NP-MRD: Showing NP-Card for (1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate (NP0235628)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 18:19:42 UTC

Updated at

2022-09-06 18:19:42 UTC

NP-MRD ID

NP0235628

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate

Description

(1S,3R)-2,2-dimethyl-4-methylidene-3-[(3E,7E)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate is found in Bupleurum fruticescens. Based on a literature review very few articles have been published on (1S,3R)-2,2-dimethyl-4-methylidene-3-[(3E,7E)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062220192D          

 28 28  0  0  1  0            999 V2000
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 70 70  0  0  0  0  0  0  0  0999 V2000
   -4.2226    0.3563   -2.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1771    0.7470   -0.7915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2745    1.4605   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6594    0.7897    1.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8231   -0.4078    1.4777 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0638   -0.7336    2.8439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6490   -1.9059    3.2546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9918   -2.7377    2.3847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3656   -0.2415    1.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875    0.4551    2.5311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7352   -1.6243    1.2761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9503    0.4575    0.0239 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2901    1.7868    0.3012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    2.5482   -0.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7638    2.0063   -1.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4638    2.7370   -3.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0475    0.9319   -1.4579 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9953    0.5112   -2.4622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3668    0.5050   -1.8152 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3957   -0.4394   -0.6772 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2330   -1.4468   -0.6761 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1918   -1.7179   -1.7893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2439   -2.3853    0.4812 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5777   -2.4314    1.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9865   -1.1331    1.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1015   -0.5022    1.4080 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0736   -1.0709    0.4485 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4379    0.8273    2.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3800   -0.1654   -2.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0741    0.5307   -2.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1345    1.5320   -0.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0264    2.5212    0.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7110    0.4347    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6708    1.4833    2.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2050   -1.2849    0.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7851   -2.0514    4.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1941   -0.1466    3.3965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1759    1.4644    2.6609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6977    0.3501    2.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9290   -2.0307    0.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2370   -2.3220    1.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6492   -1.5615    1.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2801   -0.1618   -0.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4340    1.6358    1.0299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0015    2.4467    0.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5415    3.5836   -0.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7390    2.6364   -1.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1440    3.6291   -3.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5681    3.1196   -2.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6572    2.1097   -3.8779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696    0.3704   -0.5361 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0564    1.1980   -3.3216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6911   -0.4719   -2.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5716    1.5521   -1.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1581    0.2323   -2.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -0.2736    0.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8097   -0.8448   -2.0558 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9013   -2.5200   -1.5058 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6435   -2.1212   -2.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9020   -3.3977    0.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4965   -2.0493    1.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3783   -2.8439    0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4583   -3.1765    2.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3169   -0.6447    2.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2858   -2.1620    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0792   -0.5906    0.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6867   -0.9021   -0.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7640    1.4963    1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5688    1.3076    2.4781 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3084    0.7468    2.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  1  0
 26 25  2  3
 25 24  1  0
 24 23  1  0
 23 21  1  0
 21 22  1  0
 21 20  2  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  5  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 27 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 28 69  1  0
 28 70  1  0
 25 64  1  0
 24 62  1  0
 24 63  1  0
 23 60  1  0
 23 61  1  0
 22 57  1  0
 22 58  1  0
 22 59  1  0
 20 56  1  0
 19 54  1  0
 19 55  1  0
 18 52  1  0
 18 53  1  0
 17 51  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 14 46  1  0
 14 47  1  0
 13 44  1  0
 13 45  1  0
 12 43  1  6
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  6
  7 36  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 11 42  1  0
M  END


  Mrv1652309062220192D          

 28 28  0  0  1  0            999 V2000
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0235628

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC\C=C(/C)CC[C@@H]1C(=C)CC[C@H](OC=O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C26H42O2/c1-20(2)11-10-14-21(3)12-8-9-13-22(4)15-17-24-23(5)16-18-25(28-19-27)26(24,6)7/h11-13,19,24-25H,5,8-10,14-18H2,1-4,6-7H3/b21-12+,22-13+/t24-,25+/m1/s1

> <INCHI_KEY>
BVBDSKMFBNDVTM-KWDVGDNWSA-N

> <FORMULA>
C26H42O2

> <MOLECULAR_WEIGHT>
386.62

> <EXACT_MASS>
386.318480592

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
48.890598818259676

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R)-2,2-dimethyl-4-methylidene-3-[(3E,7E)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate

> <JCHEM_LOGP>
7.621629048333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.826429698282889

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
123.0887

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R)-2,2-dimethyl-4-methylidene-3-[(3E,7E)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.004   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.338   2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      18.672   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      20.005   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.672   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9    2   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
(1S,3R)-2,2-Dimethyl-4-methylidene-3-[(3E,7E)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formic acid	Generator

Chemical Formula

C₂₆H₄₂O₂

Average Mass

386.6200 Da

Monoisotopic Mass

386.31848 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC\C=C(/C)CC[C@@H]1C(=C)CC[C@H](OC=O)C1(C)C

InChI Identifier

InChI=1S/C26H42O2/c1-20(2)11-10-14-21(3)12-8-9-13-22(4)15-17-24-23(5)16-18-25(28-19-27)26(24,6)7/h11-13,19,24-25H,5,8-10,14-18H2,1-4,6-7H3/b21-12+,22-13+/t24-,25+/m1/s1

InChI Key

BVBDSKMFBNDVTM-KWDVGDNWSA-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
Bupleurum fruticescens	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

Diterpenoid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162817023

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate (NP0235628)

MOL for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

3D MOL for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

3D SDF for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

3D-SDF for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

PDB for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

3D PDB for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

SMILES for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

INCHI for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

Structure for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)

3D Structure for NP0235628 ((1s,3r)-2,2-dimethyl-4-methylidene-3-[(3e,7e)-3,8,12-trimethyltrideca-3,7,11-trien-1-yl]cyclohexyl formate)