SE0301569D0 - Novel compounds - Google Patents

Novel compounds

Info

Publication number
SE0301569D0
SE0301569D0 SE0301569A SE0301569A SE0301569D0 SE 0301569 D0 SE0301569 D0 SE 0301569D0 SE 0301569 A SE0301569 A SE 0301569A SE 0301569 A SE0301569 A SE 0301569A SE 0301569 D0 SE0301569 D0 SE 0301569D0
Authority
SE
Sweden
Prior art keywords
novel compounds
novel
compounds
Prior art date
Application number
SE0301569A
Other languages
English (en)
Swedish (sv)
Inventor
Roger Bonnert
Rukhsana Rasul
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Priority to SE0301569A priority Critical patent/SE0301569D0/xx
Publication of SE0301569D0 publication Critical patent/SE0301569D0/xx
Priority to SE0302305A priority patent/SE0302305D0/xx
Priority to TW093114113A priority patent/TWI328004B/zh
Priority to TW099109193A priority patent/TW201024261A/zh
Priority to ARP040101792A priority patent/AR044552A1/es
Priority to AT10180348T priority patent/ATE552243T1/de
Priority to JP2006532212A priority patent/JP4541361B2/ja
Priority to DK08165755.3T priority patent/DK2025670T3/da
Priority to CA2526866A priority patent/CA2526866C/en
Priority to PT10180348T priority patent/PT2281815E/pt
Priority to EP10180348A priority patent/EP2281815B1/en
Priority to HR20090281T priority patent/HRP20090281T1/xx
Priority to AT08165755T priority patent/ATE502010T1/de
Priority to KR1020057022513A priority patent/KR101067586B1/ko
Priority to DK04734774T priority patent/DK1656346T3/da
Priority to HK06111158.9A priority patent/HK1090635B/xx
Priority to KR1020117009790A priority patent/KR20110050754A/ko
Priority to ES08165755T priority patent/ES2361485T3/es
Priority to RU2005137403/04A priority patent/RU2361860C2/ru
Priority to US10/558,228 priority patent/US7687535B2/en
Priority to DE602004020072T priority patent/DE602004020072D1/de
Priority to PL08165755T priority patent/PL2025670T3/pl
Priority to PT08165755T priority patent/PT2025670E/pt
Priority to SI200431669T priority patent/SI2025670T1/sl
Priority to MYPI20041992A priority patent/MY144483A/en
Priority to PCT/SE2004/000808 priority patent/WO2004106302A1/en
Priority to PL10180348T priority patent/PL2281815T3/pl
Priority to NZ543722A priority patent/NZ543722A/xx
Priority to DE602004031894T priority patent/DE602004031894D1/de
Priority to UAA200511010A priority patent/UA84701C2/ru
Priority to BRPI0410711A priority patent/BRPI0410711B8/pt
Priority to MXPA05012680A priority patent/MXPA05012680A/es
Priority to EP08165755A priority patent/EP2025670B1/en
Priority to SI200431120T priority patent/SI1656346T1/sl
Priority to DK10180348.4T priority patent/DK2281815T3/da
Priority to EP04734774A priority patent/EP1656346B1/en
Priority to CN2004800146027A priority patent/CN1795174B/zh
Priority to CN2011102633202A priority patent/CN102391171A/zh
Priority to SI200431874T priority patent/SI2281815T1/sl
Priority to AU2004242624A priority patent/AU2004242624B2/en
Priority to PT04734774T priority patent/PT1656346E/pt
Priority to ES10180348T priority patent/ES2382606T3/es
Priority to PL04734774T priority patent/PL1656346T3/pl
Priority to ES04734774T priority patent/ES2322650T3/es
Priority to KR1020117009788A priority patent/KR101067535B1/ko
Priority to AT04734774T priority patent/ATE425965T1/de
Priority to IL171928A priority patent/IL171928A/en
Priority to CO05118882A priority patent/CO5630030A2/es
Priority to ZA200509598A priority patent/ZA200509598B/en
Priority to IS8189A priority patent/IS2722B/is
Priority to NO20056130A priority patent/NO20056130L/no
