CN1282316A - 用作神经氨酸酶抑制剂的取代环戊烷和环戊烯化合物 - Google Patents
用作神经氨酸酶抑制剂的取代环戊烷和环戊烯化合物 Download PDFInfo
- Publication number
- CN1282316A CN1282316A CN98812351A CN98812351A CN1282316A CN 1282316 A CN1282316 A CN 1282316A CN 98812351 A CN98812351 A CN 98812351A CN 98812351 A CN98812351 A CN 98812351A CN 1282316 A CN1282316 A CN 1282316A
- Authority
- CN
- China
- Prior art keywords
- compound
- acid
- ethyl
- amino
- butyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- 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
- A61P31/12—Antivirals
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/46—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C229/48—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms of the same non-condensed ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/47—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C247/00—Compounds containing azido groups
- C07C247/14—Compounds containing azido groups with azido groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/24—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/16—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/20—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
- C07C279/24—Y being a hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
- C07C309/66—Methanesulfonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
- C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
- C07C323/59—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton with acylated amino groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/08—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Virology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pyridine Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6995697P | 1997-12-17 | 1997-12-17 | |
US60/069,956 | 1997-12-17 | ||
US8525298P | 1998-05-13 | 1998-05-13 | |
US60/085,252 | 1998-05-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1282316A true CN1282316A (zh) | 2001-01-31 |
Family
ID=26750600
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN98812351A Pending CN1282316A (zh) | 1997-12-17 | 1998-12-17 | 用作神经氨酸酶抑制剂的取代环戊烷和环戊烯化合物 |
Country Status (28)
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009021404A1 (fr) | 2007-08-14 | 2009-02-19 | Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. | Hydrates d'acide (1s, 2s, 3s, 4r)-3-[(1s)-1-acétylamino-2-éthylbutyl]-4-guanidino-2-hydroxylcyclopentyl-1-carboxylique et leurs utilisations pharmaceutiques |
CN101538228B (zh) * | 2008-03-21 | 2012-05-30 | 北京普世康医药技术有限公司 | 抗流感和禽流感病毒药物化合物帕拉米韦的合成方法 |
CN102584637A (zh) * | 2011-01-17 | 2012-07-18 | 天津药物研究院 | 帕拉米韦水合物晶体、制备方法、药用组合物及其用途 |
CN102603577A (zh) * | 2011-01-19 | 2012-07-25 | 董慧珍 | 一种抗流感和禽流感药物的衍生物及其用途 |
CN102757365A (zh) * | 2011-04-29 | 2012-10-31 | 上海泓博智源医药技术有限公司 | 一种制备帕拉米韦关键中间体的新方法 |
CN102964267A (zh) * | 2011-09-01 | 2013-03-13 | 中山大学 | 一种具有流感病毒神经氨酸酶抑制活性的环己烯化合物及其制备方法以及其应用 |
CN101486664B (zh) * | 2008-12-31 | 2013-09-04 | 北京大学深圳研究生院 | 用作流感病毒神经氨酸酶抑制剂的多取代五元环小分子化合物 |
