Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
52520 | Clemizole | 476-34-6 | 98% | ![]() |
Clemizole is a H1 histamine receptor antagonist.Recently, researchers have identified | ||||
52517 | CI-994 | 112522-64-2 | 98% | ![]() |
CI-994 (Tacedinaline) is an anti-cancer drug which inhibits HDAC1 with IC50 of 0.57 M | ||||
52506 | Chidamide | 743420-02-2 | 98% | ![]() |
Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM | ||||
52502 | CCG-1423 | 285986-88-1 | 98% | ![]() |
CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable o | ||||
52213 | CTX-0294885 | 1439934-41-4 | 98% | ![]() |
CTX-0294885 is a a novel bisanilino pyrimidine; exhibits inhibitory activity against | ||||
52234 | CX-6258 | 1202916-90-2 | 98% | ![]() |
CX-6258 is a potent, orally efficacious Pim 1/2/3 kinase(IC50=5 nM/25 nM/16 nM) inhib | ||||
52229 | CP-640186 | 591778-68-6 | 98% | ![]() |
CP-640186 is an isozyme-nonselective acetyl-CoA carboxylase (ACCase) inhibitor with I | ||||
52228 | CID-797718 | 370586-05-3 | 98% | ![]() |
CID-797718 is a compound with unknown details | ||||
51917 | CGK 733 | 905973-89-9 | 98% | ![]() |
CGK 733 is a potent and selective inhibitor ofATM/ATRwithIC50of ~200 nM. | ||||
52218 | CH-223191 | 301326-22-7 | 98% | ![]() |
CH-223191 is a potent and specificaryl hydrocarbon receptor (AhR)antagonist withIC50o | ||||
51606 | CH5424802 Hydrochloride | 1256589-74-8 | 98% | ![]() |
CH5424802 Hcl (AF 802 Hcl; Alectinib Hcl) is a potent ALK inhibitor with IC50 of 1.9 | ||||
52024 | CX-4945(Silmitasertib) | 1009820-21-6 | 98% | ![]() |
Silmitasertib (CX-4945) is a potent and selective orally bioavailable small molecule | ||||
51905 | CPI-613(Devimistat ) | 95809-78-2 | ≧98.0% | ![]() |
CPI-613( Devimistat ) is an E1 pyruvate dehydrogenase (PDH) modulator that prevents c | ||||
51906 | Cobicistat(GS-9350) | 1004316-88-4 | 98% | ![]() |
Cobicistat is a potent inhibitor of cytochrome P450 3A enzymes, including the importa |
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