ChemicalBook--->CAS DataBase List--->205687-03-2

205687-03-2

205687-03-2 Structure

205687-03-2 Structure
IdentificationBack Directory
[Name]

8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester
[CAS]

205687-03-2
[Synonyms]

Dihydrocapsiate
4-Hydroxy-3-Methoxybenzyl 8-Methylnonanoate
(4-hydroxy-3-methoxyphenyl)methyl 8-methylnonanoate
8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl este
8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester
Nonanoic acid,8-methyl-, (4-hydroxy-3-methoxyphenyl)methyl ester
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C18H28O4
[MDL Number]

MFCD29917840
[MOL File]

205687-03-2.mol
[Molecular Weight]

308.41
Chemical PropertiesBack Directory
[Boiling point ]

413.6±30.0 °C(Predicted)
[density ]

1.038
[storage temp. ]

Store at -20°C, protect from light
[form ]

Liquid
[pka]

9.51±0.20(Predicted)
[color ]

Colorless to light yellow
[LogP]

5.094 (est)
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H300-H315-H319-H335
[Precautionary statements ]

P501-P261-P270-P271-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P310+P330-P304+P340+P312-P403+P233-P405
Hazard InformationBack Directory
[Uses]

Dihydrocapsiate, is a complex that is found in chili peppers which has been used in different biological studies to determine the inhibitory effects. This includes the studies performed on cytochrome P 450 3A4 in human liver microsomes.
[Definition]

ChEBI: Dihydrocapsiate is a member of methoxybenzenes and a member of phenols.
[in vivo]

Dihydrocapsiate (2 and 10 mg/kg; p.o.) improves morphometric parameters and insulin levels, prevents high fat diet (HFD)-induced adipocyte size and enhances energy expenditure-related genes in WAT, alleviates HFD-induced hepatic steatosis, prevents HFD-induced fat deposition and enhances mitochondrial biogenesis genes in BAT and improves intestinal morphology and modulates SCFA availability.

Animal Model:HFD-fed mice[1]
Dosage:2 and 10 mg/kg
Administration:P.o.
Result:Improved morphometric parameters and insulin levels, prevented HFD-induced adipocyte size and enhanced energy expenditure-related genes in WAT, alleviated HFD-induced hepatic steatosis, prevented HFD-induced fat deposition and enhanced mitochondrial biogenesis genes in BAT and improved intestinal morphology and modulates SCFA availability.
[IC 50]

TRPV1
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