CN104387288A (zh) * | 2014-11-25 | 2015-03-04 | 广东东阳光药业有限公司 | 作为神经氨酸酶抑制剂的化合物及其在药物中的应用 |
CN104496839A (zh) * | 2014-12-03 | 2015-04-08 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN104496838A (zh) * | 2014-12-03 | 2015-04-08 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN105294589A (zh) * | 2014-06-18 | 2016-02-03 | 朱靖华 | 一种抗病毒药物及其制备方法 |
CN106220515A (zh) * | 2016-08-12 | 2016-12-14 | 郸城巨鑫生物科技有限公司 | 一种(1r,4s)‑1‑氨基‑4‑羟甲基‑2‑环戊烯盐酸盐的合成方法 |
CN108026049A (zh) * | 2015-08-10 | 2018-05-11 | 阿尔泽恩股份有限公司 | 用于治疗和预防神经退化性病症的组合物和方法 |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20000016669A (ko) | 1996-06-14 | 2000-03-25 | 몽고메리 죤 에이 | 뉴라미니다제 저해제로 유용한 치환된 시클로펜탄 화합물 |
HUP0100142A3 (en) * | 1997-12-17 | 2002-01-28 | Biocryst Pharmaceuticals Inc B | Substituted cyclopentane and cyclopentene compounds useful as neuraminidase inhibitors |
EP1087938A1 (en) * | 1998-04-23 | 2001-04-04 | Abbott Laboratories | Inhibitors of neuraminidases |
US6455571B1 (en) | 1998-04-23 | 2002-09-24 | Abbott Laboratories | Inhibitors of neuraminidases |
US6518305B1 (en) * | 1998-04-23 | 2003-02-11 | Abbott Laboratories | Five-membered carbocyclic and heterocyclic inhibitors of neuraminidases |
AU1520300A (en) | 1998-11-05 | 2000-05-29 | Biocryst Pharmaceuticals, Inc. | New cyclopentane and cyclopentene compounds and use for detecting influenza virus |
CZ20014656A3 (cs) * | 1999-06-28 | 2002-11-13 | Biocryst Pharmaceuticals, Inc. | Způsob přípravy (-)-(1S,4R) N-chráněných 4-amino-2-cyklopenten-1-karboxylát esterů |
BR0011902A (pt) * | 1999-06-28 | 2002-03-19 | Biocryst Pharm Inc | Compostos derivados de ciclopentano substituìdo, respectivos processos de preparação e formas cristalinas |
AU6056600A (en) * | 1999-06-28 | 2001-01-31 | Biocryst Pharmaceuticals, Inc. | Preparation of substituted cyclopentane and cyclopentene compounds and certain intermediates |
US6762316B1 (en) * | 1999-06-28 | 2004-07-13 | Biocryst Pharmaceuticals, Inc. | Preparation of substituted cyclopentane and cyclopentene compounds and certain intermediates |
US6593314B1 (en) | 1999-10-19 | 2003-07-15 | Abbott Laboratories | Neuraminidase inhibitors |
US6627396B1 (en) | 1999-10-28 | 2003-09-30 | The Regents Of The University Of California | Influenza sensor |
WO2001062242A1 (en) * | 2000-02-24 | 2001-08-30 | Biocryst Pharmaceuticals, Inc. | Prodrugs of substituted cyclopentane and cyclopentene compounds useful as neuraminidase inhibitors |
ES2317889T3 (es) * | 2000-03-01 | 2009-05-01 | Janssen Pharmaceutica Nv | Derivados de tiazolilo 2,4-disustituido. |
AU2001252578A1 (en) * | 2000-04-25 | 2001-11-07 | Sankyo Company Limited | Preventives for influenza |
GB0015324D0 (en) * | 2000-06-22 | 2000-08-16 | Biota Scient Management | Medicaments |
AUPR001000A0 (en) | 2000-09-08 | 2000-10-05 | Biota Scientific Management Pty Ltd | Novel chemical compounds and their use |
