AR046886A1 - Analogos de rifamicina y usos de los mismos. - Google Patents
Analogos de rifamicina y usos de los mismos.Info
- Publication number
- AR046886A1 AR046886A1 ARP040104623A ARP040104623A AR046886A1 AR 046886 A1 AR046886 A1 AR 046886A1 AR P040104623 A ARP040104623 A AR P040104623A AR P040104623 A ARP040104623 A AR P040104623A AR 046886 A1 AR046886 A1 AR 046886A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkaryl
- heteroaryl
- aryl
- alkylheteroaryl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/16—Peri-condensed systems
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
-
- 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
- A61P31/10—Antimycotics
-
- 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
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Heart & Thoracic Surgery (AREA)
- Virology (AREA)
- Pulmonology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
El presente se refiere a composición farmacéutica que los contiene y usos. Reivindicación 1: Un compuesto que tiene la fórmula (1), o una de sus sales farmacéuticamente aceptables, en donde: a) A es H, OH, O-(alquilo C1-6), O-(alcarilo C1-4), O- (arilo C6-12), O-(heteroarilo C1-9), u O-(alqheteroarilo C1-4); W es O, S o NR1, en donde R1 es H, alquilo C1-6, alcarilo C1-4 o alqheteroarilo C1-4; X es H o COR2, en donde R2 es alquilo C1-6, que puede estar sustituido con 1-5 grupos OH, O- (alquilo C3-7), que puede estar sustituido con 1-4 grupos OH, arilo C6-12, alcarilo C1-4, heteroarilo C1-9, o alqheteroarilo C1-4, en donde cada carbono del alquilo está unido a no más de un átomo de oxígeno; Y es H, Hal, u OR3, en donde R3 es alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4; R4 es OR5, SR5 o NR5R6, en donde R5 se define más abajo en relación con R7 y R6 es H, alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4, COR9, CO2R9, CONHR9, CSR9, COSR9, CSOR9, CSNHR9, SO2R9 o SO2NHR9, en donde R9 es alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo o alqheteroarilo C1-4; y Z es (CR11R12)nNR7R8, en donde n es 0 ó 1, R7 y R5 representan juntos un enlace o forman un enlace C1-4 sustituido o insustituido, R8 es H, alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4, COR10, CO2R10, CONHR10, CSR10, COSR10, CSOR10, CSNHR10, SO2R10 o SO2NHR10, en donde R10 es alquilo C1-6, arilo C6- 12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4 o R8 no existe y se forma un enlace doble entre N y un enlace de carbono C1 R5-R7, cada uno de R11 y R12 es, de modo independiente, H, alquilo C1-6, alcarilo C1-4 o alqheteroarilo C1-4 o R12 no existe y se forma un enlace doble entre N y el carbono que lleva R11; o b) A es H, OH, O-(alquilo C1-6), O-(alcarilo C1-4), O-(arilo C6-12), O-(heteroarilo C1-9), u O-(alqheteroarilo C1-4); W es O, S o NR1, en donde R1 es H, alquilo C1-6, alcarilo C1-4 o alqheteroarilo C1-4; X es H o COR2, en donde R2 es alquilo C1-6, que puede estar sustituido con 1-5 grupos OH, O-(alquilo C3-7), que puede estar sustituido con 1-4 grupos OH, arilo C6-12, alcarilo C1-4, heteroarilo C1-9, o alqheteroarilo C1-4, en donde cada carbono del alquilo