Name | 1-(2-chloro-6-fluorobenzoyl)-3-(9H-fluoren-9-yl)-urea |
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Synonyms | 2-Chloro-N-[(9H-fluoren-9-ylamino)carbonyl]-6-fluorobenzamide |
Description | TMN355 is a potent chemical cyclophilin A inhibitor and reduces foam cell formation and cytokine secretion. TMN355 is used for atherosclerosis[1]. |
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Related Catalog | |
Target |
cyclophilin A[1] |
In Vitro | TMN 355 (0.5-10 μM; 3-9 hours) results in 75.9% reduction of cyclophilin A protein expression. And 1 μM TMN 355 inhibits cyclophilin A after 6 h of activation[1]. Western Blot Analysis[1] Cell Line: THP cell lines Concentration: 0.5, 1, 2.5, 5 and 10 μM Incubation Time: 3, 6 and 9 hours Result: Resulted in 75.9% reduction of cyclophilin A protein expression. |
References |
Molecular Formula | C21H14ClFN2O2 |
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Molecular Weight | 380.79900 |
Exact Mass | 380.07300 |
PSA | 58.20000 |
LogP | 5.47030 |
Hazard Codes | Xi |
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