AR014417A1 - LA SAL DE BISULFATO DEL ÉSTER DIMETíLICO DEL ÁCIDO[3S- (3R*, 8'R*, 9'R*, 12R*)] -3,12-BIS (1,1-DIMETILETIL) -8- HIDROXI-4,11- DIOXO-9- (FENILMETIL) -6- [[4-(2-PIRIDINIL) -FENILMETIL]] -2,5,6,10,13- PENTAAZATETRADECANODIOICO Y LA COMPOSICIoN FARMACÉUTICA QUE LA CONTIENE - Google Patents

LA SAL DE BISULFATO DEL ÉSTER DIMETíLICO DEL ÁCIDO[3S- (3R*, 8'R*, 9'R*, 12R*)] -3,12-BIS (1,1-DIMETILETIL) -8- HIDROXI-4,11- DIOXO-9- (FENILMETIL) -6- [[4-(2-PIRIDINIL) -FENILMETIL]] -2,5,6,10,13- PENTAAZATETRADECANODIOICO Y LA COMPOSICIoN FARMACÉUTICA QUE LA CONTIENE

Info

Publication number
AR014417A1
AR014417A1 ARP990100179A ARP990100179A AR014417A1 AR 014417 A1 AR014417 A1 AR 014417A1 AR P990100179 A ARP990100179 A AR P990100179A AR P990100179 A ARP990100179 A AR P990100179A AR 014417 A1 AR014417 A1 AR 014417A1
Authority
AR
Argentina
Prior art keywords
pharmaceutical composition
phenylmetile
penylmentil
pentaazatetradecanodioico
dimetiletil
Prior art date
Application number
ARP990100179A
Other languages
English (en)
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22104737&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR014417(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR014417A1 publication Critical patent/AR014417A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Pyridine Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Sal de bisulfato cristalina de la formula (I) que tiene una velocidad de solubilidad disolucion inesperadamente alta y biodisponibilidad oral tambiénalta con relacion a la forma de base libre de este compuesto y composicion farmacéutica quel a comprende. Debido a dicha alta biodisponibilidad así comosu buena cristalinidad y estabilidad, la sal de bisulfato es muy util en la preparacion de formas de dosis orales. Esta sal de bisulfato, y formulacionesde la misma, se utilizan parael t ratamiento de enfermedades causadas por virus, especialmente retrovirus, como el HIV.
ARP990100179A 1998-01-20 1999-01-18 LA SAL DE BISULFATO DEL ÉSTER DIMETíLICO DEL ÁCIDO[3S- (3R*, 8'R*, 9'R*, 12R*)] -3,12-BIS (1,1-DIMETILETIL) -8- HIDROXI-4,11- DIOXO-9- (FENILMETIL) -6- [[4-(2-PIRIDINIL) -FENILMETIL]] -2,5,6,10,13- PENTAAZATETRADECANODIOICO Y LA COMPOSICIoN FARMACÉUTICA QUE LA CONTIENE AR014417A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7196898P 1998-01-20 1998-01-20

Publications (1)

Publication Number Publication Date
AR014417A1 true AR014417A1 (es) 2001-02-28

Family

ID=22104737

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP990100179A AR014417A1 (es) 1998-01-20 1999-01-18 LA SAL DE BISULFATO DEL ÉSTER DIMETíLICO DEL ÁCIDO[3S- (3R*, 8'R*, 9'R*, 12R*)] -3,12-BIS (1,1-DIMETILETIL) -8- HIDROXI-4,11- DIOXO-9- (FENILMETIL) -6- [[4-(2-PIRIDINIL) -FENILMETIL]] -2,5,6,10,13- PENTAAZATETRADECANODIOICO Y LA COMPOSICIoN FARMACÉUTICA QUE LA CONTIENE

Country Status (39)

Country Link
US (1) US6087383A (es)
EP (1) EP1056722B1 (es)
JP (2) JP4860037B2 (es)
KR (1) KR100559283B1 (es)
CN (1) CN1116282C (es)
AR (1) AR014417A1 (es)
AT (1) ATE219057T1 (es)
AU (1) AU735875B2 (es)
BG (1) BG64774B1 (es)
BR (1) BR9814736A (es)
CA (1) CA2317736C (es)
CO (1) CO4970820A1 (es)
CZ (1) CZ293507B6 (es)
DE (1) DE69806067T2 (es)
DK (1) DK1056722T3 (es)
EE (1) EE04434B1 (es)
EG (1) EG23936A (es)
ES (1) ES2178300T3 (es)
GE (1) GEP20033026B (es)
HK (2) HK1033667A1 (es)
HU (1) HU227196B1 (es)
IL (2) IL137384A0 (es)
LT (1) LT4780B (es)
LV (1) LV12522B (es)
MY (1) MY114838A (es)
NO (1) NO315605B1 (es)
NZ (1) NZ504417A (es)
PE (1) PE20000185A1 (es)
PL (1) PL190744B1 (es)
PT (1) PT1056722E (es)
RO (1) RO118869B1 (es)
RU (1) RU2186070C2 (es)
SK (1) SK283975B6 (es)
TR (1) TR200001876T2 (es)
TW (1) TW531531B (es)
UA (1) UA59432C2 (es)
UY (1) UY25345A1 (es)
WO (1) WO1999036404A1 (es)
ZA (1) ZA9956B (es)

