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Cas号索引 8

• 88069-49-2 | 吡西卡尼盐酸盐 (Catalog# : 17031016)吡西卡尼，也叫SUN 1165，是日本临床上用来治疗心律失常的一种药
• 854107-55-4 | Ponesimod (Catalog# : 17030918)Ponesimod，也被称为ACT - 128800，是一个强有力的，而且是积极的选择
• 882257-11-6 | P5091 (P005091) (Catalog# : 16122795)P5091(P005091) is a selective and potent inhibitor of ubiquitin-specific protease 7 (
• 847591-62-2 | PRI-724 (Catalog# : 16122785)PRI-724 is a potent, specific inhibitor of the canonical Wnt signaling pathway in can
• 866206-54-4 | PRX-08066 (Catalog# : 16071114)PRX-08066 is a a novel 5-hydroxytryptamine receptor 2B antagonist, reduces monocrotal
• 866323-14-0 | PXD-101 (Catalog# : 16053002)Belinostat (trade name Beleodaq, previously known as PXD101) is a histone deacetylase
• 898562-94-2 | PF-2545920 (Catalog# : 012006)PF-2545920 is a phosphodiesterase inhibitor selective for the PDE10A subtype, which i
• 802539-81-7 | PHA-848125 (Catalog# : 122916)PHA-848125 is a potent, ATP-competitive CDK inhibitor for CDK2 with IC50 of 45 nM; &g
• 871266-63-6 | PCI-27483 (Catalog# : 110401)PCI-27483 is a reversible small-molecule inhibitor of activated factor VII (factor VI
• 82508-31-4 | PSEUDOLARIC ACID B (Catalog# : 110223)Pseudolaric acid B is a diterpene acid isolated from the bark of Pseudolarix kaempfer
• 839707-37-8 | Pluripotin(SC-1) (Catalog# : 100502)SC1 (Pluripotin) was identified in a cell-based chemical library screen for small mol
• 87691-87-0 | 3-(1-Piperazinyl)-1,2-Benzisothiazole (Catalog# : 91408)The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
• 869288-64-2 | PF-573228 (Catalog# : 52816)PF-573228 is a potent and selective FAK inhibitor with IC50 of 4 nM for inhibiton of
• 873786-09-5 | PLX647 (Catalog# : 52756)PLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respe
• 827022-32-2 | Palbociclib(PD-0332991)HCl (Catalog# : 52011)Palbociclib (PD-0332991) HCl is a highly selective inhibitor ofCDK4/6withIC50of 11 nM
• 827022-33-3 | Palbociclib (PD0332991) Isethionate (Catalog# : 52012)Palbociclib (PD0332991) Isethionate is a highly selective inhibitor ofCDK4/6withIC50o
• 875320-29-9 | Quisinostat (Catalog# : 122821)Quisinostat is an orally available, potent, hydroxamate, pan-HDACi with broad activit
• 868698-49-1 | (R)-(-)-α-Methylhistamine HBr (Catalog# : 24130)(R)-(-)-α-Methylhistamine dihydrobromide is a very potent, high affinity H3 agonist
• 864814-88-0 | Resminostat (Catalog# : 20652)Resminostat, also known as 4S-201 and RAS2410, is an orally bioavailable inhibitor of
• 820957-38-8 | Retosiban (Catalog# : 192193)Retosiban，又称GSK-221149-A;是一种口服活性强、选择性强的亚纳米(Ki
• 874101-00-5 | RO4987655 (Catalog# : 17011603)RO4987655,也称为CH4987655, 是一种口服活性的小分子，靶向活性蛋白激
• 84088-42-6 | Roquinimex (Catalog# : 6111413)Roquinimex (Linomide; PNU212616; ABR212616) is a quinoline derivative immunostimulant
• 866081-62-1 | (R) QuinoxP(R) (Catalog# : 16062107)(R) QuinoxP(R)
• 847925-91-1 | RO4929097 (Catalog# : 123001)RO4929097 is a secretase inhibitor with IC50 of 4 nM, inhibiting cellular processing
• 841290-80-0 | R406 free base (Catalog# : 122927)R406 is a potent inhibitor of immunoglobulin E (IgE)- and IgG-mediated activation of
• 850807-63-5 | RSM932A (Catalog# : 90734)Choline kinase α (CHKA; here designated as ChoKα) is the first enzyme in the CDP-ch
• 88196-70-7 | (1R)-1-(3-methoxyphenyl)ethanamine (Catalog# : 91116)Coming soon!
• 856562-88-4 | (R)-1-(o-Tolyl)ethanamine hydrochloride (Catalog# : 90716)Coming soon!
• 859027-48-8 | (R)-1-Boc-3-((Dimethylamino)methyl)pyrrolidine (Catalog# : 83121)Coming soon!
• 871038-72-1 | Raltegravir potassium sal (Catalog# : 52612)Raltegravir potassium salt(MK0518 potassium salt) is a potent integrase (IN) inhibito