NP-MRD: Showing NP-Card for (3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one (NP0155325)

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Record Information

Version

2.0

Created at

2022-09-02 12:21:33 UTC

Updated at

2022-09-02 12:21:33 UTC

NP-MRD ID

NP0155325

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one

Description

(3S,4aS,4bR,7R,8aR,10aR)-3-[(1R)-2-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-tetradecahydrophenanthren-2-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one is found in Ceriops tagal. Based on a literature review very few articles have been published on (3S,4aS,4bR,7R,8aR,10aR)-3-[(1R)-2-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-tetradecahydrophenanthren-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214212D          

 43 48  0  0  1  0            999 V2000
    0.9839   -4.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8407   -5.5609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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  5  6  1  0  0  0  0
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  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
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  9 38  1  0  0  0  0
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 42 41  1  6  0  0  0
  7 42  1  0  0  0  0
 42 43  1  0  0  0  0
  3 43  1  0  0  0  0
M  END

     RDKit          3D

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  3  4  1  0
  3 43  1  0
 43 42  1  0
 42 41  1  0
 41 40  1  0
 40 38  1  0
 38 39  1  1
 38 36  1  0
 36 37  2  3
 36 34  1  0
 34 35  2  0
  3  2  1  1
  2  1  2  3
 22 23  1  0
 34 11  1  0
 22 29  1  0
 38  9  1  0
 19 31  1  0
 42  7  1  0
 24 72  1  0
 24 73  1  0
 24 74  1  0
 25 75  1  0
 25 76  1  0
 25 77  1  0
 26 78  1  0
 26 79  1  0
 27 80  1  0
 27 81  1  0
 28 82  1  0
 28 83  1  0
 30 84  1  0
 30 85  1  0
 30 86  1  0
 31 87  1  6
 32 88  1  0
 32 89  1  0
 33 90  1  0
 33 91  1  0
 17 63  1  0
 17 64  1  0
 17 65  1  0
 18 66  1  0
 20 67  1  0
 20 68  1  0
 21 69  1  0
 21 70  1  0
 22 71  1  6
 12 61  1  1
 13 62  1  0
 11 60  1  6
 10 58  1  0
 10 59  1  0
  9 57  1  1
  8 54  1  0
  8 55  1  0
  8 56  1  0
  6 52  1  0
  6 53  1  0
  5 50  1  0
  5 51  1  0
  4 47  1  0
  4 48  1  0
  4 49  1  0
 43102  1  0
 43103  1  0
 42101  1  6
 41 99  1  0
 41100  1  0
 40 97  1  0
 40 98  1  0
 39 94  1  0
 39 95  1  0
 39 96  1  0
 37 92  1  0
 37 93  1  0
  2 46  1  0
  1 44  1  0
  1 45  1  0
M  END


  Mrv1652309022214212D          

 43 48  0  0  1  0            999 V2000
    0.9839   -4.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8407   -5.5609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4727   -6.0912    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8407   -6.6215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8852   -5.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7102   -5.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227   -6.0912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5352   -5.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9477   -6.0912    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3602   -5.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1852   -5.3767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5977   -4.6622    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1852   -3.9478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4227   -4.6622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8352   -5.3767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8352   -3.9478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4671   -4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0599   -3.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9166   -2.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414   -2.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -1.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6301   -1.2282    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4869   -0.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7116   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0744    0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1189    0.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8941   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0374   -0.9801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4054   -1.5104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1806   -1.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5486   -2.3228    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3239   -2.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4671   -3.4175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5977   -6.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4227   -6.0912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1852   -6.8057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5977   -7.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3602   -6.8057    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7727   -7.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9477   -7.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227   -7.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7102   -6.8057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8852   -6.8057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  6  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 19  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 16 33  1  0  0  0  0
 11 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  9 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 41  1  6  0  0  0
  7 42  1  0  0  0  0
 42 43  1  0  0  0  0
  3 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155325

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC[C@@]2(C)[C@@H]3CC[C@@](C)(C=C3CC[C@H]12)C(=O)[C@H](O)[C@@H]1C[C@H]2[C@]3(C)CC[C@](C)(C[C@H]3CC[C@@]2(C)C(=C)C1=O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C40H60O3/c1-10-36(5)20-21-39(8)27(24-36)14-19-38(7)25(2)32(41)28(22-31(38)39)33(42)34(43)37(6)18-15-29-26(23-37)12-13-30-35(3,4)16-11-17-40(29,30)9/h10,23,27-31,33,42H,1-2,11-22,24H2,3-9H3/t27-,28-,29-,30-,31-,33-,36-,37+,38+,39-,40+/m1/s1

