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CO5160253A1 - Complejo de 1,4-benzodiazepinas sustituidas y sulfobutileter -7-ciclodextrina o 2-hidroxipropil-b-ciclodextrina . - Google Patents

Complejo de 1,4-benzodiazepinas sustituidas y sulfobutileter -7-ciclodextrina o 2-hidroxipropil-b-ciclodextrina .

Info

Publication number
CO5160253A1
CO5160253A1 CO00002434A CO00002434A CO5160253A1 CO 5160253 A1 CO5160253 A1 CO 5160253A1 CO 00002434 A CO00002434 A CO 00002434A CO 00002434 A CO00002434 A CO 00002434A CO 5160253 A1 CO5160253 A1 CO 5160253A1
Authority
CO
Colombia
Prior art keywords
cyclodextrine
substituted
cyclodextrin
complex
sulfobutileter
Prior art date
Application number
CO00002434A
Other languages
English (en)
Inventor
S Raghavan Krishnaswamy
Timothy M Malloy
A Varia Sailesh
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
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of CO5160253A1 publication Critical patent/CO5160253A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nanotechnology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Medical Informatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Un complejo del inhibidor de la rasfarnesiltransferasa que comprende el inhibidor de la rasfarnesiltransferasa o una sal farmacéuticamente aceptable del mismo<EMI FILE="00002434_1" ID="1" IMF=JPEG >en donde n es 0 o 1; R1 se selecciona de Cl, Br, fenilo, piridilo o ciano; R2 se selecciona de alquilo C1-C4, arilo o arilo sustituido o heterociclo; Z1 se selecciona de CO, SO2, C02 o SO2NR5, R5 se selecciona de hidrógeno, alquilo C1-C4 o alquilo sustituido; y sulfobutiléter-7-B-ciclodextrina o 2-hidroxipropil-B-ciclodextrina en una relación molar del inhibidor al sulfobutiléter-7-B-ciclodextrina o 2-hidroxipropil-B-ciclodextrina dentro del intervalo de 1 a 2 o superior.
CO00002434A 1999-01-21 2000-01-18 Complejo de 1,4-benzodiazepinas sustituidas y sulfobutileter -7-ciclodextrina o 2-hidroxipropil-b-ciclodextrina . CO5160253A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11664799P 1999-01-21 1999-01-21

Publications (1)

Publication Number Publication Date
CO5160253A1 true CO5160253A1 (es) 2002-05-30

Family

ID=22368422

Family Applications (1)

Application Number Title Priority Date Filing Date
CO00002434A CO5160253A1 (es) 1999-01-21 2000-01-18 Complejo de 1,4-benzodiazepinas sustituidas y sulfobutileter -7-ciclodextrina o 2-hidroxipropil-b-ciclodextrina .

Country Status (33)

Country Link
US (1) US6218375B1 (es)
EP (1) EP1143796A4 (es)
JP (1) JP2002535253A (es)
KR (1) KR100708360B1 (es)
CN (1) CN1219517C (es)
AR (1) AR022323A1 (es)
AU (1) AU772204B2 (es)
BG (1) BG105666A (es)
BR (1) BR9916566A (es)
CA (1) CA2359646C (es)
CO (1) CO5160253A1 (es)
CZ (1) CZ20012601A3 (es)
EE (1) EE200100382A (es)
GE (1) GEP20043214B (es)
HK (1) HK1038865A1 (es)
HU (1) HUP0105160A3 (es)
ID (1) ID30139A (es)
IL (1) IL144025A (es)
LT (1) LT4893B (es)
LV (1) LV12712B (es)
MY (1) MY119700A (es)
NO (1) NO20013585L (es)
NZ (1) NZ511995A (es)
PE (1) PE20001419A1 (es)
PL (1) PL195280B1 (es)
RU (1) RU2230062C2 (es)
SK (1) SK9602001A3 (es)
TR (1) TR200102109T2 (es)
TW (1) TWI232752B (es)
UA (1) UA67825C2 (es)
UY (2) UY25987A1 (es)
WO (1) WO2000042849A1 (es)
ZA (1) ZA200104416B (es)

