NP-MRD: Showing NP-Card for Capsanthin 3,6-epoxide (NP0047585)

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Record Information

Version

2.0

Created at

2022-03-17 20:42:36 UTC

Updated at

2022-03-17 20:42:36 UTC

NP-MRD ID

NP0047585

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Capsanthin 3,6-epoxide

Description

Capsanthin 3,6-epoxide 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. Capsanthin 3,6-epoxide is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Capsanthin 3,6-epoxide has been detected, but not quantified in, several different foods, such as pepper (c. Annuum), orange bell peppers, herbs and spices, green bell peppers, and italian sweet red peppers. This could make capsanthin 3,6-epoxide a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05061309242D          

 44 46  0  0  0  0            999 V2000
   -4.0901   -1.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9509   -4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5226   -3.7231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -4.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7161   -7.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8139   -7.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2522   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6764   -1.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2982   -7.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0241   -2.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9473   -1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9485   -2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0925   -2.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1932   -3.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6612   -1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2346   -2.9043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774   -2.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5219   -4.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0937   -3.7252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9070   -4.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099   -4.9616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5250   -5.3731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6233   -2.9084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -2.4949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4849   -6.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4757   -5.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5004   -1.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3762   -1.6637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2358   -3.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8087   -4.1366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6221   -3.7334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6553   -5.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1407   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5262   -6.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2000   -7.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351   -2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8123   -6.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6411   -2.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -1.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1024   -5.3336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2413   -6.6096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3839   -2.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  2  0  0  0  0
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 40 37  1  0  0  0  0
 40 39  1  0  0  0  0
 41 33  1  0  0  0  0
 42 35  2  0  0  0  0
 43 39  1  0  0  0  0
 44 34  1  0  0  0  0
 44 40  1  0  0  0  0
M  END


  Mrv0541 05061309242D          

 44 46  0  0  0  0            999 V2000
   -4.0901   -1.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9509   -4.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5226   -3.7231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -4.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7161   -7.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8139   -7.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2522   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6764   -1.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2982   -7.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0241   -2.7709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9473   -1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9485   -2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0925   -2.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1932   -3.7314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6612   -1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2346   -2.9043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774   -2.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5219   -4.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0937   -3.7252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9070   -4.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099   -4.9616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5250   -5.3731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6233   -2.9084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -2.4949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4849   -6.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4757   -5.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5004   -1.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3762   -1.6637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2358   -3.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8087   -4.1366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6221   -3.7334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6553   -5.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1407   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5262   -6.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2000   -7.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351   -2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8123   -6.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6411   -2.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -1.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1024   -5.3336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2413   -6.6096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3839   -2.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  2  0  0  0  0
 15 11  1  0  0  0  0
 16 12  1  0  0  0  0
 17 13  2  0  0  0  0
 18 14  2  0  0  0  0
 19 13  1  0  0  0  0
 20 14  1  0  0  0  0
 22 21  2  0  0  0  0
 24 23  2  0  0  0  0
 29  1  1  0  0  0  0
 29 15  2  0  0  0  0
 29 17  1  0  0  0  0
 30  2  1  0  0  0  0
 30 16  2  0  0  0  0
 30 18  1  0  0  0  0
 31  3  1  0  0  0  0
 31 19  2  0  0  0  0
 31 21  1  0  0  0  0
 32  4  1  0  0  0  0
 32 20  2  0  0  0  0
 32 23  1  0  0  0  0
 33 25  1  0  0  0  0
 33 26  1  0  0  0  0
 34 27  1  0  0  0  0
 34 28  1  0  0  0  0
 35 22  1  0  0  0  0
 36  5  1  0  0  0  0
 36  6  1  0  0  0  0
 36 25  1  0  0  0  0
 37  7  1  0  0  0  0
 37  8  1  0  0  0  0
 37 27  1  0  0  0  0
 38  9  1  0  0  0  0
 38 26  1  0  0  0  0
 38 35  1  0  0  0  0
 38 36  1  0  0  0  0
 39 10  1  0  0  0  0
 39 28  1  0  0  0  0
 40 24  1  0  0  0  0
 40 37  1  0  0  0  0
 40 39  1  0  0  0  0
 41 33  1  0  0  0  0
 42 35  2  0  0  0  0
 43 39  1  0  0  0  0
 44 34  1  0  0  0  0
 44 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0047585

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\C(=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-SPHDKFQHSA-N

> <FORMULA>
C40H56O4

> <MOLECULAR_WEIGHT>
600.8702

> <EXACT_MASS>
600.41786028

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
74.22184875127901

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,4E,6E,8Z,10E,12E,14E,16Z,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>
193.65189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.46e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E,6E,8Z,10E,12E,14E,16Z,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                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -7.635  -2.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.642  -7.729   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.309  -6.950   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.361  -7.741   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.937 -14.621   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.986 -14.403   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.471  -5.370   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.263  -3.568   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.890 -13.586   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.778  -5.172   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.635  -3.109   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.637  -4.649   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.639  -5.414   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.361  -6.965   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.968  -2.337   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.305  -5.421   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.304  -4.646   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.974  -7.733   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.642  -6.954   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.693  -7.737   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -8.978  -9.262   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -10.313 -10.030   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.030  -5.429   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.698  -4.657   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.505 -12.606   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.355 -10.936   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.934  -2.613   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.614  -2.641   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.302  -3.106   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.307  -6.961   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.976  -7.722   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.028  -6.969   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.823 -11.099   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.129  -1.772   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.316 -11.570   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -7.840 -13.374   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.252  -3.846   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -8.983 -12.342   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.063  -3.808   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.700  -3.117   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -5.791  -9.956   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0     -11.650 -12.338   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       4.450  -4.479   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       1.831  -0.250   0.000  0.00  0.00           O+0
CONECT    1   29                                                            
CONECT    2   30                                                            
CONECT    3   31                                                            
CONECT    4   32                                                            
CONECT    5   36                                                            
CONECT    6   36                                                            
CONECT    7   37                                                            
CONECT    8   37                                                            
CONECT    9   38                                                            
CONECT   10   39                                                            
CONECT   11   12   15                                                       
CONECT   12   11   16                                                       
CONECT   13   17   19                                                       
CONECT   14   18   20                                                       
CONECT   15   11   29                                                       
CONECT   16   12   30                                                       
CONECT   17   13   29                                                       
CONECT   18   14   30                                                       
CONECT   19   13   31                                                       
CONECT   20   14   32                                                       
CONECT   21   22   31                                                       
CONECT   22   21   35                                                       
CONECT   23   24   32                                                       
CONECT   24   23   40                                                       
CONECT   25   33   36                                                       
CONECT   26   33   38                                                       
CONECT   27   34   37                                                       
CONECT   28   34   39                                                       
CONECT   29    1   15   17                                                  
CONECT   30    2   16   18                                                  
CONECT   31    3   19   21                                                  
CONECT   32    4   20   23                                                  
CONECT   33   25   26   41                                                  
CONECT   34   27   28   44                                                  
CONECT   35   22   38   42                                                  
CONECT   36    5    6   25   38                                             
CONECT   37    7    8   27   40                                             
CONECT   38    9   26   35   36                                             
CONECT   39   10   28   40   43                                             
CONECT   40   24   37   39   44                                             
CONECT   41   33                                                            
CONECT   42   35                                                            
CONECT   43   39                                                            
CONECT   44   34   40                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Value	Source
Capsanthin 3,6-epoxide	MeSH

Chemical Formula

C₄₀H₅₆O₄

Average Mass

600.8702 Da

Monoisotopic Mass

600.41786 Da

IUPAC Name

(2E,4E,6E,8Z,10E,12E,14E,16Z,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

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C=C(/C)\C=C\C(=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-SPHDKFQHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Capsicum annuum	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Capsicum annuum var. annuum	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases

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
Cyclopentanol
Monosaccharide
Acryloyl-group
Cyclic alcohol
Enone
Tertiary alcohol
Tetrahydrofuran
Alpha,beta-unsaturated ketone
Secondary alcohol
Ketone
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Organic oxide
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxygen compound
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	74.22 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

HMDB0033260

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB011282

KNApSAcK ID

C00023042

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

131751400

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Capsanthin 3,6-epoxide (NP0047585)

MOL for NP0047585 (Capsanthin 3,6-epoxide)

3D MOL for NP0047585 (Capsanthin 3,6-epoxide)

3D SDF for NP0047585 (Capsanthin 3,6-epoxide)

3D-SDF for NP0047585 (Capsanthin 3,6-epoxide)

PDB for NP0047585 (Capsanthin 3,6-epoxide)

3D PDB for NP0047585 (Capsanthin 3,6-epoxide)

SMILES for NP0047585 (Capsanthin 3,6-epoxide)

INCHI for NP0047585 (Capsanthin 3,6-epoxide)

Structure for NP0047585 (Capsanthin 3,6-epoxide)

3D Structure for NP0047585 (Capsanthin 3,6-epoxide)