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R2101037 GW779439X GW779439X is an inhibitor of cyclin dependent kinase.
R2101038 RO2959 hydrochloride RO2959 hydrochloride 是一种有效的选择性 CRAC 通道抑制剂,IC50 为 402 nM。RO2959 hydrochloride 是由
R2101039 Flupenthixol dihydrochloride cis-(Z)-Flupentixol dihydrochloride 是有效、选择性的多巴胺DA D1/D2 受体的拮抗剂,其对D2 受体和 5-HT2A 的
R2101040 4BP-TQS 4BP-TQS is an allosteric agonist of α7 subunit-containing neuronal nicotinic ace
R2101041 B355252 B355252 is a neuroprotective agent that potentiates nerve growth factor (NGF)-in
R2101042 GSK 2830371 GSK 2830371 是一种选择性的Wip1磷酸酶 (Wip1 phosphatase)抑制剂,IC50 为 6 nM。
R2101043 MONNA MONNA is a potent TMEM16A (Anoctamin-1) blocker (IC50 = 80 nM). Exhibits >100
R2101044 TAE-1 TAE-1 is an inhibitor of amyloid-β fibril formation and aggregation, suggesting
R2101045 ML191 ML-191 is a potent, selective GPR55 antagonist with 160 nM potency for GPR55 and
R2101046 ML336 ML-336 is an inhibitor of of the Venezuelan equine encephalitis virus (VEEV) str
R2101047 GW280264X GW280264X is an ADAM17 inhibitor.
R2101048 TM5007 TM5007 is a poent inhibitor plasminogen activator inhibitor-1 (PAI-1) with IC50
R2101049 CYM2503 CYM2503 is a positive allosteric modulator (PAM) of the GAL2 receptor that poten
R2101050 YM26734 YM-26734 is a rabbit platelet sPLA2 inhibitor that has been used to ameliorate l
R2101051 G244-LM G244-LM is a potent and specific tankyrase 1/2 inhibitor that inhibits Wnt signa
R2101052 VK-II-86 VK-II-86 is a selective ryanodine receptor type 2 (RyR2) antagonist.
R2101053 ML298 ML298 (CID53393915) is a potent, specific inhibitor of Phospholipase D2 (PLD2) w
R2101054 SW155246 SW155246 is a potent and selective DNMT1 (DNA methyltransferase 1) inhibitor wit
R2101055 ML-299 ML299 (VU0463568) is a dual inhibitor of PLD1 and PLD2 with IC50 of 6 nM and 20
R2101056 VUF11418 VUF11418 is a nonpeptidomimetic agonist of the G protein-coupled chemokine recep
R2101057 CGS-15943 CGS15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor
R2101058 NSC177223 API-1 (NSC 177223) is a potent inhibitor of Akt that induces GSK3-dependent, β-T
R2101059 ML162 一种小分子探针,选择性杀死诱导表达突变RAS的细胞;抑制BJeLR(表达HRAS G12V)细胞系,IC50为25 nM,显示出比BJeH LT(不含HRAS
R2101060 GSK-843 GSK-843 是一种受体相互作用蛋白激酶 3 (RIP3 or RIPK3) 抑制剂,高亲和力结合 RIP3 激酶结构域,IC50 值为 8.6 nM,并抑制
R2101061 Imidazenil Imidazenil is a GABA-A modulator that blocks the sedative effects without loweri
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