 -11.120   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.689  -8.947   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.337 -11.267   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.985  -9.438   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   39                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   28                                             
CONECT    8    7                                                            
CONECT    9    7   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12   14   15   21                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   13   22                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28                                                       
CONECT   28   27   12    7   29                                             
CONECT   29   28                                                            
CONECT   30    9   31   32   39                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   35                                                            
CONECT   39   34    5   30                                                  
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
6a,16b-Diacetoxy-hopan-22-ol	Generator
6Α,16β-diacetoxy-hopan-22-ol	Generator

Chemical Formula

C₃₄H₅₆O₅

Average Mass

544.8170 Da

Monoisotopic Mass

544.41277 Da

IUPAC Name

(1R,2R,4S,5S,6S,9R,10R,13R,14R,19S,20S)-20-(acetyloxy)-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-4-yl acetate

Traditional Name

(1R,2R,4S,5S,6S,9R,10R,13R,14R,19S,20S)-20-(acetyloxy)-6-(2-hydroxypropan-2-yl)-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-4-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@]2(C)[C@H](CC[C@@H]3[C@@]4(C)CCCC(C)(C)[C@@H]4[C@H](C[C@@]23C)OC(C)=O)[C@@]2(C)CC[C@@H]([C@H]12)C(C)(C)O

InChI Identifier

InChI=1S/C34H56O5/c1-20(35)38-23-18-33(9)25(31(7)17-14-22(27(23)31)30(5,6)37)12-13-26-32(8)16-11-15-29(3,4)28(32)24(39-21(2)36)19-34(26,33)10/h22-28,37H,11-19H2,1-10H3/t22-,23-,24-,25+,26+,27+,28-,31+,32+,33+,34+/m0/s1

InChI Key

RPKCITIBMZPVBD-VQAWAFHESA-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
Physcia aipolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

Alternative Parents

Substituents

Hopane-skeleton
Triterpenoid
20-hydroxysteroid
Steroid ester
Hydroxysteroid
Steroid
Dicarboxylic acid or derivatives
Tertiary alcohol
Carboxylic acid ester
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
logP	5.9	ChemAxon
pKa (Strongest Acidic)	15.05	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	152.86 m³·mol⁻¹	ChemAxon
Polarizability	64.92 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

10197954

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21582910

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate (NP0292351)

MOL for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

3D MOL for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

3D SDF for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

3D-SDF for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

PDB for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

3D PDB for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

SMILES for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

INCHI for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

Structure for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)

3D Structure for NP0292351 ((3s,3as,4s,5ar,5br,7s,7as,11ar,11br,13ar,13br)-7-(acetyloxy)-3-(2-hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-4-yl acetate)