NP-MRD: Showing NP-Card for (2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol (NP0063874)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 08:12:22 UTC

Updated at

2022-04-28 08:12:22 UTC

NP-MRD ID

NP0063874

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol

Description

(2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. (2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol is found in Croton hieronymi . Based on a literature review very few articles have been published on (2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282210122D          

 26 25  0  0  1  0            999 V2000
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    7.4763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 13 22  1  1  0  0  0
  9 23  1  1  0  0  0
  5 24  1  1  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
M  END

     RDKit          3D

 76 75  0  0  0  0  0  0  0  0999 V2000
   -8.7059   -0.2884    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5280    0.4054    0.9680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6057    1.4346    1.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5176    2.1951    2.3832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6246    3.5322    1.9383 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1709   -0.1475    0.5840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1027   -0.0302   -0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8575   -0.4265   -1.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3371   -1.8066   -1.4896 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1314   -2.3454   -0.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0912   -1.9974   -2.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8412   -1.3561   -1.9329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2155   -1.6593   -0.6311 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0999   -0.8751   -0.4626 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1173    0.6023   -0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0299   -1.2792   -1.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3694   -0.6068   -1.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0389   -0.9696   -0.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3700   -0.1889   -0.0698 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0765   -0.5622   -1.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1316   -0.4698    1.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4289    0.2370    1.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    1.7345    1.2494 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6837    2.3934    1.3591 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5862    1.9770    0.2277 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3016    2.0857    2.7123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8469   -0.0658   -0.6841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6380   -0.0496    0.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5731   -1.3904    0.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6434    1.7892    2.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7106    2.1787    3.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4959    1.8895    2.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7613    3.9971    1.9534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2342   -1.2403    0.8618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3378    0.3168    1.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9283   -0.6931   -1.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4536    0.9974   -1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0156    0.2422   -1.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9617   -0.0839   -2.6549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1009   -2.4826   -1.9779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0232   -1.6257    0.6939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2683   -3.0715   -0.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9877   -3.0390    0.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3283   -1.7573   -3.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9186   -3.1165   -2.3180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8233   -0.2426   -2.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0803   -1.6929   -2.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8155   -1.2837    0.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9203   -2.7255   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -1.1968    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197    1.0495    0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0643    0.8198    0.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0532    1.0475   -1.4452 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6896   -0.9380   -2.5784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1472   -2.3713   -1.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0199   -0.7985   -2.2211 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2392    0.5145   -1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4346   -0.6254    0.8234 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2008   -2.0467   -0.0161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0453    0.8857   -0.0576 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8121   -1.6009   -1.6900 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1711   -0.6184   -1.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8428    0.1077   -2.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4584   -0.3343    2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3680   -1.5753    1.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8640   -0.0160    2.2990 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1661   -0.0827    0.5395 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8784    2.0853    0.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7003    2.1495    2.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5016    3.4893    1.3474 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3679    2.7508    0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9451    1.8334   -0.6648 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0069    0.9831    0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6012    1.0208    2.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1224    2.7902    2.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5013    2.2383    3.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 26  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
 25 71  1  0
 25 72  1  0
 25 73  1  0
 24 70  1  1
 26 74  1  0
 26 75  1  0
 26 76  1  0
 23 68  1  0
 23 69  1  0
 22 66  1  0
 22 67  1  0
 21 64  1  0
 21 65  1  0
 19 60  1  6
 20 61  1  0
 20 62  1  0
 20 63  1  0
 18 58  1  0
 18 59  1  0
 17 56  1  0
 17 57  1  0
 16 54  1  0
 16 55  1  0
 14 50  1  1
 15 51  1  0
 15 52  1  0
 15 53  1  0
 13 48  1  0
 13 49  1  0
 12 46  1  0
 12 47  1  0
 11 44  1  0
 11 45  1  0
  9 40  1  6
 10 41  1  0
 10 42  1  0
 10 43  1  0
  8 38  1  0
  8 39  1  0
  7 36  1  0
  7 37  1  0
  6 34  1  0
  6 35  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
M  END


  Mrv1652304282210122D          

 26 25  0  0  1  0            999 V2000
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    7.4763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 13 22  1  1  0  0  0
  9 23  1  1  0  0  0
  5 24  1  1  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0063874

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C/CO

> <INCHI_IDENTIFIER>
InChI=1S/C25H50O/c1-21(2)11-7-12-22(3)13-8-14-23(4)15-9-16-24(5)17-10-18-25(6)19-20-26/h19,21-24,26H,7-18,20H2,1-6H3/b25-19-/t22-,23-,24-/m1/s1

> <INCHI_KEY>
IRJHFRKRPYTYCQ-UAYKKUFWSA-N

> <FORMULA>
C25H50O

> <MOLECULAR_WEIGHT>
366.674

> <EXACT_MASS>
366.38616623

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
50.20845422869767

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol

> <ALOGPS_LOGP>
9.20

> <JCHEM_LOGP>
9.103844046333332

> <ALOGPS_LOGS>
-7.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.330030451338093

> <JCHEM_PKA_STRONGEST_BASIC>
-2.217044680584718

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
119.18989999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.78e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      30.840  10.106   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      36.175  10.106   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      36.175  11.646   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      34.842  12.416   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      34.842  13.956   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      37.509   9.336   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      30.840  11.646   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      25.506  11.646   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      20.171  11.646   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.503   9.336   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.836  11.646   0.000  0.00  0.00           C+0
CONECT    1    2   25   26                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7                                                       
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                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   17                                                            
CONECT   22   13                                                            
CONECT   23    9                                                            
CONECT   24    5                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₅₀O

Average Mass

366.6740 Da

Monoisotopic Mass

366.38617 Da

IUPAC Name

(2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol

Traditional Name

(2Z,7R,11R,15R)-3,7,11,15,19-pentamethylicos-2-en-1-ol

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C/CO

InChI Identifier

InChI=1S/C25H50O/c1-21(2)11-7-12-22(3)13-8-14-23(4)15-9-16-24(5)17-10-18-25(6)19-20-26/h19,21-24,26H,7-18,20H2,1-6H3/b25-19-/t22-,23-,24-/m1/s1

InChI Key

IRJHFRKRPYTYCQ-UAYKKUFWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Croton hieronymi	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Polyprenol skeleton
Long chain fatty alcohol
Fatty alcohol
Fatty acyl
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	9.2	ALOGPS
logP	9.1	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	16.33	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	119.19 m³·mol⁻¹	ChemAxon
Polarizability	50.21 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162850196

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol (NP0063874)

MOL for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

3D MOL for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

3D SDF for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

3D-SDF for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

PDB for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

3D PDB for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

SMILES for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

INCHI for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

Structure for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)

3D Structure for NP0063874 ((2E)-3,7,11,15,19-Pentamethyl-2-eicosen-1-ol)