Chemical Structure : JG-98
CAS No.: 1456551-16-8
Catalog No.: PC-62492Not For Human Use, Lab Use Only.
JG-98 is an allosteric Hsp70 inhibitor, displays >3-fold more active, greater stability than MKT-077 against the breast cancer cell lines MDA-MB-231 and MCF-7 (EC50 of 0.4 uM and 0.7 uM, respectively).
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JG-98 is an allosteric Hsp70 inhibitor, displays >3-fold more active, greater stability than MKT-077 against the breast cancer cell lines MDA-MB-231 and MCF-7 (EC50 of 0.4 uM and 0.7 uM, respectively).
JG-98 strongly affects autophagic flux, increases p62 oligomerization and reduces p62 monomer.
JG-98 destabilizes FoxM1 and relieved suppression of downstream effectors, including p21 and p27.
M.Wt | 534.532 | |
Formula | C24H21Cl2N3OS3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
Thiazolium,2-[(Z)-[(5E)-5-(6-chloro-3-methyl-2(3H)-benzothiazolylidene)-3-ethyl-4-oxo-2-thiazolidinylidene]methyl]-3-(phenylmethyl)-,chloride (1:1) |
1. Li X. et al. ACS Med Chem Lett. 2013 Nov 14;4(11).
2. Li X, et al. Mol Cancer Ther. 2015 Mar;14(3):642-8.
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