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imine

Compounds having the structure RN=CR2 (R = H, hydrocarbyl). Thus analogues of aldehydes or ketones, having NR doubly bonded to carbon; aldimines have the structure RCH=NR, ketimines have the structure R'2C=NR (where R' is not H). Imines include azomethines and Schiff bases. Imine is used as a suffix in systematic nomenclature to denote the C=NH group excluding the carbon atom.

ChEBI ID: 24783

Members (2)

MemberDefinitionRole
delta(1)-pyrroline1-pyrroline
iminoglycineA dehydroamino acid derived from glycine.dehydroglycine zwitterion; dehydroglycine

Research

Studies (18)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-199012 (66.67)18.7374
1990's1 (5.56)18.2507
2000's1 (5.56)29.6817
2010's3 (16.67)24.3611
2020's1 (5.56)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.26%)6.00%
Case Studies1 (5.26%)4.05%
Observational0 (0.00%)0.25%
Other17 (89.47%)84.16%