NP-MRD: Showing NP-Card for (1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate (NP0301769)

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Record Information

Version

2.0

Created at

2022-09-10 14:55:56 UTC

Updated at

2022-09-10 14:55:56 UTC

NP-MRD ID

NP0301769

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate

Description

(1R,4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-1-yl acetate 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. (1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate is found in Salvia phlomoides. Based on a literature review very few articles have been published on (1R,4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-1-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102216552D          

 26 28  0  0  1  0            999 V2000
    4.0145    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    3.5148    3.5212    1.0324 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401    2.4014    0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    2.4029   -1.0861 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4248    1.3089    0.5981 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0478    0.2110   -0.2473 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5954    0.1839   -0.3012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1870   -0.8183    0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4957   -2.0162    0.5277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1171   -3.0483    0.8917 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9734   -2.0277    0.5979 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5423   -3.2130    1.0731 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -1.0136    0.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1698   -1.0441    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7257   -2.2811    0.9560 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -0.8534   -1.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6753   -0.8212   -0.0249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0324   -1.7948   -1.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2958   -1.2772    1.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3503   -0.3209    1.7830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3391    0.0526    0.7014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6407    0.7230   -0.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2160    0.2953   -1.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9178    2.2290   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1640    0.5619   -0.2805 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3874    1.2353   -1.3988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    1.4787   -0.8155 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    4.5064    0.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8384    3.6336    1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5582    3.4347    1.4050 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4483    0.4582   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2122   -3.7141    1.8706 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5067   -0.1841    0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8649   -2.1633    1.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6577   -3.1919    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4105   -2.4299    2.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -0.1132   -1.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8900   -0.5063   -0.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9763   -1.8580   -1.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0246   -2.2957   -0.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9589   -1.3711   -2.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2970   -2.6257   -1.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7973   -2.2514    1.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5625   -1.4022    2.0877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9470    0.5460    2.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9364   -0.9015    2.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8983   -0.8194    0.3435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0941    0.7221    1.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5543    0.3555   -2.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6965   -0.7199   -1.6080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0947    0.9614   -1.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2228    2.7014    0.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9089    2.7175   -1.3008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9550    2.3219    0.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9012    1.1588    0.6365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3690    0.6593   -2.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8512    2.2231   -1.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6066    1.9071   -1.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130    2.1655    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 15  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  7  6  2  0
  6 26  1  0
 26 25  1  0
 25 24  1  0
 24 21  1  0
 21 22  1  0
 21 23  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  6
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 12  1  0
 16  7  1  0
 16 24  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 13 32  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 11 31  1  0
 26 57  1  0
 26 58  1  0
 25 55  1  0
 25 56  1  0
 24 54  1  1
 22 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 20 46  1  0
 20 47  1  0
 19 44  1  0
 19 45  1  0
 18 42  1  0
 18 43  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
  5 30  1  6
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652309102216552D          

 26 28  0  0  1  0            999 V2000
    4.0145    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0301769

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C(O)C(=O)C2=C(CC[C@H]3C(C)(C)CCC[C@]23C)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O4/c1-12(2)16-18(24)19(25)17-14(20(16)26-13(3)23)8-9-15-21(4,5)10-7-11-22(15,17)6/h12,15,20,24H,7-11H2,1-6H3/t15-,20+,22-/m0/s1

> <INCHI_KEY>
YGQBDNLXSFXWNB-GNSUPJDDSA-N

> <FORMULA>
C22H32O4

> <MOLECULAR_WEIGHT>
360.494

> <EXACT_MASS>
360.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.16064932314727

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-1-yl acetate

> <JCHEM_LOGP>
4.257240543666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.79010008174986

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.33011279833046

> <JCHEM_PKA_STRONGEST_BASIC>
-3.641289416102965

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
102.38069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4bS,8aS)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1H-phenanthren-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       7.494   6.105   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.724   4.771   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.184   4.771   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.494   3.437   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.883   2.630   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.831   3.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    7   17   18   24                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   16   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25    6                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(1R,4BS,8AS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-1-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₂O₄

Average Mass

360.4940 Da

Monoisotopic Mass

360.23006 Da

IUPAC Name

(1R,4bS,8aS)-3-hydroxy-4b,8,8-trimethyl-4-oxo-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthren-1-yl acetate

Traditional Name

(1R,4bS,8aS)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1H-phenanthren-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C1=C(O)C(=O)C2=C(CC[C@H]3C(C)(C)CCC[C@]23C)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C22H32O4/c1-12(2)16-18(24)19(25)17-14(20(16)26-13(3)23)8-9-15-21(4,5)10-7-11-22(15,17)6/h12,15,20,24H,7-11H2,1-6H3/t15-,20+,22-/m0/s1

InChI Key

YGQBDNLXSFXWNB-GNSUPJDDSA-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
Salvia phlomoides	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

Abietane diterpenoid
Diterpenoid
12-hydroxysteroid
Hydroxysteroid
11-oxosteroid
16-oxosteroid
Hydrophenanthrene
Phenanthrene
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	4.26	ChemAxon
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.38 m³·mol⁻¹	ChemAxon
Polarizability	41.16 Å³	ChemAxon
Number of Rings	3	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

162872613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate (NP0301769)

MOL for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

3D MOL for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

3D SDF for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

3D-SDF for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

PDB for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

3D PDB for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

SMILES for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

INCHI for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

Structure for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)

3D Structure for NP0301769 ((1r,4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-4-oxo-5,6,7,8a,9,10-hexahydro-1h-phenanthren-1-yl acetate)