CY1107913T1 - Πολυμορφικες και αλλες κρυσταλλικες μορφες cis-ftc - Google Patents
Πολυμορφικες και αλλες κρυσταλλικες μορφες cis-ftcInfo
- Publication number
- CY1107913T1 CY1107913T1 CY20081100369T CY081100369T CY1107913T1 CY 1107913 T1 CY1107913 T1 CY 1107913T1 CY 20081100369 T CY20081100369 T CY 20081100369T CY 081100369 T CY081100369 T CY 081100369T CY 1107913 T1 CY1107913 T1 CY 1107913T1
- Authority
- CY
- Cyprus
- Prior art keywords
- ftc
- cis
- forms
- manufacture
- polymorphic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (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)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Στερεές φάσεις του (-)-cis-FTC, οι οποίες ορίζονται εδώ ως άμορφο (-)-PTC και Μορφές II και III (-)-cis-FTC) παρέχονται, οι οποίες μπορεί να διακρίνονται από τη Μορφή I (-)-cis-FTC με πρότυπα διάθλασης σκόνης ακτίνων-Χ, θερμικές ιδιότητες και μεθόδους βιομηχανικής κατασκευής. Μια ένυδρη κρυσταλλική μορφή (±)-cis-FTC (δηλ. ρακεμικό cis-FTC) και αφυδατωμένη μορφή του υδρίτη, επίσης παρέχονται και μπορεί παρομοίως να διακρίνονται από άλλες μορφές FTC με πρότυπα διάθλασης σκόνης ακτίνων-Χ, θερμικές ιδιότητες και μεθόδους βιομηχανικής κατασκευής. Αυτές οι FTC μορφές μπορεί να χρησιμοποιηθούν στη βιομηχανική κατασκευή άλλων μορφών FTC ή σε φαρμακευτικές συνθέσεις. Ιδιαιτέρως προτιμώμενες χρήσεις αυτών των μορφών είναι στη θεραπεία HIV ή ηπατίτιδας Β.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27256001P | 2001-03-01 | 2001-03-01 | |
US30960501P | 2001-08-02 | 2001-08-02 | |
EP05076347A EP1574512B1 (en) | 2001-03-01 | 2002-03-01 | Polymorphic and other crystalline forms of cis-FTC |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1107913T1 true CY1107913T1 (el) | 2013-09-04 |
Family
ID=26955597
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20061100192T CY1107983T1 (el) | 2001-03-01 | 2006-02-10 | Πολυμορφικες και αλλες κρυσταλλικες μορφες cis-ftc |
CY20081100369T CY1107913T1 (el) | 2001-03-01 | 2008-03-31 | Πολυμορφικες και αλλες κρυσταλλικες μορφες cis-ftc |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20061100192T CY1107983T1 (el) | 2001-03-01 | 2006-02-10 | Πολυμορφικες και αλλες κρυσταλλικες μορφες cis-ftc |
Country Status (14)
Country | Link |
---|---|
US (3) | US6723728B2 (el) |
EP (3) | EP1574512B1 (el) |
JP (4) | JP5105689B2 (el) |
KR (4) | KR101015510B1 (el) |
CN (4) | CN1503796B (el) |
AT (2) | ATE312097T1 (el) |
AU (1) | AU2002335489B2 (el) |
CA (4) | CA2690137C (el) |
CY (2) | CY1107983T1 (el) |
DE (2) | DE60224592T2 (el) |
DK (2) | DK1389207T3 (el) |
ES (3) | ES2299950T3 (el) |
PT (2) | PT1574512E (el) |
WO (1) | WO2002070518A1 (el) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2690137C (en) | 2001-03-01 | 2012-11-13 | Gilead Sciences, Inc. | Polymorphic and other crystalline forms of cis-ftc |
TWI244393B (en) * | 2002-08-06 | 2005-12-01 | Idenix Pharmaceuticals Inc | Crystalline and amorphous forms of beta-L-2'-deoxythymidine |
ATE398455T1 (de) | 2003-01-14 | 2008-07-15 | Gilead Sciences Inc | Zusammensetzungen und verfahren zur antiviralen kombinationstherapie |
US6943249B2 (en) | 2003-03-17 | 2005-09-13 | Ash Stevens, Inc. | Methods for isolating crystalline Form I of 5-azacytidine |
US6887855B2 (en) | 2003-03-17 | 2005-05-03 | Pharmion Corporation | Forms of 5-azacytidine |
US20060014949A1 (en) * | 2004-07-13 | 2006-01-19 | Supergen Inc. | Compositions and formulations of decitabine polymorphs and methods of use thereof |
TWI375560B (en) | 2005-06-13 | 2012-11-01 | Gilead Sciences Inc | Composition comprising dry granulated emtricitabine and tenofovir df and method for making the same |
TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
WO2009005338A2 (en) * | 2007-07-05 | 2009-01-08 | Ultimorphix Technologies B.V. | Solid forms ult-i, ult-2 and ult-3 of emtricitabine |
