About 11 results found for searched term "68-26-8" (0.144 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3514 | Moxifloxacin hydrochloride | Topoisomerase |
| BAY12-8039 HCl | ||
| Moxifloxacin is a fourth-generation synthetic fluoroquinolone antibacterial agent. | ||
| M4066 | Ginsenoside-Rb3 | NF-κB |
| Gypenoside IV | ||
| Ginsenoside Rb3 is derived from Panax Notoginseng. Ginsenoside Rb3 inhibited NF-κB transcriptional activity induced by TNFα in 293T cell lines with IC50 of 8.2 μM. Ginsenoside Rb3 also inhibited the induction of COX-2 and iNOS mRNA. | ||
| M6928 | LY 2365109 hydrochloride | GlyT |
| LY 2365109 hcl | ||
| LY 2365109 hydrochloride is a potent and selective GlyT1 inhibitor. | ||
| M8712 | KIN1400 | Others |
| KIN1400 is innate immune agonists of IRF3 activation that induces IRF3 and MAVS dependent innate immune antiviral genes and IFNβ expression. | ||
| M19285 | Vitamin A | RAR/RXR |
| Vitamin A (Retinol) is a naturally occuring fat-soluble vitamin that is important for normal vision, the immune system, and reproduction. It also plays roles in normal functioning of heart, lungs, kidneys, and other organs. | ||
| M21974 | CAY-10514 | Others |
| CAY-10514 | ||
| M24968 | Manelimab | PD-1/PD-L1 |
| BCD-135 | ||
| Manelimab is a monoclonal antibody that inhibits programmed death-ligand 1 (PD-L1). | ||
| M29822 | Aha1/Hsp90-IN-1 | Microtubule |
| Aha1/Hsp90-IN-1 (Compound 17) is an Aha1/Hsp90 complex inhibitor. Aha1/Hsp90-IN-1 disrupts Aha1/Hsp90 interactions with an IC50 of 3.32 μM. Aha1/Hsp90-IN-1 inhibits tau aggregation. | ||
| M39285 | (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-serine | Amino Acid Derivatives |
| (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-serine is a serine derivative. | ||
| M40734 | Tepotinib Hydrochloride Hydrate | c-Met |
| Tepotinib Hydrochloride Hydrate is a potent, selective c-Met inhibitor with an IC50 of 4 nM and is more than 200-fold more selective for c-Met than for IRAK4, TrkA, Axl, IRAK1 and Mer. | ||
| M52789 | Astressin 2B | CFTR |
| Astressin 2B is a potent and selective corticotropin-releasing factor receptor 2 (CRF2) antagonist, with the IC50 values of 1.3 nM and > 500 nM for CRF2 and CRF1, respectively. | ||
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