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Cas号索引 1

• 1805789-54-1 (HCl) | ICEC0942 HCl (Catalog# : 204305)ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
• 1805833-75-3 (free base) | ICEC0942 free base (Catalog# : 204304)ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
• 1160521-50-5 | ITI-214 (Catalog# : 54192)ITI214 是一种选择性的PDE1抑制剂。
• 1642303-38-5 | ITI-214磷酸盐 (Catalog# : 512193)ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
• 1429179-07-6 | IDH889 (Catalog# : 19319)IDH889是一种有效的选择性IDH1抑制剂。IDH899为IDH (R132H) IC50 = 20 nM;细
• 1584121-99-2 | IT-901 (Catalog# : 186276)IT-901是一个血液恶性肿瘤抑制剂,通过阻断NF-κB-Controlled氧化应激反
• 1234490-83-5 | INX 08189 (Catalog# : 186253)INX 08189 是一种RNA引导的RNA聚合酶(NS5B)抑制剂，可用于丙型肝炎病
• 1820889-23-3 | INCB057643 (Catalog# : 185232)INCB057643是一种BET抑制剂。在卵巢癌中，INCB054329降低了同源重组效
• 1323403-33-3 | Iberdomide (Catalog# : 185216)Iberdomide,也称为CC-220，可用于治疗系统性红斑狼疮。
• 1262238-11-8 | INCB3344 (Catalog# : 185215)INCB3344是CCR2受体的一种有效的选择性拮抗剂，它在结合拮抗的IC(5
• 1668565-74-9 | IDO-IN-2 (Catalog# : 184317)IDO抑制剂1是IDO的有效抑制剂(吲哚胺-(2,3)-二氧合酶)，IC50为3nm。
• 1425043-73-7 | IPI-3063 (Catalog# : 18433)IPI-3063是一种选择性的Phosphoinoside-3-激酶p110δ 抑制剂。IPI-3063能有
• 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