Eight new amide constituents together with seven known amides were isolated from pepper and their structures were determined by spectroscopic means. They are piperamide-C5:1(2E) (2), -C7:1(6E) (3), -C7:2(2E, 6E) (4), -C9:1(8E) (5), -C9:2(2E, 8E) (6), -C9:3(2E, 4E, 8E) (7), 1-[(2E, 4E)-2, 4-decadienoyl]pyrrolidine (8), and 1-[(2E, 4E)-2, 4-dodecadienoyl]pyrrolidine (9). Among all of the amides isolated, seven (3, 4, 5, 6, 8, 9, and 15) showed larvicidal activity against second-stage larva of Toxocara canis and the others were inactive. The assay results suggested that the strongest activity was exhibited by the tertiary amides (piperidin- and pyrrolidin-amides) possessing a nine-carbon chain between the aromatic group and the amine moiety [for example, piperamide-C9: 1(8E), MLC: 0.05 mM after 24h of incubation]. The aliphatic amides 8 and 9 were also larvicidal. Mass spectra of piperamides are also discussed. © 1988, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Kiuchi, F., Nakamura, N., Tsuda, Y., Kondo, K., & Yoshimura, H. (1988). Studies on Crude Drugs Effective on Visceral Larva Migrans. IV.1) Isolation and Identification of Larvicidal Principles in Pepper. Chemical and Pharmaceutical Bulletin, 36(7), 2452–2465. https://doi.org/10.1248/cpb.36.2452
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