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Cas号索引 1

• 160162-42-5 | SR-11302 (Catalog# : 24153)SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
• 1150153-86-8 | SR 16584 (Catalog# : 24137)SR 16584 is an antagonist of the α3β4 nAChR subtype (IC50 = 10.2 μM).
• 1262873-06-2 | Sepetaprost (Catalog# : 24119)Sepetaprost is a prodrug of ONO-AG-367. It has been used in trials studying the treat
• 152121-30-7 | SB-202190 (Catalog# : 24106)SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinas
• 1648843-04-2 | SX-682 (Catalog# : 24082)SX-682 is a potent and selective Cxcr1/2 inhibitor potentially useful for castration-
• 1933514-13-6 | Sebetralstat free base (Catalog# : 24048)Sebetralstat, also known as KVD-900, is a fast-acting oral PKa inhibitor that rapidly
• 1878218-66-6 | SY-008 乙酸盐 (Catalog# : 24016)SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
• 1480443-32-0 | SY-008 (Catalog# : 24021)SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
• 194032-32-1 | (S)-1-BOC-2-甲基-[1,4]二氮杂环庚烷 (Catalog# : 20541)
• 131690-60-3 | (S)-3-氨基-3-(4-氯苯基)-丙酸 (Catalog# : 20516)
• 1980023-96-8 | (S)-1-(6-(4-氟-1H-吡唑-1-甲基)吡啶-3-甲基)乙胺 (Catalog# : 20396)
• 100874-08-6 | SB-4 agonist (Catalog# : G20378)SB 4 is a potent BMP4 agonist.
• 1310422-41-3 (HCl) | SEP-363856 盐酸盐 (Catalog# : 822222)SEP-363856 是一种新型微量胺受体 1 (TAAR1) 激动剂，具有血清素 5-HT1
• 1629138-41-5 | SRI-011381 (Catalog# : L20355)SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
• 1449597-34-5 | SMN-C3 抑制剂 (Catalog# : 20344)SMN-C3 是一种口服活性 SMN2 剪接调节剂。可用于脊椎肌肉萎缩 (SMA)
• 1619931-27-9 | Seralutinib (Catalog# : 21238)Seralutinib，也称为 PK-10571 和 GB002，是一种新型吸入性 Pdgfr 激酶抑
• 1446712-19-1 | SNG-1153 (Catalog# : 21228)SNG-1153 is a modulator of estrogen receptor ER-alpha36.
• 1293281-49-8 | Seltorexant (Catalog# : 81498)Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor
• 1401682-78-7 | Senaparib (Catalog# : 20103002)Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
• 1433953-83-3 | SAR131675 (Catalog# : 2091901)SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
• 18298-32-4 | SB 225002 (Catalog# : 2071510)
• 1369767-20-3 | ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol (Catalog# : 202331)我们可以提供公斤级定制合成。((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2
• 1393477-72-9 (free base) | Selinexor free base (Catalog# : 2051501)Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
• 1330782-76-7 | Simurosertib (Catalog# : 2041504)Simurosertib, also known as TAK-931, is an orally bioavailable inhibitor of cell divi
• 1821908-48-8 (free base) | SGC2085 free base (Catalog# : 204609)SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1
• 164991-89-3 | Segetalin B (Catalog# : 204501)Segetalin B is natural product isolated from Seeds of Vaccaria Segetalis. Segetalin B
• 1392816-46-4 | SI-113 (Catalog# : 111896)SI113 is a specific inhibitor of the Sgk1 kinase activity, counteracting cancer cell
• 1350643-72-9 | IPI145中间体 (Catalog# : 196301)
• 186611-04-1 | SU 5214 (Catalog# : 19314)SU 5214是酪氨酸激酶信号转导的调制器。
• 1423715-37-0 | Seclidemstat (Catalog# : 192147)Seclidemstat是一种抗肿瘤药物候选药物。