公开(公告)号：US20210127684A1

公开(公告)日：2021-05-06

申请号：US16639521

申请日：2018-08-15

Applicant: Bayer CropScience LP

Inventor： Milind SINGH ,  David A. LONG ,  Aveen ALKHATIB

IPC: A01N63/22 ,  C05C9/00 ,  C05C1/00 ,  C05G1/00 ,  C05G5/27 ,  C05G3/50 ,  C05G3/60 ,  C05G3/70 ,  A01N43/14 ,  A01N63/25 ,  A01N43/40 ,  A01N51/00 ,  A01N63/23 ,  A01N25/04

Abstract: The present disclosure relates to the field of agrochemical compositions and formulations. In an aspect, the present disclosure provides for a composition in combination with a fibril or microfibril or nanofibril structuring agent. In yet another aspect, the disclosure provides for a composition comprising: (a) an agricultural bioactive material, a fungicide, insecticide, herbicide, and/or plant growth regulator; (b) a fibril or microfibril or nanofibril structuring agent; and (c) optionally, an auxiliary surface active agent. The disclosure further provides for a comprising a composition described herein mixed or combined with a liquid fertilizer.

公开(公告)号：US10221137B2

公开(公告)日：2019-03-05

申请号：US15546446

申请日：2016-01-19

Applicant: BASF SE

Inventor： Matthias Witschel ,  Tobias Seiser ,  Manuel Johannes ,  Dario Massa ,  Trevor William Newton ,  Richard Evans ,  Raphael Aponte

IPC: A01N25/02 ,  A01N25/04 ,  A01N25/08 ,  A01N43/40 ,  A01N43/44 ,  A01N43/84 ,  C07D213/61 ,  C07D401/12 ,  C07D405/12 ,  C07D413/12 ,  C07D417/12 ,  A01N43/14

Abstract: The present invention relates to phenylpyridines of formula (I) wherein the variables are defined according to the description, processes and intermediates for preparing the phenylpyridines of the formula (I), compositions comprising them and their use as herbicides, i.e. for controlling harmful plants, and also a method for controlling unwanted vegetation which comprises allowing a herbicidal effective amount of at least one phenylpyridine of the formula (I) to act on plants, their seed and/or their habitat.

公开(公告)号：US08475776B2

公开(公告)日：2013-07-02

申请号：US11680292

申请日：2007-02-28

Applicant: David I. Sherris

Inventor： David I. Sherris

IPC: A61K8/00 ,  A61K39/00 ,  A61K31/517 ,  A61K31/44 ,  A01N43/14

CPC classification number: C07D311/80 ,  A61K31/192 ,  A61K31/235 ,  A61K31/352 ,  A61K31/353 ,  A61K31/366 ,  A61K31/382 ,  A61K31/4433 ,  A61K31/473 ,  A61K31/517 ,  A61K45/06 ,  C07C65/40 ,  C07C69/78 ,  C07D239/90 ,  C07D311/16 ,  C07D311/18 ,  C07D405/06 ,  C07D405/12 ,  Y02A50/401 ,  A61K2300/00

Abstract: Described herein are compositions and methods for preventing and/or treating diseases involving aberrant angiogenesis employing one or more benzo[c]chromen-6-one derivatives.

Abstract translation: 本文描述了使用一种或多种苯并[c]色酮-6-酮衍生物预防和/或治疗涉及异常血管发生的疾病的组合物和方法。

公开(公告)号：US20120122768A1

公开(公告)日：2012-05-17

申请号：US13376164

申请日：2010-06-03

Applicant: Edvar Onsoyen ,  Rolf Myrvold ,  Arne Dessen ,  David Thomas ,  Timothy Rutland Walsh

Inventor： Edvar Onsoyen ,  Rolf Myrvold ,  Arne Dessen ,  David Thomas ,  Timothy Rutland Walsh

IPC: A61K31/734 ,  A61K31/7052 ,  A61K31/7048 ,  A01N43/90 ,  A01N43/78 ,  A61P11/06 ,  A01N43/14 ,  A01N43/72 ,  A61P31/04 ,  A01P1/00 ,  A61P35/00 ,  A61P11/00 ,  A61K38/02 ,  A01N43/60

