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Chemical Structure Cat. No. Product Name CAS No.
Dimesna Chemical Structure
BCP21002 Dimesna 16208-51-8
Dimesna is an inhibitor of OAT family with IC50 value of 636 μM, 390 μM, and 590 μM for OAT1, OAT3, and OAT4, respectively.
EF-5 Chemical Structure
BCP30867 EF-5 152721-37-4
EF-5 is a hypoxia labeling agent used to identify hypoxia in cells.
D-Luciferin Chemical Structure
BCP15615 D-Luciferin 2591-17-5
D-Luciferin is a chemiluminescent substrate for luciferases. D-Luciferin produces fluorescence upon oxidation by luciferase in the presence of ATP.
BI-4464 Chemical Structure
BCP30859 BI-4464 1227948-02-8
BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC50 of 17 nM. A PTK2 ligand for PROTAC.
SRI-31215 Bis-TFA salt Chemical Structure
BCP30857 SRI-31215 Bis-TFA salt 1832686-44-8
SRI 31215 , a triplex inhibitor of matriptase, hepsin and hepatocyte growth factor activator (HGFA) with IC50s of 0.69 μM, 0.65 μM, 0.3 μM, blocks pro-HGF activation and thus mimics the activity of HAI-1/2.
TRi-1 Chemical Structure
BCP30860 TRi-1 246020-68-8
TRi-1 is a potent, specific and irreversible inhibitor of cytosolic thioredoxin reductase 1 (TXNRD1), with an IC50 of 12 nM. TRi-1 has little mitochondrial toxicity for anticancer therapy.
Boc-D-Phenylglycinol Chemical Structure
BCP30861 Boc-D-Phenylglycinol 102089-74-7
GSK2894631A Chemical Structure
BCP30833 GSK2894631A 2101626-26-8
STK16-IN-1 Chemical Structure
BCP20541 STK16-IN-1 1223001-53-3
STK16-IN-1 is a STK16 kinase inhibitor with an IC50 of 295 nM.
BPTES Chemical Structure
BCP15991 BPTES 314045-39-1
BPTES is a selective inhibitor of Glutaminase GLS1 (KGA), which is found in the kidney and brain, and is positively regulated by myc and strongly expressed in many tumors and tumor cell lines.
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