EP2350065A1 (en) | 2008-11-12 | 2011-08-03 | Lupin Ltd. | A novel polymorph of emtricitabine and a process for preparing of the same |
US8710218B2 (en) | 2009-07-15 | 2014-04-29 | Lupin Limited | Process for preparation of Efavirenz |
Family Cites Families (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
US4476248A (en) | 1983-02-28 | 1984-10-09 | The Upjohn Company | Crystallization of ibuprofen |
US5684153A (en) | 1984-08-16 | 1997-11-04 | Beecham Group Plc | Process for the preparation of purine derivatives |
EP0141927B1 (en) | 1983-08-18 | 1991-10-30 | Beecham Group Plc | Antiviral guanine derivatives |
US5223263A (en) | 1988-07-07 | 1993-06-29 | Vical, Inc. | Liponucleotide-containing liposomes |
CS264222B1 (en) | 1986-07-18 | 1989-06-13 | Holy Antonin | N-phosphonylmethoxyalkylderivatives of bases of pytimidine and purine and method of use them |
WO1989002733A1 (en) | 1987-09-22 | 1989-04-06 | The Regents Of The University Of California | Liposomal nucleoside analogues for treating aids |
US5041449A (en) | 1988-04-11 | 1991-08-20 | Iaf Biochem International, Inc. | 4-(nucleoside base)-substituted-1,3-dioxolanes useful for treatment of retroviral infections |
US5047407A (en) | 1989-02-08 | 1991-09-10 | Iaf Biochem International, Inc. | 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties |
NZ228645A (en) | 1988-04-11 | 1991-09-25 | Iaf Biochem Int | 1,3-dioxolane derivatives substituted in the 5th position by a purine or pyrimidine radical; treatment of viral infections |
US6175008B1 (en) | 1988-04-11 | 2001-01-16 | Biochem Pharma Inc. | Processes for preparing substituted 1,3-oxathiolanes with antiviral properties |
US5411947A (en) | 1989-06-28 | 1995-05-02 | Vestar, Inc. | Method of converting a drug to an orally available form by covalently bonding a lipid to the drug |
US5194654A (en) | 1989-11-22 | 1993-03-16 | Vical, Inc. | Lipid derivatives of phosphonoacids for liposomal incorporation and method of use |
US5463092A (en) | 1989-11-22 | 1995-10-31 | Vestar, Inc. | Lipid derivatives of phosphonacids for liposomal incorporation and method of use |
US5204466A (en) | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
US6703396B1 (en) | 1990-02-01 | 2004-03-09 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nuclesoside enantiomers |
US5914331A (en) | 1990-02-01 | 1999-06-22 | Emory University | Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane |
US6069252A (en) | 1990-02-01 | 2000-05-30 | Emory University | Method of resolution and antiviral activity of 1,3-oxathiolane nucleoside enantiomers |
US5700937A (en) | 1990-02-01 | 1997-12-23 | Emory University | Method for the synthesis, compositions and use of 2'-deoxy-5-fluoro-3'-thiacytidine and related compounds |
GB9009861D0 (en) | 1990-05-02 | 1990-06-27 | Glaxo Group Ltd | Chemical compounds |
AU7872491A (en) | 1990-05-07 | 1991-11-27 | Vical, Inc. | Lipid prodrugs of salicylate and nonsteroidal anti-inflammatory drugs |
EP0531452A4 (en) | 1990-05-29 | 1993-06-09 | Vical, Inc. | Synthesis of glycerol di- and triphosphate derivatives |
DK0533833T3 (da) | 1990-06-13 | 1996-04-22 | Arnold Glazier | Phosphorprolægemidler |
US5674849A (en) | 1990-10-24 | 1997-10-07 | Allelix Biopharmaceuticals Inc. | Anti-viral compositions |
US5149794A (en) | 1990-11-01 | 1992-09-22 | State Of Oregon | Covalent lipid-drug conjugates for drug targeting |
US5256641A (en) | 1990-11-01 | 1993-10-26 | State Of Oregon | Covalent polar lipid-peptide conjugates for immunological targeting |
US5543389A (en) | 1990-11-01 | 1996-08-06 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education On Behalf Of The Oregon Health Sciences University, A Non Profit Organization | Covalent polar lipid-peptide conjugates for use in salves |
