propargylaminen.

Brit.

/prəʊˈpɑːdʒᵻləmiːn/, U.S.

/proʊˈpɑrdʒələˌmin/

Origin: Formed within English, by compounding. Etymons: propargyl n., amine n.

Etymology: < propargyl n. + amine n.

Chemistry.

A pale yellow liquid amine, several substituted derivatives of which are monoamine oxidase inhibitors.Chemical name: 2-propynylamine; CH≡CCH₂NH₂.

ΚΠ

1908 N.E.D. at Propargyl Propargylamine.

1953 I. Heilbron & H. M. Bunbury Dict. Org. Compounds IV. 234/2 Propargylamine (3-Aminoallylene, 3-aminopropyne).

1975 Biochem. Pharmacol. 24 307 (title) Comparison of the inhibitory effects of propargylamine and pargyline on brain and liver monoamine oxidase activity.

1992 Jrnl. Medicinal Chem. 35 3705 A series of aliphatic propargylamine derivatives has been synthesized.

This entry has been updated (OED Third Edition, June 2007; most recently modified version published online March 2022).

单词	propargylamine
释义	propargylaminen. Brit. /prəʊˈpɑːdʒᵻləmiːn/, U.S. /proʊˈpɑrdʒələˌmin/ Origin: Formed within English, by compounding. Etymons: propargyl n., amine n. Etymology: < propargyl n. + amine n. Chemistry. A pale yellow liquid amine, several substituted derivatives of which are monoamine oxidase inhibitors.Chemical name: 2-propynylamine; CH≡CCH₂NH₂. ΚΠ 1908 N.E.D. at Propargyl Propargylamine. 1953 I. Heilbron & H. M. Bunbury Dict. Org. Compounds IV. 234/2 Propargylamine (3-Aminoallylene, 3-aminopropyne). 1975 Biochem. Pharmacol. 24 307 (title) Comparison of the inhibitory effects of propargylamine and pargyline on brain and liver monoamine oxidase activity. 1992 Jrnl. Medicinal Chem. 35 3705 A series of aliphatic propargylamine derivatives has been synthesized. This entry has been updated (OED Third Edition, June 2007; most recently modified version published online March 2022). < n.1908
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