NP-MRD: Showing NP-Card for ent-8(14),15-sandaracopimaradiene-2alpha,18-diol (NP0031333)

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Record Information

Version

2.0

Created at

2021-06-19 22:26:37 UTC

Updated at

2021-06-29 23:59:50 UTC

NP-MRD ID

NP0031333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ent-8(14),15-sandaracopimaradiene-2alpha,18-diol

Provided By

JEOL Database JEOL Logo

Description

(2Alpha)-pimara-8(14),15-diene-2,18-diol belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. ent-8(14),15-sandaracopimaradiene-2alpha,18-diol is found in Guarea rhophalocarpa. ent-8(14),15-sandaracopimaradiene-2alpha,18-diol was first documented in 2001 (Camacho, M. R., et al.). Based on a literature review very few articles have been published on (2alpha)-pimara-8(14),15-diene-2,18-diol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100263D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306202100263D          

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   -6.1927   -1.2567    0.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0262   -1.1584    3.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6320    0.3729    2.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6571   -1.5227    3.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0497   -0.2564    5.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0192    0.3007    3.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2016    1.2387    2.7174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1347   -1.5975    2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3126   -2.5216    2.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7424   -2.2417    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0706    1.4412    0.5848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4736    1.7049    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958    0.1210    2.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6812    1.8694    1.2524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4244    2.4453    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0  0  0  0
 15 17  1  0  0  0  0
 20 21  1  0  0  0  0
  6  5  2  0  0  0  0
  5  3  1  0  0  0  0
  3 22  1  0  0  0  0
 22 21  1  0  0  0  0
 14 10  1  0  0  0  0
  3  4  1  0  0  0  0
 18 20  1  0  0  0  0
  9 34  1  6  0  0  0
  9  8  1  0  0  0  0
 10 12  1  6  0  0  0
  8  7  1  0  0  0  0
 15 16  1  0  0  0  0
  7  6  1  0  0  0  0
  3  2  1  1  0  0  0
 20  6  1  0  0  0  0
  2  1  2  3  0  0  0
 10  9  1  0  0  0  0
 10 11  1  0  0  0  0
 18 17  1  0  0  0  0
 18 19  1  1  0  0  0
 18  9  1  0  0  0  0
 12 13  1  0  0  0  0
 20 50  1  6  0  0  0
 15 43  1  1  0  0  0
 14 41  1  0  0  0  0
 14 42  1  0  0  0  0
 17 45  1  0  0  0  0
 17 46  1  0  0  0  0
  8 32  1  0  0  0  0
  8 33  1  0  0  0  0
  7 30  1  0  0  0  0
  7 31  1  0  0  0  0
  5 29  1  0  0  0  0
 22 53  1  0  0  0  0
 22 54  1  0  0  0  0
 21 51  1  0  0  0  0
 21 52  1  0  0  0  0
  4 26  1  0  0  0  0
  4 27  1  0  0  0  0
  4 28  1  0  0  0  0
 12 38  1  0  0  0  0
 12 39  1  0  0  0  0
 16 44  1  0  0  0  0
  2 25  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
 11 35  1  0  0  0  0
 11 36  1  0  0  0  0
 11 37  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
 19 49  1  0  0  0  0
 13 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])C([H])([H])[C@]2(C([H])([H])[H])[C@]3([H])C(=C([H])[C@@](C([H])=C([H])[H])(C([H])([H])[H])C([H])([H])C3([H])[H])C([H])([H])C([H])([H])[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O2/c1-5-18(2)9-8-16-14(10-18)6-7-17-19(3,13-21)11-15(22)12-20(16,17)4/h5,10,15-17,21-22H,1,6-9,11-13H2,2-4H3/t15-,16-,17-,18+,19-,20+/m0/s1

> <INCHI_KEY>
YDCSRZAYXXMRIQ-YDRVBMSGSA-N

> <FORMULA>
C20H32O2

> <MOLECULAR_WEIGHT>
304.474

> <EXACT_MASS>
304.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
36.653567073305524

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R,4aR,4bS,7S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydrophenanthren-3-ol

> <ALOGPS_LOGP>
3.54

> <JCHEM_LOGP>
3.2080022963333334

> <ALOGPS_LOGS>
-4.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.473761384928327

