Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H26O4 |
Molecular Weight | 306.3966 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(COC(=O)CCCC\C=C\C(C)C)=CC=C1O
InChI
InChIKey=ZICNYIDDNJYKCP-SOFGYWHQSA-N
InChI=1S/C18H26O4/c1-14(2)8-6-4-5-7-9-18(20)22-13-15-10-11-16(19)17(12-15)21-3/h6,8,10-12,14,19H,4-5,7,9,13H2,1-3H3/b8-6+
Molecular Formula | C18H26O4 |
Molecular Weight | 306.3966 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Immunosuppressive activity of capsaicinoids: capsiate derived from sweet peppers inhibits NF-kappaB activation and is a potent antiinflammatory compound in vivo. | 2002 Jun |
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Effect of topical application of capsaicin and its related compounds on dermal insulin-like growth factor-I levels in mice and on facial skin elasticity in humans. | 2007 Apr |
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Downregulation of uncoupling protein-3 in vivo is linked to changes in muscle mitochondrial energy metabolism as a result of capsiate administration. | 2007 May |
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Capsiate, a nonpungent capsaicin-like compound, inhibits angiogenesis and vascular permeability via a direct inhibition of Src kinase activity. | 2008 Jan 1 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:27:51 GMT 2023
by
admin
on
Sat Dec 16 02:27:51 GMT 2023
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Record UNII |
PX8I7HG5I3
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Record Status |
Validated (UNII)
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Record Version |
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-
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205687-01-0
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PX8I7HG5I3
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admin on Sat Dec 16 02:27:51 GMT 2023 , Edited by admin on Sat Dec 16 02:27:51 GMT 2023
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DTXSID20174575
Created by
admin on Sat Dec 16 02:27:51 GMT 2023 , Edited by admin on Sat Dec 16 02:27:51 GMT 2023
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9839519
Created by
admin on Sat Dec 16 02:27:51 GMT 2023 , Edited by admin on Sat Dec 16 02:27:51 GMT 2023
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PRIMARY |