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Eversaeuremethylester, also known as Eversor methyl ester, is a chemical compound with the molecular formula C10H15NO2. It is a derivative of Eversor, a potent and selective inhibitor of the enzyme dipeptidyl peptidase-4 (DPP-4), which plays a crucial role in the regulation of glucose homeostasis. Eversor methyl ester is a prodrug, meaning it is converted into the active form, Eversor, within the body after administration. This conversion is facilitated by esterases, enzymes that break down the ester bond in the compound. Eversor methyl ester has been studied for its potential therapeutic applications in the treatment of type 2 diabetes and other metabolic disorders, as it can help to increase the levels of insulin-releasing hormones, such as glucagon-like peptide-1 (GLP-1), thereby improving glucose control.

3542-22-1

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3542-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3542-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3542-22:
(6*3)+(5*5)+(4*4)+(3*2)+(2*2)+(1*2)=71
71 % 10 = 1
So 3542-22-1 is a valid CAS Registry Number.

3542-22-1Relevant academic research and scientific papers

NMR Assignments of Depsides and Tridepsides of the Lichen Family Umbilicariaceae

Narui, Takao,Sawada, Keiko,Takatsuki, Satoshi,Okuyama, Toru,Culberson, Chicita F.,et al.

, p. 815 - 822 (2007/10/03)

NMR spectral analysis provides important information for the identification of secondary products of chemotaxonomic significance in the lichen genera Umbilicaria and Lasallia (Umbilicariaceae). Two depsides (evernic and lecanoric acids) and eight tridepsides (crustinic, gyrophoric, hiascic, lasallic, 4-O-methylgyrophoric, ovoic and umbilicaric acids and tenuiorin) were isolated from various unrelated lichens. Seven of the ten compounds are important taxonomic characters in the family Umbilicariaceae. 1H and 13C NMR spectral signals were assigned for the compounds and for methyl esters of lecanoric, evernic and gyrophoric acids. Using these NMR data and mass spectrometry, chemical structures were elucidated for two new compounds, papulosic acid (2,6-dihydroxy-3-carboxy-4-methylphenyl orsellinate) from the umbilicariaceous Lasallia papulosa and deliseic acid (lecanoryl 3-acetoxy-4,6-dihydroxy-2-methylbenzoate) from the parmeliaceous Cetrariella delisei.

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