UAMC-3203是ferroptosis抑制剂，在IMR-32神经母细胞瘤细胞中IC50为10 nM。 Information UAMC-3203 UAMC-3203 is an improved ferroptosis inhibitor with an IC50 value of 10 nM in IMR-32 neuroblastoma cells. Targets Ferroptosis (IMR-32 neuroblastoma cells) 10 nM In vitro UAMC-3203 has an impressive t1/2 when incubated with both human and rat microsomes (t1/2 = 20.5 h and t1/2 = 16.5 h respectively) but is found to be relatively less stable when incubated with murine microsomes (t1/2 = 3.46 h). In vivo UAMC-3203 significantly lowers the plasma levels of lactate dehydrogenase (LDH) in mice. It is rapidly removed from the bloodstream and redistributed into various tissues, as can be expected for lipophilic basic compounds. Significant concentrations of UAMC-3203 are found in all analyzed tissues (liver, kidney, and lungs).
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UAMC-3203
CAS number：2271358-64-4 molecular formula：C25H37N5O2S
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| Chinese alias | - | ||
| English alias | Benzenesulfonamide,4-(cyclohexylamino)-3-[(phenylmethyl)amino]-N-[2-(1-piperazinyl)ethyl]- | ||
| CAS number | 2271358-64-4 | molecular formula | C25H37N5O2S |
| molecular weight | 471.66 g/mol | Exact mass | ≥98% |
| PSA | 93.900 Ų | logp | 3.36 |
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