专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明申请

US20040156916A1 Methods and compositions for controlling plant pathogen 审中-公开
公开(公告)号：US20040156916A1
公开(公告)日：2004-08-12
申请号：US10771398
申请日：2004-02-05
发明人： Ran Lifshitz
IPC分类号： A01N037/12 , A01N037/44 , A01N059/26
CPC分类号： A01N59/26 , Y10S424/06 , A01N59/20 , A01N59/16 , A01N37/36 , A01N2300/00 , A01N59/00 , A01N61/00
摘要： A composition for controlling growth of pathological organisms on a plant, said composition comprises an effective amount of one or more of metal ion(s); one or more of chelating agent(s); and phosphorous acid, and/or salt or hydrate thereof, said composition is in an agriculturally compatible carrier or vehicle.

2. 发明申请

US20030078290A1 Synergistic mixtures of selected amino acids 审中-公开
公开(公告)号：US20030078290A1
公开(公告)日：2003-04-24
申请号：US10146109
申请日：2002-05-16
申请人： AGROGENE LTD.
发明人： Yigal Cohen , Moshe Korat , Dan Zvi-Tov
IPC分类号： A01N043/38 , A01N037/12 , A01N037/44
CPC分类号： A01N37/44 , A01N37/46 , A01N59/20 , A01N57/12 , A01N47/34 , A01N47/14 , A01N47/04 , A01N43/54 , A01N43/08 , A01N37/38 , A01N43/82 , A01N2300/00
摘要： Novel synergistic fungicidal compositions used for protecting seeds, plants and other vegetative material against fungi contain a mixture of one or more compounds selected from group A and one or more compounds selected from group B. Compounds from group A are selected from null-Amino butyric acid and its N-benzoyl-octyl ester derivatives. Compounds from group B are selected from the group of fosetyl aluminum, dimethomorph, a mixture of folpet and ofurace (45:5), folpet, fencaramid (Bayer SZX), mancozeb, cymoxanil, methalaxyl, the single optical isomer of metalaxyl, a mixture of cymoxamil and mancozeb (4:1), copper sulfate, copper hydroxide, copper sulfate hydrate, azoxystrobin, and acibenzolar-s-methyl.

3. 发明申请

US20020103256A1 Pesticidal and parasiticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds 失效
公开(公告)号：US20020103256A1
公开(公告)日：2002-08-01
申请号：US09920264
申请日：2001-08-01
申请人： American Cyanamid Company
发明人： William Wakefield Wood , Annmarie Enos
IPC分类号： A01N043/42 , A01N037/34 , A01N037/12
CPC分类号： C07D307/38 , A01N33/20 , A01N37/36 , A01N37/38 , A01N37/44 , A01N37/48 , A01N39/00 , A01N41/10 , A01N43/08 , A01N43/10 , A01N43/30 , A01N43/40 , C07D213/32 , C07D317/56 , C07D333/18 , C07D405/12
摘要： The present invention relates to the pesticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds having the structural formula I 1

4. 发明申请

US20020086048A1 Design and application method for enhanced oral assimilation through the oral mucosa and/or intestinal membranes, of liquids containing nutrients, nutraceuticals or drugs, which are encapsulated in natural and/or synthetic liposomal vesicles 审中-公开
标题翻译：用于通过口腔粘膜和/或肠膜，包含营养素，营养药物或药物的液体加强口服同化的设计和应用方法，其被包封在天然和/或合成的脂质体囊泡中
公开(公告)号：US20020086048A1
公开(公告)日：2002-07-04
申请号：US09750678
申请日：2001-01-02
发明人： Arnold C. Takemoto , Nikolaus J. Smeh
IPC分类号： A61K031/375 , A61K009/127 , A01N037/12 , A61K031/195
CPC分类号： A61K9/127 , A61K31/198 , A61K31/375 , A61K38/28
摘要： Method of oral administration of nutrients, nutraceuticals, and drugs to humans and animals orally by encapsulating these substances into vesicles formed by polar molecules, like phospholipids, for enhanced transport through oral mucosa or intestinal membranes into the circulatory system.
摘要翻译：通过将这些物质包封到由极性分子形成的囊泡（如磷脂）中，通过将口腔粘膜或肠膜输送到循环系统中，将口服营养素，营养物质和药物口服给人和动物的方法。

