LU90160I2 - Naratriptan facultativement sous la forme d'un sel pharmaceutiquement acceptable ou d'un solvate y compris le chlorhydrate de naratriptan - Google Patents

Naratriptan facultativement sous la forme d'un sel pharmaceutiquement acceptable ou d'un solvate y compris le chlorhydrate de naratriptan

Info

Publication number
LU90160I2
LU90160I2 LU90160C LU90160C LU90160I2 LU 90160 I2 LU90160 I2 LU 90160I2 LU 90160 C LU90160 C LU 90160C LU 90160 C LU90160 C LU 90160C LU 90160 I2 LU90160 I2 LU 90160I2
Authority
LU
Luxembourg
Prior art keywords
naratriptan
pharmaceutically acceptable
optionally
acceptable salt
hydrochloride
Prior art date
Application number
LU90160C
Other languages
English (en)
Original Assignee
Glaxo Group Ltd
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
Priority claimed from GB878719167A external-priority patent/GB8719167D0/en
Priority claimed from GB888814002A external-priority patent/GB8814002D0/en
Priority claimed from GB888814481A external-priority patent/GB8814481D0/en
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of LU90160I2 publication Critical patent/LU90160I2/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
LU90160C 1987-08-13 1997-10-31 Naratriptan facultativement sous la forme d'un sel pharmaceutiquement acceptable ou d'un solvate y compris le chlorhydrate de naratriptan LU90160I2 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB878719167A GB8719167D0 (en) 1987-08-13 1987-08-13 Chemical compounds
GB888814002A GB8814002D0 (en) 1988-06-14 1988-06-14 Chemical compounds
GB888814481A GB8814481D0 (en) 1988-06-17 1988-06-17 Chemical compounds

Publications (1)

Publication Number Publication Date
LU90160I2 true LU90160I2 (fr) 1998-01-14

Family

ID=27263551

Family Applications (1)

Application Number Title Priority Date Filing Date
LU90160C LU90160I2 (fr) 1987-08-13 1997-10-31 Naratriptan facultativement sous la forme d'un sel pharmaceutiquement acceptable ou d'un solvate y compris le chlorhydrate de naratriptan

Country Status (28)

