NP-MRD: Showing NP-Card for 11-cis-retinol (NP0310433)

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Record Information

Version

2.0

Created at

2022-09-11 05:44:31 UTC

Updated at

2022-09-11 05:44:31 UTC

NP-MRD ID

NP0310433

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-cis-retinol

Description

11-Cis-Retinol, also known as cis-11-retinol or vitamin a, belongs to the class of organic compounds known as retinoids. These are oxygenated derivatives of 3,7-dimethyl-1-(2,6,6-trimethylcyclohex-1-enyl)nona-1,3,5,7-tetraene and derivatives thereof. Thus, 11-cis-retinol is considered to be an isoprenoid lipid molecule. They showed metabolism similar to that of cells freshly isolated by nonenzymatic means. After trypsinization, confluent cultures dissociated into individual cells, but these cells showed poor retinoid metabolism, including no detectable retinyl esters or 11- cis -retinoid isomers. 11-Cis-Retinol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Within humans, 11-cis-retinol participates in a number of enzymatic reactions. In particular, 11-cis-retinol can be biosynthesized from 11-cis-retinaldehyde; which is mediated by the enzyme retinol dehydrogenase 11. In addition, 11-cis-retinol and PC(24:1(15Z)/15:0) Can be converted into glycerophosphocholine; which is mediated by the enzyme lecithin retinol acyltransferase. In humans, 11-cis-retinol is involved in retinol metabolism. Nondamaged cells cultured on thermally responsive surfaces detached in sheets upon temperature change. 11-Cis-Retinol is produce from vitamin A cycle driven by interphotoreceptor retinoid binding protein(IRBP). 11-Cis-Retinol is released from retinal pigment epithelium(RPE) membranes. 11-cis-retinol is found in Pandalus borealis. 11-cis-retinol was first documented in 1999 (PMID: 10375454). Retinoid metabolism of RPE cells freshly isolated by trypsinization showed no 11- cis -retinal and little 11- cis -retinol formation (PMID: 10655150).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 51  0  0  0  0  0  0  0  0999 V2000
   -3.3196    0.9903    2.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6764    0.5935    1.3834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7199    0.2656    0.4660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3813    0.3592    1.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2243    0.1506    0.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0514    0.2991    1.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1711    0.6843    2.6217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2035    0.0554    0.5695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767    0.1739    1.2112 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6335   -0.0233    0.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8905   -0.4022   -0.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9379   -0.6160   -1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1822   -0.5666   -0.9612 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7449   -0.9446   -2.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6154    0.0558   -2.7546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2097   -0.1074   -0.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6875    1.1547   -1.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1767   -0.7176   -1.7439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3525   -1.1164   -0.6873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3934   -0.7302    0.3034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0937    0.5818    0.9722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2779    1.2411    3.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8174    0.1226    3.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7003    1.9039    2.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2615    0.6576    2.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1885   -0.1208   -0.5394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7181   -0.1098    3.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7963    1.6291    2.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2900    0.9100    3.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0512   -0.2339   -0.4391 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4175    0.4743    2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4726    0.1391    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5128   -0.8498   -2.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    0.2991   -1.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3168   -1.5292   -1.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9216   -0.4021   -0.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1386   -1.4176   -2.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5202   -1.7797   -2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0662    0.6766   -3.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0570    1.3560   -2.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5517    2.0662   -0.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7389    0.9802   -1.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    0.0764   -2.1897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6516   -1.5329   -1.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -1.2296   -2.6182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8163   -1.3127   -1.6814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8789   -2.0670   -0.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4058   -0.6357   -0.1569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4566   -1.4933    1.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3882    1.4588    0.3709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7418    0.5832    1.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  6  2  0
  6  7  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 21  1  0
 21 20  1  0
 20 19  1  0
 19 16  1  0
 16 17  1  0
 16 18  1  0
 16  3  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 10 32  1  0
  9 31  1  0
  8 30  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
  5 26  1  0
  4 25  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
 21 50  1  0
 21 51  1  0
 20 48  1  0
 20 49  1  0
 19 46  1  0
 19 47  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 18 45  1  0
M  END