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BR0209985A (pt) * 2001-05-22 2004-06-29 Elan Pharm Inc Composto e método para o tratamento de um paciente
US7193065B2 (en) * 2001-07-13 2007-03-20 Roche Diagnostics Operations, Inc. Protease inhibitor conjugates and antibodies useful in immunoassay
US7157561B2 (en) * 2001-07-13 2007-01-02 Roche Diagnostics Operations, Inc. Methods of inhibiting transmission of a costimulatory signal of lymphocytes
EP3025718A1 (en) * 2003-01-14 2016-06-01 Gilead Sciences, Inc. Compositions and methods for combination antiviral therapy
TW200534879A (en) * 2004-03-25 2005-11-01 Bristol Myers Squibb Co Coated tablet formulation and method
CN1980666B (zh) * 2004-05-04 2011-03-30 布里斯托尔-迈尔斯斯奎布公司 制备阿扎那韦硫酸氢盐的方法和新的形式
US20050256314A1 (en) * 2004-05-04 2005-11-17 Soojin Kim Process employing controlled crystallization in forming crystals of a pharmaceutical
US7829720B2 (en) * 2004-05-04 2010-11-09 Bristol-Myers Squibb Company Process for preparing atazanavir bisulfate and novel forms
US20050288343A1 (en) * 2004-05-19 2005-12-29 Andrew Rusowicz Process of preparing substituted carbamates and intermediates thereof
TWI354569B (en) 2004-05-28 2011-12-21 Bristol Myers Squibb Co Coated tablet formulation and method
US7642049B2 (en) 2006-06-30 2010-01-05 Bristol-Myers Squibb Company Method for identifying HIV-1 protease inhibitors with reduced metabolic affects through detection of human resistin polymorphisms
NZ573887A (en) * 2006-07-21 2012-02-24 Gilead Sciences Inc Antiviral protease inhibitors
BG66056B1 (bg) * 2006-10-05 2010-12-30 Красимир ДЕЧЕВ Метод и инсталация за производство на трисезонна добавка към дизелово гориво
RU2448958C2 (ru) * 2007-06-12 2012-04-27 Консерт Фармасьютикалз, Инк. Производные азапептидов
ES2359770T3 (es) * 2007-06-22 2011-05-26 Bristol-Myers Squibb Company Composiciones en comprimidos que contienen atazanavir.
JP2010530889A (ja) * 2007-06-22 2010-09-16 ブリストル−マイヤーズ スクイブ カンパニー アタザナビルを含む錠剤組成物
US20100183715A1 (en) * 2007-06-22 2010-07-22 Bristo-Meyers Squibb Company Tableted compositions containing atazanavir
JP2010530892A (ja) * 2007-06-22 2010-09-16 ブリストル−マイヤーズ スクイブ カンパニー アタザナビルを含む錠剤組成物
KR20100028656A (ko) * 2007-06-29 2010-03-12 길리애드 사이언시즈, 인코포레이티드 치료 조성물 및 그의 용도
CN103480000A (zh) * 2007-06-29 2014-01-01 吉里德科学公司 治疗用组合物和方法
EP2288593A1 (en) * 2008-05-08 2011-03-02 Ranbaxy Laboratories Limited Process for the preparation of 3,4-epoxy-2-amino-1-substituted butane derivatives and intermediate compounds thereof
WO2010070611A1 (en) 2008-12-18 2010-06-24 Ranbaxy Laboratories Limited Atazanavir formulations
WO2010079497A2 (en) * 2009-01-12 2010-07-15 Hetero Research Foundation Novel polymorph of atazanavir sulfate
CA2762582A1 (en) 2009-05-27 2010-12-02 Merck Sharp & Dohme Corp. Hiv protease inhibitors
EP2272830A1 (en) 2009-06-18 2011-01-12 Esteve Química, S.A. Preparation process of an antivirally heterocyclic azahexane derivative
WO2011027324A1 (en) 2009-09-03 2011-03-10 Ranbaxy Laboratories Limited Polymorphic forms of atazanavir sulfate
US9649311B2 (en) 2009-10-26 2017-05-16 Merck Sharp & Dohme Corp. Solid pharmaceutical compositions containing an integrase inhibitor
WO2011080562A1 (en) 2009-12-29 2011-07-07 Hetero Research Foundation Novel aza-peptides containing 2,2-disubstituted cyclobutyl and/or substituted alkoxy benzyl derivatives as antivirals
SG10201509476RA (en) 2010-01-27 2015-12-30 Viiv Healthcare Co Antiviral therapy
EP2542527A2 (en) 2010-03-01 2013-01-09 Lupin Limited Process for the preparation of atazanavir sulfate substantially free of diastereomers
CN102917695A (zh) 2010-04-09 2013-02-06 百时美施贵宝公司 具有改进的pH效应的阿扎那韦硫酸盐制剂
EP2621472A1 (en) 2010-09-28 2013-08-07 Ratiopharm GmbH Dry processing of atazanavir
US20140343290A1 (en) 2011-07-27 2014-11-20 Rakesh Kumar Singh Process for the preparation of atazanavir or its bisulfate salt
US8461347B2 (en) 2011-08-05 2013-06-11 Scinopharm Taiwan, Ltd. Process for preparing form A of atazanavir sulfate
EP2771332B1 (en) 2011-10-26 2016-06-29 Merck Canada Inc. Thiophen and thiazol sulfonamid derivatives as HIV protease inhibitors for the treatment of AIDS
US9382207B2 (en) 2012-08-24 2016-07-05 Laurus Labs Private Limited Process for the preparation of atazanavir bisulfate
WO2014036690A1 (zh) * 2012-09-04 2014-03-13 上海迪赛诺化学制药有限公司 制备阿扎那韦硫酸氢盐a型结晶的方法
US9890121B2 (en) 2013-02-12 2018-02-13 Cipla Limited Process for preparing atazanavir sulphate
CN104250225A (zh) * 2013-06-28 2014-12-31 上海威智医药科技有限公司 阿扎那韦磷酸盐及其制备和应用
CN104250223B (zh) * 2013-06-28 2017-04-12 上海威智医药科技有限公司 阿扎那韦氢溴酸盐及其制备和应用
CN104250224A (zh) * 2013-06-28 2014-12-31 上海威智医药科技有限公司 阿扎那韦富马酸盐及其制备和应用
CN105859611A (zh) * 2016-04-18 2016-08-17 上海现代制药海门有限公司 一种阿扎那韦硫酸氢盐a型结晶的制备方法
CN109251165B (zh) * 2018-10-02 2022-09-23 国药集团川抗制药有限公司 阿扎那韦达二4-氨基苯磺酸盐及其制备方法
CN111349042B (zh) * 2018-12-20 2023-07-14 陕西理工大学 一种阿扎那韦单晶及其制备方法

