IMiD

Imid is a chemical nomenclature stem rather than a single compound. It appears in a variety of terms to denote nitrogen-containing rings or related functional groups, and its precise meaning depends on the context in which it is used. The stem is common in organic chemistry, biochemistry, and materials science.

In heterocyclic chemistry, imidazole is a five-membered aromatic ring containing two nitrogen atoms at nonadjacent positions. Imidazole is biologically significant as the side chain of the amino acid histidine and as a structural motif in many drugs and enzymes. The imidazole ring also appears in imidazole buffers used in biochemistry due to their favorable pH properties, and in various pharmaceutical agents where the ring contributes to binding or activity.

Other imid-related terms describe different functional groups or structures. An imide is a functional group with two acyl substituents attached to a single nitrogen atom (R-CO-N-CO-R′), and imide linkages are central to polyimides, a class of high-temperature polymers used in electronics and engineering. Imidazoline refers to a saturated or partially saturated ring system derived from imidazole, found in certain medicinal compounds and receptor ligands. Imidates are derivatives of imidic acids and are employed as intermediates in organic synthesis.

Overall, the term imid functions as a versatile root across chemistry to indicate nitrogen-containing heterocycles or imide-related functionalities. Its exact interpretation is governed by the surrounding chemical context, including the specific compound or class being described. See also: Imidazole, Imide, Imidazoline, Polyimide.