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About This Item
Empirical Formula (Hill Notation):
C20H30O
CAS Number:
Molecular Weight:
286.45
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
biological source
synthetic
assay
≥90% (HPLC)
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
format
neat
shipped in
dry ice
storage temp.
−20°C
SMILES string
CC(=C/CO)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Sealed ampule
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José Angel Campos-Sandoval et al.
Journal of medicinal chemistry, 54(13), 4378-4387 (2011-05-20)
Serum retinol binding protein (sRBP) is released from the liver as a complex with transthyretin (TTR), a process under the control of dietary retinol. Elevated levels of sRBP may be involved in inhibiting cellular responses to insulin and in generating
Laura H Riihimäki-Lampén et al.
Journal of medicinal chemistry, 53(1), 514-518 (2009-11-27)
The binding of therapeutically relevant synthetic retinoid derivatives to bovine and reindeer beta-lactoglobulin (betaLG) is demonstrated using fluorescence quenching and ultrafiltration/HPLC methods. Furthermore, synthesis of methyl (E)-3-[4-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)vinyl]phenyl]-acrylate 4 and (E)-3-[4-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)vinyl]phenyl]acrylic acid 5 is described. All studied compounds bind to both
George Magoulas et al.
European journal of medicinal chemistry, 44(6), 2689-2695 (2009-02-14)
Novel mono- and diacylated spermines, readily obtained using isolable succinimidyl active esters of acidic retinoids for the selective acylation of free spermine or in situ activated acidic retinoids for acylating selectively protected spermine followed by deprotection, were shown to inhibit
Synthesis and in vitro biological activity of retinyl retinoate, a novel hybrid retinoid derivative.
Hyojung Kim et al.
Bioorganic & medicinal chemistry, 16(12), 6387-6393 (2008-05-31)
A new hybrid, retinyl retinoate 1, was synthesized with a condensing reaction between retinol and retinoic acid to improve the photo-stability, and the in vitro biological activity of the hybrid was analyzed. This retinol derivative had enhanced thermal stability and
Xueliang Fang et al.
Journal of medicinal chemistry, 48(5), 1481-1488 (2005-03-04)
A comprehensive herbal medicine information system for cancer (CHMIS-C) has been developed. The current version of the database integrates information on more than 200 anticancer herbal recipes that have been used for the treatment of different types of cancer in
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