WO2002032885A1 (fr) * | 2000-10-18 | 2002-04-25 | Kuraray Co., Ltd. | Preparation d'esters d'acide amino-2-aza-1-oxybicyclo[3.3.0]oct-2-ene-6-carboxylique 4-n substitues et preparation de leurs produits intermediaires |
WO2002092555A1 (fr) * | 2001-05-11 | 2002-11-21 | Sankyo Company, Limited | Derives d'acides sialiques |
EP1831235B1 (en) | 2004-12-16 | 2013-02-20 | The Regents of The University of California | Lung-targeted drugs |
WO2007087056A2 (en) * | 2006-01-13 | 2007-08-02 | Scolr Pharma, Inc. | Peramivir derivative for oral administration |
WO2007095218A1 (en) * | 2006-02-13 | 2007-08-23 | Biocryst Pharmaceuticals, Inc. | Intravenous antiviral treatments |
US20070203241A1 (en) * | 2006-02-13 | 2007-08-30 | Babu Yarlagadda S | Antiviral treatments |
MX2008013140A (es) * | 2006-04-12 | 2009-02-12 | Biocryst Pharm Inc | Tratamientos antivirales intramusculares. |
US20070244193A1 (en) * | 2006-04-12 | 2007-10-18 | Babu Yarlagadda S | Intramuscular antiviral treatments |
CN100432047C (zh) * | 2006-07-03 | 2008-11-12 | 华南农业大学 | 一种抗流感及禽流感病毒药物帕拉米韦的合成方法 |
US8227425B2 (en) | 2007-01-23 | 2012-07-24 | Therapicon Srl | Antiviral compounds |
US20080194801A1 (en) * | 2007-02-14 | 2008-08-14 | Swanson Basil I | Robust multidentate ligands for diagnosis and anti-viral drugs for influenza and related viruses |
KR20100066475A (ko) | 2007-08-02 | 2010-06-17 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | E1 활성화 효소 억제제의 합성 방법 |
JP5849328B2 (ja) * | 2007-11-05 | 2016-01-27 | アラ ワイ ファーマ インコーポレイテッド | 経口投与極性剤の生物利用能を増強する製剤 |
AU2014200052B2 (en) * | 2007-11-05 | 2016-01-07 | Ala Wai Pharma, Inc. | Formulations for enhanced bioavailability of orally administered polar agents |
WO2010131054A1 (en) | 2009-05-15 | 2010-11-18 | Bradford Pharma Limited | Redox drug derivatives |
IT1396620B1 (it) | 2009-11-25 | 2012-12-14 | Therapicon Srl | Analoghi chimerici |
IN2012CN10271A (US06559137-20030506-C00021.png) | 2010-05-27 | 2015-04-10 | Reddy’S Lab Ltd Dr | |
WO2012145932A1 (en) * | 2011-04-29 | 2012-11-01 | Pharmaresources (Shanghai) Co., Ltd. | A novel process for the preparation of peramivir and intermediates thereof |
CN102863359B (zh) * | 2012-05-16 | 2014-05-07 | 常州制药厂有限公司 | 一种抗流感药物的合成方法 |
CN102702033A (zh) * | 2012-06-11 | 2012-10-03 | 天津泰普药品科技发展有限公司 | 无定型帕拉米韦及其制备方法与药物组合物 |
AU2013340559B2 (en) | 2012-10-29 | 2018-03-15 | Cipla Limited | Antiviral phosphonate analogues and process for preparation thereof |
RS57796B1 (sr) | 2013-03-15 | 2018-12-31 | Univ California | Diestri acikličnog nukleozid fosfonata |
EP2996685B1 (en) * | 2013-05-14 | 2019-03-27 | Biocryst Pharmaceuticals, Inc. | Anti-influenza compositions and methods |
SG11201701957XA (en) | 2014-09-15 | 2017-04-27 | Univ California | Nucleotide analogs |
CN104496857B (zh) * | 2014-12-10 | 2016-10-12 | 广东东阳光药业有限公司 | 作为神经氨酸酶抑制剂的化合物及其在药物中的应用 |
CN105198827A (zh) * | 2015-04-13 | 2015-12-30 | 广州南新制药有限公司 | 一种帕拉米韦中间体的合成方法 |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT979736B (it) | 1972-03-07 | 1974-09-30 | Ethyl Corp | Detersivo contenente un sequestran te e relativo metodo di impiego |
