NP-MRD: Showing NP-Card for 3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one (NP0028626)

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Record Information

Version

2.0

Created at

2021-06-19 20:27:48 UTC

Updated at

2021-06-29 23:55:31 UTC

NP-MRD ID

NP0028626

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one

Provided By

JEOL Database JEOL Logo

Description

3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one is found in Croton joufra. 3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one was first documented in 2001 (Sutthivaiyakit, S., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122273D          

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  Mrv1652306192122273D          

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    3.0463   -5.5500   -1.5551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760   -4.8015   -2.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -2.5434   -1.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569   -3.1975   -0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479   -1.9178    1.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092   -0.8544   -0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1403   -3.4003   -2.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4984   -4.3515   -0.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -1.0605    1.5246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0161   -0.4517    0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3802    1.0762    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2902   -0.8325    2.8307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3313   -1.4744    2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130    0.2115    3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356    1.7463    1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3970    0.6805    1.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7851    1.1067   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1593    2.5769   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1315    2.8932   -1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    4.0251    0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142   -0.1107   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7981    1.0934   -3.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6421   -0.2720   -2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6739    2.5322   -0.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    1.2411   -1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6308    5.2032   -3.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2711    3.9188   -4.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759    5.0637   -3.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 20  1  0  0  0  0
 10  8  1  0  0  0  0
  7  8  2  0  0  0  0
 18 19  1  0  0  0  0
 14 15  1  1  0  0  0
 14  7  1  0  0  0  0
  3  2  1  1  0  0  0
 13 14  1  0  0  0  0
  2  1  2  3  0  0  0
  3  9  1  0  0  0  0
 13 12  1  0  0  0  0
 20 22  1  6  0  0  0
 12 10  1  0  0  0  0
 20 21  1  0  0  0  0
  7  6  1  0  0  0  0
 10 11  2  0  0  0  0
  8  9  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
 22 23  1  0  0  0  0
  5  6  1  0  0  0  0
 23 24  1  0  0  0  0
 13 20  1  0  0  0  0
 24 25  1  0  0  0  0
 14 16  1  0  0  0  0
 24 26  2  0  0  0  0
 12 39  1  0  0  0  0
 12 40  1  0  0  0  0
  5 33  1  0  0  0  0
  5 34  1  0  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
 13 41  1  1  0  0  0
 16 45  1  0  0  0  0
 16 46  1  0  0  0  0
 17 47  1  0  0  0  0
 17 48  1  0  0  0  0
 18 49  1  6  0  0  0
 15 42  1  0  0  0  0
 15 43  1  0  0  0  0
 15 44  1  0  0  0  0
 19 50  1  0  0  0  0
  9 37  1  0  0  0  0
  9 38  1  0  0  0  0
  2 29  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
 22 54  1  0  0  0  0
 22 55  1  0  0  0  0
 21 51  1  0  0  0  0
 21 52  1  0  0  0  0
 21 53  1  0  0  0  0
  4 30  1  0  0  0  0
  4 31  1  0  0  0  0
  4 32  1  0  0  0  0
 25 56  1  0  0  0  0
 25 57  1  0  0  0  0
 25 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0028626

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C(=O)C([H])([H])[C@]2([H])[C@@]1(C([H])([H])[H])C([H])([H])OC(=O)C([H])([H])[H])C([H])([H])[C@@](C([H])=C([H])[H])(C([H])([H])[H])C([H])([H])C3([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O4/c1-6-20(3)9-7-16-15(12-20)17(24)11-18-21(16,4)10-8-19(25)22(18,5)13-26-14(2)23/h6,18-19,25H,1,7-13H2,2-5H3/t18-,19-,20+,21+,22+/m0/s1

> <INCHI_KEY>
VOMKERLMONTVKI-VNXMGFANSA-N

> <FORMULA>
C22H32O4

> <MOLECULAR_WEIGHT>
360.494

> <EXACT_MASS>
360.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.67666163698153

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,2S,4aS,7R,10aS)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-9-oxo-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthren-1-yl]methyl acetate