CPC classification number: A61K31/734 ,  A01N37/18 ,  A01N43/22 ,  A01N43/60 ,  A01N43/72 ,  A01N43/78 ,  A01N43/86 ,  A01N43/90 ,  A61K31/407 ,  A61K31/427 ,  A61K31/496 ,  A61K31/546 ,  A61K31/65 ,  A61K31/7028 ,  A61K31/7048 ,  A61K31/7052 ,  A61K45/06 ,  Y02A50/473 ,  A61K2300/00

Abstract: The invention provides a method of overcoming resistance to at least one antibiotic in a multidrug resistant bacterium, said method comprising contacting said bacterium with an alginate oligomer together with the antibiotic. The multidrug resistant bacterium may be on an animate or inanimate surface and both medical and non-medical uses and methods are provided. In one aspect the invention provides an alginate oligomer for use together with at least one antibiotic in treating a subject infected, suspected to be infected, or at risk of infection, with a multidrug resistant bacterium to overcome resistance to the antibiotic in said multidrug resistant bacterium. In another aspect the method can be used to combat contamination of a site with multidrug resistant bacteria, e.g. for disinfection and cleaning purposes.

Abstract translation: 本发明提供一种在多重耐药性细菌中克服对至少一种抗生素的抗性的方法，所述方法包括使所述细菌与抗生素一起与藻酸盐低聚物接触。 多重耐药性细菌可以是生物或无生命的表面，并且提供医疗和非医疗用途和方法。 一方面，本发明提供了一种与至少一种抗生素一起使用的藻酸盐低聚物，用于治疗受多种耐药细菌感染，怀疑感染或有感染风险的受试者，以克服对所述多重耐药细菌中抗生素的抗性 。 在另一方面，该方法可用于抵抗具有多重耐药细菌的位点的污染，例如， 用于消毒和清洁目的。

公开(公告)号：US20100093652A1

公开(公告)日：2010-04-15

申请号：US12608345

申请日：2009-10-29

Applicant: Nicholas Spring ,  Edward J. Delaney

Inventor： Nicholas Spring ,  Edward J. Delaney

IPC: A61K31/7048 ,  A01N43/14 ,  A01P1/00 ,  A61P33/00

CPC classification number: A61K9/0014 ,  A01N25/04 ,  A61K31/351 ,  A61K31/365 ,  A61K31/7048 ,  A61K45/06 ,  Y02A50/473 ,  A01N43/90 ,  A01N2300/00 ,  A61K2300/00

Abstract: A topical formulation that inhibits the growth of microorganisms comprises an effective amount of an insecticide dissolved in an oil phase comprising a water-miscible or water-soluble surface active agent, a suspending agent, and a non-ionic surfactant, and an aqueous phase comprising one or more preservatives, where the aqueous phase is buffered to a specific pH. The overall antimicrobial efficacy in an emulsion formulation can be enhanced by buffering the aqueous phase of the emulsion to a pH at which the preservative system inhibits growth for a wider variety of microorganism types in the formulation relative to the equivalent formulation in which the aqueous phase is not buffered.

Abstract translation: 抑制微生物生长的局部制剂包括有效量的溶解在油相中的杀虫剂，其包含水混溶性或水溶性表面活性剂，悬浮剂和非离子表面活性剂，以及含有 一种或多种防腐剂，其中水相被缓冲至特定pH。 通过将乳液的水相缓冲至pH，在该pH下，防腐剂体系抑制制剂中更多种类的微生物类型的生长，相对于水相为 没有缓冲。

公开(公告)号：US20090098098A1

公开(公告)日：2009-04-16

申请号：US12240755

申请日：2008-09-29

Applicant: Jih-Ru Hwu ,  Shwu-Chen Tsay

Inventor： Jih-Ru Hwu ,  Shwu-Chen Tsay

IPC: A01N59/20 ,  A01N59/16 ,  A01N55/02 ,  A01N43/14 ,  A01P1/00 ,  A01P3/00

CPC classification number: A61L2/22 ,  A61K31/28 ,  A61K33/24 ,  A61K45/06 ,  A61L2/186 ,  A61K2300/00