US4089897A (en) * | 1976-05-10 | 1978-05-16 | Minnesota Mining And Manufacturing Company | Geminal prostaglandin analogs |
US4426391A (en) | 1982-09-15 | 1984-01-17 | Merck & Co., Inc. | [(Alkoxycarbonyl)oxy]alkyl esters of methyldopa |
JPS59163365A (ja) | 1983-03-08 | 1984-09-14 | Ono Pharmaceut Co Ltd | プロスタグランジン類似化合物 |
EP0130119B1 (en) | 1983-06-23 | 1988-11-09 | Merck & Co. Inc. | (acyloxyalkoxy) carbonyl derivatives as bioreversible prodrug moieties for primary and secondary amine functions in drugs, their preparation and pharmaceutical compositions containing said derivatives |
ZA878096B (en) * | 1986-11-03 | 1988-04-26 | Merrell Dow Pharmaceuticals Inc. | Esters of hexahydro-8-hydroxy-2,6-methano-2h-quinolizin-3(4h)-one and related compounds |
JPS63179835A (ja) | 1986-12-20 | 1988-07-23 | メルク・パテント・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | シクロペンタン誘導体 |
US5362728A (en) * | 1990-02-02 | 1994-11-08 | Schering Corporation | 4,5-bridged-2,3,4,5-tetrahydro-1H-3-benzazepine-7-ols and derivatives and compositions and methods employing such compounds |
WO1992016541A1 (en) | 1991-03-12 | 1992-10-01 | Mect Corporation | Synthesis of sialic acid and synthetic intermediate therefor |
JP2951765B2 (ja) | 1991-09-10 | 1999-09-20 | 三共株式会社 | エナミノエステル類およびその製法 |
AU673824B2 (en) * | 1992-05-29 | 1996-11-28 | Bayer Aktiengesellschaft | Cyclopentane- and -pentene-beta-amino acids |
JPH07145120A (ja) * | 1993-11-25 | 1995-06-06 | Kuraray Co Ltd | cis−4−アミノ−2−シクロペンテン−1−カルボン酸の製造法 |
JPH09509664A (ja) * | 1994-02-25 | 1997-09-30 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 4−n−置換シアル酸およびそれらのシアロシド類 |
US5453533A (en) * | 1994-04-14 | 1995-09-26 | The University Of Alabama At Birmingham | Inhibitors of influenza virus neuraminidase and methods of making and using the same |
US5789434A (en) * | 1994-11-15 | 1998-08-04 | Bayer Corporation | Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors |
DK0759917T3 (da) * | 1995-02-27 | 2000-07-31 | Gilead Sciences Inc | Hidtil ukendte selektive inhibitorer af virale eller bakterielle neuraminidaser |
CA2176414A1 (en) | 1995-05-18 | 1996-11-19 | S. David Kimball | Acyl guanidine and amidine prodrugs |
JP4162712B2 (ja) * | 1995-05-19 | 2008-10-08 | バイオタ、サイアンティフィック、マネージメント、プロプライエタリ、リミテッド | 6−カルボキサミドジヒドロピラン誘導体 |
GB9516276D0 (en) * | 1995-08-08 | 1995-10-11 | Biota Scient Management | Chemical compounds |
KR20000016669A (ko) * | 1996-06-14 | 2000-03-25 | 몽고메리 죤 에이 | 뉴라미니다제 저해제로 유용한 치환된 시클로펜탄 화합물 |
CA2279927A1 (en) | 1997-02-06 | 1998-08-13 | Merck & Co., Inc. | Fibrinogen receptor antagonist prodrugs |
IL134691A0 (en) * | 1997-09-17 | 2001-04-30 | Gilead Sciences Inc | Compounds containing six-membered rings, processes for their preparation, and their use as medicaments |
