Compounds related to natural sources and their use as biopesticides
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A01N-047/40
A01N-037/34
출원번호
US-0583481
(2000-05-31)
발명자
/ 주소
Coats, Joel R.
Peterson, Christopher J.
Tsao, Rong
Eggler, Aimee L.
Tylka, Gregory L.
출원인 / 주소
Iowa State University Research Foundation, Inc.
대리인 / 주소
Schwegman, Lundberg, Woessner & Kluth, P.A.
인용정보
피인용 횟수 :
4인용 특허 :
2
초록▼
A method for suppressing target pests, comprising exposing the pests to an effective biopesticidal amount of a composition, the composition comprising a carrier and a purified glucosinolate breakdown product having a hydroxyl group attached, wherein a starting material for the purified glucosinolate
A method for suppressing target pests, comprising exposing the pests to an effective biopesticidal amount of a composition, the composition comprising a carrier and a purified glucosinolate breakdown product having a hydroxyl group attached, wherein a starting material for the purified glucosinolate breakdown product is isolated from a crambe plant or mustard plant, further wherein the target pests are plants, fungi, bacteria or root knot nematodes is disclosed. Methods for suppressing target pests without limitation as to the starting materials are also disclosed wherein the pests are exposed to an effective biopesticidal amount of a composition comprising a carrier and either an analog or a derivative of a purified glucosinolate breakdown product having a hydroxyl group attached.
대표청구항▼
A method for suppressing target pests, comprising exposing the pests to an effective biopesticidal amount of a composition, the composition comprising a carrier and a purified glucosinolate breakdown product having a hydroxyl group attached, wherein a starting material for the purified glucosinolate
A method for suppressing target pests, comprising exposing the pests to an effective biopesticidal amount of a composition, the composition comprising a carrier and a purified glucosinolate breakdown product having a hydroxyl group attached, wherein a starting material for the purified glucosinolate breakdown product is isolated from a crambe plant or mustard plant, further wherein the target pests are plants, fungi, bacteria or root knot nematodes is disclosed. Methods for suppressing target pests without limitation as to the starting materials are also disclosed wherein the pests are exposed to an effective biopesticidal amount of a composition comprising a carrier and either an analog or a derivative of a purified glucosinolate breakdown product having a hydroxyl group attached. nd, "Glycobiology: Toward Understanding the Function of Sugars," Chem. Rev. 1996, 96, pp. 683-720. Platt, Frances M., et al., "Inhibitors of Glycosphingolipid Biosynthesis," Trends in Glycoscience and Glycotechnology, vol. 7, No. 38, Nov. 1995, pp. 495-511. Dwek, Raymond A. "Glycobiology: Toward Understanding the Function of Sugars," Chem. Rev. 1996, 96, pp. 683-720. Mutchnick, et al., "Thymosin Treatment of Chronic Active Hepatitis B (CAHB): Results of a Pilot Study," Hepatology, vol. 10, No. 4, 1989. Acosta, et al., "Agents for Treating Human Immunodeficiency Virus Infection," Am. J. Hosp. Pharm., vol. 51, Sep. 15, 1994, pp. 2251-2287. Tennant, et al., "Animal Models in the Preclinical Assessment of Therapy for Viral Hepatitis," Antiviral Therapy, vol. 1, (Suppl. 4), 1996, pp. 47-52. Sachs, "Antiretroviral Chemotherapy of Human Immunodeficiency Virus Infections Other Than with Azidothymidine," Arch. Inter. Med., vol. 152, Mar. 1992, pp. 485-501. Gasparini, et al., "Clinical Importance of the Determination of Tumor Angiogenesis in Breast Carcinoma: Much More Than a New Prognostic Tool," Journal of Clinical Oncology, vol. 13, No. 3, Mar. 1995, pp. 765-782. Bruyneel, et al. "Effect of Glycosylation Inhibitors on N-Glycosylpeptides and on Invasion of Malignant Mouse MO4Cells in Vitro," Journal of Cell Science, vol. 95, 1990, pp. 279-286. Jacob, "Glycosylation Inhibitors in Biology and Medicine," Current Opinion in Structural Biology, No. 5, 1995, pp. 605-611. Senuma, et al., "Highly Effective Resolution of 1,3-Dibensl-6-hydroxy-3,3a,6,6a-tetrahydro-1H-furo[3,4-d]imidazole-2,4-dione, an intermediate for Biotin, with Optically Active Analysis and Reutilization of the Unwanted Epimer," Chem. Pharm. Bull., vol. 38, No. 4, 1990, pp. 882-887.
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이 특허에 인용된 특허 (2)
Findeisen Kurt (Leverkusen DEX) Wagner Kuno (Leverkusen DEX) Uerdingen Walter (Leverkusen DEX), Isocyanate derivatives of 1,3[oxazoles, oxazines, diazoles and diazines.
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