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ER-000444793

ER-000444793 Suppliers list
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:99.55% Package:1mg;70USD|5mg;163USD|10mg;247USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: InvivoChem
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Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:98% Package:2mg Remarks:V29295
Company Name: Aladdin Scientific
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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.  
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CAS:792957-74-5
Company Name: MedChemexpress LLC  
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Products Intro: Product Name:ER-000444793
CAS:792957-74-5
Purity:150RMB/1mg Package:>98%

ER-000444793 manufacturers

  • ER-000444793
  • ER-000444793 pictures
  • $70.00 / 1mg
  • 2025-05-01
  • CAS:792957-74-5
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  • Purity: 99.55%
  • Supply Ability: 10g
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;ER-000444793, 10 mM in DMSO
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)
form Solid
color Off-white to light yellow
Safety Information
MSDS Information
ER-000444793 Usage And Synthesis
UsesER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening. ER-000444793 inhibits mPTP with an IC50 of 2.8 μM.
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)

References[1] Briston T, et al. Identification of ER-000444793, a Cyclophilin D-independent inhibitor of mitochondrial permeability transition, using a high-throughput screen in cryopreserved mitochondria. Sci Rep. 2016 Nov 25;6:37798. DOI:10.1038/srep37798
ER-000444793 Preparation Products And Raw materials
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