> <ALOGPS_LOGP>
3.24

> <JCHEM_LOGP>
3.094093980666667

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.998747103018896

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.628483049661451

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9612826620501584

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
101.48589999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.46e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,4aS,7R,10aS)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-9-oxo-2,3,4,5,6,8,10,10a-octahydrophenanthren-1-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    0.8932   -4.8960    1.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8288   -4.6964    0.6941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543   -4.0846   -0.6968 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0267   -5.1798   -1.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6187   -2.8951   -0.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -1.7194    0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7780   -1.4035    0.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1299   -2.2654   -0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305   -3.5684   -1.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5967   -2.0003   -0.2282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4130   -2.7996   -0.6863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0652   -0.7623    0.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0424    0.3842    0.4865 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3649   -0.1452    0.9513 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2945   -0.5874    2.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3877    1.0220    0.9070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4295    1.7624   -0.4241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0610    2.3458   -0.7634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2768    3.3018    0.2461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0490    1.2587   -0.8437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8284    0.4396   -2.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4330    1.9734   -0.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4207    2.8781   -2.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5776    3.5747   -2.2737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4477    4.4979   -3.4460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5823    3.4695   -1.5851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -4.6298    1.4949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1575   -5.3488    2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8447   -5.0114    0.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456   -6.0361   -1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0463   -5.5500   -1.5551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760   -4.8015   -2.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -2.5434   -1.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569   -3.1975   -0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479   -1.9178    1.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092   -0.8544   -0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1403   -3.4003   -2.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4984   -4.3515   -0.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -1.0605    1.5246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0161   -0.4517    0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3802    1.0762    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2902   -0.8325    2.8307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3313   -1.4744    2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130    0.2115    3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356    1.7463    1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3970    0.6805    1.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7851    1.1067   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1593    2.5769   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1315    2.8932   -1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    4.0251    0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142   -0.1107   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7981    1.0934   -3.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6421   -0.2720   -2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6739    2.5322   -0.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    1.2411   -1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6308    5.2032   -3.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2711    3.9188   -4.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759    5.0637   -3.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  1  0
 17 18  1  0
 18 20  1  0
 10  8  1  0
  7  8  2  0
 18 19  1  0
 14 15  1  1
 14  7  1  0
  3  2  1  1
 13 14  1  0
  2  1  2  3
  3  9  1  0
 13 12  1  0
 20 22  1  6
 12 10  1  0
 20 21  1  0
  7  6  1  0
 10 11  2  0
  8  9  1  0
  3  4  1  0
  3  5  1  0
 22 23  1  0
  5  6  1  0
 23 24  1  0
 13 20  1  0
 24 25  1  0
 14 16  1  0
 24 26  2  0
 12 39  1  0
 12 40  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
 13 41  1  1
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  6
 15 42  1  0
 15 43  1  0
 15 44  1  0
 19 50  1  0
  9 37  1  0
  9 38  1  0
  2 29  1  0
  1 27  1  0
  1 28  1  0
 22 54  1  0
 22 55  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
  4 30  1  0
  4 31  1  0
  4 32  1  0
 25 56  1  0
 25 57  1  0
 25 58  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       0.893  -4.896   1.633  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.829  -4.696   0.694  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.654  -4.085  -0.697  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.027  -5.180  -1.716  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.619  -2.895  -0.857  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.262  -1.719   0.061  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.778  -1.403   0.163  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.130  -2.265  -0.350  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.231  -3.568  -1.028  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.597  -2.000  -0.228  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.413  -2.800  -0.686  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.065  -0.762   0.494  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.042   0.384   0.487  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.365  -0.145   0.951  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.295  -0.587   2.442  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.388   1.022   0.907  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.430   1.762  -0.424  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.061   2.346  -0.763  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.277   3.302   0.246  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.049   1.259  -0.844  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.828   0.440  -2.137  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.433   1.973  -0.984  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.421   2.878  -2.103  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.578   3.575  -2.274  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.448   4.498  -3.446  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.582   3.470  -1.585  0.00  0.00           O+0
