ER-000444793

ER-000444793 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:98.00% Package:1 mg;10 mg;100 mg;200 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:98% Package:2mg Remarks:V29295
Company Name: Aladdin Scientific
Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:98% Package:$197.9/5mg;$593.9/25mg;$1335.9/100mg;$3006.9/250mg;$10821.9/1g;Bulk package Remarks:98%
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Company Name: MedChemexpress LLC  
Tel: 021-58955995
Email: sales@medchemexpress.cn
Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:150RMB/1mg Package:>98%
ER-000444793 Basic information
Product Name:ER-000444793
Synonyms:ER-000444793;ER-000444793 (ER000444793);4-Quinolinecarboxamide, 1,2-dihydro-2-oxo-N-[2-(phenylmethyl)phenyl]-;N-(2-Benzylphenyl)-2-oxo-1,2-dihydroquinoline-4-carboxamide;Mitochondrial Metabolism,Inhibitor,ER-000444793,inhibit,ER000444793,ER 000444793
CAS:792957-74-5
MF:C23H18N2O2
MW:354.4
EINECS:
Product Categories:
Mol File:792957-74-5.mol
ER-000444793 Structure
ER-000444793 Chemical Properties
storage temp. Store at -20°C
solubility DMSO : ≥ 100 mg/mL (282.17 mM)
Safety Information
MSDS Information
ER-000444793 Usage And Synthesis
Biological ActivityER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening. It inhibits mPTP with IC50 of 2.8 μM.
in vitro

ER-000444793 is a small molecule, non-toxic mPTP inhibitor with a mechanism of action independent of CypD inhibition. It potently and dose-dependently inhibits Ca 2+ -induced mPT. It binds CypD, a CsA/CypD homogenous time-resolved fluorescence (HTRF) assay is used to study compound binding. Both CsA and SfA dose-dependently decrease HTRF signal, suggesting displacement of labelled CsA from rhCypD protein (CsA IC 50 =23 nM and SfA IC 50 = 5 nM). In contrast, ER-000444793 has no effect up to a concentration of 50 μM, indicating lack of displacement of labelled -CsA from rhCypD protein. Together, these data suggest the mechanism of it in delaying mPT is independent of CypD functional inhibition.

target

IC50: 2.8 μM (mPTP)

ER-000444793 Preparation Products And Raw materials
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