NP-MRD: Showing NP-Card for 3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene (NP0065674)

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Record Information

Version

2.0

Created at

2022-04-28 09:52:34 UTC

Updated at

2022-04-28 09:52:34 UTC

NP-MRD ID

NP0065674

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene

Description

1'-Hydroxytorulene, also known as myxocoxanthin, 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. 3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene is found in Apis cerana, Myxococcus fulvus, Myxococcus fulvus str. MXf2 and Spirochaeta aurantia J1. 3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene was first documented in 1975 (PMID: 1158846). 1'-Hydroxytorulene is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

 
  Mrv1533006051514562D          
 
 41 41  0  0  0  0            999 V2000
   11.0280  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7426  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.6011  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  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
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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  8 28  1  0  0  0  0
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  1 32  1  0  0  0  0
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  1 36  2  0  0  0  0
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 36 39  1  0  0  0  0
 13 40  1  0  0  0  0
 25 41  1  0  0  0  0
M  END

     RDKit          3D

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M  END

 
  Mrv1533006051514562D          
 
 41 41  0  0  0  0            999 V2000
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   14.6011  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3157  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0303  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7449  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4595  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1742  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8888  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6033  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3180  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0326  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7471  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4618  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1764  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8910  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6056  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3202  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0348  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.7494  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4640  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1787  -15.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8658  -15.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1718  -14.4682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0303  -14.4682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4618  -16.5296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3202  -16.5296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1787  -16.5296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3128  -15.2893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5977  -15.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5952  -16.5236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3104  -16.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0256  -16.5293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8898  -14.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7358  -14.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7378  -16.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6000  -16.5258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9744  -15.9182    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  0  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
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 27  1  0  0  0  0
  8 28  1  0  0  0  0
 17 29  1  0  0  0  0
 21 30  1  0  0  0  0
 25 31  1  0  0  0  0
  1 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
  1 36  2  0  0  0  0
 32 37  1  0  0  0  0
 32 38  1  0  0  0  0
 36 39  1  0  0  0  0
 13 40  1  0  0  0  0
 25 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065674

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\CC(C)(C)O)=C/C=C/C(/C)=C/C=C/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/C40H56O/c1-32(20-13-22-34(3)23-14-24-35(4)26-16-31-40(9,10)41)18-11-12-19-33(2)21-15-25-36(5)28-29-38-37(6)27-17-30-39(38,7)8/h11-16,18-26,28-29,41H,17,27,30-31H2,1-10H3/b12-11+,20-13+,21-15+,23-14+,26-16+,29-28+,32-18+,33-19+,34-22+,35-24+,36-25+

> <INCHI_KEY>
JLURGIFQNZBRAB-CJXMTMHDSA-N

> <FORMULA>
C40H56O

> <MOLECULAR_WEIGHT>
552.887

> <EXACT_MASS>
552.433116423

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
73.66258762957543

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohex-1-en-1-yl)pentacosa-4,6,8,10,12,14,16,18,20,22,24-undecaen-2-ol

> <ALOGPS_LOGP>
9.28

> <JCHEM_LOGP>
10.100499599333332

> <ALOGPS_LOGS>
-6.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.567969329699817

