TR200002860T2 - Bir antiviral benzimidazol terkibin yeni kristal formları. - Google Patents
Bir antiviral benzimidazol terkibin yeni kristal formları.Info
- Publication number
- TR200002860T2 TR200002860T2 TR2000/02860T TR200002860T TR200002860T2 TR 200002860 T2 TR200002860 T2 TR 200002860T2 TR 2000/02860 T TR2000/02860 T TR 2000/02860T TR 200002860 T TR200002860 T TR 200002860T TR 200002860 T2 TR200002860 T2 TR 200002860T2
- Authority
- TR
- Turkey
- Prior art keywords
- crystal forms
- new crystal
- benzimidazole composition
- antiviral
- antiviral benzimidazole
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/052—Imidazole radicals
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
-
- 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
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
Bu bulus 5,6-dikloro-2-(izopropilamino)-1-B-L-ribofuranosil-1H- benzimidazol'un fiziksel formlarina, farmasötik bilesimlere ve tibbi terapide kullanimlarina iliskindir.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9807354.7A GB9807354D0 (en) | 1998-04-07 | 1998-04-07 | Antiviral compound |
Publications (1)
Publication Number | Publication Date |
---|---|
TR200002860T2 true TR200002860T2 (tr) | 2000-12-21 |
Family
ID=10829932
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TR2000/02860T TR200002860T2 (tr) | 1998-04-07 | 1999-04-01 | Bir antiviral benzimidazol terkibin yeni kristal formları. |
Country Status (28)
Country | Link |
---|---|
US (9) | US6469160B1 (tr) |
EP (1) | EP1071693B1 (tr) |
JP (1) | JP2002510703A (tr) |
KR (1) | KR20010074472A (tr) |
CN (1) | CN1303390A (tr) |
AP (1) | AP2000001947A0 (tr) |
AT (1) | ATE261452T1 (tr) |
AU (1) | AU752877B2 (tr) |
BR (1) | BR9909474A (tr) |
CA (1) | CA2327494C (tr) |
DE (1) | DE69915461T2 (tr) |
EA (1) | EA002970B1 (tr) |
EE (1) | EE04120B1 (tr) |
ES (1) | ES2216503T3 (tr) |
GB (1) | GB9807354D0 (tr) |
HR (1) | HRP20000669A2 (tr) |
HU (1) | HUP0101669A3 (tr) |
ID (1) | ID27109A (tr) |
IL (1) | IL138697A0 (tr) |
IS (1) | IS5640A (tr) |
NO (1) | NO20005005L (tr) |
NZ (1) | NZ507173A (tr) |
PL (1) | PL343397A1 (tr) |
SK (1) | SK14832000A3 (tr) |
TR (1) | TR200002860T2 (tr) |
WO (1) | WO1999051618A1 (tr) |
YU (1) | YU60900A (tr) |
ZA (1) | ZA200005153B (tr) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9807354D0 (en) * | 1998-04-07 | 1998-06-03 | Glaxo Group Ltd | Antiviral compound |
GB9807355D0 (en) | 1998-04-07 | 1998-06-03 | Glaxo Group Ltd | Antiviral compound |
GB0008939D0 (en) | 2000-04-11 | 2000-05-31 | Glaxo Group Ltd | Process for preparing substituted benzimidazole compounds |
NZ536497A (en) | 2002-05-16 | 2006-08-31 | Tibotec Pharm Ltd | Pseudopolymorphic forms of a HIV protease inhibitor and their use as a medicament |
ES2370829T3 (es) * | 2004-06-02 | 2011-12-23 | Sandoz Ag | Producto intermedio de meropenem en forma cristalina. |
US7750153B2 (en) * | 2005-07-05 | 2010-07-06 | Hetero Drugs Limited | Process for the preparation of didanosine using novel intermediates |
WO2007052289A2 (en) * | 2005-07-22 | 2007-05-10 | Rubicon Research Pvt Ltd. | Novel dispersible tablet composition |
EP1928826B1 (en) * | 2005-09-21 | 2013-04-24 | 4Sc Ag | Sulphonylpyrrole hydrochloride salts as histone deacetylases inhibitors |
EA014905B1 (ru) * | 2005-10-31 | 2011-02-28 | Янссен Фармацевтика Н.В. | Новый способ получения пиперазинильных производных бензамида |
