NP-MRD: Showing NP-Card for (2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid (NP0179933)

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Record Information

Version

2.0

Created at

2022-09-03 18:12:22 UTC

Updated at

2022-09-03 18:12:22 UTC

NP-MRD ID

NP0179933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid

Description

2-(2,4B,6a,9,10b,12a-hexamethyl-8-oxo-1,4b,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydrochrysen-1-ylidene)acetic acid belongs to the class of organic compounds known as 16-oxosteroids. These are steroid derivatives carrying a C=O group at the 16-position of the steroid skeleton. (2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid is found in Peritassa campestris. Based on a literature review very few articles have been published on 2-(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-1,4b,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydrochrysen-1-ylidene)acetic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032220122D          

 29 32  0  0  0  0            999 V2000
   -0.1913   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7497   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2897   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0197   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8298   -3.6118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6695   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395   -4.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -1.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0787   -1.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4614   -2.2086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913   -0.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  4  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
   -5.9007    0.2700   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4066    0.0981   -0.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8405   -0.2085   -1.7356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4056   -0.4138   -1.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5766   -0.3390   -0.7959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.1648    0.5407 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3828   -1.4663    1.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3179    0.8720    1.2154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1062    1.3324    0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6887    0.1198    0.0598 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9294   -0.5770    1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1264    0.3836   -0.4140 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9546    1.1265    0.5823 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9090    0.3955    1.4373 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9566    1.4442    1.9011 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5922   -0.6240    0.6513 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8326   -0.6780    0.7086 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7941   -1.5314   -0.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7659   -0.7859   -1.0382 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7392   -0.2161   -2.1130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8704   -1.8418   -1.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4508   -1.9063   -1.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1073   -0.5493   -1.0166 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1107   -0.0348   -2.4183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5952    0.3439    0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9287    0.9938    1.6049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0513    1.6933    2.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9796    2.2357    3.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2804    1.9482    1.5403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2167    1.2462   -0.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2384   -0.4410   -1.4444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3634   -0.2006    0.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -0.3092   -2.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0488   -0.6539   -2.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4055   -1.8208    1.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1136   -1.3444    2.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7026   -2.2180    0.8666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0411    0.6674    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8822    1.8656    1.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3519    2.1200    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5660    1.8085   -0.5323 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2129   -1.1749    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8456   -1.1989    1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1814    0.2439    2.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9178    1.1593   -1.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5719    1.9102    0.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3159    1.7326    1.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    0.0309    2.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3854    1.8695    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4816    2.2044    2.5398 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7069    0.8702    2.4742 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4188   -2.4445    0.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5600   -2.0190   -0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3976    0.8164   -2.4210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7500   -0.0798   -1.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6252   -0.8415   -3.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2443   -2.8809   -1.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8743   -1.7314   -2.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1243   -2.5051   -1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4102   -2.4928   -0.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178    0.7433   -2.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1127   -0.9070   -3.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1289    0.1674   -2.7404 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.5941    2.9102    1.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
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 29 65  1  0
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 18 52  1  0
 18 53  1  0
M  END


  Mrv1652309032220122D          

 29 32  0  0  0  0            999 V2000
   -0.1913   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -1.8968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -2.2086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -2.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4796   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9395   -4.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294   -4.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3193   -4.3914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0492   -3.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -4.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8889   -1.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0787   -1.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4614   -2.2086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913   -0.8054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 13 14  1  0  0  0  0
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 10 23  1  0  0  0  0
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 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0179933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2C(C)(CCC3(C)C4=CC=C(C)C(=CC(O)=O)C4(C)CCC23C)CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O3/c1-16-7-8-20-24(4,18(16)14-22(28)29)10-12-26(6)21-13-17(2)19(27)15-23(21,3)9-11-25(20,26)5/h7-8,14,17,21H,9-13,15H2,1-6H3,(H,28,29)

> <INCHI_KEY>
YBPFFFVUQSBIIL-UHFFFAOYSA-N

> <FORMULA>
C26H36O3

> <MOLECULAR_WEIGHT>
396.571

> <EXACT_MASS>
396.266445019

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
46.35397876360223

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-1,4b,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydrochrysen-1-ylidene)acetic acid

> <JCHEM_LOGP>
5.071089678

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.769684982563785

> <JCHEM_PKA_STRONGEST_BASIC>
-7.41644357442383

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
118.10359999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.357  -5.578   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.155  -5.869   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.659  -7.324   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.171  -7.615   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.180  -6.451   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.676  -4.996   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.171  -3.541   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.684  -3.832   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.196  -4.123   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.700  -5.578   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.708  -4.414   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.212  -5.869   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.220  -4.705   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.733  -4.996   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.741  -3.832   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.237  -6.451   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.749  -6.742   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.229  -7.615   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.716  -7.324   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.220  -8.779   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.708  -8.488   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.196  -8.197   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.692  -6.742   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.684  -7.906   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.163  -4.705   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.659  -3.250   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.147  -2.959   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.861  -4.123   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.357  -1.503   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7    8   25                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   23                                             
CONECT   11   10                                                            
CONECT   12   10   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   12   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    5   10   24                                             
CONECT   24   23                                                            
CONECT   25    6    2   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
2-(2,4b,6a,9,10b,12a-Hexamethyl-8-oxo-1,4b,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydrochrysen-1-ylidene)acetate	Generator

Chemical Formula

C₂₆H₃₆O₃

Average Mass

396.5710 Da

Monoisotopic Mass

396.26645 Da

IUPAC Name

2-(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-1,4b,5,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydrochrysen-1-ylidene)acetic acid

Traditional Name

(2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid

CAS Registry Number

Not Available

SMILES

CC1CC2C(C)(CCC3(C)C4=CC=C(C)C(=CC(O)=O)C4(C)CCC23C)CC1=O

InChI Identifier

InChI=1S/C26H36O3/c1-16-7-8-20-24(4,18(16)14-22(28)29)10-12-26(6)21-13-17(2)19(27)15-23(21,3)9-11-25(20,26)5/h7-8,14,17,21H,9-13,15H2,1-6H3,(H,28,29)

InChI Key

YBPFFFVUQSBIIL-UHFFFAOYSA-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
Peritassa campestris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 16-oxosteroids. These are steroid derivatives carrying a C=O group at the 16-position of the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

16-oxosteroids

Alternative Parents

Substituents

16-hydroxysteroid
16-oxosteroid
Hydroxysteroid
Cyclic ketone
Ketone
Monocarboxylic 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	5.07	ChemAxon
pKa (Strongest Acidic)	4.77	ChemAxon
pKa (Strongest Basic)	-7.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	118.1 m³·mol⁻¹	ChemAxon
Polarizability	46.35 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

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

162986008

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid (NP0179933)

MOL for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

3D MOL for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

3D SDF for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

3D-SDF for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

PDB for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

3D PDB for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

SMILES for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

INCHI for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

Structure for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)

3D Structure for NP0179933 ((2,4b,6a,9,10b,12a-hexamethyl-8-oxo-5,6,7,9,10,10a,11,12-octahydrochrysen-1-ylidene)acetic acid)