ML346

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:ML346
CAS:100872-83-1
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:ML346
CAS:100872-83-1
Purity:99.29% Package:1mg;34USD|2mg;48USD|5mg;77USD Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:3-Chloro-6-(pyrrolidin-1-yl)pyridazine
CAS:100872-83-1
Purity:98%;crystal 604 Package:1KG;0.01USD
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CAS:100872-83-1
Purity:99% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: InvivoChem
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Products Intro: Product Name:ML346 (CID-767276)
CAS:100872-83-1
Purity:98% Package:10mg Remarks:V0090

ML346 manufacturers

  • ML346
  • ML346 pictures
  • $34.00 / 1mg
  • 2025-11-10
  • CAS:100872-83-1
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  • Purity: 99.25%
  • Supply Ability: 10g
ML346 Basic information
Product Name:ML346
Synonyms:ML346;ML346;ML 346;ML346 - CID 767276;CS-2056;2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[3-(4-methoxyphenyl)-2-propen-1-ylidene]-;5-(3-(4-Methoxyphenyl)allylidene)pyrimidine-2,4,6(1H,3H,5H)-trione;response,inhibit,probe,protein,Heat shock proteins,Inhibitor,ML346,ML 346,HSP,shock,conformational,cytotoxicity,ML-346,heat,chaperones;ML346, 10 mM in DMSO
CAS:100872-83-1
MF:C14H12N2O4
MW:272.26
EINECS:604-604-1
Product Categories:
Mol File:100872-83-1.mol
ML346 Structure
ML346 Chemical Properties
Melting point 266-268 °C(Solv: ethyl acetate (141-78-6))
density 1.374±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO:8.0(Max Conc. mg/mL);29.38(Max Conc. mM)
form A crystalline solid
pka7.42±0.20(Predicted)
color Pink to red
Safety Information
MSDS Information
ML346 Usage And Synthesis
DescriptionML-346 is an activator of the heat shock response that induces the expression of the heat shock proteins HSP70, HSP40, and HSP27. It induces the expression of the oxidative stress response genes HO1, GCLM, and BiP in mouse embryonic fibroblasts (MEFs) and pretreatment protects cells from severe heat shock-induced death and H2O2-induced apoptosis. It promotes folding of metastable proteins in models of conformational disease, including cellular models of Huntingtin aggregation and cystic fibrosis. It reduces aggregate formation in PC12 cells expressing human Huntingtin exon 1 containing a 74 glutamine expansion when used at a concentration of 10 μM. It also corrects trafficking of cystic fibrosis transmembrane conductance regulator proteins bearing the F508 deletion (ΔF508-CFTR) mutation carried by the majority of cystic fibrosis patients, leading to increased cell surface expression.
UsesML346 is an activator of Hsp70 expression and HSF-1 activity, with an EC50 of 4.6 μM for Hsp70. ML346 restores protein folding in conformational disease models, without significant cytotoxicity or lack of specificity. ML346 induces specific increases in genes and protein effectors of the heat shock response (HSR), including chaperones such as Hsp70, Hsp40, and Hsp27[1].
in vivo

ML346 suppress the aggregation of polyQ35 in a C. elegans model, suggesting the probe has efficacy in modifying protein aggregation and associated toxicity[1].

IC 50HSP70: 4.6 μM (EC50, HeLa cells)
References[1] Calamini B, et al. ML346: A Novel Modulator of Proteostasis for Protein Conformational Diseases.Probe Reports from the NIH Molecular Libraries Program. Bethesda (MD): National Center for Biotechnology Information (US); 2010-. 2012 Dec 17. PMID:23833797
[2] Calamini B, et al. Small-molecule proteostasis regulators for protein conformational diseases. Nat Chem Biol. 2011 Dec 25;8(2):185-96. DOI:10.1038/nchembio.763
ML346 Preparation Products And Raw materials
Tag:ML346(100872-83-1) Related Product Information
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