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目录号 产品名称 产品描述
R10030 MLN4924 MLN4924 is a potent and selective small molecule NEDD8-activating enzyme (NAE) i
R10031 BIIB-024; MLN2480 MLN2480(BIIB-024) is an oral, selective pan-Raf kinase inhibitor in chinical tri
R10032 SLx-2119 (KD-025) SLx-2119 (KD-025) 是选择性的 ROCK2 抑制剂,IC50 值为 105 nM。
R10033 MLN8237 Alisertib (MLN8237) is a selective Aurora A inhibitor with IC50 of 1.2 nM in a c
R10034 MK8745; MK-8745 MK-8745是极光激酶抑制剂 (aurora A),IC50 值为0.6 nM。 
R10035 MDL28170 MDL 28170 is a cell permeable selective inhibitor of Calpain 1, a Ca2+-dependent
R10036 XL880; Foretinib; GSK136308 Foretinib (GSK1363089) is an ATP-competitive inhibitor of HGFR and VEGFR, mostly
R10037 ANA12 ANA-12是有效,选择性的 TrkB 拮抗剂,对高亲和力和低亲和力位点的IC50 分别为45.6 nM和41.1 μM。 
R10038 CX-4945 CX-4945 (Silmitasertib) is a potent and selective inhibitor of CK2 (casein kinas
R10040 IP-145; Duvelisib; INK1197 Duvelisib 是一种选择性 p100δ 抑制剂,作用于 p110δ, p110γ, p110β 和 p110α,IC50 分别为 2.5 nM,27.4
R10041 Vesnarinone (OPC-8212) Vesnarinone是一种喹啉酮衍生物, 药效学效应包括抑制磷酸二酯酶III (PDE3) 活性,增加钙通量, 及减小钾通量。 
R10042 CO1686; Rociletinib Rociletinib (CO-1686, AVL-301) is an irreversible, mutant-selective EGFR inhibit
R10044 WZ4003 WZ4003 is a highly specific NUAK kinase inhibitor with IC50 of 20 nM and 100 nM
R10045 Fluoroclebopride
R10046 TORIN1 Torin 1 是一种有效的 mTOR 抑制剂,IC50 为 3 nM。Torin 1 抑制 mTORC1/2 复合物,IC50 值在 2 和 10 nM 之间
R10047 Vortioxetine Vortioxetine (Lu AA21004) is a multimodal serotonergic agent, inhibits 5-HT1A, 5
R10048 Temsavir; BMS-626529 BMS-626529 is a novel small-molecule attachment inhibitor that targets HIV-1 gp1
R10049 TP-808;TP808 TP808是影响多种四环素抗生素合成的关键中间体。
R10054 TAE684 TAE684 (NVP-TAE684) is a potent and selective ALK inhibitor with IC50 of 3 nM in
R10056 Tubastatin-A Tubastatin A is a potent and selective HDAC6 inhibitor withIC50 of 15 nM in a ce
R10058 Masitinib Masitinib is a novel inhibitor for Kit and PDGFRα/β with IC50 of 200 nM and 540
R10060 Nadifloxacin; Acuatim; Nadixa; OPC7251 Nadifloxacin is a topical fluoroquinolone antibiotic for the treatment of acne v
R10061 Nexavar; Bay 43-9006; Sorafenib Sorafenib Tosylate is a multikinase inhibitor of Raf-1, B-Raf and VEGFR-2 with I
R10062 SAR131675 SAR131675是一种VEGFR3抑制剂,无细胞试验中IC50/Ki为23 nM/12 nM,作用于VEGFR3比作用于VEGFR1/2选择性高50和10倍,
R10064 Brivanib; BMS540215 Brivanib 是一种ATP竞争性的 VEGFR2 抑制剂,IC50 值为 25 nM;可以适度抑制 VEGFR-1 和 FGFR-1,对 VEGFR2 的选
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