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Chemical Compound Review

L-alaninate     (2S)-2-aminopropanoate

Synonyms: CHEBI:32431, AC1NUU0D, L-alanine anion
This record was replaced with 5950.
 
 
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High impact information on L-alanine

  • Several adducts between Pt(II) complexes, [Pt(DA)(L-A)] (charges are omitted; DA=2,2'-bipyrimidine (bpm); A=L-arginine (L-Arg), L-alaninate (L-Ala), and AR (=indole-3-acetate (IA), gentisate (GA)) or GMP were isolated as crystals and structurally characterized by the X-ray diffraction method [1].
  • A series of low molecular weight organic gelator (LMOG) gel systems sensitive to alkaline/acidic stimuli was established by employing amino acid derivatives of cholesterol as "latent" gelators, which are cholesteryl glycinate (1), cholesteryl L-alaninate, cholesteryl D-alaninate, cholesteryl L-phenyl alaninate, and cholesteryl D-phenyl alaninate [2].

References

  1. Combined effects of electrostatic and pi-pi stacking interactions: selective binding of nucleotides and aromatic carboxylates by platinum(II)-aromatic ligand complexes. Yajima, T., Maccarrone, G., Takani, M., Contino, A., Arena, G., Takamido, R., Hanaki, M., Funahashi, Y., Odani, A., Yamauchi, O. Chemistry (Weinheim an der Bergstrasse, Germany) (2003) [Pubmed]
  2. Amino acid derivatives of cholesterol as "latent" organogelators with hydrogen chloride as a protonation reagent. Li, Y., Liu, K., Liu, J., Peng, J., Feng, X., Fang, Y. Langmuir : the ACS journal of surfaces and colloids. (2006) [Pubmed]
 
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