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TW409125B (en) * 1996-04-22 2000-10-21 Novartis Ag Antivirally active heterocyclic azahexane derivatives

Also Published As

Publication number Publication date
HK1033458A1 (en) 2001-08-31
CN1116282C (zh) 2003-07-30
TW531531B (en) 2003-05-11
BG104618A (en) 2001-02-28
EE04434B1 (et) 2005-02-15
IL137384A (en) 2006-08-01
LT2000067A (en) 2000-11-27
NO315605B1 (no) 2003-09-29
DE69806067T2 (de) 2003-01-23
LT4780B (lt) 2001-04-25
MY114838A (en) 2003-01-31
UY25345A1 (es) 2000-12-29
CZ20002564A3 (cs) 2000-10-11
NO20003692D0 (no) 2000-07-19
CN1283188A (zh) 2001-02-07
TR200001876T2 (tr) 2000-11-21
PL190744B1 (pl) 2006-01-31
JP4860037B2 (ja) 2012-01-25
SK283975B6 (sk) 2004-06-08
CA2317736C (en) 2004-11-02
EP1056722A4 (en) 2001-01-10
IL137384A0 (en) 2001-07-24
SK10622000A3 (sk) 2001-02-12
KR20010034221A (ko) 2001-04-25
ZA9956B (en) 2000-07-05
UA59432C2 (uk) 2003-09-15
AU735875B2 (en) 2001-07-19
CA2317736A1 (en) 1999-07-22
US6087383A (en) 2000-07-11
GEP20033026B (en) 2003-07-25
HUP0101389A3 (en) 2003-07-28
EE200000798A (et) 2002-06-17
EP1056722A1 (en) 2000-12-06
NZ504417A (en) 2001-09-28
AU2010199A (en) 1999-08-02
BR9814736A (pt) 2000-10-24
LV12522B (en) 2000-10-20
ES2178300T3 (es) 2002-12-16
JP2009102357A (ja) 2009-05-14
LV12522A (en) 2000-08-20
DK1056722T3 (da) 2002-09-30
CZ293507B6 (cs) 2004-05-12
EG23936A (en) 2008-01-14
NO20003692L (no) 2000-07-19
HK1033667A1 (en) 2001-09-14
KR100559283B1 (ko) 2006-03-15
PE20000185A1 (es) 2000-05-14
CO4970820A1 (es) 2000-11-07
HU227196B1 (en) 2010-10-28
PL342019A1 (en) 2001-05-07
EP1056722B1 (en) 2002-06-12
RU2186070C2 (ru) 2002-07-27
BG64774B1 (bg) 2006-03-31
WO1999036404A1 (en) 1999-07-22
RO118869B1 (ro) 2003-12-30
ATE219057T1 (de) 2002-06-15
PT1056722E (pt) 2002-09-30
DE69806067D1 (de) 2002-07-18
JP2002509136A (ja) 2002-03-26
HUP0101389A2 (hu) 2001-08-28

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