NP-MRD: Showing NP-Card for (8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid (NP0308218)

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Record Information

Version

2.0

Created at

2022-09-11 01:51:51 UTC

Updated at

2022-09-11 01:51:51 UTC

NP-MRD ID

NP0308218

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid

Description

(8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid belongs to the class of organic compounds known as diterpenoids. (8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid is found in Cochlospermum tinctorium. These are terpene compounds formed by four isoprene units (8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171521532D          

 29 29  0  0  0  0            999 V2000
    6.3677    2.4172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0855    3.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2731    3.3357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7428    2.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303    2.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    2.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    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
    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 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
    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
    0.7145   -1.2375    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
   -0.8245    0.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372    1.5246    0.0000 C   0  0  0  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
    6.6158    3.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4283    3.6811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9586    4.3131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7711    4.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0532    3.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3014    4.8018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0192    5.5771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1138    4.6586    0.0000 O   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
  3  4  1  4  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 13 21  1  0  0  0  0
 22  2  1  4  0  0  0
 22 23  2  0  0  0  0
 24 23  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
   -7.2989   -1.0609   -1.5072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2979   -0.5441   -0.5774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2408   -0.9336    0.6986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1721   -0.3170    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4999   -0.9966    2.3052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8801    1.1422    1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3874    1.5860    0.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8864    1.8695    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7726    2.8729   -0.4405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2342    0.4665   -0.9525 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4214    0.8764   -2.2791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9458   -0.2714   -0.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7670    0.2651   -0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5157   -0.4917   -0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4182   -1.9561   -0.5553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3640    0.1830   -0.3269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8507   -0.5897   -0.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9966    0.0590    0.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2228   -0.6487    0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3966   -0.1171    0.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6542    1.3329    0.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5845   -0.9796    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8086   -0.5068    0.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8907   -1.4315    0.8564 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1319   -1.1226    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1019   -2.3039    1.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6561    0.2047    1.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9201    0.3218    1.3491 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8954    1.3371    1.0703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9554   -1.7758   -0.9312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9624   -0.2928   -1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8365   -1.6050   -2.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9139   -1.6495    1.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4239    1.7039    2.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8039    1.3220    1.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4339    1.8655   -0.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3629    1.1963    0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0221    2.9099    0.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5122    2.7652   -1.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9332    3.2418    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5433    3.6650   -0.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4187    0.9622   -2.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9457   -1.3779   -0.8607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7328    1.3692   -0.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7278   -2.2395   -1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3799   -2.4412   -0.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290   -2.3723    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3653    1.2524   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8682   -1.6579   -0.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760    1.1536    0.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1856   -1.7554    0.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8521    1.6109    1.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7774    1.8910    0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5044    1.6350   -0.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4250   -2.0437    0.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9179    0.5496    0.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6515   -2.5196    0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0885   -1.9065    0.9510 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9978   -2.6965    2.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8050   -3.0754    0.4309 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1461    2.0697    0.4268 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 29  1  0
 27 28  2  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  6
 10  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 23 56  1  0
 24 57  1  0
 26 58  1  0
 26 59  1  0
 26 60  1  0
 29 61  1  0
 19 51  1  0
 18 50  1  0
 17 49  1  0
 16 48  1  0
 15 45  1  0
 15 46  1  0
 15 47  1  0
 13 44  1  0
 12 43  1  0
 11 42  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  6 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
M  END


  Mrv1533004171521532D          

 29 29  0  0  0  0            999 V2000
    6.3677    2.4172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0855    3.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2731    3.3357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7428    2.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303    2.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    2.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    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
    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 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
    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
    0.7145   -1.2375    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
   -0.8245    0.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4372    1.5246    0.0000 C   0  0  0  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
    6.6158    3.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4283    3.6811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9586    4.3131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7711    4.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0532    3.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3014    4.8018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0192    5.5771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1138    4.6586    0.0000 O   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
  3  4  1  4  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 13 21  1  0  0  0  0
 22  2  1  4  0  0  0
 22 23  2  0  0  0  0
 24 23  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0308218

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C=CC=C(C)C(O)=O)=C\C=C\C=C(/C)\C=C\C1(O)C(C)=CC(=O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O4/c1-18(12-9-13-20(3)23(27)28)10-7-8-11-19(2)14-15-25(29)21(4)16-22(26)17-24(25,5)6/h7-16,29H,17H2,1-6H3,(H,27,28)/b8-7+,12-9?,15-14+,18-10?,19-11+,20-13?

> <INCHI_KEY>
IKVOLCVFLNPJTB-WUNLQJBYSA-N

> <FORMULA>
C25H32O4

> <MOLECULAR_WEIGHT>
396.527

> <EXACT_MASS>
396.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.992309034325906

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid

> <ALOGPS_LOGP>
5.02

> <JCHEM_LOGP>
4.841049947666667

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.403064677410786

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.94620947251088

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4972976539294853

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
124.88989999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      11.886   4.512   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.360   5.959   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.843   6.227   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.853   5.047   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.337   5.314   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.347   4.135   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.830   4.402   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.303   5.849   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.840   3.222   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.344   3.490   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.539   1.594   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.816   2.846   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.350   7.139   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.866   6.871   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.856   8.051   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.373   7.784   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.899   6.337   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.363   8.963   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.836  10.411   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      18.879   8.696   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   11   19   20                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   13                                                            
CONECT   22    2   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
(8E,10E,12E)-13-(1-Hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoate	Generator

Chemical Formula

C₂₅H₃₂O₄

Average Mass

396.5270 Da

Monoisotopic Mass

396.23006 Da

IUPAC Name

(8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid

Traditional Name

(8E,10E,12E)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid

CAS Registry Number

Not Available

SMILES

CC(C=CC=C(C)C(O)=O)=C\C=C\C=C(/C)\C=C\C1(O)C(C)=CC(=O)CC1(C)C

InChI Identifier

InChI=1S/C25H32O4/c1-18(12-9-13-20(3)23(27)28)10-7-8-11-19(2)14-15-25(29)21(4)16-22(26)17-24(25,5)6/h7-16,29H,17H2,1-6H3,(H,27,28)/b8-7+,12-9?,15-14+,18-10?,19-11+,20-13?

InChI Key

IKVOLCVFLNPJTB-WUNLQJBYSA-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
Cochlospermum tinctorium	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
Long-chain fatty acid
Cyclohexenone
Methyl-branched fatty acid
Hydroxy fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Tertiary alcohol
Cyclic ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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
logP	5.02	ALOGPS
logP	4.84	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.95	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	124.89 m³·mol⁻¹	ChemAxon
Polarizability	45.99 Å³	ChemAxon
Number of Rings	1	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid (NP0308218)

MOL for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

3D MOL for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

3D SDF for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

3D-SDF for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

PDB for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

3D PDB for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

SMILES for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

INCHI for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

Structure for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)

3D Structure for NP0308218 ((8e,10e,12e)-13-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid)