NP-MRD: Showing NP-Card for Cryptocapsin (NP0048648)

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Record Information

Version

2.0

Created at

2022-03-17 20:59:55 UTC

Updated at

2022-03-17 20:59:55 UTC

NP-MRD ID

NP0048648

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cryptocapsin

Description

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

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05061309242D          

 42 43  0  0  0  0            999 V2000
   12.5419  -11.2008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2672   -7.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5887  -14.4378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2204   -4.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3067  -13.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2358  -16.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4476  -15.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8264   -4.9597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1675   -3.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6954   -3.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0321   -9.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7771   -8.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4379  -12.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3713   -6.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6236  -15.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4800  -10.2446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3291   -8.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1829  -11.6423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6262   -6.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8858  -13.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9233   -5.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3687  -14.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9477  -13.9962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8614   -4.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027  -14.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6065   -3.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0716  -15.9085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8350   -5.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9149   -4.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7350  -11.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0742   -7.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1408  -13.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6684   -4.6538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5617  -14.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6600   -5.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0097  -14.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7995   -3.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2646  -15.7370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5800   -4.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2475   -4.1392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1449   -6.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5446   -2.7415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  2  0  0  0  0
 16 11  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  2  0  0  0  0
 19 14  2  0  0  0  0
 20 13  1  0  0  0  0
 21 14  1  0  0  0  0
 22 15  1  0  0  0  0
 25 23  2  0  0  0  0
 26 24  2  0  0  0  0
 27 15  1  0  0  0  0
 30  1  1  0  0  0  0
 30 16  2  0  0  0  0
 30 18  1  0  0  0  0
 31  2  1  0  0  0  0
 31 17  2  0  0  0  0
 31 19  1  0  0  0  0
 32  3  1  0  0  0  0
 32 20  2  0  0  0  0
 32 23  1  0  0  0  0
 33  4  1  0  0  0  0
 33 21  2  0  0  0  0
 33 24  1  0  0  0  0
 34  5  1  0  0  0  0
 34 22  1  0  0  0  0
 35 28  1  0  0  0  0
 35 29  1  0  0  0  0
 36 25  1  0  0  0  0
 36 34  2  0  0  0  0
 37 26  1  0  0  0  0
 38  6  1  0  0  0  0
 38  7  1  0  0  0  0
 38 27  1  0  0  0  0
 38 36  1  0  0  0  0
 39  8  1  0  0  0  0
 39  9  1  0  0  0  0
 39 28  1  0  0  0  0
 40 10  1  0  0  0  0
 40 29  1  0  0  0  0
 40 37  1  0  0  0  0
 40 39  1  0  0  0  0
 41 35  1  0  0  0  0
 42 37  2  0  0  0  0
M  END


  Mrv0541 05061309242D          

 42 43  0  0  0  0            999 V2000
   12.5419  -11.2008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2672   -7.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5887  -14.4378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2204   -4.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3067  -13.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2358  -16.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4476  -15.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8264   -4.9597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1675   -3.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6954   -3.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0321   -9.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7771   -8.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4379  -12.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3713   -6.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6236  -15.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4800  -10.2446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3291   -8.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1829  -11.6423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6262   -6.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8858  -13.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9233   -5.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3687  -14.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9477  -13.9962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8614   -4.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2027  -14.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6065   -3.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0716  -15.9085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8350   -5.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9149   -4.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7350  -11.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0742   -7.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1408  -13.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6684   -4.6538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5617  -14.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6600   -5.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0097  -14.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7995   -3.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2646  -15.7370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5800   -4.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2475   -4.1392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1449   -6.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5446   -2.7415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  2  0  0  0  0
 16 11  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  2  0  0  0  0
 19 14  2  0  0  0  0
 20 13  1  0  0  0  0
 21 14  1  0  0  0  0
 22 15  1  0  0  0  0
 25 23  2  0  0  0  0
 26 24  2  0  0  0  0
 27 15  1  0  0  0  0
 30  1  1  0  0  0  0
 30 16  2  0  0  0  0
 30 18  1  0  0  0  0
 31  2  1  0  0  0  0
 31 17  2  0  0  0  0
 31 19  1  0  0  0  0
 32  3  1  0  0  0  0
 32 20  2  0  0  0  0
 32 23  1  0  0  0  0
 33  4  1  0  0  0  0
 33 21  2  0  0  0  0
 33 24  1  0  0  0  0
 34  5  1  0  0  0  0
 34 22  1  0  0  0  0
 35 28  1  0  0  0  0
 35 29  1  0  0  0  0
 36 25  1  0  0  0  0
 36 34  2  0  0  0  0
 37 26  1  0  0  0  0
 38  6  1  0  0  0  0
 38  7  1  0  0  0  0
 38 27  1  0  0  0  0
 38 36  1  0  0  0  0
 39  8  1  0  0  0  0
 39  9  1  0  0  0  0
 39 28  1  0  0  0  0
 40 10  1  0  0  0  0
 40 29  1  0  0  0  0
 40 37  1  0  0  0  0
 40 39  1  0  0  0  0
 41 35  1  0  0  0  0
 42 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0048648

> <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/C1=C(C)CCCC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O2/c1-30(18-13-20-32(3)23-25-36-34(5)22-15-27-38(36,6)7)16-11-12-17-31(2)19-14-21-33(4)24-26-37(42)40(10)29-35(41)28-39(40,8)9/h11-14,16-21,23-26,35,41H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20-,33-21-

