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Cas号索引 1

• 1448427-99-3 | 6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine (Catalog# : 1710123)6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine
• 1800477-30-8 | IACS-9571 (Catalog# : 1783019)IACS-9571是一种有效的选择性TRIM24和BRPF1抑制剂。布罗莫结构域包括
• 1160927-48-9 | IDE1 (Catalog# : 17030309)IDE1是一种高效的细胞渗透性明确内胚层形成诱导剂(EC50 = 125 nM,ESC
• 1072833-77-2 | Ixazomib (MLN-2238) (Catalog# : 16123024)Ixazomib, also known as MLN-2238, is a potent proteasome inhibitor (PI) with potentia
• 16051-77-7 | Isosorbide Mononitrate (Catalog# : 16123022)Isosorbide Mononitrate is a drug used principally in the treatment of angina pectoris
• 1334298-90-6 | Itacitinib (Catalog# : 6111505)Itacitinib (INCB039110) is an oral selective JAK1 inhibitor. Itacitinib is an inh
• 186611-52-9 | IC261 (Catalog# : 611914)IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50
• 160003-66-7 | Iniparib (Catalog# : 16071103)Iniparib, also known as BSI-201, is a small-molecule prodrug inhibitor of the nuclear
• 1229705-06-9 | Idasanutlin (RG7388) (Catalog# : 16070812)Idasanutlin; also known as RG7388 and RO5503781, is a highly potent and selective MDM
• 155270-99-8 | Istradefylline (Catalog# : 16070809)Istradefylline (KW-6002) is a selective antagonist at the A2A receptor. It has been f
• 142880-36-2 | Ilomastat (Catalog# : 16070104)Ilomastat (GM6001) 是一种有效、广谱的基质金属蛋白酶 (MMP) 抑制剂，
• 1448347-49-6 | Ivosidenib (Catalog# : 16053001)Ivosidenib is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1)
• 1204669-58-8 | INCB 024360 (Catalog# : 032405)INCB 024360 is a potent and novel indoleamine-2,3 dioxygenase (IDO)inhibitor with an
• 1224844-38-5 | INK-128 (Catalog# : 011121)INK 128 is a potent and selective mTOR inhibitor with IC50 of 1 nM; >200-fold less
• 1427782-89-5 | IWP L6 (Catalog# : 011109)IWP L6 is a Porcn inhibitor with EC50 of 0.5 nM.
• 1092790-21-0 | Isoquinolin-7-ylboronic acid (Catalog# : 010612)This product is for custom synthesis.
• 1186195-62-9 | IKK 16 (Catalog# : 010419)Coming soon!
• 1001753-24-7 | INH6 (Catalog# : 102620)INH6 is a potent Hec1 inhibitor, which specifically disrupts the Hec1/Nek2 interactio
• 1099644-42-4 | ITD-1 (Catalog# : 101902)ITD-1 is a selective inhibitor of TGF- signaling, displays little or no inhibition of
• 1454700-89-0 | IN00076730 (Catalog# : 91816)Coming soon!
• 1643-29-4 | 3-(4-Iodophenyl)propionic acid (Catalog# : 90711)Coming soon!
• 1100318-96-4 | 4-iodo-7H-pyrrolo[2,3-d]pyrimidine (Catalog# : 81005)Coming soon!
• 1110709-70-0 | 3-Iodo-4-(trifluoromethoxy)benzoic acid (Catalog# : 80316)Coming soon!
• 1204669-37-3 | IDO inhibitor 1 (Catalog# : 72806)IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptop
• 1029712-80-8 | INCB28060 (Catalog# : 52609)INCB28060 is a novel orally active inhibitor (IC50=0.13 nM) of c-MET kinase.
• 159752-10-0 | Ibutamoren Mesylate (Catalog# : 51804)Ibutamoren mesylate (MK-0677) is an orally active nonpeptide growth hormone (GH) secr
• 1191252-49-9 | IOWH032 (Catalog# : 52203)IOWH032 is a syntheticCFTRinhibitor withIC50of 1.01 M in CHO-CFTR cell based assays.
• 1998725-11-3 | JHU-083 (Catalog# : 24108)JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性，并防止慢
• 1404380-58-0 | JTE-151 (Catalog# : 20594)JTE-151 是一种 RORγ 抑制剂，可通过抑制与 Th17 细胞活化相关的 ROR
• 1627902-21-9 | JNJ-54175446 (Catalog# : 20534)JNJ-54175446 is a potent and selective P2X7 Receptor Antagonist. JNJ-54175446 is pote