About 8 results found for searched term "334-50-9" (0.131 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M7317 | Spermidine trihydrochloride | Autophagy |
| Spermidine trihydrochloride is a agonist at polyamine site. | ||
| M9374 | Fmoc-Trp(1-Me)-OH | Others |
| Fmoc-Trp(Me)-OH | ||
| Fmoc-Trp(1-Me)-OH is synthesized by N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and 1-Methyl-Ltrypthophan. | ||
| M10919 | Mito-TEMPO | Mitochondrial Related |
| MitoTEMPO | ||
| Mito-TEMPO (MT) is a mitochondrial-targeted superoxide dismutase mimetic that protects the early stages of acetaminophen (APAP) hepatotoxicity by inhibiting the formation of peroxynitrite. Mito-TEMPO treatment inhibits APAP-induced EXPRESSION OF RIP3 kinase. | ||
| M7247 | SAR7334 dihydrochloride | Others |
| SAR 7334 2HCl | ||
| SAR7334 dihydrochloride is a novel, highly potent and bioavailable inhibitor of TRPC6 channels, inhibiting TRPC6 currents with IC50 of 7.9 nM. | ||
| M13926 | INCB3344 | CCR |
| INCB3344 is a potent, selective and orally bioavailable CCR2 antagonist with IC50 values of 5.1 nM (hCCR2) and 9.5 nM (mCCR2) in binding antagonism and 3.8 nM (hCCR2) and 7.8 nM (mCCR2) in antagonism of chemotaxis activity. | ||
| M14473 | Prinomastat | MMP |
| AG3340; KB-R9896 | ||
| Prinomastat (AG3340) is a broad spectrum, potent, orally active metalloproteinase (MMP) inhibitor with IC50s of 79, 6.3 and 5.0 nM for MMP-1, MMP-3 and MMP-9, respectively. | ||
| M30755 | ONO-5334 | Cathepsin |
| ONO-5334 is a potent, selective and orally active cathepsin K inhibitor with Ki values of 0.10 nM, 0.049 nM and 0.85 nM for human, rabbit and rat cathepsin K, respectively. ONO 5334 is an effective antiviral compound against SAR-COV-2 virus activity with an EC50 value of 500 nM. ONO-5334 has the potential for the study of osteoporosis and COVID-19 disease. | ||
| M45317 | (S)-BAY 2965501 | DGK |
| (S)-BAY 2965501 is the left-handed isomer of BAY 2965501 (HY-153343).BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKz) inhibitor and induces pERK activation. BAY 2965501 is a potent and selective inhibitor of diacylglycerol kinase zeta (DGKz) and induces pERK activation. | ||
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