QRX 431

QRX 431
  • CAS No.:211110-63-3

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
QRX 431 Basic information
Product Name:QRX 431
Synonyms:GC-1; QRX-431;2-[4-[[4-Hydroxy-3-(1-methylethyl)phenyl]methyl]-3,5-dimethylphenoxy]acetic acid;GC-1 (Sobetirome);Anti-solute carrier family 25 (mitochondrial carrier: glutamate), member 22;[4-(4-Hydroxy-3-isopropyl-benzyl)-3,5-dimethyl-phenoxy]-acetic acid;QRX 431;GC-1;SobetiroMe
CAS:211110-63-3
MF:C20H24O4
MW:328.4
EINECS:
Product Categories:
Mol File:211110-63-3.mol
QRX 431 Chemical Properties
Melting point 122 - 124°C
Boiling point 510.2±45.0 °C(Predicted)
density 1.152±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility DMSO: soluble10mg/mL, clear
pka3.22±0.10(Predicted)
form powder
color white to beige
InChIKeyQNAZTOHXCZPOSA-UHFFFAOYSA-N
Safety Information
MSDS Information
QRX 431 Usage And Synthesis
UsesGC 1 is a high affinity thyroid receptor α (TRα) and TRβ agonist.
Biological Activitysobetirome (3,5-dimethyl-4[(4'-hydroxy-3'-isopropylbenzyl)-phenoxy] acetic acid, also known as gc-1 and qrx-431, is a member of a class of compounds known as selective thyromimetics.it was firstly developed by thomas scanlan’s group at the university of california-san francisco (ucsf) in 1995 1.in cholesterol-fed rats, sobetirome was shown to lower plasma cholesterol in a dose-dependent manner by up to 75% of untreated controls. in hypercholesterolemic mice, sobetirome was failed to induce ldl receptor mrna expression. in different mouse models, sobetirome and t-0681 were shown to promote bile acid production and biliary sterol secretion. in cynomolgus monkeys, sobetirome was shown to reduce plasma cholesterol in a dose-dependent manner by up to 30%. both sobetirome and t-0681 were shown to increase hepatic expression of the hdl receptor (scavenger receptor-bi, sr-bi) in animals.in phase i
Biochem/physiol ActionsSobetirome is also termed as 2-(4-(4-(benzyloxy)-3-isopropylbenzyl)-3,5-dimethylphenoxy)acetic acid/ GC-1. It has an inner-ring and negatively charged carboxylate groups at physiological pH. Sobetirome is considered as a cholesterol lowering agent in humans.
references1. tancevski i, demetz e, eller p. sobetirome: a selective thyromimetic for the treatment of dyslipidemia. recent pat cardiovasc drug discov. 2011 jan;6(1):16-9.
QRX 431 Preparation Products And Raw materials

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