Abstract: The present invention relates to an anti-bacterial, anti-virus, and anti-fungus composition, its preparation and use. The composition of the present invention mainly includes the following three ingredients in an adequate ratio: (A) a metal compound having a catalytic function; (B) a mixture of a coenzyme having reducing ability and quinones, and (C) an additive. The anti-bacterial, anti-virus, and anti-fungus composition of the present invention is capable of destroying viruses as well as killing bacterial and fungi. Therefore, the composition can be formulated as an aerosol and a film for applying to protection devices such as respirators, masks, gloves, filters, condoms, etc. The present composition can also be used in household, vehicle, hospital, school, restaurant, hotel, internet coffee shop for applying to filter of air-conditioner, tap, stool, interior of elevator and its keyboard. Additionally, the present composition can be applied to human being such as applying to hand, foot, genital organs, oral cavity, and the like in a lower dose to attain the effect of destroying of bacteria, viruses, and fungi.

Abstract translation: 本发明涉及抗菌，抗病毒和抗真菌组合物，其制备和应用。 本发明的组合物主要包括足够比例的以下三种成分：（A）具有催化功能的金属化合物; （B）具有还原能力的辅酶和醌类的混合物，和（C）添加剂。 本发明的抗细菌，抗病毒和抗真菌组合物能够破坏病毒以及杀死细菌和真菌。 因此，该组合物可以配制成用于应用于诸如呼吸器，面罩，手套，过滤器，避孕套等保护装置的气雾剂和膜。本发明组合物还可以用于家庭，车辆，医院，学校，餐厅， 酒店，互联网咖啡店，适用于空调，水龙头，凳子，电梯内部及其键盘。 此外，本发明的组合物可以以较低剂量施用于人，例如施用于手，脚，生殖器，口腔等，以达到破坏细菌，病毒和真菌的效果。

公开(公告)号：US20050054646A1

公开(公告)日：2005-03-10

申请号：US10863803

申请日：2004-06-08

Applicant: Diane Stephenson ,  Duncan Taylor

Inventor： Diane Stephenson ,  Duncan Taylor

IPC: A01N43/14 ,  A01N43/16 ,  A01N43/18 ,  A01N43/42 ,  A61K20060101 ,  A61K31/35 ,  A61K31/355 ,  A61K31/38 ,  A61K31/415 ,  A61K31/421 ,  A61K31/44 ,  A61K31/50

CPC classification number: A61K45/06 ,  A61K31/415 ,  A61K2300/00

Abstract: The present invention provides compositions and methods for the treatment of central nervous system disorders. In some aspects, the invention provides a combination therapy for the treatment of a central nervous system ischemic mediated disorder comprising the administration to a subject of an antioxidant agent in combination with a cyclooxygenase-2 selective inhibitor. In other aspects, the invention provides a combination therapy for the treatment of a central nervous system disorder that is neurodegenerative comprising the administration to a subject of an antioxidant agent in combination with a cyclooxygenase-2 selective inhibitor.

Abstract translation: 本发明提供了用于治疗中枢神经系统疾病的组合物和方法。 在一些方面，本发明提供了用于治疗中枢神经系统缺血性介导的病症的组合疗法，其包括与环氧合酶-2选择性抑制剂组合施用抗氧化剂的受试者。 在其它方面，本发明提供了治疗神经变性的中枢神经系统疾病的组合疗法，其包括向环氧合酶-2选择性抑制剂的组合施用抗氧化剂的受试者。