Priority to IL194872A priority patent/IL194872A0/en
Priority to US12/397,618 priority patent/US20090163518A1/en
Priority to CY20091100564T priority patent/CY1109104T1/el
Priority to HK09105852.7A priority patent/HK1126773B/en
Priority to HK11107570.0A priority patent/HK1149563B/en
Priority to JP2010082748A priority patent/JP2010155862A/ja
Priority to IS8920A priority patent/IS8920A/is
Priority to US13/047,280 priority patent/US20110263614A1/en
Priority to IL212265A priority patent/IL212265A0/en
Priority to IL212371A priority patent/IL212371A0/en
Priority to CY20111100464T priority patent/CY1111469T1/el
Priority to HR20110359T priority patent/HRP20110359T1/hr
Priority to US13/344,051 priority patent/US20120178764A1/en
Priority to HRP20120390TT priority patent/HRP20120390T1/hr
Priority to CY20121100486T priority patent/CY1112853T1/el

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/16—Central respiratory analeptics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/16—Otologicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Virology (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Rheumatology (AREA)
  • Otolaryngology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
SE0301569A 2003-05-27 2003-05-27 Novel compounds SE0301569D0 (sv)

Priority Applications (66)

Application Number Priority Date Filing Date Title
SE0301569A SE0301569D0 (sv) 2003-05-27 2003-05-27 Novel compounds
SE0302305A SE0302305D0 (sv) 2003-05-27 2003-08-27 Novel Compounds
TW093114113A TWI328004B (en) 2003-05-27 2004-05-19 Substituted indoles and use thereof
TW099109193A TW201024261A (en) 2003-05-27 2004-05-19 Substituted indoles and preparation and use thereof
ARP040101792A AR044552A1 (es) 2003-05-27 2004-05-24 Derivados del indol,composiciones farmaceuticas que los contienen y procesos para su preparacion, de utilidad para el tratamiento de trastornos respiratorios
AT10180348T ATE552243T1 (de) 2003-05-27 2004-05-25 4-(acetylamino)-3-ä(4-chlorophenyl)thioü-2-meth l-1h-indole-1-essigsäure-ethyl-ester zwischenverbindung
JP2006532212A JP4541361B2 (ja) 2003-05-27 2004-05-25 新規３位硫黄置換インドール
DK08165755.3T DK2025670T3 (da) 2003-05-27 2004-05-25 Anvendelse af 3-phenylthio-1H-indol-1-eddikesyre-derivater som modulatorer af CRTh2-receptor aktivitet
CA2526866A CA2526866C (en) 2003-05-27 2004-05-25 Substituted 3-sulfur indoles for treating a disease mediated by crth2
PT10180348T PT2281815E (pt) 2003-05-27 2004-05-25 Composto intermediário de éster etílico do ácido 4-(acetilamino)-3-[(4-clorofenil)tio]-2-metil-1h-indole- 1-acético
EP10180348A EP2281815B1 (en) 2003-05-27 2004-05-25 4-(Acetylamino)-3-[(4-chlorophenyl)thio]-2-methyl-1H-indole-1-acetic acid ethyl ester intermediate compound
HR20090281T HRP20090281T1 (hr) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituirani indol za liječenje respiratornih bolesti
AT08165755T ATE502010T1 (de) 2003-05-27 2004-05-25 Verwendung von 3-phenylthio-1h-indol-1-essigsäure-derivate als modulatoren der crth2-rezeptor- aktivität
KR1020057022513A KR101067586B1 (ko) 2003-05-27 2004-05-25 신규한 치환된 3-황 인돌
DK04734774T DK1656346T3 (da) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituerede indol til behandling af luftvejssygdomme
HK06111158.9A HK1090635B (en) 2003-05-27 2004-05-25 Substituted 3-sulfur indoles
KR1020117009790A KR20110050754A (ko) 2003-05-27 2004-05-25 신규한 치환된 3-황 인돌
ES08165755T ES2361485T3 (es) 2003-05-27 2004-05-25 Uso de derivados de ácido 3-feniltio-1h-indol-acético como moduladores de la actividad del receptor crth2.
