Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

D-alaninate (2R)-2-aminopropanoate

Synonyms: CHEBI:32435, AC1NUU0A, D-alanine anion

This record was replaced with 71080.

Li, Y. et al., Hakimelahi, G.H. et al.

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Disease relevance of D-Alanin

Phosphonoamidates 55 and 56 bearing a methyl D-alaninate moiety exhibited less cellular toxicity than 53 and 54 bearing a methyl L-alaninate moiety [1].

High impact information on D-Alanin

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

Design, synthesis, and structure-activity relationship of novel dinucleotide analogs as agents against herpes and human immunodeficiency viruses. Hakimelahi, G.H., Moosavi-Movahedi, A.A., Sadeghi, M.M., Tsay, S.C., Hwu, J.R. J. Med. Chem. (1995) [Pubmed]
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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