está unido a no más de un átomo de oxígeno; Z es H, Hal, u OR3, en donde R3 es alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4; R4 es OR5, SR5 o NR5R6, en donde R5 se define más abajo en relación con R7 y R6 es H, alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4, COR9, CO2R9, CONHR9, CSR9, COSR9, CSOR9, CSNHR9, SO2R9 o SO2NHR9, en donde R9 es alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo o alqheteroarilo C1-4; y Y es (CR11R12)nNR7R8, en donde n es 0 ó 1, R7 y R5 representan juntos un enlace o forman un enlace C1-4 sustituido o insustituido, R8 es H, alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1- 9 o alqheteroarilo C1-4, COR10, CO2R10, CONHR10, CSR10, COSR10, CSOR10, CSNHR10, SO2R10 o SO2NHR10, en donde R10 es alquilo C1-6, arilo C6-12, alcarilo C1-4, heteroarilo C1-9 o alqheteroarilo C1-4 o R8 no existe y se forma un enlace doble entre N y un enlace de carbono C1 R5-R7, cada uno de R11 y R12 es, de modo independiente, H, alquilo C1-6, alcarilo C1-4 o alqheteroarilo C1-4 o R12 no existe y se forma un enlace doble entre N y el carbono que lleva R11.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US52873303P | 2003-12-10 | 2003-12-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR046886A1 true AR046886A1 (es) | 2005-12-28 |
Family
ID=34699896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040104623A AR046886A1 (es) | 2003-12-10 | 2004-12-10 | Analogos de rifamicina y usos de los mismos. |
Country Status (9)
Country | Link |
---|---|
US (2) | US7220738B2 (es) |
EP (1) | EP1697382A4 (es) |
JP (1) | JP2007513961A (es) |
KR (1) | KR20070015506A (es) |
AR (1) | AR046886A1 (es) |
AU (1) | AU2004298983A1 (es) |
CA (1) | CA2549001A1 (es) |
TW (1) | TW200529856A (es) |
WO (1) | WO2005058231A2 (es) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200418485A (en) * | 2002-09-23 | 2004-10-01 | Activbiotics Inc | Rifalazil compositions and therapeutic regimens |
AU2004268531A1 (en) * | 2003-08-22 | 2005-03-10 | Activbiotics, Inc. | Rifamycin analogs and uses thereof |
KR20070006698A (ko) | 2003-12-23 | 2007-01-11 | 액티브 바이오틱스 인코포레이티드 | 리파마이신 유사체 및 그의 용도 |
WO2007031933A2 (en) | 2005-09-12 | 2007-03-22 | Actelion Pharmaceuticals Ltd | Stable pharmaceutical composition comprising a pyrimidine-sulfamide |
WO2007070613A2 (en) * | 2005-12-14 | 2007-06-21 | Activbiotics, Incorporated | Rifamycin analogs and uses thereof |
CN101432044A (zh) * | 2006-04-28 | 2009-05-13 | 恩迪尼国际有限公司 | 光消毒装置和方法 |
WO2009064792A1 (en) * | 2007-11-16 | 2009-05-22 | Cumbre Pharmaceuticals Inc. | Quinolone carboxylic acid-substituted rifamycin derivatives |
WO2009142719A2 (en) * | 2008-05-19 | 2009-11-26 | Massachusetts Institute Of Technology | Tympanic membrane permeating ear drops and uses thereof |
US8586029B2 (en) * | 2008-06-04 | 2013-11-19 | Trustees Of Dartmouth College | Prevention or treatment of immune-relevant disease by modification of microfloral populations |
EP2330901A4 (en) * | 2008-09-17 | 2012-03-07 | Sphingomonas Res Partners L P | TREATMENT FOR LEUKEMIA AND IDIOPATHIC APLASTIC ANEMIA |