HUP0100142A3 (en) * | 1997-12-17 | 2002-01-28 | Biocryst Pharmaceuticals Inc B | Substituted cyclopentane and cyclopentene compounds useful as neuraminidase inhibitors |
EP1087938A1 (en) | 1998-04-23 | 2001-04-04 | Abbott Laboratories | Inhibitors of neuraminidases |
CA2329422A1 (en) | 1998-04-23 | 1999-10-28 | Abbott Laboratories | Pyrrolidines as inhibitors of neuraminidases |
-
1998
- 1998-12-17 HU HU0100142A patent/HUP0100142A3/hu unknown
- 1998-12-17 CA CA002315262A patent/CA2315262C/en not_active Expired - Lifetime
- 1998-12-17 WO PCT/US1998/026871 patent/WO1999033781A1/en not_active Application Discontinuation
- 1998-12-17 JP JP2000526468A patent/JP4102022B2/ja not_active Expired - Lifetime
- 1998-12-17 AR ARP980106457A patent/AR016162A1/es not_active Application Discontinuation
- 1998-12-17 IL IL13681298A patent/IL136812A0/xx unknown
- 1998-12-17 CN CN98812351A patent/CN1282316A/zh active Pending
- 1998-12-17 EP EP98966003.0A patent/EP1040094B9/en not_active Expired - Lifetime
- 1998-12-17 PT PT98966003T patent/PT1040094E/pt unknown
- 1998-12-17 BR BR9813480-9A patent/BR9813480A/pt not_active IP Right Cessation
- 1998-12-17 DK DK98966003T patent/DK1040094T3/da active
- 1998-12-17 ZA ZA9811595A patent/ZA9811595B/xx unknown
- 1998-12-17 ES ES98966003T patent/ES2324746T3/es not_active Expired - Lifetime
- 1998-12-17 RO ROA200000635A patent/RO121815B1/ro unknown
- 1998-12-17 US US09/555,131 patent/US6562861B1/en not_active Expired - Lifetime
- 1998-12-17 SK SK871-2000A patent/SK8712000A3/sk unknown
- 1998-12-17 KR KR1020007006646A patent/KR20010024743A/ko not_active Application Discontinuation
- 1998-12-17 PL PL341431A patent/PL196674B1/pl unknown
- 1998-12-17 AT AT98966003T patent/ATE425955T1/de active
- 1998-12-17 AU AU22001/99A patent/AU2200199A/en not_active Abandoned
- 1998-12-17 DE DE69840674T patent/DE69840674D1/de not_active Expired - Lifetime
- 1998-12-17 SI SI9830919T patent/SI1040094T1/sl unknown
-
2000
- 2000-06-15 NO NO20003084A patent/NO20003084L/no not_active Application Discontinuation
-
2008
- 2008-02-05 JP JP2008025550A patent/JP5118502B2/ja not_active Expired - Lifetime
-
2009
- 2009-06-16 CY CY20091100635T patent/CY1109153T1/el unknown
-
2011
- 2011-08-12 JP JP2011177226A patent/JP5709688B2/ja not_active Expired - Lifetime
-
2018
- 2018-08-30 CY CY2018023C patent/CY2018023I1/el unknown
- 2018-09-04 BE BE2018C032C patent/BE2018C032I2/fr unknown
- 2018-09-05 FR FR18C1037C patent/FR18C1037I2/fr active Active
- 2018-09-13 LT LTPA2018513C patent/LTC1040094I2/lt unknown
- 2018-09-20 NL NL300952C patent/NL300952I2/nl unknown
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009021404A1 (fr) | 2007-08-14 | 2009-02-19 | Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. | Hydrates d'acide (1s, 2s, 3s, 4r)-3-[(1s)-1-acétylamino-2-éthylbutyl]-4-guanidino-2-hydroxylcyclopentyl-1-carboxylique et leurs utilisations pharmaceutiques |
CN101538228B (zh) * | 2008-03-21 | 2012-05-30 | 北京普世康医药技术有限公司 | 抗流感和禽流感病毒药物化合物帕拉米韦的合成方法 |
