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Related to Indole ring: tryptophan, pyrrole ring


Also known as 2,3-benzopyrrole.
C6H4-(CHNH)CH A decomposition product of tryptophan formed in the intestine during putrefaction and by certain cultures of bacteria.
(organic chemistry)
Carcinogenic, white to yellowish scales with unpleasant aroma; soluble in alcohol, ether, hot water, and fixed oils; melt at 52°C; used as a chemical reagent and in perfumery and medicine.



(2, 3-benzopyrrole), colorless crystals with an unpleasant odor. Melting point, 52°C; boiling point, 254°C. It is soluble in hot water and organic solvents. Indole is present in coal tar, from which it is extracted as salts of alkali metals, as well as in certain essential oils (for example, oil of jasmine). Along with skatole (3-methyl-indole), it is found in the intestines of human beings and mammals.

Many indole derivatives, for example, 3-indoleacetic acid (heteroauxin A, a growth substance), serotonin, and reserpine, are biologically active. Indole is a raw material for synthesizing heteroauxin and tryptophane, and is used in the perfumery industry to improve and strengthen the scents of flower essences.

References in periodicals archive ?
Considering the findings to date, it is reasonable to postulate the hemodialysis-induced cascade interaction model in fatty acid-uremic toxin-drug systems, in which a transient increase in the concentrations of long-chain fatty acids could produce a cascade displacement of both site I- and II-bound drugs by their competitive inhibitors, namely, CMPF and uremic toxins that contain an indole ring (see Fig.
Six aromatic protons provided a clue concerning the constitution of two indole rings with the substitutions.