Country Link
US (1) US4997841A (fr)
EP (1) EP0303507B1 (fr)
JP (1) JPH0633252B2 (fr)
KR (1) KR0131327B1 (fr)
AT (1) ATE92057T1 (fr)
AU (1) AU611469B2 (fr)
CA (1) CA1310968C (fr)
CY (1) CY1728A (fr)
CZ (1) CZ404291A3 (fr)
DE (2) DE3882614T2 (fr)
DK (1) DK172696B1 (fr)
ES (1) ES2058292T3 (fr)
FI (1) FI92397C (fr)
GB (1) GB2208646B (fr)
HK (1) HK86793A (fr)
HU (1) HU211576A9 (fr)
IE (1) IE61488B1 (fr)
IL (1) IL87437A0 (fr)
LU (1) LU90160I2 (fr)
LV (1) LV5736B4 (fr)
NL (1) NL970035I2 (fr)
NO (2) NO174052C (fr)
NZ (1) NZ225820A (fr)
PH (1) PH24976A (fr)
PT (1) PT88255B (fr)
SG (1) SG65393G (fr)
SK (1) SK281495B6 (fr)
UY (1) UY23657A1 (fr)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8819024D0 (en) * 1988-08-10 1988-09-14 Glaxo Group Ltd Chemical compounds
GB8903036D0 (en) * 1989-02-10 1989-03-30 Glaxo Group Ltd Chemical compounds
PT97888B (pt) * 1990-06-07 1998-12-31 Zeneca Ltd Processo para a preparacao de compostos heterociclicos derivados de indol e de composicoes farmaceuticas que os contem
DK152090D0 (da) * 1990-06-22 1990-06-22 Lundbaek A S H Piperidylsubstituerede indolderivater
US5643784A (en) * 1990-12-04 1997-07-01 H, Lundbeck A/S Indan derivatives
NZ243065A (en) 1991-06-13 1995-07-26 Lundbeck & Co As H Piperidine derivatives and pharmaceutical compositions
TW222631B (fr) * 1991-07-15 1994-04-21 Duphar Int Res
GB9209882D0 (en) * 1992-05-07 1992-06-24 Glaxo Lab Sa Compositions
GB9211277D0 (en) 1992-05-28 1992-07-15 Glaxo Group Inc Pharmaceutical compositions
FI950486A0 (fi) * 1992-08-05 1995-02-03 Wyeth John & Brother Ltd Amidijohdannaiset
GB9320115D0 (en) * 1993-09-29 1993-11-17 Glaxo Group Ltd Process
US5521196A (en) * 1994-10-05 1996-05-28 Eli Lilly And Company 5-HT1F agonists for the treatment of migraine
US5521197A (en) * 1994-12-01 1996-05-28 Eli Lilly And Company 3-<1-alkylenearyl>-4-<1,2,3,6-tetrahydropyridinyl>-and 3-<1-alkylenearyl>-4-piperidinyl-1h-indoles: new 5-HT1F agonists
FR2731224B1 (fr) * 1995-03-02 1997-05-30 Pf Medicament Nouveaux derives bi-tryptaminiques sulfonamides, leur procede de preparation et leur utilisation a titre de medicaments
FR2731222A1 (fr) * 1995-03-02 1996-09-06 Pf Medicament Nouveaux derives de piperazine aminoindoles cycliques, leur procede de preparation et leur utilisation a titre de medicaments
WO1996029075A1 (fr) * 1995-03-20 1996-09-26 Eli Lilly And Company 5-substitue-3-(1,2,3,6-tetrahydropyridine-4-yl)- et 3-(piperidine-4-yl)-1h-indoles: nouveaux antagonistes 5-ht¿1f?
WO1997033579A1 (fr) * 1996-03-13 1997-09-18 Glaxo Group Limited Medicaments comprenant des agonistes du recepteur de type 5ht1 presentant une meilleure absorption
AR013669A1 (es) * 1997-10-07 2001-01-10 Smithkline Beecham Corp Compuestos y metodos
US6066092A (en) * 1997-11-06 2000-05-23 Cady; Roger K. Preemptive prophylaxis of migraine device and method
US7189753B1 (en) 1997-11-06 2007-03-13 Cady Roger K Preemptive prophylaxis of migraine
IL153605A0 (en) 2000-07-21 2003-07-06 Lundbeck & Co As H Indole derivatives useful for the treatment of cns disorders
ATE374192T1 (de) * 2000-11-29 2007-10-15 Lilly Co Eli 1-(2-m-methansulfonamidophenylethyl)-4-(m- trifluoromethylphenyl)piperazine und ihre akzeptablen pharmazeutischen salze und solvate und ihre verwendung zur behandlung von inkontinenz
US8329734B2 (en) 2009-07-27 2012-12-11 Afgin Pharma Llc Topical therapy for migraine
EP2316468A1 (fr) 2002-02-22 2011-05-04 Shire LLC Système de distribution et méthodes de protection et d'administration de dextroamphetamine
US20070065463A1 (en) 2003-06-20 2007-03-22 Ronald Aung-Din Topical therapy for the treatment of migranes, muscle sprains, muscle spasms, spasticity and related conditions
MX2007005845A (es) * 2004-11-24 2007-07-04 Alcon Inc Metodo para entregar rocio nasal.
CA2666149A1 (fr) * 2006-10-19 2008-04-24 Auspex Pharmaceuticals, Inc. Indoles substitues
WO2008056378A2 (fr) * 2006-11-09 2008-05-15 Natco Pharma Limited Nouveau procédé destiné à la préparation de naratriptan
WO2008072257A2 (fr) * 2006-12-12 2008-06-19 Ind-Swift Laboratories Limited Procédé de préparation de dérivés de l'indole
WO2009016466A2 (fr) * 2007-07-30 2009-02-05 Orchid Chemicals & Pharmaceuticals Limited Procédé de préparation de chlorhydrate de naratriptan
WO2009118753A2 (fr) * 2008-03-07 2009-10-01 Usv Limited Procédé de préparation de chlorhydrate de naratriptane
JP2011526889A (ja) 2008-06-30 2011-10-20 アフギン ファーマ,エルエルシー 局所局部的神経作用療法
WO2010004580A2 (fr) * 2008-07-11 2010-01-14 Ind-Swift Laboratories Limited Procédé de préparation de dérivés d'indole
WO2010084507A2 (fr) * 2008-07-15 2010-07-29 Sun Pharmaceutical Industries Ltd. Procédé de synthèse du n-méthyl-2-[3-(1-méthyl-4-pipéridyl)-1h-indol-5-yl]-éthanesulfonamide et de ses sels d'addition acide
NZ597620A (en) 2009-08-20 2013-08-30 Cipla Ltd A process for the synthesis of naratriptan
CN102276581B (zh) * 2011-08-05 2013-06-12 上海师范大学 N-取代四氢吡啶连吲哚类化合物及其制备方法及应用
HK1244715A1 (zh) 2015-03-02 2018-08-17 阿福金制药有限责任公司 用大麻素的局部区域神经影响性疗法
US10383816B2 (en) 2015-03-02 2019-08-20 Afgin Pharma, Llc Topical regional neuro-affective therapy with cannabinoid combination products
US20180049994A1 (en) 2016-08-16 2018-02-22 Afgin Pharma, Llc Topical regional neuro-affective therapy with caryophyllene
EP3766483A1 (fr) 2019-07-19 2021-01-20 BioPharma Synergies, S. L. Composition de poudre orodispersible comprenant un triptane