US5543390A (en) | 1990-11-01 | 1996-08-06 | State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University | Covalent microparticle-drug conjugates for biological targeting |
US6228860B1 (en) * | 1990-11-13 | 2001-05-08 | Biochem Pharma Inc. | Substituted 1,3-oxathiolanes with antiviral properties |
US5925643A (en) | 1990-12-05 | 1999-07-20 | Emory University | Enantiomerically pure β-D-dioxolane-nucleosides |
US5444063A (en) | 1990-12-05 | 1995-08-22 | Emory University | Enantiomerically pure β-D-dioxolane nucleosides with selective anti-Hepatitis B virus activity |
US5179104A (en) | 1990-12-05 | 1993-01-12 | University Of Georgia Research Foundation, Inc. | Process for the preparation of enantiomerically pure β-D-(-)-dioxolane-nucleosides |
IL100502A (en) | 1991-01-03 | 1995-12-08 | Iaf Biochem Int | PHARMACEUTICAL PREPARATIONS CONTAINING CIS-4-AMINO-1-) 2-HYDROXIMETHIL-1,3-OXETYOLEN-5-IL (- |
NZ241625A (en) * | 1991-02-22 | 1996-03-26 | Univ Emory | 1,3-oxathiolane derivatives, anti-viral compositions containing such and method of resolving racemic mixture of enantiomers |
GB9104740D0 (en) | 1991-03-06 | 1991-04-17 | Wellcome Found | Antiviral nucleoside combination |
IT1244501B (it) | 1991-03-22 | 1994-07-15 | Sigma Tau Ind Farmaceuti | Derivati amminoacilici e oligopeptidici dell'allopurinolo dotati di attivita' immunostimolante e composizioni farmaceutiche che li contengono |
WO1992018517A1 (en) | 1991-04-17 | 1992-10-29 | Yale University | Method of treating or preventing hepatitis b virus |
GB9110874D0 (en) | 1991-05-20 | 1991-07-10 | Iaf Biochem Int | Medicaments |
ZA923641B (en) | 1991-05-21 | 1993-02-24 | Iaf Biochem Int | Processes for the diastereoselective synthesis of nucleosides |
GB9111902D0 (en) * | 1991-06-03 | 1991-07-24 | Glaxo Group Ltd | Chemical compounds |
JPH07500573A (ja) | 1991-07-12 | 1995-01-19 | ネクススター・ファーマシューティカルズ・インコーポレイテッド | 抗ウィルス性リポヌクレオシド:b型肝炎の治療 |
US5554728A (en) | 1991-07-23 | 1996-09-10 | Nexstar Pharmaceuticals, Inc. | Lipid conjugates of therapeutic peptides and protease inhibitors |
GB9116601D0 (en) * | 1991-08-01 | 1991-09-18 | Iaf Biochem Int | 1,3-oxathiolane nucleoside analogues |
US6177435B1 (en) | 1992-05-13 | 2001-01-23 | Glaxo Wellcome Inc. | Therapeutic combinations |
WO1994026273A1 (en) | 1993-05-12 | 1994-11-24 | Hostetler Karl Y | Acyclovir derivatives for topical use |
GB9311709D0 (en) | 1993-06-07 | 1993-07-21 | Iaf Biochem Int | Stereoselective synthesis of nucleoside analogues using bicycle intermediate |
US5587362A (en) | 1994-01-28 | 1996-12-24 | Univ. Of Ga Research Foundation | L-nucleosides |
IL113432A (en) | 1994-04-23 | 2000-11-21 | Glaxo Group Ltd | Process for the diastereoselective synthesis of nucleoside analogues |
US5808040A (en) | 1995-01-30 | 1998-09-15 | Yale University | L-nucleosides incorporated into polymeric structure for stabilization of oligonucleotides |
SE9500872L (sv) * | 1995-03-10 | 1996-04-01 | Tony Wiseby | Anordning vid sikte för pilbåge |
US5869461A (en) | 1995-03-16 | 1999-02-09 | Yale University | Reducing toxicity of L-nucleosides with D-nucleosides |
DE19543707A1 (de) * | 1995-11-23 | 1997-05-28 | Inst Neue Mat Gemein Gmbh | Verfahren zum Konservieren von Papier |
GB9525606D0 (en) | 1995-12-14 | 1996-02-14 | Iaf Biochem Int | Method and compositions for the synthesis of dioxolane nucleosides with - configuration |
WO1998023285A1 (en) | 1996-11-29 | 1998-06-04 | Smithkline Beecham Plc | Use of a combination of penciclovir and alpha-interferon in the manufacture of a medicament for the treatment of hepatitis b |
TW318283B (en) | 1996-12-09 | 1997-10-21 | United Microelectronics Corp | Multi-level read only memory structure and manufacturing method thereof |
US6071922A (en) | 1997-03-19 | 2000-06-06 | Emory University | Synthesis, anti-human immunodeficiency virus, and anti-hepatitis B virus activities of 1,3-oxaselenolane nucleosides |
