NP-MRD: Showing NP-Card for (E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid (NP0032506)

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Record Information

Version

2.0

Created at

2021-06-19 23:17:30 UTC

Updated at

2021-06-30 00:01:44 UTC

NP-MRD ID

NP0032506

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid

Provided By

JEOL Database JEOL Logo

Description

Coronadiene belongs to the class of organic compounds known as carboxylic acids. Carboxylic acids are compounds containing a carboxylic acid group with the formula -C(=O)OH. (E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid is found in Zingiber ottensii. (E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid was first documented in 2008 (PMID: 19043243). Based on a literature review very few articles have been published on Coronadiene.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202101173D          

 45 46  0  0  0  0            999 V2000
   -2.0683   -1.5816    2.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4049    1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3642   -1.3000   -0.2673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7441   -0.0487   -0.8962 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7654    0.0574   -0.5818 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5328    1.1368   -1.4279 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9440    2.5576   -1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.7436   -2.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    1.1535   -1.0149 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2562    1.2398    0.4881 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5506    0.1084    1.2303 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0202    0.0619    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3599    1.2597    1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.2946    1.5479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7283   -1.5350    3.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4423   -2.5797    3.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -2.8268    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928   -3.7701    5.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278   -1.9093    5.7184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9025   -1.6663    3.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -1.6514    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -1.2935   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9662   -2.1927   -0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9123   -0.1071   -1.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2790    0.8416   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1952   -0.8978   -0.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1290    2.5677   -1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    3.2159   -2.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1039    3.0338   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    1.3895   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4870    0.8398   -3.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254   -0.2891   -3.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5124    0.2376   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.9864   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3331    1.1759    0.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9364    2.2145    0.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0014   -0.8431    0.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7621    0.2130    2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219    1.3043    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5289    1.2066    2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7684    2.2215    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093   -2.1133    0.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311   -0.8136    3.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8495   -3.3227    2.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5123   -2.2154    6.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  2 14  1  0  0  0  0
 12  5  1  0  0  0  0
  2  1  2  3  0  0  0
 14 15  1  0  0  0  0
 10  9  1  0  0  0  0
 15 16  2  0  0  0  0
 10 11  1  0  0  0  0
 16 17  1  0  0  0  0
  9  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  5  1  0  0  0  0
 12 13  1  1  0  0  0
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  5 26  1  6  0  0  0
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  6  8  1  0  0  0  0
  5  4  1  0  0  0  0
 17 18  2  0  0  0  0
  4  3  1  0  0  0  0
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  9 33  1  0  0  0  0
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  4 24  1  0  0  0  0
  4 25  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
 14 42  1  6  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
 15 43  1  0  0  0  0
 16 44  1  0  0  0  0
  7 27  1  0  0  0  0
  7 28  1  0  0  0  0
  7 29  1  0  0  0  0
 13 39  1  0  0  0  0
 13 40  1  0  0  0  0
 13 41  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
 19 45  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -2.0683   -1.5816    2.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4049    1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3642   -1.3000   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441   -0.0487   -0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654    0.0574   -0.5818 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5328    1.1368   -1.4279 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9440    2.5576   -1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.7436   -2.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    1.1535   -1.0149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    1.2398    0.4881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506    0.1084    1.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0202    0.0619    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3599    1.2597    1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.2946    1.5479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7283   -1.5350    3.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4423   -2.5797    3.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -2.8268    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928   -3.7701    5.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278   -1.9093    5.7184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9025   -1.6663    3.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -1.6514    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -1.2935   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9662   -2.1927   -0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9123   -0.1071   -1.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2790    0.8416   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1952   -0.8978   -0.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1290    2.5677   -1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    3.2159   -2.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1039    3.0338   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    1.3895   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4870    0.8398   -3.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254   -0.2891   -3.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5124    0.2376   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.9864   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3331    1.1759    0.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9364    2.2145    0.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0014   -0.8431    0.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7621    0.2130    2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219    1.3043    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5289    1.2066    2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7684    2.2215    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093   -2.1133    0.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311   -0.8136    3.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8495   -3.3227    2.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5123   -2.2154    6.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2 14  1  0
 12  5  1  0
  2  1  2  3
 14 15  1  0
 10  9  1  0
 15 16  2  0
 10 11  1  0
 16 17  1  0
  9  6  1  0
  6  7  1  6
  6  5  1  0
 12 13  1  1
 12 11  1  0
  5 26  1  6
 12 14  1  0
  6  8  1  0
  5  4  1  0
 17 18  2  0
  4  3  1  0
 17 19  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
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 11 37  1  0
 11 38  1  0
  4 24  1  0
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  3 22  1  0
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 14 42  1  6
  1 20  1  0
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  7 27  1  0
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 13 39  1  0
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  8 30  1  0
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 19 45  1  0
M  END


