按首字母搜索

产品名字索引 S

• 索利霉素 (Catalog# : 17011710, Cas# : 760981-83-7)索利霉素,也称为CEM-101和OP-1068, 是一种用于治疗社区获得性肺炎(C
• SMER28 (Catalog# : 17011709, Cas# : 307538-42-7)SMER28是一种自噬的小分子调制器，在哺乳动物细胞中独立于雷帕霉
• SKF-38393盐酸盐 (Catalog# : 17011707, Cas# : 62717-42-4)SKF-38393, 也称为(+/-)-SKF-38393, 是苯偶氮化学类的合成化合物，作为
• 西他沙星 (Catalog# : 17011706, Cas# : 127254-12-0)西他沙星是一种新型的广谱口服氟喹诺酮，它对许多革兰氏阳性、
• SHP099盐酸盐 (Catalog# : 17011704, Cas# : 1801747-11-4)SHP099是一个强有力的、选择性、口服生物利用率和有效的IC50 = 0.0
• 6-姜烯酚 (Catalog# : 17011703, Cas# : 555-66-8)6-姜烯酚, 是姜的一种辛辣成分，类似于姜酚的化学结构。
• SGC707 (Catalog# : 17011702, Cas# : 1687736-54-4)SGC707是一种强效、选择性和细胞活性的蛋白质精氨酸甲基转移酶3
• SC66 (Catalog# : 17011701, Cas# : 871361-88-5)SC66是一种新型的有效的AKT抑制剂，在一定剂量和时间依赖性的方
• SBI0206965 (Catalog# : 71161, Cas# : 1884220-36-3)SBI0206965是一种有效的选择性自噬激酶ULK1抑制剂。许多肿瘤变得沉
• SB-743921盐酸盐 (Catalog# : 17011609, Cas# : 940929-33-9)SB-743921是一种具有潜在抗肿瘤性质的合成小分子。
• Sardomozide (Catalog# : 17011607, Cas# : 149400-88-4)Sardomozide，也叫SAM486A或CGP48664,是一种第二代聚胺合成抑制剂，抑制
• SAR407899 HCl (Catalog# : 17011606, Cas# : 923262-96-8)SAR407899是一种具有良好的抗高血压活性的强效和选择性的激酶抑制
• SAR131675 (Catalog# : 17011605, Cas# : 1092539-44-0)SAR131675是一种有效的选择性vegfr - 3抑制剂。
• 4SC-202 (Catalog# : 161227110, Cas# : 910462-43-0)4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone de
• SKL2001 (Catalog# : 16122784, Cas# : 909089-13-0)SKL2001 is a novel agonist of the Wnt/-catenin pathway that disrupts the Axin/-cateni
• Salicylanilide (Catalog# : 16122766, Cas# : 87-17-2)Salicylanilides are a group of compounds with a wide range of biological activities i
• Sivelestat (ONO-5046) (Catalog# : 16122760, Cas# : 127373-66-4)Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44
• Sivelestat sodium (Catalog# : 16122758, Cas# : 201677-61-4)Sivelestat sodium is a competitive inhibitor of human neutrophil elastase, also inhib
• SC75741 (Catalog# : 16122748, Cas# : 913822-46-5)SC75741 is a potent NF-B inhibitor with EC50 of 200 nM.SC75741 shows immunosuppressiv
• SQ22536 (Catalog# : 16122726, Cas# : 17318-31-9)SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE
• SIS3 (Catalog# : 16122721, Cas# : 521984-48-5)SIS3, a novel specific inhibitor of Smad3, inhibits TGF- and activin signaling by sup
• Saccharin 1-methylimidazole (SMI) (Catalog# : 16122716, Cas# : 482333-74-4)SMI is considered a general-purpose activator for DNA and RNA synthesis.
• STA-21 (Catalog# : 16122706, Cas# : 111540-00-2)STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act
• SKI II (Catalog# : 6111526, Cas# : 312636-16-1)SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
• SR1001 (Catalog# : 6111522, Cas# : 1335106-03-0)SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati
• S1P1 Agonist III (Catalog# : 61119, Cas# : 1324003-64-6)S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac
• SCH 546738 (Catalog# : 161113, Cas# : 906805-42-3)SCH 546738 is a novel, potent and non-competitive small molecule CXCR3 antagonist wit
• 4SC-202 (Catalog# : 611937, Cas# : 1186222-89-8)4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H
• SJB3-019A (Catalog# : 611930, Cas# : 2070015-29-9)SJB3-019A is a potent and novel usp1 inhibitor. SJB3-019A (IC50 = 0.0781 uM) was 5 ti
• SR-3029 (Catalog# : 611915, Cas# : 1454585-06-8)SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3