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Updated: Jun 1, 2026

Preparation and In Vivo Use of an Activity-based Probe for N-acylethanolamine Acid Amidase
Published on: November 23, 2016
(2S,4R)-4-Ammonio-5-oxopyrrolidine-2-carboxylate
Abstract:
In the crystal structure of the title compound, C(5)H(8)N(2)O(3), the mol-ecules exist in the zwitterionic form. The pyrrolidine ring adopts an envelope conformation with the unsubstituted endocyclic C atom situated at the flap. The other four endocyclic atoms are coplanar with the exocyclic carbonyl O atom, with an r.m.s. deviation from the mean plane of 0.06 Å. The carboxyl-ate substituent is located axially, while the ammonium group occupies an equatorial position. In the crystal structure, the mol-ecules are linked through N-H⋯O hydrogen bonds, forming a three-dimensional network.
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The IUPAC and common names of amides are derived from the parent carboxylic acid, by replacing the suffix “oic acid” and “ic acid,” respectively, with “amide.” In the following example, the IUPAC name ethanamide is derived from ethanoic acid, and the common name, acetamide, is obtained from acetic acid.
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