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GSK-LSD1 2HCl is an irreversible and selective LSD1 inhibitor with IC50 of 16 nM 1000 fold selective over other closely related FAD utilizing enzymes (i e LSD2 MAO-A MAO-B)
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TLR7/8 agonist 1 dihydrochloride is a toll-like receptor TLR7/TLR8 dual-agonistic imidazoquinoline TLR7/8 agonist 1 retains TLR7-agonistic activity with an EC50 of 20 nM
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BGP-15 is a nicotinic amidoxime derivative with PARP inhibitory activity It has been demonstrated that BGP-15 protects against ischemia-reperfusion injury
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H 89 2HCl is a potent PKA inhibitor with Ki of 48 nM in a cell-free assay 10-fold selective for PKA than PKG 500-fold greater selectivity than PKC MLCK calmodulin kinase II and casein kinase I/II H 89 2HCl induces autophagy
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TLR7/8 agonist 1 dihydrochloride is a toll-like receptor TLR7/TLR8 dual-agonistic imidazoquinoline TLR7/8 agonist 1 retains TLR7-agonistic activity with an EC50 of 20 nM
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Trifluoperazine (NSC-17474 RP-7623 SKF-5019) 2HCl is a dopamine D2 receptor inhibitor with IC50 of 1 1 nM Trifluoperazine also inhibits calmodulin (CaM)
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THZ1 is a covalent CDK7 inhibitor which has the unprecedented ability to target a remote cysteine residue located outside of the canonical kinase domain providing an unanticipated means of achieving selectivity for CDK7
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BGP-15 is a nicotinic amidoxime derivative with PARP inhibitory activity It has been demonstrated that BGP-15 protects against ischemia-reperfusion injury
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More