AR067850A1 - Metodos y composiciones para inhibir el factor de edema y la adenilil ciclasa y kit - Google Patents
Metodos y composiciones para inhibir el factor de edema y la adenilil ciclasa y kitInfo
- Publication number
- AR067850A1 AR067850A1 ARP080102569A ARP080102569A AR067850A1 AR 067850 A1 AR067850 A1 AR 067850A1 AR P080102569 A ARP080102569 A AR P080102569A AR P080102569 A ARP080102569 A AR P080102569A AR 067850 A1 AR067850 A1 AR 067850A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- substituted
- pyridyl
- alkyl
- unsubstituted
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Abstract
Se describen un método para tratar y/o prevenir la pérdida de fluido intestinal en un sujeto que comprende administrarle al sujeto una composicion que comprende una cantidad eficaz para el uso terapéutico de un compuesto o una sal de éste aceptable para el uso farmacéutico, donde la formula general del compuesto se selecciona del grupo que consiste en el grupo de formulas (1) a (9) y cualquier combinacion de éstas, donde 1) R es una estructura de anillo cíclico o bicíclico; 2) R1 es un hidrogeno, una estructura de anillo cíclico o bicíclico; 3) R2 es un hidrogeno, alquilo, una estructura de anillo cíclico o bicíclico; 4) R3 es un hidrogeno, o alquilo; 5) R5 es un hidrogeno, alquilo, una estructura de anillo cíclico o bicíclico; 6) X es un alquilo, oxígeno, un éster, una amina o una amida, 7) Z se selecciona del grupo que consiste en hidrogeno, alquenilo, alquinilo, fenilo, bencilo, halo, fluoro, cloro, bromo, iodo, hidroxilo, ceto, oxo, aldo. carbonato, carboxilo, alcoxilo, éster, carboxamido, amino, amonio, imino, imido, azido, azo, cianato, isociano, isocianato, isotiocianato, nitroxilo, ciano, nitrosooxilo, nitro, nitroso, 4-piridilo, 3-piridilo, 2-piridilo, tioéter, sulfanilo, sulfo, sulfinilo, mercapto, sulfanilo, sulfhidrilo, sulfonamino, tiocianato, alquil amino, ácido hidroxiámico, metilo, etilo, 1,3-dioxilanilo, propilo, iso-propilo, butilo, ter-butilo, alquilo no sustituido o sustituido, ramificado o no ramificado, alquenilo C1-3, arilo no sustituido o sustituido, ramificado o no ramificado, alquilarilo no sustituido o sustituido, ramificado o no ramificado, hidrato de carbono no sustituido a sustituido, ramificado o no ramificado; 8) W se selecciona de! grupo que consiste en CO, NH, metileno, un átomo de azufre, un átomo de oxigeno y tionilo; y 9) n es 0, 1,o más de 1. También se describen composiciones que comprenden compuestos de formula 1 y 4 y un kit o conjunto de elementos para el tratamiento de la pérdida de fluido intestinal en un sujeto, que comprende una cantidad terapéuticamente efectiva de un compuesto a una sal farmacéuticamente aceptable del mismo de formula general seleccionada del grupo que consiste de las formulas 1 a 9. Reivindicacion 2: El método de la reivindicacion 1, donde R está sustituido o no sustituido, y se selecciona del grupo que consiste en fenilo, piranonilo, piridilo, imidazolilo, 1,8-naftiridinilo y N-oxido de piridilo. Reivindicacion 4: El método de la reivindicacion 1, donde R1 esté sustituido o no sustituido, y se selecciona del grupo que consiste en fenilo, piridilo y furanilo. Reivindicacion 14: El método de la reivindicacion 1, donde la composicion se administra en combinacion con una o más drogas adicionales. Reivindicacion 15: El método de la reivindicacion 1, donde la composicion comprende además un antibiotico o un antiinflamatorio. Reivindicacion 78: El conjunto de elementos de la reivindicacion 70, que comprende además una droga seleccionada del grupo que consiste en un antibiotico, un antidiarreico y una droga inhibidora de LT.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94437507P | 2007-06-15 | 2007-06-15 | |
