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Cas号索引 4

• 471905-41-6 | MK-0752 (Catalog# : 122949)MK-0752 is a moderately potent -secretase inhibitor, which reduces A40 production wit
• 494227-37-1 | Mandyphos SL-M004-1 (Catalog# : 121502)Coming soon!
• 41100-52-1 | Memantine hydrochloride (Catalog# : 120703)Coming soon!
• 4375-15-9 | 3-methyl-2,3-dihydro-1H-indole (Catalog# : 81943)Coming soon!
• 4593-38-8 | 5-Methyl-1-indanone (Catalog# : 81942)Coming soon!
• 453562-69-1 | Motesanib (Catalog# : 52810)Motesanib (AMG-706) is a potent ATP-competitive inhibitor of VEGFR1/2/3 with IC50 of
• 423735-93-7 | ML161 (Catalog# : 52554)ML-161 is an allosteric inhibitor ofPAR1withIC50of 0.26 M.
• 473727-83-2 | Navarixin (Catalog# : 185168)Navarixin, 也称为SCH527123, PS291822和MK-7123, 是一种有效的CXCR2拮抗剂。
• 448895-37-2 | NS-1643 (Catalog# : 17030715)NS-1643是一种人类ether-a-go-go相关基因(hERG)KV11.1通道激活剂(EC50 = 10.
• 4008-48-4 | Nitroxoline (Catalog# : 16122719)Nitroxoline is a urinary antibacterial agent active against susceptible gram-positive
• 448232-80-1 | Naquotinib (Catalog# : 16071107)Naquotinib, also known as ASP8273, is an orally available, irreversible, third-genera
• 4311-88-0 | Necrostatin-1 (Catalog# : 52230)Necrostatin-1 is a specific RIP1 inhibitor and inhibits TNF--induced necroptosis with
• 412008-21-0 | O4I4 (Catalog# : 20571)O4I4 (compound 23) is a OCT4-inducing compound with metabolical stability.
• 480-11-5 | Oroxylin A (Catalog# : 2071536)Oroxylin A is a flavonoid that inhibits decreases in cell viability and increases in
• 426219-18-3 | Orteronel (外消旋) (Catalog# : 17030610)Orteronel(外消旋)是s - Orteronel和r - Orteronel异构体的混合物。Orteronel
• 457081-03-7 | Pyridone 6 (Catalog# : 193204)吡啶酮6，也被称为CMP 6或JAK抑制剂I，是一种pan-janus-激活的激酶抑
• 446022-33-9 | Pelitrexol (Catalog# : 189131)Pelitrexol是GARFT抑制剂，也是具有抗增殖活性的水溶性抗叶酸。
• 4960-10-5 | Perastine (Catalog# : 187164)Perastine是一种生物化学药。
• 404950-80-7 | 帕比司他 (Catalog# : 17022809)帕比司他(LBH-589)是一种广谱HDAC抑制剂;低纳米分子浓度(IC50 =5-20 nM
• 418805-02-4 | PYR-41 (Catalog# : 16122793)PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with
• 449811-01-2 | Pamapimod (R-1503, Ro4402257) (Catalog# : 16122774)Pamapimod (R-1503, Ro4402257) is a novel, selective inhibitor of p38 mitogen-activate
• 431898-65-6 | PS-1145 (Catalog# : 032501)Coming soon!
• 477575-56-7 | PHA-665752 (Catalog# : 121418)PHA-665752 is a potent, selective and ATP-competitive c-Met inhibitor with IC50 of 9
• 4382-63-2 | PFK-015 (Catalog# : 52824)PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFKFB3)
• 483367-10-8 | Purmorphamine (Catalog# : 52519)Purmorphamine, which directly binds and activates Smoothened, blocks BODIPY-cyclopami
• 496054-87-6 | Radiprodil (Catalog# : 25125)Radiprodil, also known as RGH-896, is an orally active and selective NMDA receptors a
• 496054-87-6 | Radiprodil (Catalog# : 25124)Radiprodil, also known as RGH-896, is an orally active and selective NMDA receptors a
• 415713-60-9 | RI-1 (Catalog# : 122404)RI-1 is a RAD51 inhibitor with IC50 ranging from 5 to 30 M.
• 449808-64-4 | R1487 (Catalog# : 102901)R1487 is a p38 MAP kinase inhibitor.
• 46022-05-3 | (1R,2R)-(-)-1,2-Cyclohexanedicarboxylic Acid (Catalog# : 91406)The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3