메뉴 건너뛰기




Volumn 63, Issue 9, 2007, Pages 928-934

Lead optimization and insecticidal activity of analogues of daphneolone isolated from Stellera chamaejasme L.

Author keywords

Aphicide; Insecticidal activity; Stellera chamaejasme; Synthesis

Indexed keywords

1,5 DIPHENYL 1 PENTANONE; 1,5 DIPHENYL 2 PENTEN 1 ONE; 1,5-DIPHENYL-1-PENTANONE; 1,5-DIPHENYL-2-PENTEN-1-ONE; ALKANONE; INSECTICIDE; LEAD; UNCLASSIFIED DRUG;

EID: 34548321234     PISSN: 1526498X     EISSN: 15264998     Source Type: Journal    
DOI: 10.1002/ps.1399     Document Type: Article
Times cited : (15)

References (23)
  • 1
    • 7044247345 scopus 로고    scopus 로고
    • Biochemical evidence that an S431F mutation in acetylcholinesterase-1 of Aphis gossypii mediates resistance to pirimicarb and omethoate
    • Benting J and Nauen R, Biochemical evidence that an S431F mutation in acetylcholinesterase-1 of Aphis gossypii mediates resistance to pirimicarb and omethoate. Pest Manag Sci 60:1051-1055 (2004).
    • (2004) Pest Manag Sci , vol.60 , pp. 1051-1055
    • Benting, J.1    Nauen, R.2
  • 2
    • 0242407299 scopus 로고    scopus 로고
    • High resistance of field populations of the cotton aphid Aphis gossypii Glover (Homoptera: Aphididae) to pyrethroid insecticides in Pakistan
    • Ahmad M, Arif MI and Denholm I, High resistance of field populations of the cotton aphid Aphis gossypii Glover (Homoptera: Aphididae) to pyrethroid insecticides in Pakistan. J Econ Entomol 96:875-878 (2003).
    • (2003) J Econ Entomol , vol.96 , pp. 875-878
    • Ahmad, M.1    Arif, M.I.2    Denholm, I.3
  • 3
    • 0032454265 scopus 로고    scopus 로고
    • Association between biochemical markers and insecticide resistance in the cotton aphid, Aphis gossypii Glover
    • Moores GD, Denholm I and Devonshire AL, Association between biochemical markers and insecticide resistance in the cotton aphid, Aphis gossypii Glover. Pestic Biochem Phys 62:164-171 (1998).
    • (1998) Pestic Biochem Phys , vol.62 , pp. 164-171
    • Moores, G.D.1    Denholm, I.2    Devonshire, A.L.3
  • 5
    • 34547835461 scopus 로고    scopus 로고
    • Natural products as leads in structural modification studies yielding new agrochemicals
    • ed. by Hedin PL, Hollingworth RM and Masle EP. American Chemical Society Publishers, Washington, DC, pp
    • Miyakado M, Watanabe K and Miyamoto J, Natural products as leads in structural modification studies yielding new agrochemicals, in Phytochemicals for Pest Control, ed. by Hedin PL, Hollingworth RM and Masle EP. American Chemical Society Publishers, Washington, DC, pp. 168-182 (1997).
    • (1997) Phytochemicals for Pest Control , pp. 168-182
    • Miyakado, M.1    Watanabe, K.2    Miyamoto, J.3
  • 6
    • 3042989151 scopus 로고    scopus 로고
    • Pesticide leads from nature
    • Crouse GD, Pesticide leads from nature. Chemtech 28:36-45 (1998).
    • (1998) Chemtech , vol.28 , pp. 36-45
    • Crouse, G.D.1
  • 7
    • 34548296768 scopus 로고    scopus 로고
    • Agrochemicals dicovered and developed from natural leads - fungicides
    • Liu CL and Li ZM, Agrochemicals dicovered and developed from natural leads - fungicides. Pesticides 42:1-4 (2003).
    • (2003) Pesticides , vol.42 , pp. 1-4
    • Liu, C.L.1    Li, Z.M.2
  • 8
    • 0035116711 scopus 로고    scopus 로고
    • Activity of the botanical aphicides 1, 5-diphenyl-1-pentanone and 1,5-diphenyl-2-penten-1-one on two species of Aphididae
    • Gao P, Hou TP, Gao R, Cui Q and Liu SG, Activity of the botanical aphicides 1, 5-diphenyl-1-pentanone and 1,5-diphenyl-2-penten-1-one on two species of Aphididae. Pest Manag Sci 57:307-310 (2001).
    • (2001) Pest Manag Sci , vol.57 , pp. 307-310
    • Gao, P.1    Hou, T.P.2    Gao, R.3    Cui, Q.4    Liu, S.G.5
  • 9
    • 34548356133 scopus 로고    scopus 로고
    • Study on extraction isolation of killing aphid components from Stellera chamaejasme L
    • Nature Ed
    • Hou TP, Cui Q, Xiang RL, Hou RT and Liu SG, Study on extraction isolation of killing aphid components from Stellera chamaejasme L. Journal of Sichuan University (Nature Ed) 38:743-747 (2001).