HETATM   27  H   UNK     0      -0.149  -4.630   1.495  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.157  -5.349   2.584  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.845  -5.011   0.938  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.346  -6.036  -1.644  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.046  -5.550  -1.555  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.976  -4.801  -2.744  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.594  -2.543  -1.898  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.657  -3.197  -0.666  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.648  -1.918   1.068  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.809  -0.854  -0.327  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.140  -3.400  -2.111  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.498  -4.351  -0.785  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.292  -1.061   1.525  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.016  -0.452   0.055  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.380   1.076   1.274  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.290  -0.833   2.831  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.331  -1.474   2.589  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.113   0.212   3.072  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.136   1.746   1.695  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.397   0.681   1.165  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.785   1.107  -1.224  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.159   2.577  -0.336  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.132   2.893  -1.711  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.372   4.025   0.193  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.114  -0.111  -2.136  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.798   1.093  -3.017  0.00  0.00           H+0
HETATM   53  H   UNK     0      -1.642  -0.272  -2.308  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.674   2.532  -0.071  0.00  0.00           H+0
HETATM   55  H   UNK     0      -3.228   1.241  -1.161  0.00  0.00           H+0
HETATM   56  H   UNK     0      -2.631   5.203  -3.274  0.00  0.00           H+0
HETATM   57  H   UNK     0      -3.271   3.919  -4.356  0.00  0.00           H+0
HETATM   58  H   UNK     0      -4.376   5.064  -3.567  0.00  0.00           H+0
CONECT    1    2   27   28                                                  
CONECT    2    3    1   29                                                  
CONECT    3    2    9    4    5                                             
CONECT    4    3   30   31   32                                             
CONECT    5    3    6   33   34                                             
CONECT    6    7    5   35   36                                             
CONECT    7    8   14    6                                                  
CONECT    8   10    7    9                                                  
CONECT    9    3    8   37   38                                             
CONECT   10    8   12   11                                                  
CONECT   11   10                                                            
CONECT   12   13   10   39   40                                             
CONECT   13   14   12   20   41                                             
CONECT   14   15    7   13   16                                             
CONECT   15   14   42   43   44                                             
CONECT   16   17   14   45   46                                             
CONECT   17   16   18   47   48                                             
CONECT   18   17   20   19   49                                             
CONECT   19   18   50                                                       
CONECT   20   18   22   21   13                                             
CONECT   21   20   51   52   53                                             
CONECT   22   20   23   54   55                                             
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24   56   57   58                                             
CONECT   26   24                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    4                                                            
CONECT   31    4                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    9                                                            
CONECT   38    9                                                            
CONECT   39   12                                                            
CONECT   40   12                                                            
CONECT   41   13                                                            
CONECT   42   15                                                            
CONECT   43   15                                                            
CONECT   44   15                                                            
CONECT   45   16                                                            
CONECT   46   16                                                            
CONECT   47   17                                                            
CONECT   48   17                                                            
CONECT   49   18                                                            
CONECT   50   19                                                            
CONECT   51   21                                                            
CONECT   52   21                                                            
CONECT   53   21                                                            
CONECT   54   22                                                            
CONECT   55   22                                                            
CONECT   56   25                                                            
CONECT   57   25                                                            
CONECT   58   25                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  120    0
END