US3526908P | 2008-03-10 | 2008-03-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR067850A1 true AR067850A1 (es) | 2009-10-28 |
Family
ID=40468705
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080102569A AR067850A1 (es) | 2007-06-15 | 2008-06-17 | Metodos y composiciones para inhibir el factor de edema y la adenilil ciclasa y kit |
Country Status (12)
Country | Link |
---|---|
US (2) | US8003692B2 (es) |
EP (1) | EP2166841A4 (es) |
CN (1) | CN101784274A (es) |
AR (1) | AR067850A1 (es) |
AU (1) | AU2008302667B2 (es) |
BR (1) | BRPI0813176A2 (es) |
CA (1) | CA2692004C (es) |
CL (1) | CL2008001782A1 (es) |
CO (1) | CO6270184A2 (es) |
DO (1) | DOP2009000272A (es) |
MX (1) | MX2009013676A (es) |
WO (1) | WO2009038842A2 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101636157A (zh) * | 2007-01-12 | 2010-01-27 | 康乃尔研究基金会有限公司 | 作为抗菌干预的新型靶的腺苷酰环化酶 |
WO2008088771A2 (en) * | 2007-01-12 | 2008-07-24 | Cornell Research Foundation, Inc. | Adenylyl cyclases as novel targets for the treatment of infection by eukaryotic pathogens |
EP2166841A4 (en) * | 2007-06-15 | 2014-05-07 | Mission Pharma Co | METHODS AND COMPOSITIONS FOR INHIBITING DOME FACTOR AND ADENYLYLCYCLASE |
EP2326953B1 (en) * | 2008-07-22 | 2018-03-21 | Promega Corporation | Adp detection based luminescent phosphotransferase or atp hydrolase assay |
KR101762574B1 (ko) * | 2009-03-31 | 2017-07-28 | 가부시키가이샤 레나사이언스 | 플라즈미노겐 액티베이터 인히비터-1 저해제 |
AU2013207510A1 (en) * | 2012-01-06 | 2014-07-31 | The Regents Of The University Of California | Compositions, methods of use, and methods of treatment |
US10092537B2 (en) | 2013-04-15 | 2018-10-09 | Renascience Co., Ltd. | Use for PAI-1 inhibitor |
US9677117B2 (en) | 2014-10-08 | 2017-06-13 | Promega Corporation | Bioluminescent succinate detection assay |
CN105218343B (zh) * | 2015-10-26 | 2017-03-22 | 乐普药业股份有限公司 | 一种3‑溴环己‑2‑烯‑1‑酮的合成方法 |
US10556853B2 (en) * | 2017-01-10 | 2020-02-11 | Owen-Barry Pharmaceuticals Inc. | Anticonvulsant compounds |
US11833156B2 (en) | 2017-09-22 | 2023-12-05 | Jubilant Epipad LLC | Heterocyclic compounds as pad inhibitors |
US10882821B1 (en) | 2017-09-26 | 2021-01-05 | The Board Of Trustees Of The Leland Stanford Junior University | Enantiomeric compound for the reduction of the deleterious activity of extended nucleotide repeat containing genes |
FI3697785T3 (fi) | 2017-10-18 | 2023-04-03 | Jubilant Epipad LLC | Imidatsopyridiiniyhdisteitä pad:n estäjinä |
EP3707135A1 (en) | 2017-11-06 | 2020-09-16 | Jubilant Prodel LLC | Pyrimidine derivatives as inhibitors of pd1/pd-l1 activation |
JP7368369B2 (ja) | 2017-11-24 | 2023-10-24 | ジュビラント・エピスクライブ・エルエルシー | Prmt5阻害剤としてのヘテロ環式化合物 |
JP7279063B6 (ja) | 2018-03-13 | 2024-02-15 | ジュビラント プローデル エルエルシー | Pd1/pd-l1相互作用/活性化の阻害剤としての二環式化合物 |
Family Cites Families (22)
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US4066834A (en) * | 1974-01-24 | 1978-01-03 | Miles Laboratories, Inc. | Cycloalkenyl analogues of prostaglandins E |
US4222944A (en) * | 1978-07-31 | 1980-09-16 | Hoffmann-La Roche Inc. | Halo-3-dibenzofuran alkanonitriles |
KR20000068415A (ko) * | 1996-09-04 | 2000-11-25 | 로즈 암스트롱, 크리스틴 에이. 트러트웨인 | 매트릭스 메탈로프로테이나제 억제용 화합물 및 방법 |
CA2366877A1 (en) * | 1999-03-22 | 2000-09-28 | Stanley Michael Roberts | Chemical compounds and their uses |
AU2001274858A1 (en) * | 2000-06-08 | 2001-12-17 | Board Of Regents, The University Of Texas System | Heterocycle derivatives and methods of use for treating anthrax infection |
AU2002239277A1 (en) * | 2000-11-20 | 2002-05-27 | Cor Therapeutics, Inc. | Adenine based inhibitors of adenylyl cyclase, pharmaceutical compositions and method of use thereof |
AU2002217316A1 (en) * | 2001-01-03 | 2002-07-30 | Medpharma Plc | Use of terpenes for the treatment of digestive tract infections |
