NP-MRD: Showing NP-Card for [(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate (NP0187644)

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Record Information

Version

2.0

Created at

2022-09-04 03:50:46 UTC

Updated at

2022-09-04 03:50:47 UTC

NP-MRD ID

NP0187644

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate

Description

(1S,3Z,7E,11S,12S)-(+)-verticilla-3,7-dien-12,20-diol 20-acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. [(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate is found in Bursera suntui. [(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate was first documented in 2005 (PMID: 16309306). Based on a literature review very few articles have been published on (1S,3Z,7E,11S,12S)-(+)-verticilla-3,7-dien-12,20-diol 20-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042205502D          

 25 26  0  0  1  0            999 V2000
    3.7767    4.8517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    4.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620    4.1744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9260    3.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    1.9484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1464    2.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7259    3.1977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2539    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    1.6619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5175    2.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7834    0.8818    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
  4  5  1  0  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  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 15 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
M  END

     RDKit          3D

 61 62  0  0  0  0  0  0  0  0999 V2000
    5.3168   -3.5764    1.9106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993   -2.1472    1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9389   -1.3017    1.9773 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0409   -1.6919    0.8154 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9231   -0.3235    0.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989   -0.0190   -0.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9461   -1.0642   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8248   -1.0972   -1.5544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5352   -1.4048   -0.9662 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6245   -1.9991   -1.6631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7059   -2.2422   -0.5855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3025   -0.9520   -0.0330 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7969   -1.2888    1.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5248   -0.8536   -0.7794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4863    0.2207   -0.2139 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4275    1.2747    0.8879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7414    2.5000    0.7937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6430    3.0925    0.0581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1224    4.0067   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6683    3.1091    0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8208    2.2703    0.3497 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4096    1.3702   -0.6769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9925   -0.0328   -0.5015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8630    0.7262   -1.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5282   -0.1448    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9289   -4.2557    1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9332   -3.8346    2.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4146   -3.7408    1.9226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148    0.2695    1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8394    0.0407    0.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1802   -2.0358   -0.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0151   -2.0494   -2.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9322   -0.3450   -2.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2837   -2.1453   -0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1538   -1.5537   -2.4859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3685   -3.0408   -1.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1949   -2.7664    0.2439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4685   -2.9385   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2049   -2.1296    1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8346   -1.7495    1.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9207   -0.4194    2.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1701   -1.5224   -0.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9924    0.8297   -1.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3168    0.7899    1.9019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5511    1.4965    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4374    2.7552    1.8970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5762    3.3069    0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9055    3.5836   -2.0745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2133    4.1763   -1.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6791    5.0182   -0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0577    4.1599   -0.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6190    1.6475    1.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    2.9153    0.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0995    1.5182   -1.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4802    1.8082   -0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0818    1.3406   -2.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7721    1.3803   -2.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0127    0.0554   -2.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3776   -0.7627    1.1177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2265   -0.9121    1.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3874    0.6784    1.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 12 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 15 23  1  0
 23 24  1  0
 23 25  1  0
 22  6  1  0
 23  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  1
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  6
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 19 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 24 56  1  0
 24 57  1  0
 24 58  1  0
 25 59  1  0
 25 60  1  0
 25 61  1  0
M  END


  Mrv1652309042205502D          

 25 26  0  0  1  0            999 V2000
    3.7767    4.8517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    4.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620    4.1744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9260    3.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    1.9484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1464    2.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7259    3.1977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    2.3645    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2539    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    1.6619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5175    2.5240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7834    0.8818    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
  4  5  1  0  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  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 15 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0187644

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC\C1=C/C[C@@H]2CC[C@](C)(O)[C@@H](CC\C(C)=C\CC1)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O3/c1-16-7-6-8-18(15-25-17(2)23)10-11-19-13-14-22(5,24)20(12-9-16)21(19,3)4/h7,10,19-20,24H,6,8-9,11-15H2,1-5H3/b16-7+,18-10-/t19-,20+,22+/m1/s1

> <INCHI_KEY>
ONBYNDRDNDICPR-NHUDBVNLSA-N

> <FORMULA>
C22H36O3

> <MOLECULAR_WEIGHT>
348.527

> <EXACT_MASS>
348.266445019

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
40.70741045022153

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,3Z,7E,11S,12S)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate

> <JCHEM_LOGP>
4.371816506333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4365558184326651

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
104.0858

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,3Z,7E,11S,12S)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.050   9.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.594   7.479   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.969   7.792   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.329   5.608   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.874   3.637   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.517   1.746   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.747   0.413   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.207   0.413   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.437   1.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.897   1.746   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.127   3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.897   4.414   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.273   4.740   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.355   5.969   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.437   4.414   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.207   5.747   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.747   5.747   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.517   4.414   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.628   3.102   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.057   4.414   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.827   3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.057   1.746   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.207   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.699   4.711   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.196   1.646   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                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    6                                                       
CONECT   23   15    9   24   25                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
(1S,3Z,7E,11S,12S)-(+)-Verticilla-3,7-dien-12,20-diol 20-acetic acid	Generator

Chemical Formula

C₂₂H₃₆O₃

Average Mass

348.5270 Da

Monoisotopic Mass

348.26645 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC\C1=C/C[C@@H]2CC[C@](C)(O)[C@@H](CC\C(C)=C\CC1)C2(C)C

InChI Identifier

InChI=1S/C22H36O3/c1-16-7-6-8-18(15-25-17(2)23)10-11-19-13-14-22(5,24)20(12-9-16)21(19,3)4/h7,10,19-20,24H,6,8-9,11-15H2,1-5H3/b16-7+,18-10-/t19-,20+,22+/m1/s1

InChI Key

ONBYNDRDNDICPR-NHUDBVNLSA-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
Bursera suntui	LOTUS Database	35616633

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

Verticillane diterpenoid
Diterpenoid
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

4483795

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5326321

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hernandez-Hernandez JD, Roman-Marin LU, Cerda-Garcia-Rojas CM, Joseph-Nathan P: Verticillane derivatives from Bursera suntui and Bursera kerberi. J Nat Prod. 2005 Nov;68(11):1598-602. doi: 10.1021/np050323e. [PubMed:16309306 ]
LOTUS database [Link]

Showing NP-Card for [(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate (NP0187644)

MOL for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

3D MOL for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

3D SDF for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

3D-SDF for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

PDB for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

3D PDB for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

SMILES for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

INCHI for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

Structure for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)

3D Structure for NP0187644 ([(1s,3z,7e,11s,12s)-12-hydroxy-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-4-yl]methyl acetate)