  Mrv1652306202101173D          

 45 46  0  0  0  0            999 V2000
   -2.0683   -1.5816    2.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4049    1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3642   -1.3000   -0.2673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7441   -0.0487   -0.8962 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7654    0.0574   -0.5818 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5328    1.1368   -1.4279 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9440    2.5576   -1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.7436   -2.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    1.1535   -1.0149 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2562    1.2398    0.4881 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5506    0.1084    1.2303 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0202    0.0619    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3599    1.2597    1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.2946    1.5479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7283   -1.5350    3.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4423   -2.5797    3.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -2.8268    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1018   -1.6514    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -1.2935   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
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  3  2  1  0  0  0  0
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 12  5  1  0  0  0  0
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 14 15  1  0  0  0  0
 10  9  1  0  0  0  0
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  7 29  1  0  0  0  0
 13 39  1  0  0  0  0
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 13 41  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
 19 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0032506

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O2/c1-12-6-8-14-16(2,3)10-5-11-17(14,4)13(12)7-9-15(18)19/h7,9,13-14H,1,5-6,8,10-11H2,2-4H3,(H,18,19)/b9-7+/t13-,14-,17+/m0/s1

> <INCHI_KEY>
GZRHZZSARAUGHK-VIJNKSRKSA-N

> <FORMULA>
C17H26O2

> <MOLECULAR_WEIGHT>
262.393

> <EXACT_MASS>
262.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
30.928246942412443

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-decahydronaphthalen-1-yl]prop-2-enoic acid

> <ALOGPS_LOGP>
4.49

> <JCHEM_LOGP>
4.347086382666667

> <ALOGPS_LOGS>
-4.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.1809312258167655

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
78.43719999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.86e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]prop-2-enoic acid

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -2.0683   -1.5816    2.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4049    1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3642   -1.3000   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441   -0.0487   -0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654    0.0574   -0.5818 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5328    1.1368   -1.4279 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9440    2.5576   -1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.7436   -2.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    1.1535   -1.0149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    1.2398    0.4881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506    0.1084    1.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0202    0.0619    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3599    1.2597    1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.2946    1.5479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7283   -1.5350    3.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4423   -2.5797    3.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -2.8268    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928   -3.7701    5.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278   -1.9093    5.7184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9025   -1.6663    3.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -1.6514    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -1.2935   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9662   -2.1927   -0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9123   -0.1071   -1.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2790    0.8416   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1952   -0.8978   -0.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1290    2.5677   -1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    3.2159   -2.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1039    3.0338   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    1.3895   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4870    0.8398   -3.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254   -0.2891   -3.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5124    0.2376   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.9864   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3331    1.1759    0.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9364    2.2145    0.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0014   -0.8431    0.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7621    0.2130    2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219    1.3043    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5289    1.2066    2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7684    2.2215    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093   -2.1133    0.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311   -0.8136    3.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8495   -3.3227    2.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5123   -2.2154    6.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2 14  1  0
 12  5  1  0
  2  1  2  3
 14 15  1  0
 10  9  1  0
 15 16  2  0
 10 11  1  0
 16 17  1  0
  9  6  1  0
  6  7  1  6
  6  5  1  0
 12 13  1  1
 12 11  1  0
  5 26  1  6
 12 14  1  0
  6  8  1  0
  5  4  1  0
 17 18  2  0
  4  3  1  0
 17 19  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
  9 34  1  0
 11 37  1  0
 11 38  1  0
  4 24  1  0
  4 25  1  0
  3 22  1  0
  3 23  1  0
 14 42  1  6
  1 20  1  0
  1 21  1  0
 15 43  1  0
 16 44  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
 19 45  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      -2.068  -1.582   2.090  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.066  -1.405   1.211  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.364  -1.300  -0.267  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.744  -0.049  -0.896  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.765   0.057  -0.582  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.533   1.137  -1.428  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.944   2.558  -1.343  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.492   0.744  -2.930  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.026   1.153  -1.015  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.256   1.240   0.488  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.551   0.108   1.230  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.020   0.062   0.978  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.360   1.260   1.710  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.424  -1.295   1.548  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.728  -1.535   3.015  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.442  -2.580   3.467  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.740  -2.827   4.885  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.393  -3.770   5.295  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.228  -1.909   5.718  0.00  0.00           O+0
HETATM   20  H   UNK     0      -1.903  -1.666   3.159  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.102  -1.651   1.763  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.444  -1.294  -0.459  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.966  -2.193  -0.767  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.912  -0.107  -1.976  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.279   0.842  -0.549  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.195  -0.898  -0.929  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.129   2.568  -1.558  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.420   3.216  -2.081  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.104   3.034  -0.377  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.151   1.389  -3.523  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.487   0.840  -3.352  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.825  -0.289  -3.082  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.512   0.238  -1.378  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.546   1.986  -1.505  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.333   1.176   0.686  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.936   2.215   0.870  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.001  -0.843   0.918  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.762   0.213   2.302  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.722   1.304   1.558  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.529   1.207   2.791  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.768   2.221   1.408  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.909  -2.113   0.993  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.331  -0.814   3.726  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.849  -3.323   2.791  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.512  -2.215   6.604  0.00  0.00           H+0
CONECT    1    2   20   21                                                  
CONECT    2    3   14    1                                                  
CONECT    3    2    4   22   23                                             
CONECT    4    5    3   24   25                                             
CONECT    5   12    6   26    4                                             
CONECT    6    9    7    5    8                                             
CONECT    7    6   27   28   29                                             
CONECT    8    6   30   31   32                                             
CONECT    9   10    6   33   34                                             
CONECT   10    9   11   35   36                                             
CONECT   11   10   12   37   38                                             
CONECT   12    5   13   11   14                                             
CONECT   13   12   39   40   41                                             
CONECT   14    2   15   12   42                                             
CONECT   15   14   16   43                                                  
CONECT   16   15   17   44                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   45                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    4                                                            
CONECT   26    5                                                            
CONECT   27    7                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32    8                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   15                                                            
CONECT   44   16                                                            
CONECT   45   19                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   92    0
END