> <INCHI_KEY>
ITZNDVRDABSNRE-JLPYQHGFSA-N

> <FORMULA>
C40H56O2

> <MOLECULAR_WEIGHT>
568.8714

> <EXACT_MASS>
568.428031036

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
72.77620480721643

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,4Z,6E,8E,10E,12E,14E,16Z,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-19-(2,6,6-trimethylcyclohex-1-en-1-yl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

> <ALOGPS_LOGP>
8.94

> <JCHEM_LOGP>
9.892089687666665

> <ALOGPS_LOGS>
-6.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.20725097551032

> <JCHEM_PKA_STRONGEST_BASIC>
-2.708148423311787

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
193.2943

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.02e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4Z,6E,8E,10E,12E,14E,16Z,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-19-(2,6,6-trimethylcyclohex-1-en-1-yl)nonadeca-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      23.412 -20.908   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.032 -13.585   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.766 -26.951   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.678  -7.543   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.839 -25.302   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.707 -30.915   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.236 -29.590   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.476  -9.258   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.113  -7.298   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.098  -6.582   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.460 -17.979   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.984 -16.514   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      21.351 -23.197   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      23.093 -11.296   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.297 -28.551   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.429 -19.123   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.014 -15.370   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.875 -21.732   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      23.569 -12.761   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.320 -24.342   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.123 -10.152   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.822 -27.087   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.302 -26.126   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      22.141  -8.367   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      22.778 -27.591   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      21.665  -6.902   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      26.267 -29.696   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.359 -10.096   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.374  -8.632   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      21.905 -20.588   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      22.539 -13.905   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.796 -25.806   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      23.648  -8.687   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      25.315 -26.767   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      19.899 -10.096   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      24.285 -27.911   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      20.159  -6.582   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      24.761 -29.376   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.883  -8.632   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      19.129  -7.727   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      20.804 -11.342   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      19.683  -5.117   0.000  0.00  0.00           O+0
CONECT    1   30                                                            
CONECT    2   31                                                            
CONECT    3   32                                                            
CONECT    4   33                                                            
CONECT    5   34                                                            
CONECT    6   38                                                            
CONECT    7   38                                                            
CONECT    8   39                                                            
CONECT    9   39                                                            
CONECT   10   40                                                            
CONECT   11   12   16                                                       
CONECT   12   11   17                                                       
CONECT   13   18   20                                                       
CONECT   14   19   21                                                       
CONECT   15   22   27                                                       
CONECT   16   11   30                                                       
CONECT   17   12   31                                                       
CONECT   18   13   30                                                       
CONECT   19   14   31                                                       
CONECT   20   13   32                                                       
CONECT   21   14   33                                                       
CONECT   22   15   34                                                       
CONECT   23   25   32                                                       
CONECT   24   26   33                                                       
CONECT   25   23   36                                                       
CONECT   26   24   37                                                       
CONECT   27   15   38                                                       
CONECT   28   35   39                                                       
CONECT   29   35   40                                                       
CONECT   30    1   16   18                                                  
CONECT   31    2   17   19                                                  
CONECT   32    3   20   23                                                  
CONECT   33    4   21   24                                                  
CONECT   34    5   22   36                                                  
CONECT   35   28   29   41                                                  
CONECT   36   25   34   38                                                  
CONECT   37   26   40   42                                                  
CONECT   38    6    7   27   36                                             
CONECT   39    8    9   28   40                                             
CONECT   40   10   29   37   39                                             
CONECT   41   35                                                            
CONECT   42   37                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

View in JSmol

Synonyms

Value	Source
(3's,5'r)-3'-Hydroxy-beta,kappa-caroten-6'-one	HMDB
3'-Hydroxy-b,K-caroten-6'-one	HMDB
Kryptocapsin	HMDB

Chemical Formula

C₄₀H₅₆O₂

Average Mass

568.8714 Da

Monoisotopic Mass

568.42803 Da

IUPAC Name

(2E,4Z,6E,8E,10E,12E,14E,16Z,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-19-(2,6,6-trimethylcyclohex-1-en-1-yl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Traditional Name

(2E,4Z,6E,8E,10E,12E,14E,16Z,18E)-1-(4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-19-(2,6,6-trimethylcyclohex-1-en-1-yl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

CAS Registry Number

7044-42-0

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/C1=C(C)CCCC1(C)C

InChI Identifier

InChI=1S/C40H56O2/c1-30(18-13-20-32(3)23-25-36-34(5)22-15-27-38(36,6)7)16-11-12-17-31(2)19-14-21-33(4)24-26-37(42)40(10)29-35(41)28-39(40,8)9/h11-14,16-21,23-26,35,41H,15,22,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20-,33-21-

InChI Key

ITZNDVRDABSNRE-JLPYQHGFSA-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
Alpha,beta-unsaturated ketone
Enone
Cyclic alcohol
Acryloyl-group
Secondary alcohol
Ketone
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	8.94	ALOGPS
logP	9.89	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	15.21	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	193.29 m³·mol⁻¹	ChemAxon
Polarizability	72.78 Å³	ChemAxon
Number of Rings	2	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

HMDB0036923

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015892

KNApSAcK ID

C00022984

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

131752094

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Cryptocapsin (NP0048648)

MOL for NP0048648 (Cryptocapsin)

3D MOL for NP0048648 (Cryptocapsin)

3D SDF for NP0048648 (Cryptocapsin)

3D-SDF for NP0048648 (Cryptocapsin)

PDB for NP0048648 (Cryptocapsin)

3D PDB for NP0048648 (Cryptocapsin)

SMILES for NP0048648 (Cryptocapsin)

INCHI for NP0048648 (Cryptocapsin)

Structure for NP0048648 (Cryptocapsin)

3D Structure for NP0048648 (Cryptocapsin)