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Pest Management Science | 2001

Recent advances in the chemistry of spinosyns

Gary D. Crouse; Thomas C. Sparks; Joseph R. Schoonover; James M. Gifford; James Edwin Dripps; Tim Bruce; Larry L. Larson; Joseph Garlich; Christopher J. Hatton; Robert L. Hill; Thomas V. Worden; Jacek G. Martynow

The spinosyns are a new class of fermentation-derived insect control agents that are effective against a variety of chewing insect pests. The successful introduction of spinosad into the agricultural marketplace represents an important milestone in the use of natural products for commercial pest control. The development of a natural product presents additional limitations relative to a synthetic material. While the latter affords some degree of control in building appropriate physical attributes such as photostability, a natural product, designed to function in a different environment, is often less suited for traditional spray applications. Despite its intrinsic photolability, spinosad is stable enough to perform under field conditions. In an effort to generate analogs with improved physical characteristics, we have developed a variety of conditions for selectively modifying different portions of the molecule, and we have discovered analogs with greater activity against a broader spectrum of pests. The inability to translate improved greenhouse activity to actual field conditions resulted in a detailed study of the effects of formulations and crystallinity on biological activity. Through this effort, measurably improved field performance of synthetic spinosyn analogs relative to the natural product have now been observed.


Current Topics in Medicinal Chemistry | 2002

Evaluation and Development of Spinosyns to Control Ectoparasites on Cattle and Sheep

Herbert A. Kirst; Lawrence Creemer; Sharon A. Naylor; Paul T. Pugh; Daniel E. Snyder; Joseph Raymond Winkle; L. Barry Lowe; J. T. Rothwell; Thomas C. Sparks; Thomas V. Worden

The spinosyns are a novel family of fermentation-derived natural products that exhibit potent insecticidal activities. Spinosad, a naturally-occurring mixture of spinosyn A and spinosyn D, has successfully established its utility for crop protective applications in the agrochemical field. Potential applications of this unique chemical family of macrolides also have been investigated in the field of animal health. Applications for the control of blowfly strike and lice on sheep have now been commercially developed and registered in Australia and potential applications for the control of ectoparasites on cattle are being studied.


Journal of Economic Entomology | 1998

Biological Activity of the Spinosyns, New Fermentation Derived Insect Control Agents, on Tobacco Budworm (Lepidoptera: Noctuidae) Larvae

Thomas C. Sparks; Gary D. Thompson; Herbert A. Kirst; Mark Hertlein; Larry L. Larson; Thomas V. Worden; Stephen T. Thibault


Archive | 1996

Synthetic modification of Spinosyn compounds

Carl Deamicis; Peter Biagio Anzeveno; Jacek G. Martynow; Kevin L. McLaren; Frederick Richard Green; Thomas C. Sparks; Herbert A. Kirst; Lawrence Camillo Creemer; Thomas V. Worden; Joe Raymond Schoonover; James M. Gifford; Christopher J. Hatton; Vidyadhar B. Hegde; Gary D. Crouse; Brian R. Thoreen; Michael John Ricks


Archive | 1999

Fermentation-Derived Insect Control Agents

Thomas C. Sparks; Gary D. Thompson; Herbert A. Kirst; Mark Hertlein; Jon S. Mynderse; Jan R. Turner; Thomas V. Worden


Bioorganic & Medicinal Chemistry | 2009

Discovery of the butenyl-spinosyn insecticides: Novel macrolides from the new bacterial strain Saccharopolyspora pogona

Paul Lewer; Donald R. Hahn; Laura L. Karr; Dennis O. Duebelbeis; Jeffrey R. Gilbert; Gary D. Crouse; Thomas V. Worden; Thomas C. Sparks; Pat McKamey Rex Edwards; Paul R. Graupner


The Journal of Antibiotics | 2000

Synthesis and insecticidal activity of spinosyn analogs functionally altered at the 2'-,3'- and 4'-positions of the rhamnose moiety.

Lawrence Creemer; Herbert A. Kirst; Jonathan W. Paschal; Thomas V. Worden


Pesticide Chemistry and Bioscience#R##N#The Food-Environment Challenge | 1999

Chemistry and Insecticidal Activity of the Spinosyns

Gary D. Crouse; Tom Sparks; Carl Deamicis; Herbert A. Kirst; Jacek G. Martynow; Lawrence Camillo Creemer; Thomas V. Worden; Peter Biagio Anzeveno


Pesticide Biochemistry and Physiology | 2000

The Application of Artificial Neural Networks to the Identification of New Spinosoids with Improved Biological Activity toward Larvae of Heliothis virescens

Thomas C. Sparks; Peter Biagio Anzeveno; Jacek G. Martynow; James M. Gifford; Mark Hertlein; Thomas V. Worden; Herbert A. Kirst


Archive | 2008

SYNTHETIC MODIFICATION OF SPINOSYN COMPOUND AND ITS USE

Peter Biagio Anzeveno; Lawrence Creemer; Gary D Crouse; Carl Deamicis; James M. Gifford; Frederick Richard Green; Christopher J. Hatton; Vidyadhar B. Hegde; Herbert A. Kirst; Jacek G. Martynow; Kevin L. McLaren; Michael John Ricks; Joe Raymond Schoonover; Thomas C. Sparks; Brian R. Thoreen; Thomas V. Worden; カール・ビンセント・デイーミシス; クリストフアー・ジエイ・ハツトン; ゲイリー・デイ・クルーズ; ケビン・エル・マクラレン; ジエイセク・ジー・マーテイナウ; ジエイムズ・マイケル・ギフオード; ジヨー・レイモンド・スクーノーバー・ジユニア; トーマス・シー・スパークス; トーマス・ブイ・ワーデン; ハーバート・エイ・カースト; ピーター・ビアジオ・アンゼベノ; ビドヤドハル・ビー・ヘグデ; ブライアン・アール・ソレーン; フレデリク・リチヤード・グリーン・ザサード

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