US20100311686A1 (en) * | 2009-06-03 | 2010-12-09 | Kasper Lloyd H | Nutraceutical composition and methods for preventing or treating multiple sclerosis |
US8580278B2 (en) | 2009-06-03 | 2013-11-12 | Trustees Of Dartmouth College | Nutraceutical composition and methods for preventing or treating multiple sclerosis |
EP2731617A4 (en) | 2011-07-12 | 2015-07-01 | Brigham & Womens Hospital | LIPID-CONTAINING PSA COMPOSITIONS, METHODS OF ISOLATION AND METHODS OF USING SAME |
CA2858372A1 (en) * | 2011-11-10 | 2013-05-16 | Lankenau Institute For Medical Research | Compositions and methods for the prevention of microbial infections |
AU2016304585B2 (en) | 2015-08-05 | 2023-04-06 | Children's Medical Center Corporation | Compositions with permeation enhancers for drug delivery |
EP3337321A4 (en) | 2015-08-19 | 2019-07-17 | President and Fellows of Harvard College | LIPIDED PSA COMPOSITIONS AND METHOD |
US11491181B2 (en) | 2016-07-15 | 2022-11-08 | President And Fellows Of Harvard College | Glycolipid compositions and methods of use |
CN110467629B (zh) * | 2018-05-09 | 2022-04-08 | 上海迪诺医药科技有限公司 | 苯醌衍生物、其药物组合物及应用 |
Family Cites Families (30)
Publication number | Priority date | Publication date | Assignee | Title |
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NL130099C (es) * | 1963-10-11 | |||
JPS58225093A (ja) | 1982-06-25 | 1983-12-27 | Kanegafuchi Chem Ind Co Ltd | ベンゾチアジノリフアマイシン誘導体およびその製造法 |
JPS59231092A (ja) | 1983-06-11 | 1984-12-25 | Kanebo Ltd | フエノチアジン型リフアマイシンおよびその医薬用途 |
US4690919A (en) * | 1984-01-04 | 1987-09-01 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Benzoxazinorifamycin derivative, process for preparing the same and antibacterial agent containing the same |
JPS6122090A (ja) | 1984-07-09 | 1986-01-30 | Kanebo Ltd | アミノ置換フエノチアジン型リフアマイシンおよびその医薬用途 |
JPS62240688A (ja) | 1986-04-12 | 1987-10-21 | Kanegafuchi Chem Ind Co Ltd | ヒドロキシメチル基を有するアミノベンゾキサジノおよびアミノベンゾチアジノリフアマイシン誘導体 |
JPS62242687A (ja) | 1986-04-15 | 1987-10-23 | Kanegafuchi Chem Ind Co Ltd | 置換ベンゾキサジノおよび置換ベンゾチアジノリフアマイシン誘導体 |
JP2544375B2 (ja) * | 1986-07-14 | 1996-10-16 | 鐘淵化学工業株式会社 | アルキル置換ベンゾキサジノリフアマイシン誘導体 |
JPS6335579A (ja) | 1986-07-31 | 1988-02-16 | Kanegafuchi Chem Ind Co Ltd | 含硫ベンゾキサジノリフアマイシン誘導体 |
JPS6335578A (ja) * | 1986-07-31 | 1988-02-16 | Kanegafuchi Chem Ind Co Ltd | ベンゾキサジノまたはベンゾチアジノリフアマイシン誘導体 |
JPS63233987A (ja) | 1987-03-23 | 1988-09-29 | Kanegafuchi Chem Ind Co Ltd | 4′−tert−ブチルベンゾキサジノリフアマイシン誘導体 |
DE68924722T2 (de) * | 1988-03-18 | 1996-04-18 | Kanegafuchi Chemical Ind | Substituiertes Benzoxazinorifamycinderivat, Verfahren zur Herstellung und dieses Derivat enthaltende Bakterizidmittel. |
CA1304363C (en) * | 1988-11-01 | 1992-06-30 | Takehiko Yamane | 3'-hydroxybenzoxazinorifamycin derivative, process for preparing the same and antibacterial agent containing the same |
WO1994008709A1 (en) * | 1992-10-09 | 1994-04-28 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Production method for fine granulate |
US5981522A (en) | 1995-09-01 | 1999-11-09 | Kaneka Corporation | Treatment of disease caused by infection of Helicobacter |
WO1997009047A1 (fr) | 1995-09-01 | 1997-03-13 | Kaneka Corporation | Medicament contre des maladies causees par une infection par helicobacter |
