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

Modify Date: 2024-01-11 22:03:47

8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester Structure
8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester structure
Common Name 8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester
CAS Number 205687-03-2 Molecular Weight 308.41300
Density N/A Boiling Point N/A
Molecular Formula C18H28O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of 8-Methylnonanoic acid (4-hydroxy-3-methoxyphenyl)methyl ester


Dihydrocapsiate, as a compound of capsinoid family, is an orally active TRPV1 agonist. Dihydrocapsiate can be used for the research of metabolism disease[1].

 Names

Name (4-hydroxy-3-methoxyphenyl)methyl 8-methylnonanoate
Synonym More Synonyms

  Biological Activity

Description Dihydrocapsiate, as a compound of capsinoid family, is an orally active TRPV1 agonist. Dihydrocapsiate can be used for the research of metabolism disease[1].
Related Catalog
Target

TRPV1

In Vitro Dihydrocapsiate (10, 25 and 50 μM; 48 hours; human preadipocytes) does not affect cell viability[1]. Dihydrocapsiate (10 and 20 μM; 8 days; mature adipocytes) markedly decreases the expression levels of other adipogenic markers (such as SREBP1, FABP4, PLIN1, ADIPOQ and LEPTIN) and inflammatory markers (MCP1 and TNFα), whereas it enhances the expression levels of PGC1α (master regulator of mitochondrial biogenesis) and TBX1 (marker of “brite” cell) [1]. Dihydrocapsiate (25~200 μM; RAW 264.7 cells) prevents NO release and intracellular ROS generation[1]. Cell Viability Assay[1] Cell Line: Human preadipocytes Concentration: 10, 25 and 50 μM Incubation Time: 48 hours Result: Did not affect cell viability. RT-PCR[1] Cell Line: Mature adipocytes Concentration: 10 and 20 μM Incubation Time: 8 days Result: Markedly decreased the expression levels of other adipogenic markers (such as SREBP1, FABP4, PLIN1, ADIPOQ and LEPTIN) and inflammatory markers (MCP1 and TNFα), whereas it enhanced the expression levels of PGC1α (master regulator of mitochondrial biogenesis) and TBX1 (marker of “brite” cell).
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.
References

[1]. Baboota RK, et al. Dihydrocapsiate supplementation prevented high-fat diet-induced adiposity, hepatic steatosis, glucose intolerance, and gut morphological alterations in mice. Nutr Res. 2018;51:40-56.

 Chemical & Physical Properties

Molecular Formula C18H28O4
Molecular Weight 308.41300
Exact Mass 308.19900
PSA 55.76000
LogP 4.44060
Index of Refraction n20/D 1.483-1.489

 Synonyms

UNII-W2F7769AEU
dihydrocapsiate
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