RU2005137403/04A RU2361860C2 (ru) 2003-05-27 2004-05-25 Новые замещенные 3-сера-индолы
US10/558,228 US7687535B2 (en) 2003-05-27 2004-05-25 Substituted 3-sulfur indoles
DE602004020072T DE602004020072D1 (de) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituiertes indol zur behandlung von atemwegserkrankungen
PL08165755T PL2025670T3 (pl) 2003-05-27 2004-05-25 Zastosowanie pochodnych kwasu 3-fenylotio-1H-indolo-1-octowego jako modulatorów aktywności receptora CRTh2
PT08165755T PT2025670E (pt) 2003-05-27 2004-05-25 Utiliza??o de derivados do ?cido 3-feniltio-1h-indole-1-ac?tico como moduladores da actividade dos receptores crth2
SI200431669T SI2025670T1 (sl) 2003-05-27 2004-05-25 Uporaba derivatov 3-feniltio-1H-indol-1-ocetne kisline kot modulatorjev aktivnosti CRTh2 receptorja
MYPI20041992A MY144483A (en) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituted indole for the treatment of respiratory diseases
PCT/SE2004/000808 WO2004106302A1 (en) 2003-05-27 2004-05-25 Novel substituted 3-sulfur indoles
PL10180348T PL2281815T3 (pl) 2003-05-27 2004-05-25 Związek pośredni, ester etylowy kwasu 4-(acetyloamino)-3-[(4-chlorofenylo}tio]-2-metylo-1H-indolooctowego
NZ543722A NZ543722A (en) 2003-05-27 2004-05-25 Novel substituted 3-sulfur indoles
DE602004031894T DE602004031894D1 (de) 2003-05-27 2004-05-25 Verwendung von 3-Phenylthio-1H-indol-1-essigsäure-Derivate als Modulatoren der CRTh2-Rezeptor-Aktivität
UAA200511010A UA84701C2 (ru) 2003-05-27 2004-05-25 Замещенные индолы, способ их получения, их использования
BRPI0410711A BRPI0410711B8 (pt) 2003-05-27 2004-05-25 ácido 4-(acetilamina)-3-[(4-clorofenil)tio]-2-metil-1h-indol-1-acético
MXPA05012680A MXPA05012680A (es) 2003-05-27 2004-05-25 Indoles novedosos de 3-azufre sustituidos.
EP08165755A EP2025670B1 (en) 2003-05-27 2004-05-25 Use of 3-phenylthio-1H-indole-1-acetic acid derivatives as modulators of CRTh2 receptor activity
SI200431120T SI1656346T1 (sl) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituiran indol za zdravljenje respiratornih bolezni
DK10180348.4T DK2281815T3 (da) 2003-05-27 2004-05-25 4-(Acetylamino)-3-[(4-chlorophenyl)thio]-2-methyl-1H-indole-1-acetic acid ethyl ester intermediate compound
EP04734774A EP1656346B1 (en) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituted indole for the treatment of respiratory diseases
CN2004800146027A CN1795174B (zh) 2003-05-27 2004-05-25 取代的3-硫吲哚
CN2011102633202A CN102391171A (zh) 2003-05-27 2004-05-25 新型取代的3-硫吲哚
SI200431874T SI2281815T1 (sl) 2003-05-27 2004-05-25 Vmesna spojina etil estra 4-(acetilamino)-3-((4-klorofenil)tio)-2-metil-1H-indol-1-ocetne kisline
AU2004242624A AU2004242624B2 (en) 2003-05-27 2004-05-25 Novel substituted 3-sulfur indoles
PT04734774T PT1656346E (pt) 2003-05-27 2004-05-25 Indole 1,2,3,4-tetrassubstituído para o tratamento de doenças respiratórias
ES10180348T ES2382606T3 (es) 2003-05-27 2004-05-25 Compuesto intermedio éster etílico del ácido 4-(acetilamino)-3-[(4-clorofenil)tio]-2-metil-1H-indol-acético
PL04734774T PL1656346T3 (pl) 2003-05-27 2004-05-25 1,2,3,4-Tetrapodstawiony indol do leczenia chorób dróg oddechowych
ES04734774T ES2322650T3 (es) 2003-05-27 2004-05-25 Indol 1,2,3,4-tetrasustituido para el tratamiento de enfermedades respiratorias.
