7ACC-2

7ACC-2 Suppliers list
Company Name: Hubei XinRunde Chemical Co., Ltd.
Tel: +8615102730682
Email: bruce@xrdchem.cn
Products Intro: Product Name:7ACC-2
CAS:1472624-85-3
Purity:99 Package:1KG;10USD
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:1472624-85-3
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: Hebei Binshare New Material Co. Ltd
Tel: +8618633865755
Email: china01@hbbinshare.com
Products Intro: Product Name:7ACC2
CAS:1472624-85-3
Purity:99.99% Package:1g;1USD
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:7ACC2
CAS:1472624-85-3
Purity:100.00% Package:1 mg;1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Career Henan Chemica Co
Tel: +86-0371-86658258 15093356674;
Email: laboratory@coreychem.com
Products Intro: Product Name:7ACC2
CAS:1472624-85-3
Purity:98%;604crystal Package:1KG;0.01USD

7ACC-2 manufacturers

  • 7ACC-2
  • 7ACC-2 pictures
  • $15.00 / 1KG
  • 2021-07-02
  • CAS:1472624-85-3
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
  • 7ACC-2
  • 7ACC-2 pictures
  • $10.00 / 1KG
  • 2019-01-15
  • CAS:1472624-85-3
  • Min. Order: 100G
  • Purity: 99
  • Supply Ability: 10MT
7ACC-2 Basic information
Product Name:7ACC-2
Synonyms:7ACC 2;7ACC2;7ACC-2;7-[Benzyl(methyl)amino]-2-oxo-2H-chromene-3-carboxylic acid;7ACC 2; 7ACC-2; 7ACC 2; 7ACC-2;7-[benzyl(methyl)amino]-2-oxochromene-3-carboxylic acid;2H-1-Benzopyran-3-carboxylic acid, 7-[methyl(phenylmethyl)amino]-2-oxo-;7ACC2,MPC,MCT1,7ACC-2,Monocarboxylate Transporter,Inhibitor,lactate,pyruvate,Mitochondrial Metabolism,radiosensitizes,antitumor,mitochondrial,inhibit
CAS:1472624-85-3
MF:C18H15NO4
MW:309.32
EINECS:604-604-1
Product Categories:Inhibitors
Mol File:1472624-85-3.mol
7ACC-2 Structure
7ACC-2 Chemical Properties
Boiling point 548.9±50.0 °C(Predicted)
density 1.368±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility insoluble in EtOH; insoluble in H2O; ≥47.5 mg/mL in DMSO
form Powder
pka-98.37±0.20(Predicted)
Safety Information
HS Code 2932990090
MSDS Information
7ACC-2 Usage And Synthesis
Biological Activity7acc2, a carboxycoumarin derivative, is a potent inhibitor of monocarboxylate transporter 1 (mct1), with an ic50 value of ~ 10 nm for lactate uptake in the human cervix carcinoma cell line siha. the family of mct is composed of 14 members, among which only four isoforms (i.e. mct1-4) have been documented to act as proton-linked transporters carrying short chain monocarboxylates such as lactate and pyruvate across cell membranes. in cancer cells, mct1 and mct4 are the most widely expressed, and mct1 shows a better affinity for l-lactate than mct4, enabling lactate entry into oxidative tumor cells. thus, mct1 blockade could serve as a potential therapeutic strategy to limit cancer progression. in addition, 7acc2 is also a potent inhibitor of mitochondrial pyruvate transport, which interferes with pyruvate import into mitochondria and ultimately prevents extracellular lactate uptake as efficiently as a mct1 inhibitor.1. draoui n, schicke o, fernandes a, et al. synthesis and pharmacological evaluation of carboxycoumarins as a new antitumor treatment targeting lactate transport in cancer cells. bioorganic & medicinal chemistry, 2013, 21(22): 7107-7117.2. corbet c, bastien e, draoui n, et al. interruption of lactate uptake by inhibiting mitochondrial pyruvate transport unravels direct antitumor and radiosensitizing effects. nature communications, 2018, 9(1): 1208.
in vitro

7ACC-2 (compound 19; 72 hours) inhibits SiHa cells proliferation in lactate-containing medium with an EC50 of 0.22 μM. In SiHa cells, lactate uptake primarily depends on the high affinity MCT1 transporter.
It (compound 19) shows an excellent chemical stability in simulated gastric (SGF) and intestinal (SIF) fluids, a good apparent permeability coefficient (Papp) through Caco-2 monolayer and a high metabolic stability on mouse (MLM) and human liver microsomes ( HLM) as well as on human hepatocytes.
It is a potent inhibitor of mitochondrial pyruvate transport which consecutively blocks extracellular lactate uptake by promoting intracellular pyruvate accumulation.

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in vivo

7ACC-2 (3 mg/kg; intraperitoneal administration; daily; for 5 days or 10days) treatment significantly inhibits tumor growth in mice. It radiosensitizes tumor cells by reducing hypoxia in vivo.
The intraperitoneal administration of it (compound 19; 3 mg/kg) to mice leads to a C max of 1246 ng/ml (4 μM) in a very short time (T max =10 min) associated with a plasma half-life of 4.5 h.

Animal Model: 7-week-old female NMRI nude mice with radiotherapy administered
Dosage: 3 mg/kg
Administration: Intraperitoneal administration; daily; for 5 days or 10days
Result: A significant increase in tumor growth delay was observed.
target
TargetValue
MCT1
()
7ACC-2 Preparation Products And Raw materials
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