Chemical Structure : DDL-357
Catalog No.: PC-24532Not For Human Use, Lab Use Only.
DDL-357 is a small molecule secreted isoform of clusterin (sCLU) enhancer with EC50 of 223 nM, increases brain sCLU in the murine ApoE4TR-5XFAD model of AD.
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DDL-357 is a small molecule secreted isoform of clusterin (sCLU) enhancer with EC50 of 223 nM, increases brain sCLU in the murine ApoE4TR-5XFAD model of AD.
DDL-357 is a BET inhibitor (+)-JQ1 analog with IC50 of 161/20 nM for BRD2/4 respectively.
DDL-357 does not show overt toxicity at concentrations as high as 50 µM in CNS gliotoxicity (U-87 MG), neurotoxicity (SH-SY5Y), nephrotoxicity (HEK 293 T), and hepatotoxicity (HEPG2).
DDL-357 increase sCLU in brain in the ApoE4TR-5XFAD murine model of AD, and both decrease phospho-tau (p-tau) and improve memory in the 3xTg-AD murine model of AD.
DDL-357 increased proteins related to mitochondrial function, synaptic plasticity and protein aggregate clearance in ApoE4TR-5XFAD mice.
DDL-357 increased mitochondrial oxygen consumption, and HN and SirT1 expression in U-87 and SH-SY5Y cells, and neurite outgrowth in iPSC-derived neurons.
M.Wt | 440.95 | |
Formula | C22H21ClN4O2S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Cohn W, et al. NPJ Drug Discov. 2025;2(1):7.
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