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Cas号索引 8

• 866598-45-0 | AZD-2207 (Catalog# : 20440)AZD-2207 is a cannabinoid receptor CB1 antagonist and highly lipophilic compound for
• 851845-37-9 | AZD6703 (Catalog# : 20439)AZD6703 is a potent, selective and reversible orally bioavailable inhibitor of p38 mi
• 882697-00-9 | Anle138b (Catalog# : 171553)Anle138b 是一种口服的、可透过血脑屏障的蛋白质抑制剂。在 α-突
• 83265-53-6 | 2-氨基-5-三氟甲基苯甲酸 (Catalog# : 20312)
• 88349-90-0 | A2793 (Catalog# : 20286)A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK). A2793 inhibited TW
• 868623-40-9 | ABT-384 (Catalog# : 20281)ABT-384 是 11β-羟基类固醇脱氢酶 1 (HSD-1) 的有效选择性抑制剂，该
• 872044-70-7 | AN 0128 (Catalog# : 20269)AN 0128, also known as CRM-0005 and ONT-0001, is a tumour necrosis factor alpha (TNF-
• 870087-36-8 | Apilimod mesylate ( STA-5326 ) (Catalog# : 23948)Apilimod, also known as STA-5326, is a potent IL-12/IL-23 inhibitor. Apilimod inhibit
• 875446-37-0 | Anacetrapib (Catalog# : 2061701)Anacetrapib, also known as MK-0859, is a CETP inhibitor being developed to treat hype
• 898800-26-5 | AZ876 (Catalog# : 19356)AZ876，又称AZ-876，是一种肝脏X受体激动剂。AZ876可预防病理性心肌
• 836620-48-5 | AS1842856 (Catalog# : 1811265)AS1842856是一种细胞可渗透的Foxo1抑制剂，IC50为33 nM，阻断Foxo1的转
• 880549-30-4 | AMD-070盐酸盐 (Catalog# : 18741)AMD11070，也称为 AMD070, X4P-001和mavorixafor, 是一种有效的口服生物活
• 841301-32-4 | 阿莫奈韦 (Catalog# : 186252)阿莫奈韦是一种 helicase-primase 抑制剂，对 HSVs 具有强效的抗病毒活
• 851881-60-2 | ADX-47273 (Catalog# : 185173)ADX-47273是一种强有力的和选择性mGluR5受体PAM(积极的变构调制器),E
• 80306-38-3 | AR-7 (Catalog# : 179158)AR-7，亦称非典型维甲酸7，是一种有效的和选择性的自噬（CMA）增
• 811803-05-1 | 阿帕替尼 (Catalog# : 17022301)阿帕替尼是一种具有生物口服、选择性的IC50为1 nM的VEGFR2 抑制剂。
• 878385-84-3 | AZD-5069 (Catalog# : 16122864)AZD-5069 is a potent and selective CXCR2 antagonist with the potential to inhibit neu
• 848141-11-7 | Alvelestat (AZD9688) (Catalog# : 16122854)Avelestat, also known as AZD9668, is a novel, oral inhibitor of neutrophil elastase (
• 88321-09-9 | Aloxistatin (E-64d) (Catalog# : 16122801)Aloxistatin (E-64d), is a selective cysteine protease inhibitor or calpain and autoph
• 859498-05-8 | AGN 205728 (Catalog# : 6111520)AGN 205728 is a potent and selective RAR antagonist with Ki/IC95 values of 3 nM/ 0.6
• 893422-47-4 | Akt1 and Akt2-IN-1 (Catalog# : 611804)Akt1 and Akt2-IN-1 is an allosteric inhibitor of Akt1 (IC50 = 3.5 nM) and Akt2 (IC50
• 857531-00-1 (free base); 1431697-86-7 (2HCl) | AT7867 (Catalog# : 161009021)This ATP-competitive small molecule potently inhibits both AKT and p70S6K activity at
• 870281-34-8 | Acalisib (Catalog# : 16071413)Acalisib, also known as GS-9820, is an inhibitor of the beta and delta isoforms of th
• 865305-30-2 | AF-353 (Catalog# : 16071021)AF-353 is a novel, potent and orally bioavailable P2X3/P2X2/3 receptor antagonist, in
• 89924-69-6 | ascorbic acid (Catalog# : 16070919)(2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one
• 844499-71-4 | A-769662 (Catalog# : 16070701)A-769662 is a potent, reversible AMP-activated protein kinase (AMPK) activator with a
• 848344-36-5 | AS 602801 (Catalog# : 011913)AS 602801 is a novel, orally active inhibitor of JNK.
• 878739-06-1 | AZ 628 (Catalog# : 011120)AZ628 is a new pan-Raf inhibitor for BRAF, BRAFV600E, and c-Raf-1 with IC50 of 105 nM
• 882663-88-9 | AMG-47a (Catalog# : 011107)AMG-47a is a potent inhibitor of Lck and T cell proliferation.
• 869357-68-6 | AZD8330 (Catalog# : 010809)AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 n