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ERLOTINIB MESYLATE

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ERLOTINIB MESYLATE manufacturers

  • Erlotinib mesylate
  • Erlotinib mesylate pictures
  • 2019-12-25
  • CAS:248594-19-6
  • Min. Order: 1KG
  • Purity: 95%-99%
  • Supply Ability: 1kg; 100kg; 1000kg
ERLOTINIB MESYLATE Basic information
Product Name:ERLOTINIB MESYLATE
Synonyms:ERLOTINIB MESYLATE;Erlotinib (OSI-744) mesylate;TARCEVA; CP-358774; OSI-774; NSC 718781; R 1415;Erlotinib mesylate (CP-358774;CP-358774;OSI-774;NSC 718781;R 1415;CP-358
CAS:248594-19-6
MF:C23H27N3O7S
MW:489.54
EINECS:
Product Categories:
Mol File:248594-19-6.mol
ERLOTINIB MESYLATE Structure
ERLOTINIB MESYLATE Chemical Properties
storage temp. Store at -20°C
solubility 25℃: DMSO
form Powder
Safety Information
MSDS Information
ERLOTINIB MESYLATE Usage And Synthesis
UsesErlotinib mesylate (CP-358774 mesylate) inhibits purified EGFR kinase with an IC50 of 2 nM. Erlotinib (mesylate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
in vivo

There is a 1.49-fold statistically significant difference between AUC0-inf after p.o. administration of Erlotinib (5 mg/kg) comparing Bcrp1/Mdr1a/1b-/- and WT mice (7,419±1,720 versus 4,957±1,735 ng*h/mL respectively, P=0.01)[3]. The administration of Erlotinib (10 mg/kg/day, or 20 mg/kg/day) to Bleomycin (BLM)-treated rats shows no exacerbation of lung injuries in indices such as macroscopic findings, lung weights, histopathological scores (lung lesion density and lung fibrosis score), and pulmonary hydroxyproline (HyP) level. The result suggests that Erlotinib does not have any exacerbating effects on lung injuries induced by BLM in rats[4].

IC 50EGFR: 2 nM (IC50)
References[1] Moyer JD, et al. Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase. Cancer Res. 1997 Nov 1;57(21):4838-48. PMID:9354447
[2] Ali S, et al. Apoptosis-inducing effect of erlotinib is potentiated by 3,3'-diindolylmethane in vitro and in vivo using an orthotopic model of pancreatic cancer. Mol Cancer Ther, 2008, 7(6), 1708-1719. DOI:10.1158/1535-7163.MCT-08-0354
[3] Marchetti S, et al. Effect of the ATP-binding cassette drug transporters ABCB1, ABCG2, and ABCC2 on erlotinib hydrochloride (Tarceva) disposition in in vitro and in vivo pharmacokinetic studies employing Bcrp1-/-/Mdr1a/1b-/- (triple-knockout) and wild-type mice.Mol Cancer Ther. 2008 Aug;7(8):2280-7. DOI:10.1158/1535-7163.MCT-07-2250
[4] Adachi K, et al. Effects of erlotinib on lung injury induced by intratracheal administration of bleomycin (BLM) in rats. J Toxicol Sci. 2010 Aug;35(4):503-14. DOI:10.2131/jts.35.503
ERLOTINIB MESYLATE Preparation Products And Raw materials
Tag:ERLOTINIB MESYLATE(248594-19-6) Related Product Information
Erlotinib DesMethyl Erlotinib Carboxylate Acid 4-Chloro-6,7-bis(2-methoxyethoxy)quinazoline Erlotinib D6 HCl Erlotinib iMpurity 2 Erlotinib Impurity Q Erlotinib 6-O-DesMethoxyethyl-6-O-chloroethyl Erlotinib Hydrochloride Erlotinib iMpurity Desmethyl Erlotinib Acetate 4-QuinazolinaMine, 7-(2-chloroethoxy)-N-(3-ethynylphenyl)-6-(2-Methoxyethoxy)- Erlotinib Impurity G Erlotinib CP 373413 4-Chloro-6,7-bis-(2-chloroethoxy)quinazoline Erlotinib Impurity 22 4-Quinazolinamine,N-(3-ethylphenyl)-6,7-bis(2-methoxyethoxy)- 4-Chloro-6-(2-chloro-ethoxy)-7-(2-methoxy-ethoxy)-quinazoline