5. 发明申请

US20030206968A1 Fungicidal mixtures 失效
标题翻译：杀菌混合物
公开(公告)号：US20030206968A1
公开(公告)日：2003-11-06
申请号：US10314594
申请日：2002-12-10
发明人： Henry Van Tuyl Cotter , Leslie May , Gunter Reichert , Ewald Sieverding
IPC分类号： A01N043/90 , A01N043/64 , A01N037/12 , A01N037/44 , A01N059/20 , A01N059/02 , A01N037/18
CPC分类号： A01N43/90 , A01N2300/00
摘要： Fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I 1 nullin which R1, R2, L1, L2 and L3 have the meaning given in claim 1; and (b) at least one fungicidal active ingredient selected from benomyl, carboxin, captan, chlorothalonil, copper oxychloride, cyprodinil, dimethomorph, dithianon, dodine, famoxadone, fenhexamid, fenpiclonil, fenpropimorph, fluazinam, mancozeb, metalaxyl, pyrimethanil, quinoxifen, sulfur, triforine, vinclozolin, a fungicidal triazole derivative, and a synthetic strobilurine derivative. The invention also provides a method of controlling the growth of phytopathogenic fungi at a locus by applying synergistically effective amounts of at least one azolopyrimidine of formula I and at least one fungicidal active ingredient (b) to the locus.
摘要翻译：包含可接受的载体和/或表面活性剂和协同有效量的（a）至少一种式I的偶氮嘧啶的杀真菌组合物，其中R 1，R 2，L 1，L 2和L <3>具有权利要求1中给出的含义; 和（b）至少一种杀真菌活性成分，其选自苯菌灵，呋喃丹，克拉曼，百菌清，氯氧化铜，西酞替尼，烯酰吗啉，二噻吩，十二烷，恶唑酮，芬己酰，芬替尼，芬卡芬，氟啶胺，代森锰锌，甲霜灵，嘧霉胺，喹喔啉，，triperine，长春菌素，杀真菌三唑衍生物和合成次溴酸衍生物。本发明还提供了一种通过将协同有效量的至少一种式I的偶氮嘧啶和至少一种杀真菌活性成分（b）施用于该基因座来控制植物病原真菌在一个场所生长的方法。

6. 发明申请

US20030083340A1 Plant protection agents 失效
标题翻译：植物保护剂
公开(公告)号：US20030083340A1
公开(公告)日：2003-05-01
申请号：US10191584
申请日：2002-07-09
发明人： Paul Margot , Gertrude Knauf-Beiter
IPC分类号： A01N043/54 , A01N043/42 , A01N043/82 , A01N043/76 , A01N037/12 , A01N037/44 , A01N043/12 , A01N043/26 , A01N043/36
CPC分类号： A01N37/50 , A01N43/82 , A01N43/76 , A01N43/54 , A01N43/42 , A01N43/36 , A01N43/30 , A01N37/24 , A01N2300/00
摘要： Microbicide composition for plants, containing at least two active ingredient components in an amount producing synergistic activity, together with an appropriate filler, characterized in that component I is the compound 2-nullnull-nullnull(null-methyl-3-trifluoromethyl-benzyl)iminonull-oxynull-o-tolylnull-glyoxylic acid-methylester-O-methyloxime, and component II is a compound selected from the group IIA) 5,7-dichloro-4-(4-fluorophenoxy)quinoline (nullQuinoxyfennull); IIB) 4-cyclopropyl-6-methyl-N-phenyl-2-pyrimidinamine (nullCyprodinilnull); IIC) benzo(1,2,3)thiadiazole-7-carbothio-acid-S-methylester (nullAcibenzolar-S-methylnull); IID) 3-anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione (nullFamoxadonenull); IIE) 8-(1,1-dimethylethyl)-N-ethyl-N-propyl-1,4-dioxaspironull4.5nulldecane-2-methanamine (nullSpiroxaminnull); IIF) 4-(2,2-difluoro-1,3-benzodioxol-4-yl)pyrrole-3-carbonitrile (nullFludioxonilnull); IIG) 4-(2,3-dichlorophenyl)pyrrole-3-carbonitrile (nullFenpiclonilnull); IIH) 1-methyl-cyclohexanecarboxylic acid-(2,3-dichloro-4-hydroxy-phenyl)-amide (nullFenhexamidnull); IIJ) 2-null2-null6-(2-cyano-phenoxy)-pyrimidin-4-yloxynull-phenylnull-3-methoxy-acrylic acid methyl ester (nullAzoxystrobinnull); IIK) Methoximino-(2-o-tolyloxymethyl-phenyl)-acetic acid methyl ester (nullKresoxim-methylnull); or repectively one of the salts or metal complexes of components I and II.
摘要翻译：用于植物的杀微生物剂组合物，其含有至少两种产生协同活性的量的活性成分组分以及合适的填充剂，其特征在于组分I是化合物2-[{[（α-甲基-3-三氟甲基 - 苄基）亚氨基] - 氧基} - 对 - 甲苯基] - 乙醛酸 - 甲酯-O-甲基肟，组分II是选自IIA）5,7-二氯-4-（4-氟苯氧基）喹啉（“Quinoxyfen “）; IIB）4-环丙基-6-甲基-N-苯基-2-嘧啶胺（“Cyprodinil”）; IIC）苯并（1,2,3）噻二唑-7-硫代硫酸S-甲酯（“Acibenzolar-S-甲基”）; IID）3-苯胺基-5-甲基-5-（4-苯氧基苯基）-1,3-恶唑烷-2,4-二酮（“Famoxadone”）; IIE）8-（1,1-二甲基乙基）-N-乙基-N-丙基-1,4-二氧杂螺[4.5]癸烷-2-甲胺（“螺螺心”）; IIF）4-（2,2-二氟-1,3-苯并间二氧杂环戊烯-4-基）吡咯-3-腈（“Fludioxonil”）; IIG）4-（2,3-二氯苯基）吡咯-3-腈（“Fenpiclonil”）; IIH）1-甲基 - 环己烷羧酸 - （2,3-二氯-4-羟基 - 苯基） - 酰胺（“Fenhexamid”）; IIJ）2- {2- [6-（2-氰基 - 苯氧基） - 嘧啶-4-基氧基] - 苯基} -3-甲氧基 - 丙烯酸甲酯（“嘧菌酯”）; IIK）甲肟基 - （2-邻甲苯氧基甲基 - 苯基） - 乙酸甲酯（“Kresoxim-methyl”）; 或分别是组分I和II的盐或金属络合物之一。

