BR0212214A - Base livre de clindamicina cristalina - Google Patents
Base livre de clindamicina cristalinaInfo
- Publication number
- BR0212214A BR0212214A BR0212214-6A BR0212214A BR0212214A BR 0212214 A BR0212214 A BR 0212214A BR 0212214 A BR0212214 A BR 0212214A BR 0212214 A BR0212214 A BR 0212214A
- Authority
- BR
- Brazil
- Prior art keywords
- free base
- crystalline
- clindamycin free
- crystalline clindamycin
- clindamycin
- Prior art date
Links
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 title abstract 6
- 229960002227 clindamycin Drugs 0.000 title abstract 6
- 239000012458 free base Substances 0.000 title abstract 6
- 238000000034 method Methods 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
- C07H13/10—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals directly attached to heterocyclic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/14—Acyclic radicals, not substituted by cyclic structures attached to a sulfur, selenium or tellurium atom of a saccharide radical
- C07H15/16—Lincomycin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/26—Acyclic or carbocyclic radicals, substituted by hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
"BASE LIVRE DE CLINDAMICINA CRISTALINA". A droga antibiótica clindamicina é fornecida como uma base livre cristalina. Três formas polimórfica/pseudopolimórfica de base livre de clindamicina cristalina são reveladas. São também fornecidas composições farmacêuticas que compreendem a base livre de clindamicina, cristalina. São também fornecidos os processos para a preparação de base livre de clindamicina cristalina e composições da mesma, juntamente com métodos para tratar condições médicas com as composições farmacêuticas.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31537501P | 2001-08-28 | 2001-08-28 | |
| US37789202P | 2002-05-01 | 2002-05-01 | |
| PCT/US2002/027159 WO2003020736A1 (en) | 2001-08-28 | 2002-08-26 | Crystaline clindamycin free base |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR0212214A true BR0212214A (pt) | 2004-10-19 |
Family
ID=26979857
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR0212214-6A BR0212214A (pt) | 2001-08-28 | 2002-08-26 | Base livre de clindamicina cristalina |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US20030073647A1 (pt) |
| EP (1) | EP1421093B1 (pt) |
| JP (1) | JP2005504785A (pt) |
| AR (1) | AR037654A1 (pt) |
| AT (1) | ATE298758T1 (pt) |
| BR (1) | BR0212214A (pt) |
| CA (1) | CA2458644A1 (pt) |
| DE (1) | DE60204897T2 (pt) |
| ES (1) | ES2243763T3 (pt) |
| MX (1) | MXPA04001964A (pt) |
| MY (1) | MY134083A (pt) |
| TW (1) | TWI232865B (pt) |
| WO (1) | WO2003020736A1 (pt) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6544555B2 (en) | 2000-02-24 | 2003-04-08 | Advancis Pharmaceutical Corp. | Antibiotic product, use and formulation thereof |
| US6565882B2 (en) * | 2000-02-24 | 2003-05-20 | Advancis Pharmaceutical Corp | Antibiotic composition with inhibitor |
| US20020068078A1 (en) | 2000-10-13 | 2002-06-06 | Rudnic Edward M. | Antifungal product, use and formulation thereof |
| US6541014B2 (en) * | 2000-10-13 | 2003-04-01 | Advancis Pharmaceutical Corp. | Antiviral product, use and formulation thereof |
