WebMar 15, 2005 · All of the new analogues, Pifithrin-like and polycyclic dehydrated derivatives were assessed for their p53 inactivation potency by measuring survival of cortical neurons, whose death was induced by the DNA-damaging agent etoposide. Pifithrin-alpha like 2f as well as the cyclic dehydrated 6b analogue were found to be one log more potent p53 ... WebCyclic Pifithrin-α hydrobromide. Synonym(s): 2-(4-Methylphenyl)imidazo[2,1-b]-5,6,7,8-tetrahydrobenzothiazole hydrobromide, Cyclic PFT-α hydrobromide, Pifithrin-α, cyclic, QB102. Empirical Formula (Hill Notation): C 16 H 16 N 2 S · HBr. CAS No.: 511296-88-1. Molecular Weight: 349.29. Compare Product No. Description SDS Pricing; P4236:
Pifithrin-α, p-Nitro, Cyclic (PFN-α) p53 Inhibitor MedChemExpress
WebCyclic Pifithrin-α hydrobromide is the hydrobromide salt form of Cyclic Pifithrin-α, which is a transcriptional inhibitor of p53. CAS No. 511296-88-1 Selleck's Cyclic Pifithrin-α … WebCyclic pifithrin-alpha sensitizes wild type p53 tumor cells to antimicrotubule agent-induced apoptosis Authors Valentina Zuco 1 , Franco Zunino Affiliation 1 Department of … hmi manassas
Cyclic Pifithrin-alpha Hydrobromide 98.0+%, TCI …
WebPifithrin-α (PFT-α; Item No. 13326) is an inactivator of p53 that blocks p53-dependent transcriptional activation and apoptosis. 1 Cyclic PFT-α (Item No. 14748) is a stable analog of PFT-α. 2 p -nitro-Cyclic PFT-α is a cell-permeable form of cyclic PFT-α. 3 It is one order of magnitude more active that PFT-α in protecting cortical neurons exposed … WebPifithrin-α, p-nitro, cyclic Pifithrin-α, p-nitro, cyclic is A cell-permeable p53 inhibitor that is more potent & has a longer half-life than Pifithrin-α. 60477-38-5 sc-222177 sc-222177A sc-222177B sc-222177C : 5 mg 10 mg 25 mg 50 mg: $164.00 $300.00 $600.00 1 WebPifithrin-α (PFT-α; Item No. 13326) is a reversible inhibitor of p53-dependent transcription and apoptosis. 1 Cyclic PFT-α, also known as PFT-β, is a stable analog of PFT-α, formed by the condensation of pifithrin-α in solution. 2 It inhibits the growth of the cancer cell lines IGROV-1, A2780, and HCT116 (IC 50 = 23, 77, and 103 μM, respectively). 2,3 At doses … hmi masterclass