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(2E,4E,6Z,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraenal
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ChemBase ID:
134305
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Molecular Formular:
C20H28O
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Molecular Mass:
284.43572
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Monoisotopic Mass:
284.21401552
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SMILES and InChIs
SMILES:
CC1=C(C(CCC1)(C)C)/C=C/C(=C\C=C\C(=C\C=O)\C)/C
Canonical SMILES:
O=C/C=C(/C=C/C=C(\C=C\C1=C(C)CCCC1(C)C)/C)\C
InChI:
InChI=1S/C20H28O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,15H,7,10,14H2,1-5H3/b9-6+,12-11+,16-8-,17-13+
InChIKey:
NCYCYZXNIZJOKI-MKOSUFFBSA-N
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Cite this record
CBID:134305 http://www.chembase.cn/molecule-134305.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(2E,4E,6Z,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraenal
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IUPAC Traditional name
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Synonyms
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9-cis-Retinal
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9-Z-Retinal
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9-cis-Retinaldehyde
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9-cis-Vitamin A Aldehyde
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Isoretinene a
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9-cis-Retinal
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维生素 A 醛
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9-顺式视黄醛
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CAS Number
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EC Number
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
H Acceptors
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1
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H Donor
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0
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LogD (pH = 5.5)
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4.8557515
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LogD (pH = 7.4)
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4.8557515
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Log P
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4.8557515
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Molar Refractivity
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96.8654 cm3
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Polarizability
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35.792797 Å3
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Polar Surface Area
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17.07 Å2
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Rotatable Bonds
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5
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Sigma Aldrich
TRC
Sigma Aldrich -
R5754
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Biochem/physiol Actions Retinal, retinol and retinoic acid are the aldehyde, alcohol and acid forms of vitamin A. The retinoids exist as many geometric isomers due to the unsaturated bonds in the aliphatic chain.9-cis retinal is a natural ligand (chromophore) of the vertebrate rod visual pigment. 9-cis retinal is used in studies on the mechanisms of visual function. Other Notes Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. R5754.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin. |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Yan, E., et al.: Biochemistry, 43, 10867 (2004)
- • Kukura, P., et al.: Science, 310, 1006 (2004)
- • Ridge, K., et al.: J. Biol. Chem., 282, 9297 (2004)
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PATENTS
PATENTS
PubChem Patent
Google Patent