| AU2003284942A1 (en) * | 2002-10-30 | 2004-06-07 | Pharmacia Corporation | Oral extended release tablets and methods of making and using the same |
| EP1613333A1 (en) * | 2003-04-04 | 2006-01-11 | Pharmacia Corporation | Oral extended release compressed tablets of multiparticulates |
| WO2005009365A2 (en) | 2003-07-21 | 2005-02-03 | Advancis Pharmaceutical Corporation | Antibiotic product, use and formulation thereof |
| CA2533358C (en) * | 2003-07-21 | 2014-03-11 | Advancis Pharmaceutical Corporation | Antibiotic product, use and formulation thereof |
| AU2004258953B2 (en) * | 2003-07-21 | 2011-02-10 | Shionogi, Inc. | Antibiotic product, use and formulation thereof |
| US8758820B2 (en) * | 2003-08-11 | 2014-06-24 | Shionogi Inc. | Robust pellet |
| JP2007502294A (ja) | 2003-08-12 | 2007-02-08 | アドバンシス ファーマスーティカル コーポレイション | 抗生物質製剤、その使用法及び作成方法 |
| US8246996B2 (en) | 2003-08-29 | 2012-08-21 | Shionogi Inc. | Antibiotic product, use and formulation thereof |
| JP2007513869A (ja) | 2003-09-15 | 2007-05-31 | アドバンシス ファーマスーティカル コーポレイション | 抗生物質製剤、その使用法及び作成方法 |
| JP2007517039A (ja) * | 2003-12-24 | 2007-06-28 | アドバンシス ファーマスーティカル コーポレイション | 変性放出製剤の吸収増強 |
| US8715727B2 (en) | 2004-07-02 | 2014-05-06 | Shionogi Inc. | Tablet for pulsed delivery |
| US7976517B2 (en) * | 2004-09-30 | 2011-07-12 | Codman & Shurtleff, Inc. | Fluid management flow implants of improved occlusion resistance |
| CN100446774C (zh) * | 2005-05-31 | 2008-12-31 | 黑龙江龙桂制药有限公司 | 盐酸克林霉素阴道泡腾片及其制备方法 |
| JP4892915B2 (ja) * | 2005-10-04 | 2012-03-07 | 大日本印刷株式会社 | エパルレスタット製造法 |
| US8357394B2 (en) | 2005-12-08 | 2013-01-22 | Shionogi Inc. | Compositions and methods for improved efficacy of penicillin-type antibiotics |
| US8778924B2 (en) | 2006-12-04 | 2014-07-15 | Shionogi Inc. | Modified release amoxicillin products |
| US8299052B2 (en) | 2006-05-05 | 2012-10-30 | Shionogi Inc. | Pharmaceutical compositions and methods for improved bacterial eradication |
| US7923021B2 (en) * | 2007-07-24 | 2011-04-12 | University Of Memphis Research Foundation | Local delivery method and composition |
| EP2313083A1 (en) * | 2008-07-22 | 2011-04-27 | Lupin Limited | Oral compositions of clindamycin |
| US10105320B2 (en) * | 2013-10-03 | 2018-10-23 | Altria Client Services | Soluble fiber lozenge |
| CN111825729B (zh) * | 2020-07-14 | 2023-08-29 | 天方药业有限公司 | 克林霉素磷酸酯的纯化方法 |
| CN112206212B (zh) * | 2020-10-16 | 2023-04-28 | 海南锦瑞制药有限公司 | 一种注射用克林霉素磷酸酯的制备方法 |
| CN112569196B (zh) * | 2020-12-30 | 2023-05-12 | 海南海神同洲制药有限公司 | 一种克林霉素磷酸酯阴道片及其制备工艺 |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3380992A (en) * | 1965-06-14 | 1968-04-30 | Upjohn Co | Lincomycin derivatives and process for preparing same |
| NL126594C (pt) * | 1964-09-12 | |||
| US3496163A (en) * | 1965-02-08 | 1970-02-17 | Upjohn Co | 7-halo-7-deoxylincomycins and process for preparing the same |
| US3508904A (en) * | 1965-04-29 | 1970-04-28 | Owens Illinois Inc | Glass feeding orifice with multichamber combustion zones |
| US3435025A (en) * | 1966-03-18 | 1969-03-25 | Upjohn Co | 7-deoxylincomycin and analogs and isomers thereof and process for making the same |
| US3426012A (en) * | 1966-04-01 | 1969-02-04 | Upjohn Co | Process for preparing lincomycin-2-acylates and novel intermediate compounds |