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2362628A1 (fr) * 1976-08-26 1978-03-24 Roussel Uclaf Nouveaux derives du piperidyl-indole et leurs sels, procede de preparation et application a titre de medicaments
FR2421899A1 (fr) * 1978-01-16 1979-11-02 Roussel Uclaf Nouveaux derives du tetrahydropyridinyl-indole et leurs sels, le procede de preparation et l'application a titre de medicaments de ces nouveaux produits
IT1170387B (it) * 1982-06-07 1987-06-03 Glaxo Group Ltd Composti eterociclici, procedimento per prepararli e composizioni farmaceutiche che li contengono
FR2533924A1 (fr) * 1982-10-05 1984-04-06 Roussel Uclaf Nouveaux derives du 4-(1h-indol-3-yl)a-methyl piperidine-1-ethanol, leurs sels, le procede de preparation, l'application a titre de medicaments et les compositions les renfermant
GB8332435D0 (en) * 1983-12-06 1984-01-11 Glaxo Group Ltd Chemical compounds
GB8332437D0 (en) * 1983-12-06 1984-01-11 Glaxo Group Ltd Chemical compounds
DE3419935A1 (de) * 1984-05-28 1985-11-28 Merck Patent Gmbh, 6100 Darmstadt Verwendung von hydroxyindolderivaten bei der senkung des blutdrucks
GB2162522B (en) * 1984-08-01 1988-02-24 Glaxo Group Ltd An indole derivative
US4548939A (en) * 1984-10-01 1985-10-22 Janssen Pharmaceutica N. V. 1H-Indol-3-yl containing 1,3-dimethyl-1H-purine-2,6-diones
IT1181741B (it) * 1984-12-04 1987-09-30 Glaxo Group Ltd Derivati di indolo,procedimento per prepararli e composizioni farmaceutiche che li contengono
IE58370B1 (en) * 1985-04-10 1993-09-08 Lundbeck & Co As H Indole derivatives
GB8819024D0 (en) * 1988-08-10 1988-09-14 Glaxo Group Ltd Chemical compounds
GB8903036D0 (en) * 1989-02-10 1989-03-30 Glaxo Group Ltd Chemical compounds

Also Published As

Publication number Publication date
KR0131327B1 (en) 1998-04-17
CA1310968C (fr) 1992-12-01
DE3882614T2 (de) 1993-11-18
PT88255A (pt) 1989-06-30
FI92397C (fi) 1994-11-10
HU211576A9 (en) 1995-12-28
GB2208646A (en) 1989-04-12
DK455488D0 (da) 1988-08-12
SG65393G (en) 1993-08-06
EP0303507B1 (fr) 1993-07-28
NZ225820A (en) 1990-09-26
IE61488B1 (en) 1994-11-02
NL970035I1 (nl) 1997-11-03
ES2058292T3 (es) 1994-11-01
SK281495B6 (sk) 2001-04-09
NL970035I2 (nl) 1998-01-05
NO174052C (no) 1994-03-09
JPH0633252B2 (ja) 1994-05-02
PH24976A (en) 1990-12-26
PT88255B (pt) 1995-03-01
LV5736B4 (lv) 1997-06-20
NO883587D0 (no) 1988-08-12
AU2069288A (en) 1989-02-16
EP0303507A2 (fr) 1989-02-15
KR890003731A (ko) 1989-04-17
UY23657A1 (es) 1994-02-25
FI883744A0 (fi) 1988-08-12
NO883587L (no) 1989-02-14
ATE92057T1 (de) 1993-08-15
GB8819200D0 (en) 1988-09-14
DK455488A (da) 1989-02-14
CZ404291A3 (en) 1993-04-14
JPH01207288A (ja) 1989-08-21
IL87437A0 (en) 1989-01-31
DE3882614D1 (de) 1993-09-02
NO1998008I1 (no) 1998-02-05
FI92397B (fi) 1994-07-29
IE882477L (en) 1989-02-13
AU611469B2 (en) 1991-06-13
LV5736A4 (lv) 1996-06-20
NO174052B (no) 1993-11-29
HK86793A (en) 1993-08-27
CY1728A (en) 1994-05-06
DE19775082I2 (de) 2006-04-27
EP0303507A3 (en) 1990-09-19
FI883744L (fi) 1989-02-14
GB2208646B (en) 1991-06-26
US4997841A (en) 1991-03-05
SK404291A3 (en) 2000-09-12
DK172696B1 (da) 1999-05-31

Similar Documents

Publication Publication Date Title
LU90160I2 (fr) Naratriptan facultativement sous la forme d&#39;un sel pharmaceutiquement acceptable ou d&#39;un solvate y compris le chlorhydrate de naratriptan
DK391289D0 (da) Indolderivater
ATE103812T1 (de) Zusammensetzung zur behandlung von ischaemischen stoerungen in organen.
CA2203274A1 (fr) Inhibiteurs de synthese d&#39;apolipoproteines-b
DE69008142D1 (de) 4-Substituierten Imidazolen zur Senkung des intraokularen Druckes.
MY132062A (en) Apolipoprotein-b synthesis inhibitors
IL106445A0 (en) 4-substituted 1,2,4-triazole derivatives,their preparation and pharmaceutical compositions containing them
EP0555479A4 (fr)
MY103509A (en) Indole derivatives.
TNSN93081A1 (fr) Procede de preparation de derives de la n-(phenylethyl-b-ol) amine