1227163-56-5 | AZD3839 (Catalog# : 17022710)AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for the treatment of Alzheimer disease. AZD3839 inhibits BACE1 activity, A and sAPP release from
1620576-64-8 | AZD-8835 (Catalog# : 102703)AZD8835 is a selective, oral inhibitor of PI3K isoforms and with the following activity in enzymatic assays: PI3K C IC50 = 6nM (equipotent vs wt and E545K / H1047R mutants); P
1472624-85-3 | 7ACC2 (Catalog# : 17011302)7ACC2 is a potent MCT inhibitor. Monocarboxylate transporters (MCTs) catalyze the proton-linked transport of monocarboxylates such as L-lactate, pyruvate, and the ketone bodies a
1442684-77-6 | AM-2394 (Catalog# : 16122855)AM-2394 is a potent and selective Glucokinase agonist (GKA), which catalyzes the phosphorylation of glucose to glucose-6-phosphate. AM-2394 activates GK with an EC50 of 60 nM, in
106566-58-9 | AS101 (Catalog# : 161227106)AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1beta converting enzyme.AS101 downregulates IL-18 and IL-1 serum levels in a mouse model of lipop
1527503-11-2 | A-366 (Catalog# : 16122743)A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor with IC50 of 3.3nM, exhibiting >1000-fold selectivity for G9a/GLP over 21 other methyltransf
1337878-62-2 | ATI-2341 (Catalog# : 6111101)ATI-2341, pepducin targeting the C-X-C chemokine receptor type 4 (CXCR4), is an allosteric agonist activating the inhibitory heterotrimeric G protein (Gi) to promote inhibition o
Sun-shinechem(SSC) provides a wide range of research chemicals and biochemicals including novel life-science reagents, reference compounds, APIs, building blocks and Natural compounds for laboratory and scientific use.