| US3395139A (en) * | 1966-06-17 | 1968-07-30 | Upjohn Co | Lincomycin s and process for producing the same |
| US3487068A (en) * | 1966-12-16 | 1969-12-30 | Upjohn Co | Lincomycin-2-phosphates,7-substituted compounds and salts thereof |
| US3475407A (en) * | 1967-12-22 | 1969-10-28 | Upjohn Co | Process for preparing 7(r)- and 7(s)-halolincomycins |
| US3726858A (en) * | 1968-01-09 | 1973-04-10 | Upjohn Co | Delta 4',alpha-analogs of lincomycin |
| US3514440A (en) * | 1968-01-23 | 1970-05-26 | Upjohn Co | 7-epimers of lincomycin and related compounds and processes for making the same |
| US3544551A (en) * | 1968-04-30 | 1970-12-01 | Upjohn Co | 7-mercapto-7-deoxylincomycins and process for preparing the same |
| US3509127A (en) * | 1968-04-30 | 1970-04-28 | Upjohn Co | Isologs of lincomycins and process for preparing the same |
| US3513155A (en) * | 1968-05-07 | 1970-05-19 | Upjohn Co | Sulfoxides of 7-halo-7-deoxylincomycins and process |
| US3580904A (en) * | 1969-04-03 | 1971-05-25 | Upjohn Co | 7-halo-7-deoxy-lincomycin derivatives |
| BE758393A (fr) * | 1969-11-03 | 1971-05-03 | Upjohn Co | Procede de preparation de cis-1-thioglucosides et nouveaux produits en derivant |
| US3702322A (en) * | 1970-04-06 | 1972-11-07 | Upjohn Co | Derivatives of lincomycin and its analogs and process |
| US3705889A (en) * | 1970-04-28 | 1972-12-12 | Upjohn Co | Lincomycin analogs and process |
| US3714141A (en) * | 1970-05-26 | 1973-01-30 | Upjohn Co | Process for making 7-halolincomycins |
| US3655885A (en) * | 1970-06-10 | 1972-04-11 | Upjohn Co | Antibacterial compositions and methods of treating bacterial infections |
| US3715346A (en) * | 1970-11-18 | 1973-02-06 | Upjohn Co | Process for the preparation of lincomycin compounds |
| US3671647A (en) * | 1971-03-24 | 1972-06-20 | Upjohn Co | Lincomycin 3-nucleotides and the salts thereof |
| US3892729A (en) * | 1971-06-23 | 1975-07-01 | Upjohn Co | 1{40 (Beta-hydroxyethyl)-1{40 -demethyl clindamycin 2-phosphates |
| US3892730A (en) * | 1971-06-23 | 1975-07-01 | Upjohn Co | 1{40 -({62 -hydroxyethyl)-1{40 -demethyl clindamycin 2-acylates |
| US3915954A (en) * | 1971-11-15 | 1975-10-28 | Upjohn Co | Derivatives of lincomycin and its analogs and process |
| US3853843A (en) * | 1972-12-13 | 1974-12-10 | Upjohn Co | Derivatives of thiolincosaminide compounds |
| US3870699A (en) * | 1973-03-06 | 1975-03-11 | Upjohn Co | Lincomycin analogs |
| US4271266A (en) * | 1974-06-10 | 1981-06-02 | The Upjohn Manufacturing Company | Process for preparing lincomycin |
| US3969516A (en) * | 1974-12-19 | 1976-07-13 | Nelson Research & Development Company | Composition and method for treatment of acne |
| US4031304A (en) * | 1976-01-30 | 1977-06-21 | The Upjohn Company | Process for preparing lincomycin derivatives |
| US4278789A (en) * | 1979-11-23 | 1981-07-14 | The Upjohn Company | Lincomycin compounds |
| US4310660A (en) * | 1980-05-19 | 1982-01-12 | The Upjohn Company | Lincomycin compounds |
| US4309533A (en) * | 1980-05-19 | 1982-01-05 | The Upjohn Company | Lincomycin compounds |
| US4317903A (en) * | 1981-01-26 | 1982-03-02 | The Upjohn Company | Process for the purification of lincomycin |