RDKit          3D

58 60  0  0  0  0  0  0  0  0999 V2000
    0.8932   -4.8960    1.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8288   -4.6964    0.6941 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543   -4.0846   -0.6968 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0267   -5.1798   -1.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6187   -2.8951   -0.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -1.7194    0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7780   -1.4035    0.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1299   -2.2654   -0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305   -3.5684   -1.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5967   -2.0003   -0.2282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4130   -2.7996   -0.6863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0652   -0.7623    0.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0424    0.3842    0.4865 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3649   -0.1452    0.9513 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2945   -0.5874    2.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3877    1.0220    0.9070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4295    1.7624   -0.4241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0610    2.3458   -0.7634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2768    3.3018    0.2461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0490    1.2587   -0.8437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8284    0.4396   -2.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4330    1.9734   -0.9836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4207    2.8781   -2.1028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5776    3.5747   -2.2737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4477    4.4979   -3.4460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5823    3.4695   -1.5851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -4.6298    1.4949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1575   -5.3488    2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8447   -5.0114    0.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3456   -6.0361   -1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0463   -5.5500   -1.5551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760   -4.8015   -2.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5937   -2.5434   -1.8981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569   -3.1975   -0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479   -1.9178    1.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092   -0.8544   -0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1403   -3.4003   -2.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4984   -4.3515   -0.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -1.0605    1.5246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0161   -0.4517    0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3802    1.0762    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2902   -0.8325    2.8307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3313   -1.4744    2.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130    0.2115    3.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356    1.7463    1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3970    0.6805    1.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7851    1.1067   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1593    2.5769   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1315    2.8932   -1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3724    4.0251    0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142   -0.1107   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7981    1.0934   -3.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6421   -0.2720   -2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6739    2.5322   -0.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    1.2411   -1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6308    5.2032   -3.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2711    3.9188   -4.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759    5.0637   -3.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  1  0
 17 18  1  0
 18 20  1  0
 10  8  1  0
  7  8  2  0
 18 19  1  0
 14 15  1  1
 14  7  1  0
  3  2  1  1
 13 14  1  0
  2  1  2  3
  3  9  1  0
 13 12  1  0
 20 22  1  6
 12 10  1  0
 20 21  1  0
  7  6  1  0
 10 11  2  0
  8  9  1  0
  3  4  1  0
  3  5  1  0
 22 23  1  0
  5  6  1  0
 23 24  1  0
 13 20  1  0
 24 25  1  0
 14 16  1  0
 24 26  2  0
 12 39  1  0
 12 40  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
 13 41  1  1
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  6
 15 42  1  0
 15 43  1  0
 15 44  1  0
 19 50  1  0
  9 37  1  0
  9 38  1  0
  2 29  1  0
  1 27  1  0
  1 28  1  0
 22 54  1  0
 22 55  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
  4 30  1  0
  4 31  1  0
  4 32  1  0
 25 56  1  0
 25 57  1  0
 25 58  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₄

Average Mass

360.4940 Da

Monoisotopic Mass

360.23006 Da

IUPAC Name

[(1S,2S,4aS,7R,10aS)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-9-oxo-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthren-1-yl]methyl acetate

Traditional Name

[(1S,2S,4aS,7R,10aS)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-9-oxo-2,3,4,5,6,8,10,10a-octahydrophenanthren-1-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C([H])([H])C([H])([H])[C@@]2(C3=C(C(=O)C([H])([H])[C@]2([H])[C@@]1(C([H])([H])[H])C([H])([H])OC(=O)C([H])([H])[H])C([H])([H])[C@@](C([H])=C([H])[H])(C([H])([H])[H])C([H])([H])C3([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H32O4/c1-6-20(3)9-7-16-15(12-20)17(24)11-18-21(16,4)10-8-19(25)22(18,5)13-26-14(2)23/h6,18-19,25H,1,7-13H2,2-5H3/t18-,19-,20+,21+,22+/m0/s1

InChI Key

VOMKERLMONTVKI-VNXMGFANSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Croton joufra	JEOL database	Sutthivaiyakit, S., et al, Phytochemistry 56, 811 (2001)

Chemical Taxonomy

Classification

Not classified

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	3.24	ALOGPS
logP	3.09	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	14.63	ChemAxon
pKa (Strongest Basic)	-3	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	4	ChemAxon
Refractivity	101.49 m³·mol⁻¹	ChemAxon
Polarizability	40.68 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

Not Available

References

General References

Sutthivaiyakit, S., et al. (2001). Sutthivaiyakit, S., et al, Phytochemistry 56, 811 (2001). Phytochem..

Showing NP-Card for 3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one (NP0028626)

MOL for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

3D MOL for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

3D SDF for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

3D-SDF for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

PDB for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

3D PDB for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

SMILES for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

INCHI for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

Structure for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)

3D Structure for NP0028626 (3beta-hydroxy-19-O-acetyl-pimara-8(9),15-diene-7-one)