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Product Description
– SCH-202676 is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). SCH-202676 has antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 µM[1][2][3][4].
Web ID
– HY-133862
Shipping
– Room temperature
Applications
– COVID-19-anti-virus
Molecular Formula
– C15H13N3S
References
– [1]Ren P, et al. Discovery, synthesis and mechanism study of 2,3,5-substituted [1,2,4]-thiadiazoles as covalent inhibitors targeting 3C-Like protease of SARS-CoV-2. Eur J Med Chem. 2023 Jan 18;249:115129.|[2]Lewandowicz AM, et al. The ‘allosteric modulator’ SCH-202676 disrupts G protein-coupled receptor function via sulphydryl-sensitive mechanisms. Br J Pharmacol. 2006 Feb;147(4):422-9.|[3]Fawzi A B, et al. SCH-202676: an allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors[J]. Molecular Pharmacology, 2001, 59(1): 30-37.|[4]Gao ZG, et al. Effects of the allosteric modulator SCH-202676 on adenosine and P2Y receptors. Life Sci. 2004 May 7;74(25):3173-80.
CAS Number
– 70375-43-8
Molecular Weight
– 267.35
SMILES
– C/N=C1N=C(C2=CC=CC=C2)N(C3=CC=CC=C3)S/1
Clinical Information
– No Development Reported
Research Area
– Infection
Solubility
– 10 mM in DMSO
Target
– Adenosine Receptor;G protein-coupled Bile Acid Receptor 1;Influenza Virus
Isoform
– Adenosine A3 receptor (A3R)
Pathway
– Anti-infection;GPCR/G Protein
Product type
– Reference compound
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