NP-MRD: Showing NP-Card for methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate (NP0148870)

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Record Information

Version

2.0

Created at

2022-09-02 04:40:51 UTC

Updated at

2022-09-02 04:40:51 UTC

NP-MRD ID

NP0148870

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate

Description

Methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]Pentadecane-12-carboxylate belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. Based on a literature review very few articles have been published on methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0²,⁷.0¹²,¹⁴]Pentadecane-12-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206402D          

 28 31  0  0  1  0            999 V2000
   -1.7563   -4.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1081   -3.5631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3420   -3.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2242   -4.6858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3062   -3.3589    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2041   -2.7107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124   -2.5929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7351   -1.7089    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248   -1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310   -0.2946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9393   -3.1232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7558   -3.0054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2455   -2.3571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8786   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3889   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0827   -3.5357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8903   -3.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0570   -4.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -3.6536    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9600   -4.4196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331   -3.8893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3269   -4.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8165   -4.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103   -4.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 13  8  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  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
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    6.5701   -2.1327   -0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1808   -1.9254   -0.4289 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5406   -0.7859    0.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2745    0.1315    0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0646   -0.6622   -0.0729 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4579   -1.8902   -0.6453 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4667   -0.6421   -1.3455 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1053    0.0246   -1.4841 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2815    1.4056   -1.5738 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0421    2.2201   -2.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3043    3.6760   -2.4987 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6081    1.6919   -3.6954 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3318   -0.3520   -0.2522 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1410   -0.3560   -0.3864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6675    0.7065   -1.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5626   -1.6748   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0225   -1.8602   -1.1515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8921   -1.2278   -0.1604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2868   -0.4451    0.9453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906   -1.0456    2.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8256    0.9918    0.9873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7941   -0.4350    0.9625 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2447    0.5671    1.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    0.0726    2.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9432    0.3346    0.9224 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1782    1.7959    0.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -0.2751    1.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7603   -0.4404    2.2300 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0393   -1.2655    0.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -3.1079    0.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9254   -2.1549   -1.4574 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0574   -0.6367   -2.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6858   -0.4386   -2.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6850    4.2428   -3.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9848    4.0640   -1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3828    3.9176   -2.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6089   -1.4492   -0.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3481    1.7232   -1.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7761    0.7238   -1.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3729    0.4259   -2.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0446   -2.4681   -0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0611   -1.6497   -2.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3421   -1.4998   -2.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2052   -2.9765   -1.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5490   -2.0326    0.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6767   -0.5640   -0.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7815   -0.2455    3.0677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9537   -1.7654    2.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7013   -1.4973    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0570    1.7436    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3417    1.2348    1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6010    1.1225    0.1758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4901   -1.4470    1.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1577    1.5927    1.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8634    0.5837    2.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1458   -0.9953    2.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6053    0.7214    2.9949 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2204    2.0359    0.4534 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4163    2.3994    0.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2369    2.1952    1.8879 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  8 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  6
 25 27  1  0
 27 28  2  0
  7  5  1  0
 25 13  1  0
 27  5  1  0
 22 14  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  7 32  1  6
  8 33  1  6
 11 34  1  0
 11 35  1  0
 11 36  1  0
 13 37  1  1
 15 38  1  0
 15 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 18 45  1  0
 18 46  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  1
 23 54  1  0
 23 55  1  0
 24 56  1  0
 24 57  1  0
 26 58  1  0
 26 59  1  0
 26 60  1  0
M  END


  Mrv1652309022206402D          

 28 31  0  0  1  0            999 V2000
   -1.7563   -4.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1081   -3.5631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3420   -3.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2242   -4.6858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3062   -3.3589    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2041   -2.7107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124   -2.5929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7351   -1.7089    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248   -1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4083   -1.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5310   -0.2946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9393   -3.1232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7558   -3.0054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2455   -2.3571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8786   -2.1214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3889   -2.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0827   -3.5357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8903   -3.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0570   -4.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -3.6536    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9600   -4.4196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331   -3.8893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3269   -4.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8165   -4.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5103   -4.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 13  8  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  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
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0148870