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.857828827945234

> <JCHEM_PKA_STRONGEST_BASIC>
-2.702259225151705

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
92.06179999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4aR,4bS,7S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-3-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    4.0060   -1.8646    0.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1844   -0.5354    0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2851    0.5271   -0.4345 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1192    1.2877   -1.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0658   -0.0615   -1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8177   -0.0379   -0.6137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3578   -0.5133   -1.4304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.3729   -0.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7388   -0.7010    0.6919 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0002   -1.3331    1.3950 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9153   -2.8604    1.6015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2571   -1.0653    0.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4531   -1.4607    1.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2393   -0.6411    2.7609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9944   -0.5339    3.6337 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3143    0.2045    4.8129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8756    0.2063    2.9077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4542   -0.4641    1.5790 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3108   -1.7743    1.9034 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959    0.5150    0.7700 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7550    0.9507    1.5577 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8286    1.5403    0.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -2.3431   -0.2437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7296   -2.5111    0.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0790   -0.1503    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5232    2.0593   -1.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818    1.7859   -1.0258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032    0.6133   -2.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2330   -0.4926   -2.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283   -1.0749   -2.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8855    0.3731   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9201   -2.3664   -0.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2269   -1.5253   -1.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0771    0.3132    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8689   -3.2639    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1782   -3.1525    2.3478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6849   -3.3835    0.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3467    0.0007    0.2697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2087   -1.6233   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1927   -1.2567    0.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0262   -1.1584    3.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6320    0.3729    2.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6571   -1.5227    3.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0497   -0.2564    5.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0192    0.3007    3.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2016    1.2387    2.7174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1347   -1.5975    2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3126   -2.5216    2.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7424   -2.2417    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0706    1.4412    0.5848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4736    1.7049    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958    0.1210    2.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6812    1.8694    1.2524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4244    2.4453    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 15 17  1  0
 20 21  1  0
  6  5  2  0
  5  3  1  0
  3 22  1  0
 22 21  1  0
 14 10  1  0
  3  4  1  0
 18 20  1  0
  9 34  1  6
  9  8  1  0
 10 12  1  6
  8  7  1  0
 15 16  1  0
  7  6  1  0
  3  2  1  1
 20  6  1  0
  2  1  2  3
 10  9  1  0
 10 11  1  0
 18 17  1  0
 18 19  1  1
 18  9  1  0
 12 13  1  0
 20 50  1  6
 15 43  1  1
 14 41  1  0
 14 42  1  0
 17 45  1  0
 17 46  1  0
  8 32  1  0
  8 33  1  0
  7 30  1  0
  7 31  1  0
  5 29  1  0
 22 53  1  0
 22 54  1  0
 21 51  1  0
 21 52  1  0
  4 26  1  0
  4 27  1  0
  4 28  1  0
 12 38  1  0
 12 39  1  0
 16 44  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 13 40  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       4.006  -1.865   0.211  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.184  -0.535   0.191  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.285   0.527  -0.435  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.119   1.288  -1.485  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.066  -0.062  -1.120  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.818  -0.038  -0.614  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.358  -0.513  -1.430  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.348  -1.373  -0.642  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.739  -0.701   0.692  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.000  -1.333   1.395  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.915  -2.860   1.601  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.257  -1.065   0.507  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.453  -1.461   1.172  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.239  -0.641   2.761  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.994  -0.534   3.634  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.314   0.205   4.813  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.876   0.206   2.908  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.454  -0.464   1.579  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.311  -1.774   1.903  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.496   0.515   0.770  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.755   0.951   1.558  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.829   1.540   0.644  0.00  0.00           C+0
HETATM   23  H   UNK     0       3.145  -2.343  -0.244  0.00  0.00           H+0
HETATM   24  H   UNK     0       4.730  -2.511   0.698  0.00  0.00           H+0
HETATM   25  H   UNK     0       5.079  -0.150   0.681  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.523   2.059  -1.987  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.982   1.786  -1.026  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.503   0.613  -2.260  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.233  -0.493  -2.106  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.028  -1.075  -2.313  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.886   0.373  -1.806  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.920  -2.366  -0.471  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.227  -1.525  -1.276  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.077   0.313   0.420  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.869  -3.264   1.963  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.178  -3.152   2.348  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.685  -3.384   0.668  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.347   0.001   0.270  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.209  -1.623  -0.433  0.00  0.00           H+0
HETATM   40  H   UNK     0      -6.193  -1.257   0.574  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.026  -1.158   3.326  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.632   0.373   2.597  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.657  -1.523   3.959  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.050  -0.256   5.253  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.019   0.301   3.588  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.202   1.239   2.717  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.135  -1.597   2.602  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.313  -2.522   2.388  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.742  -2.242   1.014  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.071   1.441   0.585  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.474   1.705   2.303  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.196   0.121   2.116  0.00  0.00           H+0
HETATM   53  H   UNK     0       3.681   1.869   1.252  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.424   2.445   0.169  0.00  0.00           H+0
CONECT    1    2   23   24                                                  
CONECT    2    3    1   25                                                  
CONECT    3    5   22    4    2                                             
CONECT    4    3   26   27   28                                             
CONECT    5    6    3   29                                                  
CONECT    6    5    7   20                                                  
CONECT    7    8    6   30   31                                             
CONECT    8    9    7   32   33                                             
CONECT    9   34    8   10   18                                             
CONECT   10   14   12    9   11                                             
CONECT   11   10   35   36   37                                             
CONECT   12   10   13   38   39                                             
CONECT   13   12   40                                                       
CONECT   14   15   10   41   42                                             
CONECT   15   14   17   16   43                                             
CONECT   16   15   44                                                       
CONECT   17   15   18   45   46                                             
CONECT   18   20   17   19    9                                             
CONECT   19   18   47   48   49                                             
CONECT   20   21   18    6   50                                             
CONECT   21   20   22   51   52                                             
CONECT   22    3   21   53   54                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    4                                                            
CONECT   27    4                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    7                                                            
CONECT   31    7                                                            
CONECT   32    8                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35   11                                                            
CONECT   36   11                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   12                                                            
CONECT   40   13                                                            
CONECT   41   14                                                            
CONECT   42   14                                                            
CONECT   43   15                                                            
CONECT   44   16                                                            
CONECT   45   17                                                            
CONECT   46   17                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   19                                                            
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   21                                                            
CONECT   53   22                                                            
CONECT   54   22                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  112    0
END

