NP-MRD: Showing NP-Card for 1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid (NP0256866)

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Record Information

Version

2.0

Created at

2022-09-07 21:49:47 UTC

Updated at

2022-09-07 21:49:48 UTC

NP-MRD ID

NP0256866

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid

Description

14-Acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-ene-6-carboxylic acid belongs to the class of organic compounds known as 20-oxosteroids. These are steroid derivatives carrying a C=O group at the 20-position of the steroid skeleton. Based on a literature review very few articles have been published on 14-acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-ene-6-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223492D          

 27 30  0  0  0  0            999 V2000
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539    1.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6857    2.5951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4978    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  8 27  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    6.0590    1.0251    0.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8175    0.7679    0.8838 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6630    1.4204    1.8983 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8881   -0.2459    0.3659 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3688    0.0899   -1.0330 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2954   -0.9976   -1.1657 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7533   -1.1771    0.2593 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3062   -0.8774    0.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1251    0.3023    0.5343 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396    1.2485    1.3277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0963    1.0300    1.4103 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5849   -0.3356    1.1316 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9022   -1.1143    2.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5142    0.6251    0.0299 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3973    0.7423   -1.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0516    1.8916    0.5919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4097    2.1655   -0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2308    0.9544   -0.2735 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3708    0.5247   -1.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7730   -0.1575    0.6895 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7602   -1.2355    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6463   -2.4234    0.4133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0591   -0.8668    1.1351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3474   -0.5240    0.5543 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0226   -1.8221   -0.0706 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6515   -2.0918   -1.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5619   -2.0085   -0.2328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3605    2.0809    0.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9500    0.7190   -0.9542 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8947    0.4150    0.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3539   -1.2530    0.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1373   -0.0257   -1.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9437    1.0979   -1.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7290   -1.9204   -1.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246   -0.5882   -1.8490 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9428   -2.2475    0.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    2.2949    0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1794    1.3115    2.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4151    1.2844    2.4667 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6215    1.7983    0.7891 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4758   -0.4908    3.1158 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9604   -1.5036    2.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5179   -1.9766    2.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3274    0.9236   -1.7717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9038    1.6740   -1.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7425   -0.0873   -2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    1.7761    1.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4193    2.7939    0.3511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3150    2.8359   -0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9286    2.8362    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2863    1.1691    0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7746   -0.3678   -1.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9164    0.3781    1.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6284   -0.3028    0.5298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9729   -0.6645    1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622   -2.6477    0.6308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817   -3.0688   -1.4041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1659   -2.9207    0.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2990   -2.2338   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
  9 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 20 21  1  0
 21 23  1  0
 21 22  2  0
 12  4  1  0
 24 14  1  0
 12  7  1  0
 27  8  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  6
  5 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  1
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 15 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  1
 19 52  1  0
 20 53  1  1
 24 55  1  1
 25 56  1  1
 26 57  1  0
 27 58  1  0
 27 59  1  0
 23 54  1  0
M  END


  Mrv1652309072223492D          

 27 30  0  0  0  0            999 V2000
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539    1.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6857    2.5951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4978    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  8 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256866

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C1CCC2C3=C(CCC12C)C1(C)CCC(O)C(C1C(O)C3)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-11(23)13-4-5-14-12-10-17(25)19-18(20(26)27)16(24)7-9-22(19,3)15(12)6-8-21(13,14)2/h13-14,16-19,24-25H,4-10H2,1-3H3,(H,26,27)

> <INCHI_KEY>
WQQALAOCZONREL-UHFFFAOYSA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.81423657042568

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-ene-6-carboxylic acid

> <JCHEM_LOGP>
1.6075878043333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.597350385297112

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.51761646911912

> <JCHEM_PKA_STRONGEST_BASIC>
-2.877649016945883

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
101.16849999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
14-acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-ene-6-carboxylic acid

> <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      11.407  -1.269   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.882  -1.480   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.302  -2.907   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.069  -1.700   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.373  -0.949   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.698   1.312   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.287   3.667   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.280   4.844   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.229   3.938   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.319   3.125   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.796   4.573   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.835   2.854   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    4    7   13                                             
CONECT   13   12                                                            
CONECT   14    9   15   16   24                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   20   14   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    8                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
14-Acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadec-1(10)-ene-6-carboxylate	Generator

Chemical Formula

C₂₂H₃₂O₅

Average Mass

376.4930 Da

Monoisotopic Mass

376.22497 Da

IUPAC Name

14-acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-ene-6-carboxylic acid

Traditional Name

14-acetyl-5,8-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-ene-6-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=O)C1CCC2C3=C(CCC12C)C1(C)CCC(O)C(C1C(O)C3)C(O)=O

InChI Identifier

InChI=1S/C22H32O5/c1-11(23)13-4-5-14-12-10-17(25)19-18(20(26)27)16(24)7-9-22(19,3)15(12)6-8-21(13,14)2/h13-14,16-19,24-25H,4-10H2,1-3H3,(H,26,27)

InChI Key

WQQALAOCZONREL-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 20-oxosteroids. These are steroid derivatives carrying a C=O group at the 20-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

20-oxosteroids

Alternative Parents

Substituents

20-oxosteroid
4-carboxy steroid
Steroid acid
Androgen-skeleton
Androstane-skeleton
7-hydroxysteroid
Hydroxysteroid
15-hydroxysteroid
6-hydroxysteroid
3-hydroxysteroid
Beta-hydroxy acid
Hydroxy acid
Cyclic alcohol
Secondary alcohol
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	1.61	ChemAxon
pKa (Strongest Acidic)	4.52	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	101.17 m³·mol⁻¹	ChemAxon
Polarizability	41.81 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

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

163054809

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid (NP0256866)

MOL for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

3D MOL for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

3D SDF for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

3D-SDF for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

PDB for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

3D PDB for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

SMILES for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

INCHI for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

Structure for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)

3D Structure for NP0256866 (1-acetyl-5,7-dihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,4h,5h,5ah,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-6-carboxylic acid)