|
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. |