MX2008016008A (es) * | 2006-06-16 | 2009-01-16 | Lundbeck & Co As H | Formas cristalinas de 4-[2-(4-metilfenilsulfonil)-fenil] piperidina con inhibicion combinada de la recaptacion de serotonina y norepinefrina para el tratamiento del dolor neuropatico. |
US7919598B2 (en) * | 2006-06-28 | 2011-04-05 | Bristol-Myers Squibb Company | Crystal structures of SGLT2 inhibitors and processes for preparing same |
BRPI0717394A2 (pt) * | 2006-10-27 | 2013-10-15 | Signal Pharm Llc | Forma cristalina, composição farmacêutica, forma de dosagem unitária única, método para tratar ou prevenir uma doença ou condição, e, processo para preparar um composto |
EP2085397A1 (en) * | 2008-01-21 | 2009-08-05 | Esteve Quimica, S.A. | Crystalline form of abacavir |
US7935817B2 (en) * | 2008-03-31 | 2011-05-03 | Apotex Pharmachem Inc. | Salt form and cocrystals of adefovir dipivoxil and processes for preparation thereof |
AR071318A1 (es) * | 2008-04-15 | 2010-06-09 | Basilea Pharmaceutica Ag | Benzhidril ester del acido (6r,7r)-7-{2-(5-amino-[1,2,4]tiadiazol-3-il)-2-[(z)-tritiloxiimino]-acetilamino}-3-[(r)-1'-terc-butoxicarbonil-2-oxo-[1,3']bipirrolidinil-(3e)-ilidenometil]-8-oxo-5-tia-1-aza-biciclo[4.2.0]oct-2-eno-2-carboxilico cristalino; su elaboracion y uso |
US8097719B2 (en) * | 2008-07-15 | 2012-01-17 | Genesen Labs | Meropenem intermediate in novel crystalline form and a method of manufacture of meropenem |
KR101043794B1 (ko) * | 2009-04-13 | 2011-06-27 | 청우산업 주식회사 | 황토판재로 제공되는 기능성 황토방 |
KR101713453B1 (ko) | 2010-03-12 | 2017-03-07 | 오메로스 코포레이션 | Pde10 억제제 및 관련 조성물 및 방법 |
WO2012030957A2 (en) * | 2010-09-01 | 2012-03-08 | Arena Pharmaceuticals, Inc. | Non-hygroscopic salts of 5-ht2c agonists |
US8940707B2 (en) | 2010-10-28 | 2015-01-27 | Viropharma Incorporated | Maribavir isomers, compositions, methods of making and methods of using |
US8541391B2 (en) | 2010-10-28 | 2013-09-24 | Viropharma Incorporated | Crystalline phases of 5,6-dichloro-2-(isopropylamino)-1-β-L-ribofuranosyl-1H-benzimidazole |
US8546344B2 (en) | 2010-10-28 | 2013-10-01 | Viropharma Incorporated | Crystalline phases of 5,6-dichloro-2-(isopropylamino)-1-β-L-ribofuranosyl)-1H-benzimidazole |
CN103930419B (zh) * | 2011-09-30 | 2016-06-01 | 广东东阳光药业有限公司 | 阿齐沙坦的晶型及其制备方法 |
NZ716462A (en) * | 2014-04-28 | 2017-11-24 | Omeros Corp | Optically active pde10 inhibitor |
NZ630810A (en) | 2014-04-28 | 2016-03-31 | Omeros Corp | Processes and intermediates for the preparation of a pde10 inhibitor |
AU2016250843A1 (en) | 2015-04-24 | 2017-10-12 | Omeros Corporation | PDE10 inhibitors and related compositions and methods |
JP2018535969A (ja) | 2015-11-04 | 2018-12-06 | オメロス コーポレーション | Pde10阻害剤の固体状態形態 |
CN111303230B (zh) * | 2020-03-09 | 2021-07-13 | 中国食品药品检定研究院 | 一种黄体酮共晶物及其制备方法和用途 |
WO2024081308A1 (en) * | 2022-10-12 | 2024-04-18 | Takeda Pharmaceutical Company Limited | Method of preparing maribavir |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3399987A (en) * | 1965-08-02 | 1968-09-03 | United States Borax Chem | 2-alkylaminobenzimidazoles as herbicides |
CH443777A (de) * | 1965-08-06 | 1968-02-15 | Agripat Sa | Verfahren zum Schützen textiler Keratinfasern vor Insektenfrass und Mittel zur Durchführung dieses Verfahrens |
US3655901A (en) * | 1970-07-30 | 1972-04-11 | Merck & Co Inc | Method of inhibiting the formation of phenylethanalamine-n-methyl transferase with 2-aminobenzimidazoles |
SE9003151D0 (sv) * | 1990-10-02 | 1990-10-02 | Medivir Ab | Nucleoside derivatives |
