Cis-trans Relationship between the Two Amino-acids Obtained by Hydrogenation of p-Aminomethyl Benzoic Acid.
- 1 January 1965
- journal article
- research article
- Published by Danish Chemical Society in Acta Chemica Scandinavica
- Vol. 19 (7) , 1709-1714
- https://doi.org/10.3891/acta.chem.scand.19-1709
Abstract
In order to establish which of the two isomers of 1,4-aminomethyl-cyclohexane-carboxylic acid is the cis and which the trans form, the crystal structure of the hydrobromide of the amino-acid which is "inactive" as an anti-fibrinolytic agent has been determined. It was found that the inactive amino-acid is the cis isomer and consequently the "active" amino-acid the trans form. Details of the crystal structure of the hydro-bromide of the "inactive" amino-acid are presented.This publication has 1 reference indexed in Scilit:
- Biochemistry and Toxicology of Amikapron ®; The Antifibrinolytically Active Isomer of AMCHA. (A Comparative Study with ε‐Aminocaproic Acid)Acta Pharmacologica et Toxicologica, 1965