N-(2,3-Diphenyl-1,2,4-thiadiazol-5-(2H)-ylidene)methanamine, hydrobromide
70375-43-8
348.26
C15H13N3S • HBr
DMSO
-20°C
SCH-202676 is a reversible inhibitor of both agonist and antagonist binding to G protein-coupled receptors (GPCRs). Modification of GPCRs is mediated via sulfhydryl modification. IC50= 0.1-1.7 μM for nine GPCRs. Differentially modulates the activity of adenosine and P2Y receptors.
Research or further manufacturing use only, not for food or drug use.
