Ethyl L-leucinate HCl

  • CAT Number: I014374
  • CAS Number: 2743-40-0
  • Molecular Formula: C8H18ClNO2
  • Molecular Weight: 195.68
  • Purity: ≥95%
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Ethyl L-leucine hydrochloride(Cat No.:I014374) is a compound that has been employed as a hypertrophic agent in the study of myotubes, aiming to assess its impact on muscle fiber growth. Additionally, it has found utility as a constituent of PMG (Pantothenate Medium supplemented with Glycerol) media for yeast cultivation. By incorporating Ethyl L-leucine HCl, researchers can explore its potential effects on muscle development and utilize it as a component to support yeast growth in specific culture conditions.

Catalog Number I014374
CAS Number 2743-40-0
Synonyms

Ethyl L-leucinate hydrochloride; AI3-28816; Ethyl L-leucinate HCl;;ethyl L-leucinate hydrochloride

Molecular Formula

C8H18ClNO2

Purity 95%
Solubility Soluble in DMSO
Storage Room Temperature
IUPAC Name ethyl (2S)-2-amino-4-methylpentanoate;hydrochloride
InChI InChI=1S/C8H17NO2.ClH/c1-4-11-8(10)7(9)5-6(2)3;/h6-7H,4-5,9H2,1-3H3;1H/t7-;/m0./s1
InChIKey NOUDPBCEONUCOV-FJXQXJEOSA-N
SMILES CCOC(=O)C(CC(C)C)N.Cl
Reference

</br>1: Vujić JM, Cvijović M, Kaluderović GN, Milovanović M, Zmejkovski BB, Volarević V, Arsenijević N, Sabo TJ, Trifunović SR. Palladium(II) complexes with R(2)edda derived ligands. Part IV. O,O’-dialkyl esters of (S,S)-ethylenediamine-N,N’-di-2-(4-methyl)-pentanoic acid dihydrochloride and their palladium(II) complexes: synthesis, characterization and in vitro antitumoral activity against chronic lymphocytic leukemia (CLL) cells. Eur J Med Chem. 2010 Sep;45(9):3601-6. doi: 10.1016/j.ejmech.2010.05.005. Epub 2010 May 12. PubMed PMID: 20570025.</br>2: Chen G, Li J, Sun Z, Zhang S, Li G, Song C, Suo Y, You J. Rapid and sensitive ultrasonic-assisted derivatisation microextraction (UDME) technique for bitter taste-free amino acids (FAA) study by HPLC-FLD. Food Chem. 2014 Jan 15;143:97-105. doi: 10.1016/j.foodchem.2013.07.099. Epub 2013 Jul 27. PubMed PMID: 24054218.</br>3: Smith CB, Medzihradsky F, Woods JH. Dihydromorphine-peptide hybrids have mu receptor antagonistic and delta receptor agonistic activity on the mouse vas deferens and bind with high affinity to opioid receptors in rat brain. NIDA Res Monogr. 1986;75:189-92. PubMed PMID: 2828970.</br>4: Chipley JR, Mabee MS, Alegate KL, Dreyfuss MS. Further characterization of tissue distribution and metabolism of (14C)aflatoxin B1 in chickens. Appl Microbiol. 1974 Dec;28(6):1027-9. PubMed PMID: 4615634; PubMed Central PMCID: PMC186876. </br> </br>

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