DE10123163A1 (de) * | 2001-05-09 | 2003-01-16 | Gruenenthal Gmbh | Substituierte Cyclohexan-1,4-diaminderivate |
CA2457468A1 (en) * | 2001-08-09 | 2003-02-27 | Ono Pharmaceutical Co., Ltd. | Carboxylic acid derivatives and pharmaceutical agent comprising the same as active ingredient |
EP1456214A2 (en) * | 2001-12-14 | 2004-09-15 | Charterhouse Therapeutics Limited | Improvements in pharmaceutical compositions |
US20030157159A1 (en) * | 2002-01-15 | 2003-08-21 | Franklin Lanny Udell | Prevention and treatment of digestive tract infections |
US20030224403A1 (en) * | 2002-02-27 | 2003-12-04 | Popov Serguei G. | Lethal toxin cytopathogenicity and novel approaches to anthrax treatment |
EP1479666A4 (en) * | 2002-02-28 | 2010-10-13 | Japan Tobacco Inc | ESTER CONNECTION AND THEIR MEDICAL USE |
KR20050065624A (ko) * | 2002-10-23 | 2005-06-29 | 그렌마크 파머수티칼스 엘티디. | 염증성 및 알레르기 질환의 치료에 유용한 신규한트리사이클릭 화합물, 이의 제조 방법 및 이를 함유하는약제 조성물 |
CA2528626A1 (en) * | 2003-07-09 | 2005-01-20 | Biolipox Ab | Indoles useful in the treatment of inflammation |
US7223759B2 (en) * | 2003-09-15 | 2007-05-29 | Anadys Pharmaceuticals, Inc. | Antibacterial 3,5-diaminopiperidine-substituted aromatic and heteroaromatic compounds |
LT2489659T (lt) * | 2004-06-24 | 2018-03-26 | Vertex Pharmaceuticals Incorporated | Atp rišančios kasetės transporterių moduliatoriai |
US20080096848A1 (en) * | 2004-09-29 | 2008-04-24 | Cytovia Inc. | Substituted N-Aryl-9-Oxo-9H-Fluorene-1-Carboxamides and Analogs as Activators of Caspases and Inducers of Apoptosis |
US7091231B2 (en) * | 2004-12-10 | 2006-08-15 | Allergan, Inc. | 12-Aryl prostaglandin analogs |
WO2007076055A2 (en) * | 2005-12-22 | 2007-07-05 | Entremed, Inc. | Compositions and methods comprising proteinase activated receptor antagonists |
WO2007135120A1 (en) * | 2006-05-23 | 2007-11-29 | Neurosearch A/S | Novel 1,4-diaza-bicyclo[3.2.2]nonane derivatives and their medical use |
EP2166841A4 (en) * | 2007-06-15 | 2014-05-07 | Mission Pharma Co | METHODS AND COMPOSITIONS FOR INHIBITING DOME FACTOR AND ADENYLYLCYCLASE |
-
2008
- 2008-06-13 EP EP08832293.8A patent/EP2166841A4/en not_active Withdrawn
- 2008-06-13 WO PCT/US2008/066898 patent/WO2009038842A2/en active Application Filing
- 2008-06-13 BR BRPI0813176-7A2A patent/BRPI0813176A2/pt not_active Application Discontinuation
- 2008-06-13 CN CN200880024507A patent/CN101784274A/zh active Pending
- 2008-06-13 US US12/139,212 patent/US8003692B2/en not_active Expired - Fee Related
- 2008-06-13 MX MX2009013676A patent/MX2009013676A/es active IP Right Grant
- 2008-06-13 AU AU2008302667A patent/AU2008302667B2/en not_active Ceased
- 2008-06-13 CA CA2692004A patent/CA2692004C/en not_active Expired - Fee Related
- 2008-06-16 CL CL2008001782A patent/CL2008001782A1/es unknown
- 2008-06-17 AR ARP080102569A patent/AR067850A1/es unknown
-
2009
- 2009-12-03 DO DO2009000272A patent/DOP2009000272A/es unknown
-
2010
- 2010-01-12 CO CO10002271A patent/CO6270184A2/es active IP Right Grant
-
2011
- 2011-06-07 US US13/154,923 patent/US20120010233A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
MX2009013676A (es) | 2010-06-01 |
CA2692004C (en) | 2013-04-09 |
CN101784274A (zh) | 2010-07-21 |
EP2166841A4 (en) | 2014-05-07 |
AU2008302667A1 (en) | 2009-03-26 |
WO2009038842A3 (en) | 2009-12-30 |
US20120010233A1 (en) | 2012-01-12 |
US8003692B2 (en) | 2011-08-23 |
WO2009038842A2 (en) | 2009-03-26 |
EP2166841A2 (en) | 2010-03-31 |
CA2692004A1 (en) | 2009-03-26 |
CL2008001782A1 (es) | 2008-11-03 |
US20090093519A1 (en) | 2009-04-09 |
AU2008302667B2 (en) | 2014-07-10 |
BRPI0813176A2 (pt) | 2014-12-30 |
CO6270184A2 (es) | 2011-04-20 |
DOP2009000272A (es) | 2010-02-15 |
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