> <INCHI_KEY>
HABLYLGYDIJAPY-SIUSXJPSSA-N

> <FORMULA>
C40H60O3

> <MOLECULAR_WEIGHT>
588.917

> <EXACT_MASS>
588.454245792

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
70.84307398259901

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4aS,4bR,7R,8aR,10aR)-3-[(1R)-2-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydrophenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-tetradecahydrophenanthren-2-one

> <ALOGPS_LOGP>
6.35

> <JCHEM_LOGP>
9.697872143999998

> <ALOGPS_LOGS>
-7.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.200286715859136

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.949646323728178

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6943008107994766

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
177.0145

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.48e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aS,4bR,7R,8aR,10aR)-3-[(1R)-2-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3H-phenanthren-2-one

> <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       1.837  -8.864   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.569 -10.380   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.749 -11.370   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.569 -12.360   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.519 -10.037   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.059 -10.037   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.829 -11.370   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.599 -10.037   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.369 -11.370   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.139 -10.037   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.679 -10.037   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.449  -8.703   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.679  -7.369   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.989  -8.703   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.759 -10.037   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      12.759  -7.369   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.939  -8.359   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.312  -6.842   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.044  -5.326   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.597  -4.799   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.330  -3.283   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.510  -2.293   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.242  -0.776   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.795  -1.303   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.472   0.558   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.422   0.214   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.869  -0.313   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.136  -1.829   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.957  -2.819   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.404  -3.346   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.224  -4.336   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.671  -4.863   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.939  -6.379   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.449 -11.370   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      11.989 -11.370   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       9.679 -12.704   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.449 -14.038   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.139 -12.704   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.909 -14.038   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.369 -14.038   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.829 -14.038   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.059 -12.704   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.519 -12.704   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   43                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   42                                             
CONECT    8    7                                                            
CONECT    9    7   10   38                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   34                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   33                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   31                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   22   30   31                                             
CONECT   30   29                                                            
CONECT   31   29   19   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   16                                                       
CONECT   34   11   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36    9   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41    7   43                                                  
CONECT   43   42    3                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₆₀O₃

Average Mass

588.9170 Da

Monoisotopic Mass

588.45425 Da

IUPAC Name

Traditional Name

(3S,4aS,4bR,7R,8aR,10aR)-3-[(1R)-2-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3H-phenanthren-2-one

CAS Registry Number

Not Available

SMILES

CC1(C)CCC[C@@]2(C)[C@@H]3CC[C@@](C)(C=C3CC[C@H]12)C(=O)[C@H](O)[C@@H]1C[C@H]2[C@]3(C)CC[C@](C)(C[C@H]3CC[C@@]2(C)C(=C)C1=O)C=C

InChI Identifier

InChI=1S/C40H60O3/c1-10-36(5)20-21-39(8)27(24-36)14-19-38(7)25(2)32(41)28(22-31(38)39)33(42)34(43)37(6)18-15-29-26(23-37)12-13-30-35(3,4)16-11-17-40(29,30)9/h10,23,27-31,33,42H,1-2,11-22,24H2,3-9H3/t27-,28-,29-,30-,31-,33-,36-,37+,38+,39-,40+/m1/s1

InChI Key

HABLYLGYDIJAPY-SIUSXJPSSA-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
Ceriops tagal	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
18-oxosteroid
Oxosteroid
Steroid
Phenanthrene
Hydrophenanthrene
Acyloin
Alpha-hydroxy ketone
Cyclic ketone
Secondary alcohol
Ketone
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Alcohol
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	6.35	ALOGPS
logP	9.7	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	12.95	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	177.01 m³·mol⁻¹	ChemAxon
Polarizability	70.84 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162999483

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one (NP0155325)

MOL for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

3D MOL for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

3D SDF for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

3D-SDF for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

PDB for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

3D PDB for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

SMILES for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

INCHI for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

Structure for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)

3D Structure for NP0155325 ((3s,4as,4br,7r,8ar,10ar)-3-[(1r)-2-[(2s,4ar,4br,8ar)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3h-phenanthren-2-yl]-1-hydroxy-2-oxoethyl]-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-octahydro-3h-phenanthren-2-one)