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TWI310684B (en) * 2000-03-27 2009-06-11 Bristol Myers Squibb Co Synergistic pharmaceutical kits for treating cancer
JP2003063965A (ja) * 2001-06-13 2003-03-05 Otsuka Pharmaceut Factory Inc 注射用シロスタゾール水性製剤
US6566347B1 (en) * 2001-08-22 2003-05-20 Duquesne University Of The Holy Ghost Controlled release pharmaceutical
US7074921B2 (en) * 2001-11-13 2006-07-11 Bristol Myers Squibb Company Process for the preparation of 3,7-disubstituted-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine compounds
KR100451485B1 (ko) 2002-03-28 2004-10-06 주식회사종근당 푸마질롤 유도체 또는 그 염의 포접 화합물, 및 이를포함하는 약제학적 조성물
US6869939B2 (en) * 2002-05-04 2005-03-22 Cydex, Inc. Formulations containing amiodarone and sulfoalkyl ether cyclodextrin
US6818662B2 (en) * 2002-05-28 2004-11-16 Taisho Pharmaceutical Co., Ltd. Pharmaceutical composition
US20040009972A1 (en) * 2002-06-17 2004-01-15 Ding Charles Z. Benzodiazepine inhibitors of mitochondial F1F0 ATP hydrolase and methods of inhibiting F1F0 ATP hydrolase
US7157446B2 (en) * 2003-05-02 2007-01-02 Bristol Myers Squibb Company Complex of ras-farnesyltransferase inhibitor, a cyclodextrin, and ethanol
US20070020299A1 (en) 2003-12-31 2007-01-25 Pipkin James D Inhalant formulation containing sulfoalkyl ether cyclodextrin and corticosteroid
MX2008004287A (es) * 2005-09-30 2008-10-23 Ovation Pharmaceuticals Inc Formulacion de carbamazepina parenteral novedosa.
US20100204178A1 (en) * 2006-10-02 2010-08-12 James Cloyd Novel parenteral carbamazepine formulation
CN100503647C (zh) * 2005-11-02 2009-06-24 南京师范大学 羟丙基-磺丁基-β-环糊精及其制备方法、分析方法以及在药学上的应用
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
KR20090087079A (ko) * 2006-11-21 2009-08-14 노파르티스 아게 벤조디아제핀 구조의 rsv 억제제를 포함하는 안정한 비경구 제형
US12370352B2 (en) 2007-06-28 2025-07-29 Cydex Pharmaceuticals, Inc. Nasal and ophthalmic delivery of aqueous corticosteroid solutions
PT2725028T (pt) 2008-10-22 2016-08-31 Array Biopharma Inc Compostos de pirazolo[1,5-]pirimidina substituídos como intermediários na síntese de inibidores de cinase trk
JP5798621B2 (ja) 2010-05-26 2015-10-21 ニューロフィキシア ベー.フェー. 2−イミノビオチン製剤およびその使用
WO2012034038A2 (en) * 2010-09-09 2012-03-15 H. Lee Moffitt Cancer Center And Research Institute, Inc. Dual inhibitors of farnesyltransferase and geranylgeranyltransferase i
RU2632097C2 (ru) * 2011-10-07 2017-10-02 ПАЙСИЗ ТЕРАПЬЮТИКЗ ЭлЭлСи Лечение злокачественных и незлокачественных заболеваний с помощью антагонистов ras
CN105194685A (zh) * 2015-10-15 2015-12-30 重庆大学 磺胺脒的磺丁基醚-β-环糊精包合物及其粉针制剂
FI3389653T3 (fi) 2015-12-16 2023-12-18 Neurophyxia B V 2-iminobiotiini käytettäväksi aivosoluvaurion hoidossa
RS65987B1 (sr) 2016-04-04 2024-10-31 Loxo Oncology Inc Tečne formulacije (s)-n-(5-((r)-2-(2,5-difluorofenil)-pirolidin-1-il)-pirazolo[1,5-]pirimidin-3-il)-3-hidroksipirolidin-1-karboksamida
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
EP3800189B1 (en) 2016-05-18 2023-06-28 Loxo Oncology, Inc. Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide
JOP20190092A1 (ar) 2016-10-26 2019-04-25 Array Biopharma Inc عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها
US20210145816A1 (en) * 2019-11-15 2021-05-20 Cyclolab Cyclodextrin Research And Development Laboratory Ltd. Pharmaceutical formulation of lonafarnib with a sulfobutylether beta-cyclodextrin
CA3162106A1 (en) 2019-12-27 2021-07-01 Yuli Xie Spiro ring-containing quinazoline compound
US20250049926A1 (en) * 2021-12-15 2025-02-13 Sillajen, Inc. Pharmaceutical compositions comprising modified betacyclodextrins
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
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US4596795A (en) * 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
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Also Published As

Publication number Publication date
BR9916566A (pt) 2001-11-13
IL144025A0 (en) 2002-04-21
KR100708360B1 (ko) 2007-04-17
UA67825C2 (uk) 2004-07-15
CA2359646A1 (en) 2000-07-27
HUP0105160A2 (hu) 2002-05-29
EP1143796A1 (en) 2001-10-17
PL366338A1 (en) 2005-01-24
NO20013585D0 (no) 2001-07-20
PL195280B1 (pl) 2007-08-31
EE200100382A (et) 2002-12-16
BG105666A (en) 2002-04-30
KR20010101611A (ko) 2001-11-14
LV12712A (lv) 2001-09-20
RU2230062C2 (ru) 2004-06-10
TR200102109T2 (tr) 2001-12-21
PE20001419A1 (es) 2001-02-21
HUP0105160A3 (en) 2003-01-28
SK9602001A3 (en) 2002-06-04
EP1143796A4 (en) 2002-03-20
AU772204B2 (en) 2004-04-22
WO2000042849A1 (en) 2000-07-27
ZA200104416B (en) 2002-05-29
CN1219517C (zh) 2005-09-21
IL144025A (en) 2004-05-12
AU2374000A (en) 2000-08-07
NO20013585L (no) 2001-09-04
CA2359646C (en) 2008-12-02
TWI232752B (en) 2005-05-21
UY25987A1 (es) 2000-09-29
UY25986A1 (es) 2000-09-29
JP2002535253A (ja) 2002-10-22
LT4893B (lt) 2002-02-25
CZ20012601A3 (cs) 2002-05-15
ID30139A (id) 2001-11-08
LV12712B (en) 2002-01-20
GEP20043214B (en) 2004-04-26
AR022323A1 (es) 2002-09-04
HK1038865A1 (zh) 2002-04-04
MY119700A (en) 2005-06-30
NZ511995A (en) 2003-11-28
LT2001064A (en) 2001-10-25
CN1333651A (zh) 2002-01-30
US6218375B1 (en) 2001-04-17

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