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Cat.No.	Name	Information
M21539	TC LPA5 4	TC LPA5 4 is a specific non-lipid LPA5 (GPR92) antagonist (IC50=0.8 μM in LPA5-RH7777 cells). Shows selectivity for LPA5 against 80 other screening targets.TC LPA5 4 was shown to inhibit LPA-induced aggregation of isolated human platelets.TC LPA5 4 inhibits proliferation and migration of thyroid cancer cells.
M21538	Diphenyl diselenide	Diphenyl diselenide inhibits δ-aminolevulinic acid dehydrase (δ-ALA-D) in brain, liver, and kidney in vivo.
M21537	Urokinase	Urokinase (urokinase) is a proteolytic enzyme. It can be used as a highly effective thrombolytic agent and also has a local vasodilating effect. Used as an antithrombotic compound.
M21536	BAY-069	BAY-069 is a branched-chain amino acid transaminase (BCAT) 1/2 inhibitor. Involved in the synthesis and catabolism of branched-chain amino acids.
M21535	UCB7362	UCB7362 is an oral plasma protease X (PMX) inhibitor that is being developed as an anti-malarial compound.
M21534	AN15368	AN15368 is an oral cleavage and polyadenylate specific factor (CPSF3) inhibitor being developed for use in Chagas disease (also known as American trypanosomiasis).
M21533	BI-0474	BI-0474 is a covalent KRASG12C inhibitor. The IC50 value for GDP-KRAS::SOS1 protein-protein interaction was 7.0 nM. BI-0474 also showed better antitumor activity in non-small cell lung cancer xenograft models.
M21532	JNJ-64264681	JNJ-64264681 is a covalent Bruton tyrosine kinase (BTK) inhibitor under development for hematological malignancies.