7. 发明申请

US20010051743A1 ESTERS OF 5-AMINOLEVULINIC ACID AS PHOTOSENSITIZING AGENTS IN PHOTOCHEMOTHERAPY 失效
标题翻译： 5-氨基酸在光化学疗法中作为光敏剂使用
公开(公告)号：US20010051743A1
公开(公告)日：2001-12-13
申请号：US09471620
申请日：1999-12-21
发明人： KARL E. GIERSKCKY , JOHAN MOAN , QIAN PENG , HARALD STEEN , TROND WARLOE , ALF BJORSETH
IPC分类号： C07C229/00 , A61K031/24 , A01N037/12 , A01N037/44 , A61K031/22 , A01N025/00
CPC分类号： A61K49/0021 , A61K31/22 , A61K41/0061 , C07C229/22 , Y10S514/863 , Y10S514/947
摘要： The present invention relates to compounds being esters of 5-aminolevulinic acids or pharmaceutically acceptable salts thereof, including compounds of formula (I) R22NnullCH2COCH2nullCH2COnullOR1 (wherein R1 may represent alkyl optionally substituted by hydroxy, alkoxy, acyloxy, alkoxycarbonyloxy, amino, aryl, oxo or fluoro groups and optionally interrupted by oxygen, nitrogen, sulphur or phosphorus atoms; and R2 represents a hydrogen atom or a group R1, and both R2 groups may be the identical or different), and their use in diagnosis and photochemotherapy of disorders or abnormalities of external or internal surfaces of the body, and products and kits for performing the invention.
摘要翻译：本发明涉及作为5-氨基乙酰丙酸的酯或其药学上可接受的盐的化合物，包括式（I）R 22 N-CH 2 COCH 2 -CH 2 CO-OR 1的化合物（其中R 1可以表示任选被羟基，烷氧基，酰氧基，烷氧基羰基氧基，氨基，芳基，氧代或氟基团，并且任选地被氧，氮，硫或磷原子间隔;并且R 2表示氢原子或基团R 1，并且两个R 2基团可以相同或不同），以及它们在诊断和身体的外表面或内表面的紊乱或异常的光化学疗法，以及用于实施本发明的产品和试剂盒。

8. 发明申请

US20010044465A1 Use of L-carnitine and its alkanoyl derivatives in the preparation of medicaments with anticancer activity 失效
标题翻译： L-肉碱及其烷酰基衍生物在制备具有抗癌活性的药物中的应用
公开(公告)号：US20010044465A1
公开(公告)日：2001-11-22
申请号：US09769488
申请日：2001-01-26
发明人： Claudio Cavazza , Caudio Pisano , Loredana Vesci
IPC分类号： A61K031/335 , A01N043/02 , A61K031/24 , A01N037/12 , A01N037/44
CPC分类号： A61K45/06 , A61K31/205 , A61K31/221 , A61K31/28 , A61K31/335 , A61K31/475 , A61K31/555 , A61K33/24 , A61K38/14 , A61K2300/00
摘要： Alkanoyl L-carnitines of the formula: 1 where R is hydrogen or a C2-8 alkanoyl group and Xnull is an anion of a pharmaceutically acceptable salt, are used in conjunction with anticancer agents such as taxol or bleomycin to improve the therapeutic index and reduce side effects typical of anticancer chemotherapy.
摘要翻译：其中R为氢或C2-8烷酰基，X为药学上可接受的盐的阴离子的烷酰基L-肉碱与抗癌剂如紫杉醇或博来霉素结合使用，以改善治疗指数并减少抗癌化疗典型的副作用。

