• 제목/요약/키워드: guineensine

검색결과 4건 처리시간 0.017초

후추 열매 유래 화합물들의 배추좀나방 유충에 대한 살충 활성 (Larvicidal Activity of Constituents Identified in Piper nigrum L. Fruit Against the Diamondback moth, Plutella xylostella)

  • 박일권
    • 한국응용곤충학회지
    • /
    • 제51권2호
    • /
    • pp.149-152
    • /
    • 2012
  • 잎침지법을 이용하여 후추 열매 메탄올 추출물 및 분리된 화합물들의 배추좀나방(Plutellaxylostella) 유충에 대한 살충 활성을 검정하였다. 후추 열매 메탄올 추출물은 배추좀나방 유충에 대해 5.0과 2.5 mg/mL 농도에서 각각 100%와 97%의 살충 활성을 보였다. 후추 열매에서 유래된 화합물들의 배추좀나방에 대한 살충 활성을 조사한 결과, guineensine ($LC_{50}$=0.013 mg/mL)의 살충 활성이 가장 높았으며, 다음으로 retrofractamide A (0.020 mg/mL), pipercide (0.033 mg/mL) 그리고 pellitorine (0.046 mg/mL) 순이었다. Piperine의 반수치사농도는 0.5 mg/mL 이상이었다.

ACAT inhibitory effect of Guineensine isolated from Piper longum L.

  • Lee, Seung-Woong;Kim , Koan-Hoi;Kim, Young-Ho;Rho, Mun-Chual;Lee, Hyun-Sun;Kim, Young-Kook
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
    • /
    • pp.201.1-201.1
    • /
    • 2003
  • Study of Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors from medicinal plants, we found strong inhibitory activity of ACAT enzyme from rat liver microsome by the CHC1$_3$ extract of Piper longum. Bioactivity-guided fractionation led to the isolation of Guineensine (1), its structure was elucidated by spectroscopic (IR, UV, MS and NMR) means. It inhibited ACAT activity in a dose-dependent manner with IC$\sub$50/ values of 1.2 $\mu\textrm{g}$/ml on in vitro assay using rat liver microsome.

  • PDF

Pesticidal Constituents Derived from Piperaceae Fruits

  • Lee, Hoi-Seon
    • Journal of Applied Biological Chemistry
    • /
    • 제48권2호
    • /
    • pp.65-74
    • /
    • 2005
  • Fungicidal, insecticidal, and mosquito larvicidal activities of piperidine alkaloids, pipernonaline and piperoctadecalidine, and isobutylamide alkaloids, pellitorine, guineensine, pipercide, and retrofractaminde A, derived from Piperaceae fruits were studied. Pipernonaline and piperoctadecalidine showed potent fungicidal activities against Puccinia recondita with 91 and 80% control values at 500 ppm. Against Phytophthora infestans, pipernonaline showed strong fungicidal activity with 91 and 80% control values at 1,000 and 500 ppm. $LD_{50}$ values of pipernonaline and piperoctadecalidine against Plutella xylostella were 125 and 95.5 ppm, respectively, and that of piperoctadecalidine against Tetranychus urticae was 246 ppm. Against larvae of Aedes aegypti and Culex pipiens pallens, $LD_{50}$ values of pipernonaline were 0.35 and 0.21 ppm, respectively. Highest larvicidal activities of pipercide and retrofractamide A were found against A. aegypti, A. togoi, and C. pipiens pallens. $LD_{50}$ values of pipercide and retrofractamide A were 0.10 and 0.039 ppm against A. aegypti, 0.26 and 0.01 ppm against A. togoi, and 0.004 and 0.028 ppm against C. pipiens pallens, respectively. Based upon these results and earlier findings, bioactive components derived from Piperaceae fruits may be valuable for development of useful lead product of possibly safer fungicidal, insecticidal, and mosquito larvicidal agents.

Piperoctadecalindine, a New Piperidine Alkaloid from Piper retrofractum Fruits

  • Ahn Jong Woong;Lee Chong Ock;Kim Eun Joo;Zee Ok Pyo;Kim Hyung Jin
    • Bulletin of the Korean Chemical Society
    • /
    • 제13권4호
    • /
    • pp.388-391
    • /
    • 1992
  • A chemical investigation of the fruits of Piper retrofractum (Piperaceae) has led to the isolation and characterization of a novel piperidine alkaloid, piperoctadecalidine together with three known alkaloids piperine, pipernonaline and guineensine. The structure of the new compound was detemined to be (2E,4E,14Z)-N-(2,4,14-Octadecatrienoyl) piperidine by spectral and synthetic methods.