产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 17011709 | SMER28 | 307538-42-7 | 98% |  |
| 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 | ||||
| 17011707 | SKF-38393盐酸盐 | 62717-42-4 | 98% |  |
| SKF-38393, 也称为(+/-)-SKF-38393, 是苯偶氮化学类的合成化合物，作为 | ||||
| 17011706 | 西他沙星 | 127254-12-0 | 98% |  |
| 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、 | ||||
| 17011704 | SHP099盐酸盐 | 1801747-11-4 | 98% |  |
| 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 | ||||
| 17011703 | 6-姜烯酚 | 555-66-8 | 98% | -cas-555-66-8.png) |
| 6-姜烯酚, 是姜的一种辛辣成分，类似于姜酚的化学结构。 | ||||
| 17011702 | SGC707 | 1687736-54-4 | 98% |  |
| 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 | ||||
| 17011701 | SC66 | 871361-88-5 | 98% |  |
| 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 | ||||
| 71161 | SBI0206965 | 1884220-36-3 | 98% |  |
| 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 | ||||
| 17011609 | SB-743921盐酸盐 | 940929-33-9 | 98% |  |
| SB-743921是一种具有潜在抗肿瘤性质的合成小分子。 | ||||
| 17011607 | Sardomozide | 149400-88-4 | 98% |  |
| Sardomozide，也叫SAM486A或CGP48664,是一种第二代聚胺合成抑制剂，抑制 | ||||
| 17011606 | SAR407899 HCl | 923262-96-8 | 98% |  |
| 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 | ||||
| 17011605 | SAR131675 | 1092539-44-0 | 98% |  |
| SAR131675是一种有效的选择性vegfr - 3抑制剂。 | ||||
| 161227110 | 4SC-202 | 910462-43-0 | 98% |  |
| 4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone de | ||||
| 16122784 | SKL2001 | 909089-13-0 | 98% | |
| SKL2001 is a novel agonist of the Wnt/-catenin pathway that disrupts the Axin/-cateni | ||||
| 16122766 | Salicylanilide | 87-17-2 | 98% |  |
| Salicylanilides are a group of compounds with a wide range of biological activities i | ||||
| 16122760 | Sivelestat (ONO-5046) | 127373-66-4 | 98% | -cas-127373-66-4.png) |
| Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44 | ||||
| 16122758 | Sivelestat sodium | 201677-61-4 | 98% |  |
| Sivelestat sodium is a competitive inhibitor of human neutrophil elastase, also inhib | ||||
| 16122748 | SC75741 | 913822-46-5 | 98% |  |
| SC75741 is a potent NF-B inhibitor with EC50 of 200 nM.SC75741 shows immunosuppressiv | ||||
| 16122726 | SQ22536 | 17318-31-9 | 98% |  |
| SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE | ||||
| 16122721 | SIS3 | 521984-48-5 | 98% |  |
| SIS3, a novel specific inhibitor of Smad3, inhibits TGF- and activin signaling by sup | ||||
| 16122716 | Saccharin 1-methylimidazole (SMI) | 482333-74-4 | 98% | |
| SMI is considered a general-purpose activator for DNA and RNA synthesis. | ||||
| 16122706 | STA-21 | 111540-00-2 | 98% |  |
| STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act | ||||
| 6111526 | SKI II | 312636-16-1 | 98% |  |
| SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M | ||||
| 6111522 | SR1001 | 1335106-03-0 | 98% |  |
| SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati | ||||
| 61119 | S1P1 Agonist III | 1324003-64-6 | 98% | |
| S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac | ||||
| 161113 | SCH 546738 | 906805-42-3 | 98% |  |
| SCH 546738 is a novel, potent and non-competitive small molecule CXCR3 antagonist wit | ||||
| 611937 | 4SC-202 | 1186222-89-8 | 98% | |
| 4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H | ||||
| 611930 | SJB3-019A | 2070015-29-9 | 98% |  |
| SJB3-019A is a potent and novel usp1 inhibitor. SJB3-019A (IC50 = 0.0781 uM) was 5 ti | ||||
| 611915 | SR-3029 | 1454585-06-8 | 98% | |
| SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3 | ||||
| 161009026 | SB-216763 | 280744-09-4 | 98% by HPLC |  |
| SB-216763 is a glycogen synthase kinase-3 (GSK3) inhibitor, which can maintain mouse | ||||