NP-MRD: Showing NP-Card for (1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid (NP0321544)

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Record Information

Version

2.0

Created at

2022-09-11 23:48:18 UTC

Updated at

2022-09-11 23:48:18 UTC

NP-MRD ID

NP0321544

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid

Description

(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosane-5,18-dicarboxylic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid is found in Schefflera actinophylla. Based on a literature review very few articles have been published on (1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosane-5,18-dicarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122201482D          

 35 39  0  0  1  0            999 V2000
    1.9163   -2.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1279   -2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5233   -2.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7071   -1.5565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9442   -3.7263    0.0000 C   0  0  2  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  0  0  0  0  0  0  0  0  0  0
    1.0635   -5.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5685   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8925   -6.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506   -5.6171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651   -5.7765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2900   -5.7890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    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
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    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  1  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
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    6.9147   -6.2396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4238   -4.9044    0.0000 O   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  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  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  2  1  1  0  0  0
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  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 19 20  1  0  0  0  0
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 27 28  2  0  0  0  0
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 25 30  1  0  0  0  0
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 30 31  1  6  0  0  0
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 32 33  1  0  0  0  0
 19 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  1  6  0  0  0
 16 35  1  0  0  0  0
 35  5  1  6  0  0  0
  8 35  1  0  0  0  0
M  END

     RDKit          3D

 83 87  0  0  0  0  0  0  0  0999 V2000
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 11 48  1  0
M  END


  Mrv1652309122201482D          

 35 39  0  0  1  0            999 V2000
    1.9163   -2.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1279   -2.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    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  1  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
    6.9147   -6.2396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4238   -4.9044    0.0000 O   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  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  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  1  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 19 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  1  6  0  0  0
 16 35  1  0  0  0  0
 35  5  1  6  0  0  0
  8 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321544

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=C)[C@@H]1CCC2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC[C@](C)([C@@H]5CC[C@@]34C)C(O)=O)[C@@H]12)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H48O4/c1-7-19(2)20-11-16-31(26(34)35)18-17-29(5)21(24(20)31)9-10-23-27(3)13-8-14-28(4,25(32)33)22(27)12-15-30(23,29)6/h20-24H,2,7-18H2,1,3-6H3,(H,32,33)(H,34,35)/t20-,21+,22+,23+,24+,27-,28+,29+,30+,31?/m0/s1

> <INCHI_KEY>
OVMIVBJJVBSTIJ-GDQINFEWSA-N

> <FORMULA>
C31H48O4

> <MOLECULAR_WEIGHT>
484.721

> <EXACT_MASS>
484.355260026

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
56.66804040330758

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

> <JCHEM_LOGP>
7.506811410999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.0585219982947045

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.455913245713857

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
137.4282

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       3.577  -5.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.105  -5.454   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.977  -4.407   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.320  -2.905   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.762  -6.956   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.346  -7.561   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.484  -9.094   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.985  -9.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.061 -10.670   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.666 -12.086   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -0.468 -10.485   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.735 -10.783   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.275 -10.806   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.065  -9.484   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.814 -10.830   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.315  -8.139   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.105  -6.817   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.645  -6.841   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.395  -8.186   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.935  -8.209   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.185  -6.864   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.725  -6.888   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.265  -6.911   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.907 -11.647   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      13.858  -9.155   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.775  -8.116   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12   35                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   33                                             
CONECT   15   14                                                            
CONECT   16   14   17   35                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   33                                                  
CONECT   20   19   21   22   30                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   30                                             
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   20   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   19   14   34                                             
CONECT   34   33                                                            
CONECT   35   16    5    8                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(But-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0,.0,.0,]henicosane-5,18-dicarboxylate	Generator

Chemical Formula

C₃₁H₄₈O₄

Average Mass

484.7210 Da

Monoisotopic Mass

484.35526 Da

IUPAC Name

(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

Traditional Name

(1R,2R,8R,9R,10R,13R,14R,18R,19R)-8-(but-1-en-2-yl)-1,2,14,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosane-5,18-dicarboxylic acid

CAS Registry Number

Not Available

SMILES

CCC(=C)[C@@H]1CCC2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC[C@](C)([C@@H]5CC[C@@]34C)C(O)=O)[C@@H]12)C(O)=O

InChI Identifier

InChI=1S/C31H48O4/c1-7-19(2)20-11-16-31(26(34)35)18-17-29(5)21(24(20)31)9-10-23-27(3)13-8-14-28(4,25(32)33)22(27)12-15-30(23,29)6/h20-24H,2,7-18H2,1,3-6H3,(H,32,33)(H,34,35)/t20-,21+,22+,23+,24+,27-,28+,29+,30+,31?/m0/s1

InChI Key

OVMIVBJJVBSTIJ-GDQINFEWSA-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
Schefflera actinophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
18-hydroxysteroid
18-oxosteroid
Oxosteroid
Hydroxysteroid
Steroid
Dicarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	7.51	ChemAxon
pKa (Strongest Acidic)	4.46	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	137.43 m³·mol⁻¹	ChemAxon
Polarizability	56.67 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

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

162968553

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid (NP0321544)

MOL for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D MOL for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D SDF for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D-SDF for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

PDB for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D PDB for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

SMILES for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

INCHI for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

Structure for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)

3D Structure for NP0321544 ((1r,5ar,5br,7ar,8r,11ar,11br,13ar,13br)-1-(but-1-en-2-yl)-5a,5b,8,11a-tetramethyl-hexadecahydrocyclopenta[a]chrysene-3a,8-dicarboxylic acid)