Others 11

Others 11

Others 11 related products

Structure Cat No. Product Name CAS No. Product Description
V56644 HPPE 1325721-55-8 HPPE is a specific non-electrophilic physiological Bach1 inhibitor through the heme-binding site of Bach1 protein.
V56773 HS94 1892594-93-2 HS94 is a selective DAPK3 inhibitor.
V56749 HUN39963 893739-96-3 HUN39963, also known as LDH-IN-2, is an inhibitor (blocker/antagonist) of glycolate oxidase.
V56607 HUP30 312747-21-0 HUP30 is a vasodilator.
V56669 iGOT1-01 882256-55-5 iGOT1-01 is a potent inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate aminotransferase 1; GOT1) with IC50 of 85 μM in the MDH-coupled GOT1 enzymatic assay and IC50 in the GOT1/GLOX/HRP assay is 11.3 μM.
V56762 iJak-381 1831144-46-7 iJak-381, also known as GDC-0214, is a specific, inhalable inhibitor of Janus kinase-1 (JAK-1), with lung concentrations approximately 950 times higher than plasma concentrations in mice after inhalation .
V56802 ikB 77500-04-0 MeIQx, also known as 8-methyl-IQX, is a synthetic light orange to brown crystalline solid that is soluble in dimethyl sulfoxide and methanol.
V54376 Iodobananin 858956-95-3 Iodobananin is a potent inhibitor of the ATPase activity of SARS virus helicase, with IC50 of 0.54 μM.
V56620 Isavuconazonium Free Base 742049-41-8 Isavuconazole (BAL4815; trade name Cresemba) is a triazole antifungal drug.
V56671 JNJ-63576253 2110426-27-0 JNJ63576253, also known as TRC253, is a potent orally bioactive androgen receptor antagonist.
V56761 KHS-101 free base 1262770-73-9 KHS-101 is a selective inducer of neuronal differentiation.
V56735 KL-11743 1369452-53-8 KL-11743 is a representative compound that blocks glucose metabolism, triggering an acute collapse of NADH pools and a significant accumulation of aspartate.
V56787 KR-32568 852146-73-7 KR-32568 is an inhibitor (blocker/antagonist) of sodium-hydrogen exchanger-1 (NHE-1; IC50 = 230 nM).
V56683 L-Tyrosinol HCl 87745-27-5 L-Tyrosine is an aromatic, polar, non-essential amino acid (AA) containing highly reactive α-amino, α-carboxyl and phenolic hydroxyl groups.
V56617 Lenalidomide-acetylene-Br 2619512-84-2 Lenalidomide-acetylene-Br is the PROTAC (PROteolysis TArgeting Chimera) linker that makes up HJM-561.
V56713 LZWL02003 1371564-45-2 LZWL02003 is a neuro-protection agent and an analogue of N-salicyloyltryptamine.
V56794 MAO-B-IN-19 152897-41-1 MAO-B-IN-19) is a selective MAO-B inhibitor (antagonist) with IC50 of 0.67 μM.
V56668 MAO-B-IN-22 2902600-76-2 MAO-B-IN-22 (compound 6h) is a potent MAO-B inhibitor (antagonist) with IC50 of 0.014 μM.
V56783 MCUF-651 2747162-85-0 MCUF-651 is a small molecule guanylate cyclase A receptor PAM (positive allosteric modulator) (GC-A PAM).
V56798 ML-339 2579689-83-9 ML339 is a selective CXCR6 antagonist (inhibitor) with IC50 of 140 nM.
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