9. 发明申请

US20010000513A1 Biphenyl butyric acids and their derivatives as inhibitors of matrix metalloproteinases 失效
标题翻译：联苯丁酸及其衍生物作为基质金属蛋白酶抑制剂
公开(公告)号：US20010000513A1
公开(公告)日：2001-04-26
申请号：US09736802
申请日：2000-12-14
发明人： Claude Forsey Purchase JR. , Bruce David Roth , Gerald Paul Schielke , Lary Craswell Walker , Andrew David White
IPC分类号： C07C229/00 , C07C233/00 , C07C235/00 , C07C237/00 , C07C239/00 , C07C255/00 , A61K031/275 , A01N037/34 , A61K031/24 , A01N037/12
CPC分类号： C07C323/63 , C07C59/56 , C07C59/84 , C07C59/88 , C07C59/90 , C07C69/738 , C07C251/48 , C07C251/86 , C07C255/64
摘要： Biphenyl butyric acid compounds and derivatives are described as well as acid methods for the preparation and pharmaceutical compositions of same, which are useful as inhibitors of matrix metalloproteinases, particularly gelatinase A (72 kD gelatinase) and stromelysin-1 and for the treatment of multiple sclerosis, atherosclerotic plaque rupture, aortic aneurism, heart failure, restenosis, periodontal disease, corneal ulceration, treatment of burns, decubital ulcers, wound healing, cancer, inflammation, pain, arthritis, or other autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes or other activated migrating cells.
摘要翻译：描述了联苯丁酸化合物和衍生物以及用于制备的酸法和其药物组合物，其可用作基质金属蛋白酶抑制剂，特别是明胶酶A（72kD明胶酶）和基质溶素-1和用于治疗多发性硬化症，动脉粥样硬化斑块破裂，主动脉瘤，心力衰竭，再狭窄，牙周病，角膜溃疡，烧伤治疗，褥疮性溃疡，伤口愈合，癌症，炎症，疼痛，关节炎或依赖于白细胞组织侵袭的其他自身免疫性或炎症性疾病或其他激活的迁移细胞。

10. 发明申请

US20030108927A1 Compositions and methods for the prevention, treatment and detection of tuberculosis and other diseases 审中-公开
标题翻译：预防，治疗和检测结核病等疾病的组成和方法
公开(公告)号：US20030108927A1
公开(公告)日：2003-06-12
申请号：US10265190
申请日：2002-10-07
发明人： Kathryn Leishman
IPC分类号： A61K048/00 , A61K031/325 , A61K031/198 , A61K039/395 , A61K039/00 , C12Q001/68 , A61K031/70 , A01N043/04 , A61K039/38 , A61K031/27 , A01N047/10 , A61K031/195 , A01N037/12 , A01N037/44
CPC分类号： A61K31/198 , A61K31/325 , A61K38/44 , A61K39/04 , A61K2039/505 , C12Y102/99002
摘要： Methods and compositions are provided for the prevention and treatment of infectious diseases such as syphilis, tuberculosis, pneumonia, other bacterial infections, AIDS, and other viral infections. Many of the compositions are active against carbon monoxide dehydrogenase (nullCODHnull), and include substances such as antigens, antibodies specific for CODH, and other inhibitors of CODH such as nickel and molybdenum metal chelators. The methods and compositions are particularly suited for treatment of diseases from previously under recognized anaerobic or facultative anaerobic pathogens such as Mycobacterium tuberculosis and Mycobacterium pneumonia.
摘要翻译：提供方法和组合物用于预防和治疗感染性疾病如梅毒，肺结核，肺炎，其他细菌感染，艾滋病和其他病毒感染。许多组合物对一氧化碳脱氢酶（“CODH”）具有活性，并且包括诸如抗原的物质，对CODH特异的抗体，以及其它CODH抑制剂如镍和钼金属螯合剂。所述方法和组合物特别适用于治疗先前在识别的厌氧或兼性厌氧病原体如结核分枝杆菌和肺炎支原体之间的疾病。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式