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1220-77-5 | 3,5,7-Octatrien-2-one, 6-methyl-8-(2,6,6-trimethyl-1-cyclohexen-1-yl)-
CAS No: 1220-77-5 Catalog No: AG0016JI MDL No:
Product Description
Catalog Number:
AG0016JI
Chemical Name:
3,5,7-Octatrien-2-one, 6-methyl-8-(2,6,6-trimethyl-1-cyclohexen-1-yl)-
CAS Number:
1220-77-5
Molecular Formula:
C18H26O
Molecular Weight:
258.3984
IUPAC Name:
6-methyl-8-(2,6,6-trimethylcyclohexen-1-yl)octa-3,5,7-trien-2-one
InChI:
InChI=1S/C18H26O/c1-14(8-6-10-16(3)19)11-12-17-15(2)9-7-13-18(17,4)5/h6,8,10-12H,7,9,13H2,1-5H3
InChI Key:
UBTNVRPIHJRBCI-UHFFFAOYSA-N
SMILES:
CC(=CC=CC(=O)C)C=CC1=C(C)CCCC1(C)C
Properties
Complexity:
456
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
258.198g/mol
Formal Charge:
0
Heavy Atom Count:
19
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
258.405g/mol
Monoisotopic Mass:
258.198g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
3
XLogP3:
4.8
Literature
| Title | Journal |
|---|---|
| Naturally occurring eccentric cleavage products of provitamin A β-carotene function as antagonists of retinoic acid receptors. | The Journal of biological chemistry 20120504 |
| Beta-carotene reduces body adiposity of mice via BCMO1. | PloS one 20110101 |
| The eccentric cleavage product of β-carotene, β-apo-13-carotenone, functions as an antagonist of RXRα. | Archives of biochemistry and biophysics 20101201 |
| The Mycobacterium tuberculosis ORF Rv0654 encodes a carotenoid oxygenase mediating central and excentric cleavage of conventional and aromatic carotenoids. | The FEBS journal 20101101 |
| {beta}-Apocarotenoids do not significantly activate retinoic acid receptors {alpha} or {beta}. | Experimental biology and medicine (Maywood, N.J.) 20100301 |
| In vitro characterization of Synechocystis CYP120A1 revealed the first nonanimal retinoic acid hydroxylase. | The FEBS journal 20091001 |
| Carotenoid oxygenases involved in plant branching catalyse a highly specific conserved apocarotenoid cleavage reaction. | The Biochemical journal 20081201 |
| Reaction of retinol with peroxynitrite. | Bioscience, biotechnology, and biochemistry 20071001 |
| The biochemical characterization of two carotenoid cleavage enzymes from Arabidopsis indicates that a carotenoid-derived compound inhibits lateral branching. | The Journal of biological chemistry 20041105 |
| [Initial stages of trisporic acid synthesis in Blakeslea trispora]. | Prikladnaia biokhimiia i mikrobiologiia 20020101 |
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