Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 1812134 | SAR260301 | 1260612-13-2 | >98% |  |
| SAR260301 is potent and selective Class I phosphatidylinositol-3-kinase (PI3K)β spec | ||||
| 1812132 | Sparsentan | 254740-64-2 | >98% |  |
| Sparsentan, also known as RE-021, PS433540 and DARA-a, is a Dual angiotensin II and e | ||||
| 1810263 | SR-0987 | 303126-97-8 | >98% |  |
| SR-0987 is a T cell-specific RORγ (RORγt) agonist. SR-0987 induces IL-17 expression | ||||
| 1810244 | SGC-CBP30 | 1613695-14-9 | >98% |  |
| SGC-CBP30 is a potent and selective inhibitor of CREBBP (CBP) and EP300; which are ge | ||||
| 1810243 | ST2825 | 894787-30-5 | >98% |  |
| ST-2825 is MyD88 inhibitor. ST2825 provides neuroprotection after experimental trauma | ||||
| 1810221 | Seletalisib | 1362850-20-1 | >98% |  |
| Seletalisib, also known as UCB-5857, is a potent and selective PI3 kinase inhibitor, | ||||
| 1810172 | Simenepag | 910562-15-1 | >98% |  |
| Simenepag, also known as AGN-210676, is a small molecule prostaglandin E2 receptor ag | ||||
| 186221 | SB-273005 | 205678-31-5 | >98% |  |
| SB-273005 is an inhibitor of integrin αvβ3. | ||||
| 185151 | STF-083010 | 307543-71-1 | >98% |  |
| STF-083010, also known as IRE1 Inhibitor I, is an inhibitor of the IRE1/XBP1 pathway. | ||||
| 185115 | SAR407899 free base | 923359-38-0 | >98% |  |
| SAR407899 is a potent and selective Rho kinase inhibitor with promising antihypertens | ||||
| 185114 | SB-334867 free base | 792173-99-0 | >98% |  |
| SB-334867 is an orexin antagonist. | ||||
| 185113 | SC-560 | 188817-13-2 | >98% |  |
| SC-560 is a potent, orally active and selective inhibitor of COX-1. | ||||
| 185112 | Seladelpar | 851528-79-5 | >98% |  |
| Seladelpar, also known as MBX-8025 and RWJ-800025, is a selective peroxisome prolifer | ||||
| 18574 | SEL120-34A HCl | 1609452-30-3 | >98% |  |
| SEL120-34A is a potent and selective CDK8 inhibitor active in AML cells with high lev | ||||
| 1842814 | SR-4370 | 1816294-67-3 | >98% |  |
| SR-4370 is an HDAC inhibitor. | ||||
| 184287 | SGC2085 HCl | 1821908-49-9 | >98% |  |
| SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1 | ||||
| 184176 | S38093 HCl | 1222097-72-4 | >98% |  |
| S38093 is an inverse agonist at histamine H3 receptors. | ||||
| 184123 | STO-609 acetate | 1173022-21-3 | >98% |  |
| STO-609 is a cell-permeable inhibitor of calcium/calmodulin-dependent kinase kinases | ||||
| 18495 | Super-TDU | 1599441-71-0 | >98% |  |
| Super-TDU is an inhibitory polypeptide targeting yap-teads interaction. | ||||
| 18427 | SSD114 HCl | N/A | >98% |  |
| SSD114 is a GABAB positive allosteric modulator. SSD114 potentiated GABA-stimulated [ | ||||
| 183219 | (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)methyl 2,4-dimethylbenzoate | 1253955-19-9 | >98% |  |
| (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)met | ||||
| 183218 | (S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic acid | 2097334-20-6 | >98% |  |
| (S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic aci | ||||
| 1712291 | (S)-Butyl 2-hydroxybutanoate | 132513-51-0 | >96% |  |
| butyl (2S)-2-hydroxybutanoate is building blocks. | ||||
| 1712261 | SCR7 pyrazine | 14892-97-8 | >98% |  |
| SCR7 pyrazine is a small molecule inhibitor of DNA ligase IV that prevents nonhomolog | ||||
| 17101615 | S38093 | 862896-30-8 | >98% |  |
| S 38093 is a brain-penetrant antagonist of H3 receptor, with Ki of 8.8, 1.44 and 1.2 | ||||
| 17101610 | SAR-7334 HCl | 1333207-63-8 | >98% |  |
| SAR7334 is a novel, highly potent and bioavailable inhibitor of TRPC6 channels that o | ||||
| 1710168 | SEN-826 | 1160833-51-1 | >98% |  |
| SEN-826 is a potential anticancer agent. | ||||
| 17101310 | SRT3025 HCl | 2070015-26-6 | >98% |  |
| SRT3025 is an orally available small molecule activator of the SIRT1 enzyme. | ||||
| 1710136 | Senexin A | 1366002-50-7 | >98% |  |
| Senexin A is a potent and selective CDK8 inhibitor (IC50 = 280 nM). Senexin A binds t | ||||
| 171071 | S63845 | 1799633-27-4 | >98% |  |
| S63845 is a small molecule that specifically binds with high affinity to the BH3-bind | ||||