| US4464466A (en) * | 1981-04-20 | 1984-08-07 | The Upjohn Company | Process of producing lincomycin nucleotides |
| US4568741A (en) * | 1984-05-15 | 1986-02-04 | The Upjohn Company | Synthesis of 7-halo-7-deoxylincomycins |
| CN1004002B (zh) * | 1984-11-29 | 1989-04-26 | 厄普约翰公司 | 制备7-卤-7-去氧林可霉素及其类似化合物的改进方法 |
| US4857337A (en) * | 1988-05-24 | 1989-08-15 | American Home Products Corp. (Del) | Enteric coated aspirin tablets |
| US4895934A (en) * | 1988-08-22 | 1990-01-23 | E. I. Du Pont De Nemours And Company | Process for the preparation of clindamycin phosphate |
| US4849515A (en) * | 1988-08-22 | 1989-07-18 | E. I. Du Pont De Nemours And Company | Clindamycin-2-phosphoryl benzylate |
| US5182374A (en) * | 1990-03-21 | 1993-01-26 | American Cyanamid Company | Clindamycin phosphate synthesis |
| US5811547A (en) * | 1992-10-14 | 1998-09-22 | Nippon Shinyaju Co., Ltd. | Method for inducing crystalline state transition in medicinal substance |
| US6224911B1 (en) * | 1993-03-16 | 2001-05-01 | Syntex (U.S.A.) Llc | Process for the preparation of enteric coated pharmaceutical dosage forms |
| US6207679B1 (en) * | 1997-06-19 | 2001-03-27 | Sepracor, Inc. | Antimicrobial agents uses and compositions related thereto |
| DE19737348C2 (de) * | 1997-08-27 | 2002-07-25 | Dan-Gabriel Vulpescu | Neue Clindamycin und Clotrimazol enthaltende pharmazeutische Zusammensetzung |
| DK1083885T3 (da) * | 1998-06-11 | 2007-02-26 | Pharmacia & Upjohn Co Llc | Delavirdintabletformulering |
| MXPA02006029A (es) * | 1999-12-15 | 2004-08-23 | Cubist Pharm Inc | Lipopeptidos novedosos como agentes antibacterianos. |
-
2002
- 2002-08-26 DE DE60204897T patent/DE60204897T2/de not_active Expired - Fee Related
- 2002-08-26 EP EP02768713A patent/EP1421093B1/en not_active Expired - Lifetime
- 2002-08-26 WO PCT/US2002/027159 patent/WO2003020736A1/en not_active Ceased
- 2002-08-26 US US10/227,901 patent/US20030073647A1/en not_active Abandoned
- 2002-08-26 JP JP2003525006A patent/JP2005504785A/ja active Pending
- 2002-08-26 BR BR0212214-6A patent/BR0212214A/pt not_active IP Right Cessation
- 2002-08-26 CA CA002458644A patent/CA2458644A1/en not_active Abandoned
- 2002-08-26 US US10/227,902 patent/US20030073826A1/en not_active Abandoned
- 2002-08-26 ES ES02768713T patent/ES2243763T3/es not_active Expired - Lifetime
- 2002-08-26 US US10/228,356 patent/US20030073648A1/en not_active Abandoned
- 2002-08-26 AT AT02768713T patent/ATE298758T1/de not_active IP Right Cessation
- 2002-08-26 MX MXPA04001964A patent/MXPA04001964A/es unknown
- 2002-08-27 MY MYPI20023184A patent/MY134083A/en unknown
- 2002-08-28 TW TW091119546A patent/TWI232865B/zh not_active IP Right Cessation
- 2002-08-28 AR ARP020103235A patent/AR037654A1/es unknown
-
2005
- 2005-05-02 US US11/120,264 patent/US20050192236A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ES2243763T3 (es) | 2005-12-01 |
| US20050192236A1 (en) | 2005-09-01 |
| MY134083A (en) | 2007-11-30 |
| US20030073647A1 (en) | 2003-04-17 |
| US20030073648A1 (en) | 2003-04-17 |
| MXPA04001964A (es) | 2004-06-07 |
| EP1421093B1 (en) | 2005-06-29 |
| DE60204897T2 (de) | 2006-05-11 |
| DE60204897D1 (de) | 2005-08-04 |
| WO2003020736A1 (en) | 2003-03-13 |
| TWI232865B (en) | 2005-05-21 |
| US20030073826A1 (en) | 2003-04-17 |
| AR037654A1 (es) | 2004-12-01 |