  Mrv1652303192021392D          

 21 21  0  0  0  0            999 V2000
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    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  1  0  0  0  0
  2  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
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0310433

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(=C/CO)\C=C/C=C(\C)/C=C/C1=C(C)CCCC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6-,12-11+,16-8+,17-13+

> <INCHI_KEY>
FPIPGXGPPPQFEQ-IOUUIBBYSA-N

> <FORMULA>
C20H30O

> <MOLECULAR_WEIGHT>
286.4516

> <EXACT_MASS>
286.229665582

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.685679783607306

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4Z,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol

> <ALOGPS_LOGP>
6.38

> <JCHEM_LOGP>
4.694093173000001

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.435769749539965

> <JCHEM_PKA_STRONGEST_BASIC>
-2.1707943115512176

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
97.9234

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.58e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
vitamin a

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.057   3.670   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13   20   21                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
11-cis-Vitamin a alcohol	HMDB
cis-11-Retinol	HMDB
3,7-Dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol, (all-e)-isomer	HMDB
all trans Retinol	HMDB
all-trans-Retinol	HMDB
Aquasol a	HMDB
Retinol	HMDB
Vitamin a	HMDB
Vitamin a1	HMDB

Chemical Formula

C₂₀H₃₀O

Average Mass

286.4516 Da

Monoisotopic Mass

286.22967 Da

IUPAC Name

(2E,4Z,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol

Traditional Name

vitamin a

CAS Registry Number

Not Available

SMILES

C\C(=C/CO)\C=C/C=C(\C)/C=C/C1=C(C)CCCC1(C)C

InChI Identifier

InChI=1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6-,12-11+,16-8+,17-13+

InChI Key

FPIPGXGPPPQFEQ-IOUUIBBYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, CDCl₃, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Pandalus borealis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as retinoids. These are oxygenated derivatives of 3,7-dimethyl-1-(2,6,6-trimethylcyclohex-1-enyl)nona-1,3,5,7-tetraene and derivatives thereof.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Retinoids

Direct Parent

Retinoids

Alternative Parents

Substituents

Retinoid skeleton
Diterpenoid
Fatty alcohol
Fatty acyl
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

retinol (CHEBI:16302 )
Retinoids (C00899 )
Retinoids (LMPR01090005 )

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	6.38	ALOGPS
logP	4.69	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	16.44	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	5	ChemAxon
Refractivity	97.92 m³·mol⁻¹	ChemAxon
Polarizability	35.69 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0006216

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB023840

KNApSAcK ID

Not Available

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5280382

PDB ID

Not Available

ChEBI ID

16302

Good Scents ID

Not Available

References

General References

Edwards RB, Adler AJ: IRBP enhances removal of 11- cis -retinaldehyde from isolated RPE membranes. Exp Eye Res. 2000 Feb;70(2):235-45. doi: 10.1006/exer.1999.0781. [PubMed:10655150 ]
von Recum HA, Okano T, Kim SW, Bernstein PS: Maintenance of retinoid metabolism in human retinal pigment epithelium cell culture. Exp Eye Res. 1999 Jul;69(1):97-107. doi: 10.1006/exer.1999.0682. [PubMed:10375454 ]
LOTUS database [Link]

Showing NP-Card for 11-cis-retinol (NP0310433)

MOL for NP0310433 (11-cis-retinol)

3D MOL for NP0310433 (11-cis-retinol)

3D SDF for NP0310433 (11-cis-retinol)

3D-SDF for NP0310433 (11-cis-retinol)

PDB for NP0310433 (11-cis-retinol)

3D PDB for NP0310433 (11-cis-retinol)

SMILES for NP0310433 (11-cis-retinol)

INCHI for NP0310433 (11-cis-retinol)

Structure for NP0310433 (11-cis-retinol)

3D Structure for NP0310433 (11-cis-retinol)