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Cas号索引 2

• 2101700-15-4 | Pirtobrutinib (Catalog# : 20618)
• 2904682-19-3 | PDS-0330 (Catalog# : 231106)PDS-0330 是一种特异性、有效的Claudin-1抑制剂。PDS-0330 干扰 claudin-1
• 2253123-16-7 | Pimicotinib (Catalog# : 20548)Pimicotinib是一种新型的 CSF-1R 小分子抑制剂，可口服、高选择性、
• 260415-63-2 | PD-173955 (Catalog# : 20499)PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce
• 217171-01-2 | PD-173212 (Catalog# : 20468)PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced
• 2172870-89-0 | Paltusotine ( CRN-00808 ) (Catalog# : 20294)Paltusotine 是一类新型的、口服、选择性、非肽类2型生长抑素受体
• 26305-03-3 | Pepstatin (Catalog# : 2071607)Pepstatin inhibits the aspartic protease endothiapepsin.
• 2227425-05-8 | PF-06869206 (Catalog# : 2071506)PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
• 26033-20-5 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE (Catalog# : 2062020)
• 248282-01-1 | Paquinimod (Catalog# : 2061706)Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
• 2170608-82-7 | PZ-2891 (Catalog# : 193282)PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂，
• 2102501-84-6 | PF-06835919 ( MDK-1846 ) (Catalog# : 193264)MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
• 2185857-97-8 | PF-06873600 (Catalog# : 191145)PF-06873600是一种口服生物利用的细胞周期蛋白依赖性激酶(CDK)抑制
• 2070014-93-4 | PF-CBP1盐酸 (Catalog# : 179112)PF-CBP1，也称为 PF06670910，是强效、高选择性的CREB结合蛋白布罗莫
• 25606-41-1 | 霜霉威盐酸盐 (Catalog# : 2017080115)霜霉威盐酸盐是一种高效、广谱、氨基甲酸酯类杀菌剂。
• 257933-82-7 | 培利替尼 (Catalog# : 17022702)培利替尼(EKB-569; WAY-EKB 569)是一种有效且不可逆转的IC50为38.5 nM的E
• 202350-68-3 | PNU-159682 (Catalog# : 16071409)PNU-159682 is a major active metabolite of nemorubicin (MMDX) in human liver microsom
• 269718-84-5 | Pardoprunox (Catalog# : 122523)Pardoprunox is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT
• 219580-11-7 | PD173074 (Catalog# : 122212)PD173074 is a small-molecule FGFR3-selective tyrosine kinase inhibitor (TKI), as a th
• 269718-83-4 | Pardoprunox hydrochloride (Catalog# : 111010)Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and
• 20062-91-3 | 3-(4-phenoxyphenyl)propanoic acid (Catalog# : 90709)Coming soon!
• 212844-53-6 | Purvalanol A (Catalog# : 52564)Purvalanol A(NG-60) is a potent, cell-permeable, and selective inhibitor of cyclin-de
• 212844-54-7 | Purvalanol B (Catalog# : 52559)Purvalanol B(NG-95) is a cyclin-dependent kinase inhibitor with IC50 values of 6, 6,
• 2645-32-1 | PR-619 (Catalog# : 52227)PR-619 is a broad-range DUB inhibitor with potential for further development as a che
• 2169919-21-3 | Revumenib (Catalog# : 25140)Revumenib, also known as SNDX-5613, is a potent and specific Menin-MLL inhibitor. It
• 206885-38-3 | Ronopterin (Catalog# : 25084)Ronopterin is a potent Nitric oxide synthase inhibitor and Neuroprotectant.
• 2765081-21-6 | RMC-6236 (Catalog# : 25074)Daraxonrasib, also known as RMC-6236 and RAS-IN-2, is a potent and selective RAS(ON)
• 266359-83-5 | Reparixin (Catalog# : 25050)Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
• 2794934-49-7 | RGT-018 (Catalog# : 24148)RGT-018 is a potent and orally active SOS1 inhibitor with anti-tumor effects.
• 2204289-53-0 | (Rac)-SHIN2 (Catalog# : 24136)(Rac)-SHIN2 is a serine hydroxymethyltransferase (SHMT) inhibitor having 1,4-dihydrop