| ATE298758T1 (de) | 2005-07-15 |
| JP2005504785A (ja) | 2005-02-17 |
| CA2458644A1 (en) | 2003-03-13 |
| EP1421093A1 (en) | 2004-05-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BR0212214A (pt) | Base livre de clindamicina cristalina | |
| BRPI0413452A (pt) | composto, composição farmacêutica, kit, artigo de fabricação, e, métodos de inibir dpp-iv, terapêutico e de tratar um estado de doença, cáncer, distúrbios autoimunes, uma condição einfecção por hiv | |
| AR023423A1 (es) | Derivados de adamantano, procedimientos para su preparacion, composicion farmaceutica, procedimiento para la preparacion de la composicion farmaceutica, yuso de dichos derivados para la manufactura de medicamentos | |
| BRPI0409136A (pt) | composto heteroaromático pentacìclico e uso medicinal do mesmo | |
| CL2007002450A1 (es) | Forma polimorfica i del enantiomero levogiro o dextrogiro de modafinilo; su procedimiento de preparacion; y composicion farmaceutica que los comprende (divisional solicitud 2693-03). | |
| BR0012450A (pt) | Benzimidazóis substituìdos | |
| PA8442001A1 (es) | Derivados de pirimidina biciclica condensada | |
| HN1999000124A (es) | Derivados de pirazol substituido. | |
| UY28150A1 (es) | Agentes terapeuticos | |
| UY28691A1 (es) | Derivados de difenilazetidona | |
| CY1114708T1 (el) | Παραγωγα πυραζολο-κιναζολινης, διαδικασια για την παρασκευη τους και η χρηση τους ως αναστολεων κινασης | |
| CY1111504T1 (el) | Αζαδικυκλοαλκανια ως ρυθμιστες του ccr5 | |
| CO5180642A1 (es) | Compuestos sustituidos de piperidina, procesos para su prepa racion, composiciones farmaceuticas que los contienen y su utilizacion | |
| SV2004001690A (es) | Nuevos derivados de fluoroglicosidos heterociclicos, medicamentos que contienen estos compuestos, y el uso de los mismos | |
| PA8451801A1 (es) | Derivados de la 9-oxima eritromicina | |
| UY28695A1 (es) | Derivados de difenilazetidona | |
| UY27455A1 (es) | Derivados n-(1,4,5,6-tetrahidro-ciclopentapirazol -3-il)- sustituidos. su obtención y uso como fármacos. | |
| PA8465901A1 (es) | Nuevos derivados de la eritromicina | |
| ECSP055701A (es) | Nuevos derivados de pirimidinamida y el uso de los mismos | |
| CR7195A (es) | Nuevos derivados de oxazolidinonas como antibacterianos | |
| AR012504A1 (es) | Utilizacion de derivados de tetrahidropiridina, para la preparacion de medicamentos para el tratamiento de las enfermedades que provocan unadesmielinizacion. | |
| BR0308133A (pt) | Forma polimórfica cristalina de cloridrato de irinotecan | |
| HN2003000162A (es) | Derivados de isoindolona, proceso de preparacion y compuestos intermedios de este proceso, su uso como medicamentos, y composiciones farmaceuticas que los contienen. | |
| BRPI0413013A (pt) | composto, seus sais, solvatos, e derivados farmaceuticamente funcionais, composição farmacêutica, uso de um composto, e, métodos para o tratamento ou profilaxia de condições ou distúrbios, e de doenças | |
| BR0211739A (pt) | Novas formas polimórficas cristalinas de cloridrato de lercanidipina e processo para preparação das mesmas |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 6A,7A E 8A ANUIDADES. |
|
| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2060 DE 29/06/2010. |