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12O[C@H]1[C@H](OC(C)=O)[C@@H]1[C@@]3(C)CCCC(C)(C)[C@@H]3CC[C@@]1(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O6/c1-12(23)27-14-15-20(4)10-7-9-19(2,3)13(20)8-11-21(15,5)17(24)22(16(14)28-22)18(25)26-6/h13-16H,7-11H2,1-6H3/t13-,14+,15+,16-,20-,21+,22-/m0/s1

> <INCHI_KEY>
XQWPWNOLICOIOA-WSPPHXGASA-N

> <FORMULA>
C22H32O6

> <MOLECULAR_WEIGHT>
392.492

> <EXACT_MASS>
392.21988875

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.404533139639945

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecane-12-carboxylate

> <ALOGPS_LOGP>
3.53

> <JCHEM_LOGP>
3.8503116339999988

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.368720333784768

> <JCHEM_POLAR_SURFACE_AREA>
82.19999999999999

> <JCHEM_REFRACTIVITY>
100.01529999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.54e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecane-12-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.278  -7.604   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.068  -6.651   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.638  -7.223   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.418  -8.747   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.572  -6.270   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.381  -5.060   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.143  -4.840   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.239  -3.190   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.286  -1.980   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.762  -2.200   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.858  -0.550   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.620  -5.830   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.144  -5.610   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.192  -4.400   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.716  -4.180   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.240  -3.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.193  -5.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.621  -6.600   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.129  -6.915   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.573  -8.139   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.097  -6.820   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.525  -8.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.048  -7.260   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.477  -8.690   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.524  -7.480   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.953  -8.910   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   27                                             
CONECT    6    5    7                                                       
CONECT    7    6    5    8                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14   25                                                  
CONECT   14   13   15   16   22                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   14   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   13   26   27                                             
CONECT   26   25                                                            
CONECT   27   25    5   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0,.0,]pentadecane-12-carboxylic acid	Generator

Chemical Formula

C₂₂H₃₂O₆

Average Mass

392.4920 Da

Monoisotopic Mass

392.21989 Da

IUPAC Name

methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecane-12-carboxylate

Traditional Name

methyl (1R,2S,7S,10R,12S,14S,15R)-15-(acetyloxy)-2,6,6,10-tetramethyl-11-oxo-13-oxatetracyclo[8.5.0.0^{2,7}.0^{12,14}]pentadecane-12-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12O[C@H]1[C@H](OC(C)=O)[C@@H]1[C@@]3(C)CCCC(C)(C)[C@@H]3CC[C@@]1(C)C2=O

InChI Identifier

InChI=1S/C22H32O6/c1-12(23)27-14-15-20(4)10-7-9-19(2,3)13(20)8-11-21(15,5)17(24)22(16(14)28-22)18(25)26-6/h13-16H,7-11H2,1-6H3/t13-,14+,15+,16-,20-,21+,22-/m0/s1

InChI Key

XQWPWNOLICOIOA-WSPPHXGASA-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 oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

17-oxosteroid
Oxosteroid
Oxepane
Dicarboxylic acid or derivatives
Oxirane carboxylic acid
Oxirane carboxylic acid or derivatives
Methyl ester
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	3.53	ALOGPS
logP	3.85	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	82.2 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	100.02 m³·mol⁻¹	ChemAxon
Polarizability	42.4 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

10476913

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15346713

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate (NP0148870)

MOL for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

3D MOL for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

3D SDF for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

3D-SDF for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

PDB for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

3D PDB for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

SMILES for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

INCHI for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

Structure for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)

3D Structure for NP0148870 (methyl (4as,6ar,7as,8as,9r,9ar,9bs)-9-(acetyloxy)-4,4,6a,9b-tetramethyl-7-oxo-octahydro-1h-phenanthro[2,3-b]oxirene-7a-carboxylate)