NP-MRD: Showing NP-Card for (10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one (NP0224057)

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Record Information

Version

2.0

Created at

2022-09-06 02:19:04 UTC

Updated at

2022-09-06 02:19:04 UTC

NP-MRD ID

NP0224057

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Description

(10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]Heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. (10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one is found in Capsicum annuum. Xanthophylls arise by oxygenation of the carotene backbone (10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]Heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004161515382D          

 44 46  0  0  0  0            999 V2000
    6.0826    8.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    8.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    8.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    7.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392    6.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392    5.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247    5.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    5.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247    4.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    4.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    3.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    3.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    2.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    1.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    1.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2875    0.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813   -0.6243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668    0.6132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4577    0.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0704    1.3129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957   -0.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.6132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6202    0.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2329    1.3129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    9.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0826    9.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0826   10.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   10.9257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   10.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   11.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   12.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   12.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2260   13.4007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   13.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2820   14.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4615   12.6470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6410   12.7333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890   12.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4695   13.5403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1840   13.9528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8563   14.7099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6619   14.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  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  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27  2  1  4  0  0  0
 27 28  2  0  0  0  0
 29 28  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 32 30  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END


  Mrv1533004161515382D          

 44 46  0  0  0  0            999 V2000
    6.0826    8.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    8.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    8.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6536    7.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392    6.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392    5.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247    5.5632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    5.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247    4.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    4.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5102    3.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    3.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    2.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    1.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    1.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2875    0.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813   -0.6243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668    0.6132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4577    0.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0704    1.3129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957   -0.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.6132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6202    0.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2329    1.3129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3681    9.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0826    9.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0826   10.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   10.9257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   10.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   11.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   12.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5115   12.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2260   13.4007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   13.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2820   14.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4615   12.6470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6410   12.7333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0890   12.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4695   13.5403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1840   13.9528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8563   14.7099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6619   14.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  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  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27  2  1  4  0  0  0
 27 28  2  0  0  0  0
 29 28  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 32 30  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224057

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C=CC=C(C)C=CC(=O)C1(C)CC(O)CC1(C)C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C12OC(CC1(C)C)CC2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O4/c1-29(17-13-19-31(3)21-22-35(42)38(9)26-33(41)25-36(38,5)6)15-11-12-16-30(2)18-14-20-32(4)23-24-40-37(7,8)27-34(44-40)28-39(40,10)43/h11-24,33-34,41,43H,25-28H2,1-10H3/b12-11+,17-13?,18-14+,22-21?,24-23+,29-15?,30-16+,31-19?,32-20+

> <INCHI_KEY>
TWTPPPZIWNGQCQ-KYHIUUMWSA-N

> <FORMULA>
C40H56O4

> <MOLECULAR_WEIGHT>
600.884

> <EXACT_MASS>
600.417860283

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
73.77200488682436

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

> <ALOGPS_LOGP>
7.77

> <JCHEM_LOGP>
7.958779693

> <ALOGPS_LOGS>
-6.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.220802717430466

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.694703534997782

> <JCHEM_PKA_STRONGEST_BASIC>
-2.708148423311787

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
193.65190000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.46e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      11.354  15.005   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.020  15.775   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.687  15.005   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.687  13.465   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.353  12.695   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.353  11.155   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.019  10.385   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.686  11.155   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.019   8.845   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.686   8.075   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.686   6.535   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.352   5.765   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.018   6.535   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.352   4.225   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.018   3.455   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.018   1.915   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.403   0.375   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.018  -1.165   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.685  -0.395   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.685   1.145   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.854   1.198   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.131   2.451   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.352  -0.395   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.352   1.145   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.891   1.198   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.168   2.451   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.020  17.315   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.354  18.085   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.354  19.625   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.688  20.395   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.021  19.625   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.688  21.935   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.021  22.705   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.021  24.245   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      15.355  25.015   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.688  25.015   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.593  26.261   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.061  23.608   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.530  23.769   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.499  22.624   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      10.210  25.275   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.543  26.045   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.932  27.458   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.435  27.300   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
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                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   20   24                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   16   21   22                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24                                                       
CONECT   24   23   16   25   26                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27    2   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38   42                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   36   43   44                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₆O₄

Average Mass

600.8840 Da

Monoisotopic Mass

600.41786 Da

IUPAC Name

(10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Traditional Name

(10E,12E,14E,16E,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

CAS Registry Number

Not Available

SMILES

CC(C=CC=C(C)C=CC(=O)C1(C)CC(O)CC1(C)C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C12OC(CC1(C)C)CC2(C)O

InChI Identifier

InChI=1S/C40H56O4/c1-29(17-13-19-31(3)21-22-35(42)38(9)26-33(41)25-36(38,5)6)15-11-12-16-30(2)18-14-20-32(4)23-24-40-37(7,8)27-34(44-40)28-39(40,10)43/h11-24,33-34,41,43H,25-28H2,1-10H3/b12-11+,17-13?,18-14+,22-21?,24-23+,29-15?,30-16+,31-19?,32-20+

InChI Key

TWTPPPZIWNGQCQ-KYHIUUMWSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Capsicum annuum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Tetraterpenoids

Direct Parent

Xanthophylls

Alternative Parents

Substituents

Xanthophyll
Monosaccharide
Cyclopentanol
Alpha,beta-unsaturated ketone
Tetrahydrofuran
Tertiary alcohol
Enone
Cyclic alcohol
Acryloyl-group
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	7.77	ALOGPS
logP	7.96	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	193.65 m³·mol⁻¹	ChemAxon
Polarizability	73.77 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 (10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one (NP0224057)

MOL for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D MOL for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D SDF for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D-SDF for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

PDB for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D PDB for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

SMILES for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

INCHI for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

Structure for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)

3D Structure for NP0224057 ((10e,12e,14e,16e,18e)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-19-{2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl}-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one)