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

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Chemical Compound Review:

AEPD 2-amino-2-ethyl-propane-1,3- diol

Synonyms: CHEMBL119482, NSC-8803, ACMC-1CA9Z, AG-K-66559, ANW-16898, ...

Iwama, M. et al., Beck, W.F. et al.

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High impact information on Aminoethyl propanediol

In contrast, the hyperfine line pattern and temperature dependence of the S2-state multiline EPR spectrum in the presence of tris(hydroxymethyl)aminomethane, 2-amino-2-ethyl-1,3-propanediol, or CH3NH2 at pH 7.5 were the same as those observed in untreated PSII membranes [1].
Hydrolysis of maltose by the glucoamylases was inhibited competitively by aminoalcohols at pH 5.0, and tris(hydroxymethyl)aminomethane, 2-amino-2-ethyl-1,3-propanediol and 2-aminocyclohexanol were relatively good inhibitors of the glucoamylases among the aminoalcohol derivatives tested [2].

References

Binding of amines to the O2-evolving center of photosystem II. Beck, W.F., Brudvig, G.W. Biochemistry (1986) [Pubmed]
Inhibition of glucoamylases from a Rhizopus sp. and Aspergillus saitoi by aminoalcohol derivatives. Iwama, M., Takahashi, T., Inokuchi, N., Koyama, T., Irie, M. J. Biochem. (1985) [Pubmed]

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