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2381702151892995

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
196.8116000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.86e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
myxocoxanthin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-JUN-15   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-JUN-15         0                                  
HETATM    1  C   UNK     0      20.586 -29.316   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.920 -28.546   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      23.253 -29.316   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.587 -28.546   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      25.922 -29.316   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      27.255 -28.546   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      28.589 -29.316   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      29.923 -28.546   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      31.257 -29.316   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      32.591 -28.546   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      33.925 -29.316   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      35.259 -28.546   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      36.593 -29.316   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      37.927 -28.546   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      39.261 -29.316   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      40.595 -28.546   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      41.929 -29.316   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      43.263 -28.546   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      44.596 -29.316   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      45.931 -28.546   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      47.264 -29.316   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      48.598 -28.546   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      49.932 -29.316   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      51.266 -28.546   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      52.600 -29.316   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      53.883 -28.546   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      24.587 -27.007   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      29.923 -27.007   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      41.929 -30.855   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      47.264 -30.855   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      52.600 -30.855   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      19.251 -28.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      17.916 -29.305   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      17.911 -30.844   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      19.246 -31.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      20.581 -30.855   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      20.328 -27.463   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      18.173 -27.463   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      21.911 -31.628   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      36.587 -30.848   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      54.086 -29.714   0.000  0.00  0.00           C+0
CONECT    1    2   32   36                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   27                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   40                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   29                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   31   41                                             
CONECT   26   25                                                            
CONECT   27    4                                                            
CONECT   28    8                                                            
CONECT   29   17                                                            
CONECT   30   21                                                            
CONECT   31   25                                                            
CONECT   32    1   33   37   38                                             
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35    1   39                                                  
CONECT   37   32                                                            
CONECT   38   32                                                            
CONECT   39   36                                                            
CONECT   40   13                                                            
CONECT   41   25                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   82    0
END

View in JSmol

Synonyms

Value	Source
1',2'-Dihydro-1'-hydroxytorulene	ChEBI
1'-OH-Torulene	ChEBI
3',4'-Didehydro-1',2'-dihydro-beta,psi-caroten-1'-ol	ChEBI
Myxocoxanthin	ChEBI
3',4'-Didehydro-1',2'-dihydro-b,psi-caroten-1'-ol	Generator
3',4'-Didehydro-1',2'-dihydro-β,psi-caroten-1'-ol	Generator

Chemical Formula

C₄₀H₅₆O

Average Mass

552.8870 Da

Monoisotopic Mass

552.43312 Da

IUPAC Name

(4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2,6,10,14,19,23-hexamethyl-25-(2,6,6-trimethylcyclohex-1-en-1-yl)pentacosa-4,6,8,10,12,14,16,18,20,22,24-undecaen-2-ol

Traditional Name

myxocoxanthin

CAS Registry Number

Not Available

SMILES

C\C(\C=C\CC(C)(C)O)=C/C=C/C(/C)=C/C=C/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/C40H56O/c1-32(20-13-22-34(3)23-14-24-35(4)26-16-31-40(9,10)41)18-11-12-19-33(2)21-15-25-36(5)28-29-38-37(6)27-17-30-39(38,7)8/h11-16,18-26,28-29,41H,17,27,30-31H2,1-10H3/b12-11+,20-13+,21-15+,23-14+,26-16+,29-28+,32-18+,33-19+,34-22+,35-24+,36-25+

InChI Key

JLURGIFQNZBRAB-CJXMTMHDSA-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
Apis cerana	LOTUS Database	35616633
Myxococcus fulvus	LOTUS Database	35616633
Myxococcus fulvus str. MXf2	Bacteria	KNApSAcK
Spirochaeta aurantia J1	--	KNApSAcK

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
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

xanthophyll (CHEBI:80134 )

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	9.28	ALOGPS
logP	10.1	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	18.57	ChemAxon
pKa (Strongest Basic)	-1.2	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	13	ChemAxon
Refractivity	196.81 m³·mol⁻¹	ChemAxon
Polarizability	73.66 Å³	ChemAxon
Number of Rings	1	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

C00022845

Chemspider ID

Not Available

KEGG Compound ID

C15860

BioCyc ID

CPD-17309

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23724599

PDB ID

Not Available

ChEBI ID

80134

Good Scents ID

Not Available

References

General References

Greenberg EP, Canale-Parola E: Carotenoid pigments of facultatively anaerobic spirochetes. J Bacteriol. 1975 Sep;123(3):1006-12. doi: 10.1128/jb.123.3.1006-1012.1975. [PubMed:1158846 ]

Showing NP-Card for 3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene (NP0065674)

MOL for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

3D MOL for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

3D SDF for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

3D-SDF for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

PDB for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

3D PDB for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

SMILES for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

INCHI for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

Structure for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)

3D Structure for NP0065674 (3',4'-Didehydro-1',2'-dihydro-1'-hydroxy-beta,psi-carotene)