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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3042 | JAK2 Inhibitor V | JAK2 Inhibitor V Z3,Z3 | JAK |
JAK2 Inhibitor V (JAK2 Inhibitor V Z3) is a novel specific inhibitor of Jak2, inhibiting Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner. | |||
T77678 | TZ3O | AChR | |
TZ3O is an anticholinergic compound with neuroprotective activity.TZ3O ameliorates memory impairment and cognitive decay in Scopolamine-induced Alzheimer's type model in rats, and can be used in the study of Alzheimer's ... | |||
T4443 | AZ32 | ATM/ATR | |
AZ32 is an orally bioavailable and blood-brain barrier-penetrating ATM inhibitor with an IC50 of <6.2 nM for ATM enzyme, and an IC50 of 0.31 μM for ATM in cell. | |||
T5172 | AZ304 | c-Fms , Raf , p38 MAPK , Autophagy | |
AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits BRAF (WT), BRAF (V600E), and wild type CRAF (IC50s: 79/38/68 nM). | |||
T19671 | AZ31 | AZ 31,AZ-31 | ATM/ATR |
AZ31 is an ATM inhibitor with potency, high selectivity, and oral activity.AZ31 inhibits ATM enzymes, intracellular ATM, with IC50 values of <1.2 nM and 46 nM, respectively.AZ31 exhibits excellent ATR selectivity, PIKK f... | |||
T2689 | AZ3146 | AZ 3146 | Kinesin |
AZ3146 is a selective Mps1 inhibitor with IC50 of ~35 nM. | |||
TQ0012 | AZ3451 | Protease-activated Receptor | |
AZ3451 is an allosteric antagonist of protease-activated receptor-2 (PAR2, IC50: 23 nM). | |||
T23764 | AZ3976 | AZ 3976,AZ-3976 | PAI-1 |
AZ3976 is an inhibitor of PAI-1 with an IC50 of 16 μM in a plasma clot lysis assay. AZ3976 displays profibrinolytic activities. | |||
T9658 | DCZ3301 | NPS ALX Compound 4a hydrochloride(1:1)(299433-10-6 Free base) | Others |
DCZ3301 is a novel aryl-guanidino inhibitor. | |||
T5182 | AMZ30 | Others | |
AMZ30 is a selective inhibitor of PME-1 (IC50: 600 nM). It also reduces the demethylated form of PP2A in living cells. | |||
T81725 | Mz325 | HDAC | |
Mz325 serves as a dual inhibitor of both HDAC and Sirt2, exhibiting an IC50 of 9.7 µM against Sirt2, which are implicated in the pathogenesis of cancer and neurodegenerative diseases [1]. | |||
T71098 | AZ3971 | ||
AZ3971 is a potent BACE1 inhibitor. AZ3971 blocks BACE1-mediated cleavage of APP and inhibits Aβ42 production HEK cells overexpressing the APP protein which carries the Swedish mutation (HEK.APPswe). | |||
T126167 | Kudinoside LZ3 | ||
Kudinoside LZ3 is a useful organic compound for research related to life sciences. The catalog number is T126167 and the CAS number is 1239453-03-2. | |||
T62511 | AZ3391 | ||
AZ3391 is a quinoxaline derivative that is a potent inhibitor of PARP. AZ3391 has potential for the study of diseases and conditions occurring in central nervous system tissues (e.g., brain and spinal cord). | |||
T27522 | GZ389988 | GZ-389988,GZ 389988 | |
GZ389988 is a potent Trk inhibitor. | |||
T71151 | Z36 | ||
Z36 is a novel Bcl-xL inhibitor, upregulating the expression levels of FAM134B, LC3, and Atg9, inducing autophagy along with autophagic cell death, resulting in ER stress and the unfolded protein response (UPR). | |||
T69783 | Z30529104 | ||
Z30529104 is a Rpn11 inhibitor. |