JP3963976B2 (ja) * | 1995-12-08 | 2007-08-22 | 株式会社カネカ | クラミジア感染症治療剤 |
JPH10258509A (ja) * | 1997-03-19 | 1998-09-29 | Fujitsu Ltd | インクジェットヘッド及びその製造方法 |
US6486161B1 (en) * | 1998-07-29 | 2002-11-26 | Kaneka Corporation | Use of rifamycin derivative for treating mastitis in a domestic animal |
US6316433B1 (en) * | 1998-12-18 | 2001-11-13 | Kaneka Corporation | Method for treatment of bacterial infections with once or twice-weekly administered rifalazil |
AU2002368203A1 (en) * | 2001-09-06 | 2004-05-04 | Activbiotics, Inc. | Antimicrobial agents and uses thereof |
WO2003045319A2 (en) * | 2001-11-21 | 2003-06-05 | Activbiotics, Inc. | Targeted therapeutics and uses thereof |
WO2003051299A2 (en) * | 2001-12-13 | 2003-06-26 | Activbiotics, Inc. | Sulfhydryl rifamycins and uses thereof |
US20040014750A1 (en) * | 2001-12-13 | 2004-01-22 | Michaelis Arthur F. | Metal complexes and formulations of rifamycin analogues and uses thereof |
US20040077533A1 (en) * | 2002-05-23 | 2004-04-22 | Sayada Chalom B. | Methods and compositions for treating bacterial infections and diseases associated therewith |
WO2003099217A2 (en) * | 2002-05-23 | 2003-12-04 | Activbiotics, Inc. | Methods of treating bacterial infections and diseases associated therewith |
WO2003101445A1 (en) * | 2002-06-03 | 2003-12-11 | Activbiotics, Inc. | Intravenous rifalazil formulation and methods of use thereof |
AU2003268330A1 (en) * | 2002-08-29 | 2004-03-19 | Activbiotics, Inc. | Methods and reagents for treating infections of clostridium difficile and diseases associated therewith |
AU2004268531A1 (en) * | 2003-08-22 | 2005-03-10 | Activbiotics, Inc. | Rifamycin analogs and uses thereof |
KR20070006698A (ko) | 2003-12-23 | 2007-01-11 | 액티브 바이오틱스 인코포레이티드 | 리파마이신 유사체 및 그의 용도 |
-
2004
- 2004-12-09 EP EP04813534A patent/EP1697382A4/en not_active Withdrawn
- 2004-12-09 JP JP2006543971A patent/JP2007513961A/ja not_active Withdrawn
- 2004-12-09 KR KR1020067013721A patent/KR20070015506A/ko not_active Application Discontinuation
- 2004-12-09 CA CA002549001A patent/CA2549001A1/en not_active Abandoned
- 2004-12-09 AU AU2004298983A patent/AU2004298983A1/en not_active Abandoned
- 2004-12-09 WO PCT/US2004/041222 patent/WO2005058231A2/en active Application Filing
- 2004-12-09 US US11/008,597 patent/US7220738B2/en not_active Expired - Fee Related
- 2004-12-10 AR ARP040104623A patent/AR046886A1/es unknown
- 2004-12-10 TW TW093138355A patent/TW200529856A/zh unknown
-
2007
- 2007-05-17 US US11/804,141 patent/US7494991B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US7494991B2 (en) | 2009-02-24 |
KR20070015506A (ko) | 2007-02-05 |
AU2004298983A1 (en) | 2005-06-30 |
US20050137189A1 (en) | 2005-06-23 |
US7220738B2 (en) | 2007-05-22 |
CA2549001A1 (en) | 2005-06-30 |
EP1697382A4 (en) | 2008-11-05 |
US20070238747A1 (en) | 2007-10-11 |
WO2005058231A2 (en) | 2005-06-30 |
TW200529856A (en) | 2005-09-16 |
JP2007513961A (ja) | 2007-05-31 |
WO2005058231A3 (en) | 2005-12-22 |
EP1697382A2 (en) | 2006-09-06 |
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