CN101486664B (zh) * | 2008-12-31 | 2013-09-04 | 北京大学深圳研究生院 | 用作流感病毒神经氨酸酶抑制剂的多取代五元环小分子化合物 |
CN102584637A (zh) * | 2011-01-17 | 2012-07-18 | 天津药物研究院 | 帕拉米韦水合物晶体、制备方法、药用组合物及其用途 |
CN102603577A (zh) * | 2011-01-19 | 2012-07-25 | 董慧珍 | 一种抗流感和禽流感药物的衍生物及其用途 |
CN102757365A (zh) * | 2011-04-29 | 2012-10-31 | 上海泓博智源医药技术有限公司 | 一种制备帕拉米韦关键中间体的新方法 |
CN102757365B (zh) * | 2011-04-29 | 2013-10-30 | 上海泓博智源医药技术有限公司 | 一种制备帕拉米韦关键中间体的方法 |
CN102964267A (zh) * | 2011-09-01 | 2013-03-13 | 中山大学 | 一种具有流感病毒神经氨酸酶抑制活性的环己烯化合物及其制备方法以及其应用 |
CN102964267B (zh) * | 2011-09-01 | 2015-06-10 | 中山大学 | 一种具有流感病毒神经氨酸酶抑制活性的环己烯化合物及其制备方法以及其应用 |
CN105294589A (zh) * | 2014-06-18 | 2016-02-03 | 朱靖华 | 一种抗病毒药物及其制备方法 |
CN105294589B (zh) * | 2014-06-18 | 2017-06-30 | 朱靖华 | 一种抗病毒药物及其制备方法 |
CN104387288A (zh) * | 2014-11-25 | 2015-03-04 | 广东东阳光药业有限公司 | 作为神经氨酸酶抑制剂的化合物及其在药物中的应用 |
CN104496838A (zh) * | 2014-12-03 | 2015-04-08 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN104496838B (zh) * | 2014-12-03 | 2016-04-20 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN104496839B (zh) * | 2014-12-03 | 2016-04-20 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN104496839A (zh) * | 2014-12-03 | 2015-04-08 | 广东东阳光药业有限公司 | 取代环丁烷类神经氨酸酶抑制剂及其使用方法和用途 |
CN108026049A (zh) * | 2015-08-10 | 2018-05-11 | 阿尔泽恩股份有限公司 | 用于治疗和预防神经退化性病症的组合物和方法 |
US11053192B2 (en) | 2015-08-10 | 2021-07-06 | Alzheon, Inc. | Compositions and methods for treating and preventing neurodegenerative disorders |
CN108026049B (zh) * | 2015-08-10 | 2021-08-31 | 阿尔泽恩股份有限公司 | 用于治疗和预防神经退化性病症的组合物和方法 |
CN106220515A (zh) * | 2016-08-12 | 2016-12-14 | 郸城巨鑫生物科技有限公司 | 一种(1r,4s)‑1‑氨基‑4‑羟甲基‑2‑环戊烯盐酸盐的合成方法 |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1282316A (zh) | 用作神经氨酸酶抑制剂的取代环戊烷和环戊烯化合物 | |
CN1154650C (zh) | 三唑并[4,5-d]嘧啶类化合物、其制备、用途和含有其的药物组合物 | |
CN1067683C (zh) | 取代的吗啉衍生物及其作为治疗剂的用途 | |
CN1207288C (zh) | 逆病毒蛋白酶抑制化合物 | |
CN1114596C (zh) | 联苯基衍生物 | |
CN1305839C (zh) | 苯基甘氨酸衍生物 | |
CN1046268C (zh) | 二氢吲哚-2-酮衍生物 | |
CN1324025C (zh) | 作为ccr5调节剂的托烷衍生物 | |
CN1214011C (zh) | 作为整联蛋白拮抗剂的间-氮杂环氨基苯甲酸化合物及其衍生物 | |
CN1571786A (zh) | 烷基醚衍生物或其盐 | |
CN1227466A (zh) | 用作神经氨酸酶抑制剂的取代环戊烷化合物 | |
CN1774419A (zh) | 制备吡咯烷羧酸类化合物的方法和中间体 | |
CN1439006A (zh) | 具有抗细菌、抗真菌或抗肿瘤活性的新的化合物 | |
CN1950343A (zh) | 胺系碱性化合物及其用途 | |
CN1832948A (zh) | 1-烷基-1-氮鎓双环[2.2.2]辛烷氨基甲酸酯衍生物及其用作蕈毒碱受体拮抗剂的用途 | |
CN1107839A (zh) | 甲酰胺类化合物 | |
CN1330637A (zh) | 用于治疗炎性疾病的化合物 | |
CN1358171A (zh) | 包含氨基氧基的化合价平台分子 | |
CN1533388A (zh) | 取代的哌嗪化合物及其作为脂肪酸氧化抑制剂的应用 | |
CN1774245A (zh) | 用于视网膜神经疾病的含有烷基醚衍生物或其盐的预防剂/治疗剂 | |
CN1062536A (zh) | 从3-氯-2-氯甲基-1-丙烯衍生的逆转录酶病毒蛋白酶抑制剂 | |
CN1226243A (zh) | 苯并二氢吡喃衍生物 | |
CN1054071A (zh) | 口服的活性肾素抑制剂 | |
CN1254334A (zh) | 新颖的对苯二甲酰胺衍生物 | |
CN1035509A (zh) | 头孢菌素类衍生物及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: GR Ref document number: 1017194 Country of ref document: HK |
|
REG | Reference to a national code |
Ref country code: HK Ref legal event code: WD Ref document number: 1034506 Country of ref document: HK |