RDKit          3D

54 56  0  0  0  0  0  0  0  0999 V2000
    4.0060   -1.8646    0.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7550    0.9507    1.5577 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8286    1.5403    0.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5232    2.0593   -1.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818    1.7859   -1.0258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5032    0.6133   -2.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2330   -0.4926   -2.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283   -1.0749   -2.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8855    0.3731   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9201   -2.3664   -0.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2269   -1.5253   -1.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0771    0.3132    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8689   -3.2639    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1782   -3.1525    2.3478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6849   -3.3835    0.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3467    0.0007    0.2697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2087   -1.6233   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1927   -1.2567    0.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0262   -1.1584    3.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6320    0.3729    2.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6571   -1.5227    3.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0497   -0.2564    5.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0192    0.3007    3.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2016    1.2387    2.7174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1347   -1.5975    2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3126   -2.5216    2.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7424   -2.2417    1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0706    1.4412    0.5848 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4736    1.7049    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958    0.1210    2.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6812    1.8694    1.2524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4244    2.4453    0.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 15 17  1  0
 20 21  1  0
  6  5  2  0
  5  3  1  0
  3 22  1  0
 22 21  1  0
 14 10  1  0
  3  4  1  0
 18 20  1  0
  9 34  1  6
  9  8  1  0
 10 12  1  6
  8  7  1  0
 15 16  1  0
  7  6  1  0
  3  2  1  1
 20  6  1  0
  2  1  2  3
 10  9  1  0
 10 11  1  0
 18 17  1  0
 18 19  1  1
 18  9  1  0
 12 13  1  0
 20 50  1  6
 15 43  1  1
 14 41  1  0
 14 42  1  0
 17 45  1  0
 17 46  1  0
  8 32  1  0
  8 33  1  0
  7 30  1  0
  7 31  1  0
  5 29  1  0
 22 53  1  0
 22 54  1  0
 21 51  1  0
 21 52  1  0
  4 26  1  0
  4 27  1  0
  4 28  1  0
 12 38  1  0
 12 39  1  0
 16 44  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 13 40  1  0
M  END

View in JSmol

Synonyms

Value	Source
(2a)-Pimara-8(14),15-diene-2,18-diol	Generator
(2Α)-pimara-8(14),15-diene-2,18-diol	Generator

Chemical Formula

C₂₀H₃₂O₂

Average Mass

304.4740 Da

Monoisotopic Mass

304.24023 Da

IUPAC Name

(1R,3R,4aR,4bS,7S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydrophenanthren-3-ol

Traditional Name

(1R,3R,4aR,4bS,7S,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-3-ol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@]1(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])C([H])([H])[C@]2(C([H])([H])[H])[C@]3([H])C(=C([H])[C@@](C([H])=C([H])[H])(C([H])([H])[H])C([H])([H])C3([H])[H])C([H])([H])C([H])([H])[C@@]12[H]

InChI Identifier

InChI=1S/C20H32O2/c1-5-18(2)9-8-16-14(10-18)6-7-17-19(3,13-21)11-15(22)12-20(16,17)4/h5,10,15-17,21-22H,1,6-9,11-13H2,2-4H3/t15-,16-,17-,18+,19-,20+/m0/s1

InChI Key

YDCSRZAYXXMRIQ-YDRVBMSGSA-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
Guarea rhophalocarpa	JEOL database	Camacho, M. R., et al, Phytochemistry 56, 203 (2001)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Pimarane diterpenoid
Diterpenoid
Phenanthrene
Hydrophenanthrene
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.54	ALOGPS
logP	3.21	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	14.86	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.06 m³·mol⁻¹	ChemAxon
Polarizability	36.65 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

553437

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

637854

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Camacho, M. R., et al. (2001). Camacho, M. R., et al, Phytochemistry 56, 203 (2001) . Phytochem..

Showing NP-Card for ent-8(14),15-sandaracopimaradiene-2alpha,18-diol (NP0031333)

MOL for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

3D MOL for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

3D SDF for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

3D-SDF for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

PDB for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

3D PDB for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

SMILES for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

INCHI for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

Structure for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)

3D Structure for NP0031333 (ent-8(14),15-sandaracopimaradiene-2alpha,18-diol)