    • (2001) Journal of Sichuan University , vol.38 , pp. 743-747
    • Hou, T.P.1    Cui, Q.2    Xiang, R.L.3    Hou, R.T.4    Liu, S.G.5
  • 12
    • 84989683676 scopus 로고
    • Pesticidal compounds from higher plants
    • Benner JP, Pesticidal compounds from higher plants. Pestic Sci 39:95-102 (1993).
    • (1993) Pestic Sci , vol.39 , pp. 95-102
    • Benner, J.P.1
  • 14
    • 0041589258 scopus 로고    scopus 로고
    • Antileishmanial activities of dihydrochalcones from Piper elongatum and synthetic related compounds. Structural requirements for activity
    • Hermoso A, Jimenez IA, Mamani ZA, Bazzocchi IL, Pinero JE, Ravelo AG, et al, Antileishmanial activities of dihydrochalcones from Piper elongatum and synthetic related compounds. Structural requirements for activity. Bioorgan Med Chem 11:3975-3980 (2003).
    • (2003) Bioorgan Med Chem , vol.11 , pp. 3975-3980
    • Hermoso, A.1    Jimenez, I.A.2    Mamani, Z.A.3    Bazzocchi, I.L.4    Pinero, J.E.5    Ravelo, A.G.6
  • 15
    • 34548336126 scopus 로고    scopus 로고
    • Acaricides or mite repellents containing diphenyl compounds. Japan
    • Patent JP 90-312890 19901120 1992
    • Kenjiro I, Masayoshi Y, Wataru K and Yoshiaki S, Acaricides or mite repellents containing diphenyl compounds. Japan Patent JP 90-312890 19901120 (1992).
    • Kenjiro, I.1    Masayoshi, Y.2    Wataru, K.3    Yoshiaki, S.4
  • 16
    • 7744243992 scopus 로고    scopus 로고
    • Bioisosterism: A rational appoach in drug design
    • Patani GA and LaVoie EJ, Bioisosterism: a rational appoach in drug design. Chem Rev 96:3147-3106 (1996).
    • (1996) Chem Rev , vol.96 , pp. 3147-3106
    • Patani, G.A.1    LaVoie, E.J.2
  • 17
    • 0035813439 scopus 로고    scopus 로고
    • Solvent-free Claisen and Cannizzaro reactions
    • Yoshizawa K, Toyota K and Toda F, Solvent-free Claisen and Cannizzaro reactions. Tetrahedron Lett 42:7983-7985 (2001).
    • (2001) Tetrahedron Lett , vol.42 , pp. 7983-7985
    • Yoshizawa, K.1    Toyota, K.2    Toda, F.3
  • 18
    • 4444342444 scopus 로고    scopus 로고
    • Acyl derivatives of 2-aminobenzimidazole and their fungicide activity
    • Pilyugin VS, Sapozhnikov YE and Sapozhnikova NA, Acyl derivatives of 2-aminobenzimidazole and their fungicide activity. Russ J Gen Chem 74:804-810 (2004).
    • (2004) Russ J Gen Chem , vol.74 , pp. 804-810
    • Pilyugin, V.S.1    Sapozhnikov, Y.E.2    Sapozhnikova, N.A.3
  • 20
    • 0000722909 scopus 로고
    • A method for computing the effectiveness of an insecticide
    • Abbott WS, A method for computing the effectiveness of an insecticide. J Econ Entomol 18:265-267 (1925).
    • (1925) J Econ Entomol , vol.18 , pp. 265-267
    • Abbott, W.S.1
  • 21
    • 0037185616 scopus 로고    scopus 로고
    • A mild and efficient method for esterification and transesterification catalyzed by iodine
    • Ramalinga K, Vijayalakshmi P and Kaimal TNB, A mild and efficient method for esterification and transesterification catalyzed by iodine. Tetrahedron Lett 43:879-882 (2002).
    • (2002) Tetrahedron Lett , vol.43 , pp. 879-882
    • Ramalinga, K.1    Vijayalakshmi, P.2    Kaimal, T.N.B.3
  • 22
    • 0034234818 scopus 로고    scopus 로고
    • Diphenylammonium triflate (DPAT): Efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols
    • Wakasugi K, Misaki T, Yamada K and Tanabe Y, Diphenylammonium triflate (DPAT): efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols. Tetrahedron Lett 41:5249-5252 (2000).
    • (2000) Tetrahedron Lett , vol.41 , pp. 5249-5252
    • Wakasugi, K.1    Misaki, T.2    Yamada, K.3    Tanabe, Y.4
  • 23
    • 0035825050 scopus 로고    scopus 로고
    • An unprecedented and highly chemoselective esterification method
    • Lee ASY, Yang HC and Su FY, An unprecedented and highly chemoselective esterification method. Tetrahedron Lett 42:301-303 (2001).
    • (2001) Tetrahedron Lett , vol.42 , pp. 301-303
    • Lee, A.S.Y.1    Yang, H.C.2    Su, F.Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.