US5248672A (en) * | 1990-11-01 | 1993-09-28 | The Regents Of The University Of Michigan | Polysubstituted benzimidazole nucleosides as antiviral agents |
AU5447094A (en) * | 1992-10-21 | 1994-05-09 | Regents Of The University Of Michigan, The | Polysubstituted benzimidazoles as antiviral agents |
GB9413724D0 (en) * | 1994-07-07 | 1994-08-24 | Wellcome Found | Therapeutic nucleosides |
GB9600143D0 (en) | 1996-01-05 | 1996-03-06 | Wellcome Found | Therapeutic compounds |
GB9807354D0 (en) * | 1998-04-07 | 1998-06-03 | Glaxo Group Ltd | Antiviral compound |
GB9807355D0 (en) | 1998-04-07 | 1998-06-03 | Glaxo Group Ltd | Antiviral compound |
-
1998
- 1998-04-07 GB GBGB9807354.7A patent/GB9807354D0/en not_active Ceased
-
1999
- 1999-04-01 IL IL13869799A patent/IL138697A0/xx unknown
- 1999-04-01 JP JP2000542339A patent/JP2002510703A/ja active Pending
- 1999-04-01 SK SK1483-2000A patent/SK14832000A3/sk unknown
- 1999-04-01 BR BR9909474-6A patent/BR9909474A/pt not_active IP Right Cessation
- 1999-04-01 NZ NZ507173A patent/NZ507173A/en unknown
- 1999-04-01 KR KR1020007011089A patent/KR20010074472A/ko not_active Application Discontinuation
- 1999-04-01 EP EP99917935A patent/EP1071693B1/en not_active Expired - Lifetime
- 1999-04-01 CN CN99806894A patent/CN1303390A/zh active Pending
- 1999-04-01 CA CA2327494A patent/CA2327494C/en not_active Expired - Lifetime
- 1999-04-01 DE DE69915461T patent/DE69915461T2/de not_active Expired - Lifetime
- 1999-04-01 AP APAP/P/2000/001947A patent/AP2000001947A0/en unknown
- 1999-04-01 EA EA200000911A patent/EA002970B1/ru not_active IP Right Cessation
- 1999-04-01 AU AU36034/99A patent/AU752877B2/en not_active Ceased
- 1999-04-01 EE EEP200000584A patent/EE04120B1/xx not_active IP Right Cessation
- 1999-04-01 US US09/647,962 patent/US6469160B1/en not_active Expired - Lifetime
- 1999-04-01 ID IDW20002036A patent/ID27109A/id unknown
- 1999-04-01 WO PCT/EP1999/002214 patent/WO1999051618A1/en not_active Application Discontinuation
- 1999-04-01 PL PL99343397A patent/PL343397A1/xx unknown
- 1999-04-01 HU HU0101669A patent/HUP0101669A3/hu unknown
- 1999-04-01 AT AT99917935T patent/ATE261452T1/de not_active IP Right Cessation
- 1999-04-01 ES ES99917935T patent/ES2216503T3/es not_active Expired - Lifetime
- 1999-04-01 YU YU60900A patent/YU60900A/sh unknown
- 1999-04-01 TR TR2000/02860T patent/TR200002860T2/tr unknown
-
2000
- 2000-09-26 ZA ZA200005153A patent/ZA200005153B/en unknown
- 2000-09-26 IS IS5640A patent/IS5640A/is unknown
- 2000-10-04 NO NO20005005A patent/NO20005005L/no not_active Application Discontinuation
- 2000-10-09 HR HR20000669A patent/HRP20000669A2/hr not_active Application Discontinuation
-
2001
- 2001-10-29 US US10/007,272 patent/US7297683B2/en not_active Expired - Fee Related
-
2007
- 2007-10-25 US US11/924,204 patent/US7714123B2/en not_active Expired - Fee Related
-
2010
- 2010-03-26 US US12/732,302 patent/US20100179101A1/en not_active Abandoned
-
2011
- 2011-01-25 US US13/012,924 patent/US9163052B2/en not_active Expired - Fee Related
-
2013
- 2013-02-01 US US13/756,612 patent/US20130261294A1/en not_active Abandoned
-
2015
- 2015-10-12 US US14/880,600 patent/US20160030460A1/en not_active Abandoned
-
2016
- 2016-09-19 US US15/268,949 patent/US20170002035A1/en not_active Abandoned
-
2017
- 2017-10-05 US US15/725,785 patent/US20180044366A1/en not_active Abandoned
Also Published As
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