RU2439069C2 (ru) * | 1998-08-12 | 2012-01-10 | Гайлид Сайенсиз, Инк. | Способ получения 1,3-оксатиолановых нуклеозидов |
PT1119635E (pt) | 1998-10-09 | 2012-07-24 | Gilead Sciences Inc | Sistemas não homogéneos para a resolução de misturas enantioméricas |
CA2690137C (en) * | 2001-03-01 | 2012-11-13 | Gilead Sciences, Inc. | Polymorphic and other crystalline forms of cis-ftc |
US6600044B2 (en) * | 2001-06-18 | 2003-07-29 | Brantford Chemicals Inc. | Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers |
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2002
- 2002-03-01 CA CA2690137A patent/CA2690137C/en not_active Expired - Fee Related
- 2002-03-01 WO PCT/US2002/006184 patent/WO2002070518A1/en active IP Right Grant
- 2002-03-01 DE DE60224592T patent/DE60224592T2/de not_active Expired - Lifetime
- 2002-03-01 DE DE60207850T patent/DE60207850T2/de not_active Expired - Lifetime
- 2002-03-01 CN CN028082850A patent/CN1503796B/zh not_active Expired - Fee Related
- 2002-03-01 EP EP05076347A patent/EP1574512B1/en not_active Expired - Lifetime
- 2002-03-01 JP JP2002569838A patent/JP5105689B2/ja not_active Expired - Fee Related
- 2002-03-01 AT AT02748367T patent/ATE312097T1/de active
- 2002-03-01 CA CA2867970A patent/CA2867970A1/en not_active Abandoned
- 2002-03-01 PT PT05076347T patent/PT1574512E/pt unknown
- 2002-03-01 DK DK02748367T patent/DK1389207T3/da active
- 2002-03-01 CN CN201210146877.2A patent/CN102911166B/zh not_active Expired - Fee Related
- 2002-03-01 US US10/086,830 patent/US6723728B2/en not_active Expired - Lifetime
- 2002-03-01 DK DK05076347T patent/DK1574512T3/da active
- 2002-03-01 ES ES05076347T patent/ES2299950T3/es not_active Expired - Lifetime
- 2002-03-01 CN CN201210146874.9A patent/CN102911165B/zh not_active Expired - Fee Related
- 2002-03-01 CA CA2788498A patent/CA2788498C/en not_active Expired - Fee Related
- 2002-03-01 ES ES02748367T patent/ES2253544T3/es not_active Expired - Lifetime
- 2002-03-01 CN CN2012101468804A patent/CN102942563A/zh active Pending
- 2002-03-01 KR KR1020087016002A patent/KR101015510B1/ko active IP Right Grant
- 2002-03-01 KR KR1020107016624A patent/KR101150250B1/ko not_active IP Right Cessation
- 2002-03-01 CA CA002439831A patent/CA2439831C/en not_active Expired - Fee Related
- 2002-03-01 AU AU2002335489A patent/AU2002335489B2/en not_active Ceased
- 2002-03-01 ES ES08000264.5T patent/ES2537007T3/es not_active Expired - Lifetime
- 2002-03-01 PT PT80002645T patent/PT1903041E/pt unknown
- 2002-03-01 KR KR1020087016003A patent/KR100927024B1/ko active IP Right Grant
- 2002-03-01 KR KR10-2003-7011355A patent/KR20040002871A/ko not_active Application Discontinuation
- 2002-03-01 EP EP08000264.5A patent/EP1903041B1/en not_active Expired - Lifetime
- 2002-03-01 EP EP02748367A patent/EP1389207B1/en not_active Expired - Lifetime
- 2002-03-01 AT AT05076347T patent/ATE383355T1/de active
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2004
- 2004-04-19 US US10/827,615 patent/US7544692B2/en not_active Expired - Lifetime
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2006
- 2006-02-10 CY CY20061100192T patent/CY1107983T1/el unknown
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2008
- 2008-03-31 CY CY20081100369T patent/CY1107913T1/el unknown
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2009
- 2009-04-14 JP JP2009097656A patent/JP2009197005A/ja active Pending
- 2009-06-09 US US12/481,003 patent/US8637535B2/en not_active Expired - Fee Related
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2012
- 2012-10-17 JP JP2012229555A patent/JP2013040192A/ja active Pending
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2014
- 2014-09-10 JP JP2014184339A patent/JP2015028045A/ja active Pending
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