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Cas号索引 2

• 2102196-57-4 | MDK6574 (Catalog# : 18421)MDK6574,也称为FAA1 agonist-1,FAA1受体激动剂。
• 23612-48-8 | 2-甲基-7-氮杂吲哚 (Catalog# : 183131)2-甲基-7-氮杂吲哚是一种医药中间体。
• 2060530-16-5 | MDK30165 (Catalog# : 179138)MDK30165，也称为K-Ras（G12C）抑制剂6。
• 203849-91-6 | 单甲基澳瑞他汀 D (Catalog# : 20179132)MMAD又称为单甲基澳瑞他汀 D，是一种高效的微管蛋白抑制剂。MMAD
• 2070015-13-1 | ML241 HCl (Catalog# : 179111)ML241是强有力的和有选择性的蛋白酶抑制剂。ML241抑制P97 ATPase与IC
• 210110-90-0 | 米格鲁特盐酸盐 (Catalog# : 2017824)米格鲁特, 也称为OGT 918,是Actelion开发的一种药物，主要用于治疗I
• 21516-68-7 | 红曲素 (Catalog# : 201708015)它是一种有效的抑制剂，是由car纤维组织形成来测量不利的化学或
• 23007-85-4 | MPTP hydrochloride (Catalog# : 16122796)MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of do
• 2029049-79-2 | ML390 (Catalog# : 16122749)ML390 is a human DHODH inhibitor that induces differentiation in acute myeloid leukem
• 219832-49-2 | MP-A08 (Catalog# : 6111524)MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and S
• 292057-76-2 | Mcl1-IN-2 (Catalog# : 6111404)Mcl1-IN-2 is a Mcl-1 inhibitor without reported IC50 value.
• 256373-96-3 | MCC950 sodium (Catalog# : 6111014)MCC950 (CP 456773) sodium is a potent, selective, small molecule inhibitor of NLRP3 w
• 29906-67-0 | 1-METHYL-5-NITRO-1H-INDOLE (Catalog# : 169701)1-METHYL-5-NITRO-1H-INDOLE CAS#29906-67-0
• 210826-40-7 | MCC950 (Catalog# : 030101)MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM
• 208538-73-2 | Micafungin sodium (Catalog# : 120712)Micafungin is an antifungal drug that belongs to the antifungal class of compounds kn
• 23012-17-1 | 2-Methyl-1,3-oxazole-4-carboxylic acid (Catalog# : 91828)Coming soon!
• 24623-20-9 | 6-methyl-2,3-dihydroinden-1-one (Catalog# : 81929)Coming soon!
• 24644-78-8 | 4-methyl-2,3-dihydroinden-1-one (Catalog# : 81923)Coming soon!
• 29415-97-2 | Methyl 3-bromo-4-hydroxybenzoate (Catalog# : 80319)Coming soon!
• 2375840-87-0 | NDI-091143 (Catalog# : 24057)NDI-091143 is a novel potent inhibitor of human ATP-citrate lyase, indirectly disrupt
• 2354321-33-6 | NMD670 (Catalog# : 24050)NMD670 is an orally bioavailable skeletal muscle-specific chloride ion channel (ClC-1
• 2739866-40-9 | NVL-655 ( ALK-IN-27 ) (Catalog# : 24003)NVL-655是一种新型脑渗透性ALK选择性抑制剂，旨在解决目前可用的
• 2244614-14-8 | Navacaprant (Catalog# : 23122601)Navacaprant (NMRA-335140, BTRX-140) 是一种口服、选择性、可逆的 kappa 阿
• 2254741-41-6 | Ninerafaxstat (Catalog# : 20608)Ninerafaxstat is a biochemical that decreases fatty acid oxidation and improves mitoc
• 2154406-04-7 | NBI-921352 (Catalog# : 20602)NBI-921352 is a potent, highly selective Nav1.6 sodium channel inhibitor being develo
• 2143096-93-7 | Navitoclax-piperazine (Catalog# : 20559)Navitoclax-piperazine, also known as ABT-263-piperazine, is a Navitoclax derative and
• 2411819-82-2 | NBD-14270 (Catalog# : 20448)
• 2055599-51-2 | NTP42 (Catalog# : 2051509)NTP42 is a novel antagonist of the thromboxane prostanoid receptor (TP), currently in
• 2349367-89-9 (free base) | NVS-ZP7-4 (Catalog# : 204506)NVS-ZP7-4 is a potent ZIP7 Inhibitor, which inhibits Notch signaling with IC50 of 0.1
• 2231098-99-8 | NCT-506 (Catalog# : 19354)NCT-506是一种口服生物可利用醛脱氢酶1A1 (ALDH1A1)抑制剂，IC50为7nm。