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Dihydrocapsiate

Catalog No. T60741 CAS 205687-03-2

Dihydrocapsiate is a compound of capsinoid family that can be used in metabolism diseas research. Dihydrocapsiate is an orally active agonist of TRPV1 [1].

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Dihydrocapsiate, CAS 205687-03-2

Pack Size	Availability	Price/USD
25 mg	6-8 weeks	$ 970.00
50 mg	6-8 weeks	$ 1,260.00
100 mg	6-8 weeks	$ 1,910.00

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This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.

Biological Description

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Description	Dihydrocapsiate is a compound of capsinoid family that can be used in metabolism diseas research. Dihydrocapsiate is an orally active agonist of TRPV1 [1].
In vitro	Dihydrocapsiate treatment at concentrations of 10, 25, and 50 μM for 48 hours does not impact the viability of human preadipocytes, indicating its non-toxic nature at these levels [1]. At lower concentrations of 10 and 20 μM, but over a longer period of 8 days, dihydrocapsiate significantly reduces the expression of various adipogenic (like SREBP1, FABP4, PLIN1, ADIPOQ, and LEPTIN) and inflammatory markers (MCP1 and TNFα) in mature adipocytes. Conversely, it increases the expression of PGC1α, crucial for mitochondrial biogenesis, and TBX1, a marker of "brite" cells, highlighting its potential role in adipocyte metabolism and inflammation modulation [1]. Interestingly, in RAW 264.7 cells, dihydrocapsiate concentrations ranging from 25 to 200 μM effectively inhibit the release of nitric oxide (NO) and the generation of intracellular reactive oxygen species (ROS), providing evidence of its anti-inflammatory and antioxidative properties [1].
In vivo	Dihydrocapsiate administered orally at doses of 2 and 10 mg/kg effectively improves morphometric parameters and insulin levels in HFD-fed mice [1]. It counteracts the enlargement of adipocytes and upregulates energy expenditure-related genes in white adipose tissue (WAT), mitigates hepatic steatosis, and inhibits fat accumulation prompted by a high-fat diet (HFD). Furthermore, it elevates the expression of mitochondrial biogenesis-related genes in brown adipose tissue (BAT), ameliorates intestinal morphology, and modulates the availability of short-chain fatty acids (SCFAs), showcasing its broad pharmacological potential in metabolic regulation.

Molecular Weight	308.41
Formula	C18H28O4
CAS No.	205687-03-2

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Powder: -20°C for 3 years | In solvent: -80°C for 1 year

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Keywords

Dihydrocapsiate 205687-03-2 inhibitor inhibit

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