RDKit          3D

45 46  0  0  0  0  0  0  0  0999 V2000
   -2.0683   -1.5816    2.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4049    1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3642   -1.3000   -0.2673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441   -0.0487   -0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7654    0.0574   -0.5818 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5328    1.1368   -1.4279 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9440    2.5576   -1.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923    0.7436   -2.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    1.1535   -1.0149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    1.2398    0.4881 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5506    0.1084    1.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0202    0.0619    0.9783 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3599    1.2597    1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4243   -1.2946    1.5479 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7283   -1.5350    3.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4423   -2.5797    3.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -2.8268    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928   -3.7701    5.2950 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278   -1.9093    5.7184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9025   -1.6663    3.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -1.6514    1.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4440   -1.2935   -0.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9662   -2.1927   -0.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9123   -0.1071   -1.9761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2790    0.8416   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1952   -0.8978   -0.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1290    2.5677   -1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201    3.2159   -2.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1039    3.0338   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1507    1.3895   -3.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4870    0.8398   -3.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8254   -0.2891   -3.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5124    0.2376   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.9864   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3331    1.1759    0.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9364    2.2145    0.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0014   -0.8431    0.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7621    0.2130    2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219    1.3043    1.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5289    1.2066    2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7684    2.2215    1.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093   -2.1133    0.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3311   -0.8136    3.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8495   -3.3227    2.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5123   -2.2154    6.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2 14  1  0
 12  5  1  0
  2  1  2  3
 14 15  1  0
 10  9  1  0
 15 16  2  0
 10 11  1  0
 16 17  1  0
  9  6  1  0
  6  7  1  6
  6  5  1  0
 12 13  1  1
 12 11  1  0
  5 26  1  6
 12 14  1  0
  6  8  1  0
  5  4  1  0
 17 18  2  0
  4  3  1  0
 17 19  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
  9 34  1  0
 11 37  1  0
 11 38  1  0
  4 24  1  0
  4 25  1  0
  3 22  1  0
  3 23  1  0
 14 42  1  6
  1 20  1  0
  1 21  1  0
 15 43  1  0
 16 44  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
  8 30  1  0
  8 31  1  0
  8 32  1  0
 19 45  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆O₂

Average Mass

262.3930 Da

Monoisotopic Mass

262.19328 Da

IUPAC Name

(2E)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-decahydronaphthalen-1-yl]prop-2-enoic acid

Traditional Name

(2E)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)C(\[H])=C(/[H])[C@@]1([H])C(=C([H])[H])C([H])([H])C([H])([H])[C@@]2([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]12C([H])([H])[H]

InChI Identifier

InChI=1S/C17H26O2/c1-12-6-8-14-16(2,3)10-5-11-17(14,4)13(12)7-9-15(18)19/h7,9,13-14H,1,5-6,8,10-11H2,2-4H3,(H,18,19)/b9-7+/t13-,14-,17+/m0/s1

InChI Key

GZRHZZSARAUGHK-VIJNKSRKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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
Zingiber ottensii	JEOL database	Akiyama, K., et al, J. Nat. Prod. 69, 1637 (2006)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carboxylic acids. Carboxylic acids are compounds containing a carboxylic acid group with the formula -C(=O)OH.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acids

Direct Parent

Carboxylic acids

Alternative Parents

Substituents

Monocarboxylic acid or derivatives
Carboxylic acid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.49	ALOGPS
logP	4.35	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	5.18	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	78.44 m³·mol⁻¹	ChemAxon
Polarizability	30.93 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

10167536

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11995069

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nakamura S, Okazaki Y, Ninomiya K, Morikawa T, Matsuda H, Yoshikawa M: Medicinal flowers. XXIV. Chemical structures and hepatoprotective effects of constituents from flowers of Hedychium coronarium. Chem Pharm Bull (Tokyo). 2008 Dec;56(12):1704-9. doi: 10.1248/cpb.56.1704. [PubMed:19043243 ]
Akiyama, K., et al. (2006). Akiyama, K., et al, J. Nat. Prod. 69, 1637 (2006) . J. Nat. Prod..

Showing NP-Card for (E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid (NP0032506)

MOL for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

3D MOL for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

3D SDF for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

3D-SDF for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

PDB for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

3D PDB for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

SMILES for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

INCHI for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

Structure for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )

3D Structure for NP0032506 ((E)-14,-15,16-trinorlabda-8(17),11-dien-13-oic acid )