公开(公告)号：US4719227A

公开(公告)日：1988-01-12

申请号：US834287

申请日：1986-02-27

Applicant: Gerold Schade ,  Wilfried Paulus ,  Hans-Georg Schmitt

Inventor： Gerold Schade ,  Wilfried Paulus ,  Hans-Georg Schmitt

IPC: A01N43/02 ,  A01N43/08 ,  A01N43/14 ,  A01N43/16 ,  A01N43/20 ,  A01N43/28 ,  A01N43/30 ,  A01N43/32 ,  A61K31/335 ,  C07D305/06 ,  C07D307/12 ,  C07D307/20 ,  C07D309/06 ,  C07D317/18 ,  C07D317/22 ,  C07D317/34 ,  C07D317/72 ,  C07D319/06 ,  C07D319/08 ,  C07D325/00

CPC classification number: C07D317/72 ,  A01N43/08 ,  A01N43/16 ,  A01N43/20 ,  A01N43/28 ,  A01N43/30 ,  A01N43/32 ,  C07D305/06 ,  C07D307/12 ,  C07D307/20 ,  C07D309/06 ,  C07D317/22 ,  C07D319/06

Abstract: Iodopropargyl ethers of the formula ##STR1## wherein A represents oxygen or a methylene group,R.sup.1 denotes hydrogen or lower alkyl,R.sup.2 and R.sup.3 are identical or different and represent hydrogen, lower alkyl, alkenyl or unsubstituted or halogen-substituted phenyl, or R.sup.2 and R.sup.3 together form a carbocyclic ring with 4 to 7 C atoms,L and m represent 0, 1 or 2,k denotes 0 or 1 andn denotes an integer from 0 to 4, with the proviso that if 1 is 0, n represents 1, 2, 3 or 4,can be prepared by reaction of the corresponding propargyl ethers with iodinating agents. The iodopropargyl ethers are active compounds in microbicidal agents.

Abstract translation: 其中A表示氧或亚甲基，R1表示氢或低级烷基，R2和R3相同或不同，表示氢，低级烷基，烯基或未取代的或卤素取代的苯基，或R2和 R3一起形成具有4至7个C原子的碳环，L和m表示0,1或2，k表示0或1，n表示0至4的整数，条件是如果1为0，则n表示1 ，2,3或4可以通过相应的炔丙基醚与碘化剂的反应来制备。 碘代炔丙基醚是杀菌剂中的活性化合物。

公开(公告)号：US4599351A

公开(公告)日：1986-07-08

申请号：US575971

申请日：1984-02-01

Applicant: David C. K. Chan

Inventor： David C. K. Chan

IPC: A01N43/08 ,  A01N43/10 ,  A01N43/14 ,  C07D307/33 ,  C07D333/36 ,  C07D307/32 ,  A61K31/365

CPC classification number: C07D307/33 ,  A01N43/08 ,  A01N43/10 ,  A01N43/14 ,  C07D333/36

Abstract: 3-(N-butyryl or valeryl-N-arylamino)-gamma-butyrolactones and their thio analogs. These compounds are useful as fungicides.

Abstract translation: 3-（N-丁酰基或戊酰基-N-芳基氨基） - γ-丁内酯及其硫代类似物。 这些化合物可用作杀真菌剂。

公开(公告)号：US4537623A

公开(公告)日：1985-08-27

申请号：US594497

申请日：1984-03-29

Applicant: Carl E. Ward

Inventor： Carl E. Ward

IPC: A01N43/08 ,  A01N43/10 ,  A01N43/14 ,  C07D409/04 ,  A01N43/02 ,  A01N43/00 ,  C07D333/00

CPC classification number: C07D409/04 ,  A01N43/08 ,  A01N43/10 ,  A01N43/14

Abstract: Herbicidal 2-(oxaheterocycle or thiaheterocycle)-5-amino-3-oxo-4-(substituted-phenyl)-2,3-dihydrofurans and derivatives thereof. The compounds generally exhibit both pre-emergence and post-emergence phytotoxicity and are useful as herbicides and also plant growth regulating agents at low dosages.

Abstract translation: 除草2-（氧杂环或硫杂环）-5-氨基-3-氧代-4-（取代苯基）-2,3-二氢呋喃及其衍生物。 化合物通常表现出出苗前和芽后植物毒性，并且可用作除草剂以及低剂量的植物生长调节剂。