Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 17011713 | Sugammadex sodium | 343306-79-6 | 98% | |
| Sugammadex soidum is an agent for reversal of neuromuscular blockade by the agent roc | ||||
| 17011712 | Streptozocin | 18883-66-4 | 98% |  |
| Streptozocin is a methylnitrosourea antineoplastic antibiotic isolated from the bacte | ||||
| 17011711 | Sotagliflozin | 1018899-04-1 | 98% |  |
| Sotagliflozin, also known as LX4211, is an orally active and a dual SGLT1/SGLT2 inhib | ||||
| 17011710 | Solithromycin | 760981-83-7 | 98% |  |
| Solithromycin, also known as CEM-101 and OP-1068, is a ketolide antibiotic undergoing | ||||
| 17011709 | SMER28 | 307538-42-7 | 98% |  |
| SMER28 is a small molecule modulator of autophagy, inducing autophagy independently o | ||||
| 17011707 | SKF-38393 hydrochloride | 62717-42-4 | 98% |  |
| SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine | ||||
| 17011706 | Sitafloxacin anhydrous | 127254-12-0 | 98% |  |
| Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone that is very ac | ||||
| 17011704 | SHP099 HCl | 1801747-11-4 | 98% |  |
| SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi | ||||
| 17011703 | Shogaol (6-Shogaol) | 555-66-8 | 98% | -cas-555-66-8.png) |
| Shogaol, also known as (6)-shogaol, is a pungent constituent of ginger similar in che | ||||
| 17011702 | SGC707 | 1687736-54-4 | 98% |  |
| SGC707 is a potent, selective and cell-active allosteric inhibitor of protein arginin | ||||
| 17011701 | SC66 | 871361-88-5 | 98% |  |
| SC66 is a novel and potent AKT inhibitor, which reduced cell viability in a dose- and | ||||
| 71161 | SBI0206965 | 1884220-36-3 | 98% |  |
| SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec | ||||
| 17011609 | SB-743921 HCl | 940929-33-9 | 98% |  |
| SB-743921 is a synthetic small molecule with potential antineoplastic properties. SB- | ||||
| 17011608 | Sarecycline | 1035654-66-0 | 98% |  |
| Sarecycline, also known as P005672, is a novel, tetracycline-derived, narrow-spectrum | ||||
| 17011607 | Sardomozide | 149400-88-4 | 98% |  |
| Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn | ||||
| 17011606 | SAR407899 HCl | 923262-96-8 | 98% |  |
| SAR407899 is a potent and selective Rho kinase inhibitor with promising antihypertens | ||||
| 17011605 | SAR131675 | 1092539-44-0 | 98% |  |
| SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine | ||||
| 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 | ||||