Ethylhydrocupreine

For research use only. Not for therapeutic Use.

  • CAT Number: I015201
  • CAS Number: 522-60-1
  • Molecular Formula: C₂₁H₂₈N₂O₂
  • Molecular Weight: 340.46
  • Purity: ≥95%
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Ethylhydrocupreine(Cat No.:I015201)is a chemical compound used primarily in biochemical and pharmaceutical research. This organic molecule, a derivative of hydrocupreine, exhibits a range of properties, including the ability to inhibit certain enzymes and participate in redox reactions. Ethylhydrocupreine is utilized in studies related to the modulation of oxidative stress, cell signaling, and enzymatic activity. It serves as a valuable tool in exploring the biological effects of copper complexes and their potential therapeutic applications, particularly in neurodegenerative diseases and conditions involving oxidative damage.


Catalog Number I015201
CAS Number 522-60-1
Molecular Formula C₂₁H₂₈N₂O₂
Purity ≥95%
Target Bacterial
IUPAC Name (R)-(6-ethoxyquinolin-4-yl)-[(2S,4S,5R)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]methanol
InChI InChI=1S/C21H28N2O2/c1-3-14-13-23-10-8-15(14)11-20(23)21(24)17-7-9-22-19-6-5-16(25-4-2)12-18(17)19/h5-7,9,12,14-15,20-21,24H,3-4,8,10-11,13H2,1-2H3/t14-,15-,20-,21+/m0/s1
InChIKey SUWZHLCNFQWNPE-LATRNWQMSA-N
SMILES CC[C@H]1CN2CC[C@H]1C[C@H]2[C@@H](C3=C4C=C(C=CC4=NC=C3)OCC)O
Reference

[1]. J A Kolmer, et al. CHEMOTHERAPEUTIC STUDIES WITH ETHYLHYDROCUPREINE HYDROCHLORIDE IN EXPERIMENTAL PNEUMOCOCCUS PLEURITIS. J Exp Med. 1921 May 31;33(6):693-711.<br>[2]. Paulo R Cortes, et al. Subinhibitory Concentrations of Penicillin Increase the Mutation Rate to Optochin Resistance in Streptococcus Pneumoniae. J Antimicrob Chemother. 2008 Nov;62(5):973-7.<br>[3]. Nassira Mahmoudi, et al. Identification of New Antimalarial Drugs by Linear Discriminant Analysis and Topological Virtual Screening. J Antimicrob Chemother. 2006 Mar;57(3):489-97.<br>[4]. Antonella Di Pizio, et al. Molecular Features Underlying Selectivity in Chicken Bitter Taste Receptors. Front Mol Biosci. 2018 Jan 31;5:6.

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