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Compound - d-glutamic acid


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(R)-2-Aminopentanedioic acid
(R)-2-Aminopentanedioic acid

Formula: C5H9NO4 
CAS#: 138-16-9 
MW: 147.13 

[MS]  [ NMR ]  [Behavioural function]  [Chemdraw

Dots surface:

Reference(s) for synthesis of (R)-2-Aminopentanedioic acid

Frank, H., Woiwode, W., Nicholson, G., and Bayer, E. 1981. Liebigs Ann. Chem. 3:354-365.
Hafenbradi, D., Keller, M., Waechtershaeuser, G., and Stetter, K.O. 1995. Primordial amino acids by reductive amination of -oxo acids in conjunction with the oxidative formation of pyrite. Tetrahedron Lett. 36:5179-5182.
Huber, C., and Waechtershaeuser, G. 2003. Primordial reductive amination revisited. Tetrahedron Lett. 44:1695-1697.
Oikawa, T., Watanabe, M., Makiura, H., Kusakabe, H., Yamade, K., and Soda, K. 1999. Production of D-glutamate from L-glutamate with glutamate racemase and L-glutamate oxidase. Biosci. Biotechnol. Biochem. 63:2168-2173.
Qi, D., Kuang, H., and Distefano, M.D. 1998. Effects of metal ions on the rates and enantioselectivities of reactions catalyzed by a series of semisynthetic transaminases created by site directed mutagenesis. Bioorg. Med. Chem. Lett. 8:875-880.

Citation: El-Sayed AM 2018. The Pherobase: Database of Pheromones and Semiochemicals. <>.
2003-2018 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
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