KR1020117009788A KR101067535B1 (ko) 2003-05-27 2004-05-25 신규한 치환된 3-황 인돌
AT04734774T ATE425965T1 (de) 2003-05-27 2004-05-25 1,2,3,4-tetrasubstituiertes indol zur behandlung von atemwegserkrankungen
IL171928A IL171928A (en) 2003-05-27 2005-11-14 Compounds of 4 - (acetylamino) - 3 - [(4 - chlorophenyl) thio] - 2 - methyl - 1H - indole - 1 - acetic acid, salts and their solvates, and their uses in the preparation of medicine
CO05118882A CO5630030A2 (es) 2003-05-27 2005-11-23 Acido 4-(acetilamino)-3-{(4-clorofenil)tio}-2-metil-1h-indol-1-acetico y composicion farmaceutica que lo contiene
ZA200509598A ZA200509598B (en) 2003-05-27 2005-11-28 Novel substituted 3-sulfur indoles
IS8189A IS2722B (is) 2003-05-27 2005-12-20 1, 2, 3, 4- Tetrasetin indól til meðhöndlunar á öndunarfærasjúkdómum
NO20056130A NO20056130L (no) 2003-05-27 2005-12-22 Nye substituerte 3-svovelindoler
IL194872A IL194872A0 (en) 2003-05-27 2008-10-23 Novel substituted 3-sulfur indoles
US12/397,618 US20090163518A1 (en) 2003-05-27 2009-03-04 Novel Compounds
CY20091100564T CY1109104T1 (el) 2003-05-27 2009-05-28 1,2,3,4 τετρα-υποκατεστημενη ινδολη για την αντιμετωπιση ασθενειων του αναπνευστικου
HK09105852.7A HK1126773B (en) 2003-05-27 2009-06-30 Use of 3-phenylthio-1h-indole-1-acetic acid derivatives as modulators of crth2 receptor activity
HK11107570.0A HK1149563B (en) 2003-05-27 2009-06-30 4-(acetylamino)-3-[(4-chlorophenyl)thio]-2-methyl-1h-indole-1-acetic acid ethyl ester intermediate compound
JP2010082748A JP2010155862A (ja) 2003-05-27 2010-03-31 新規３位硫黄置換インドール
IS8920A IS8920A (is) 2003-05-27 2010-08-09 3-(Fenýl eða kínólyl)þíó- 1H-idnól-1-ediksýru afleður sem mótarar á virkni CRTh2 vitaka.
US13/047,280 US20110263614A1 (en) 2003-05-27 2011-03-14 Novel compounds
IL212265A IL212265A0 (en) 2003-05-27 2011-04-11 Novel compounds
IL212371A IL212371A0 (en) 2003-05-27 2011-04-14 Novel compounds
CY20111100464T CY1111469T1 (el) 2003-05-27 2011-05-16 ΧΡΗΣΗ ΠΑΡΑΓΩΓΩΝ 3-ΦΑΙΝΥΛΘΕΙΟ-1Η-ΙΝΔΟΛΗ-1-ΟΞΙΚΟΥ ΟΞΕΟΣ ΩΣ ΡΥΘΜΙΣΤΕΣ ΤΗΣ ΔΡΑΣΗΣ ΤΟΥ ΥΠΟΔΟΧΕΑ CRTh2
HR20110359T HRP20110359T1 (hr) 2003-05-27 2011-05-16 Upotreba derivata 3-feniltio-1h-indol-1-octene kiseline kao modulatora crth2 receptorske aktivnosti
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Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200307542A (en) 2002-05-30 2003-12-16 Astrazeneca Ab Novel compounds
SE0201635D0 (sv) 2002-05-30 2002-05-30 Astrazeneca Ab Novel compounds
SE0202241D0 (sv) 2002-07-17 2002-07-17 Astrazeneca Ab Novel Compounds
SE0301569D0 (sv) * 2003-05-27 2003-05-27 Astrazeneca Ab Novel compounds
SE0302232D0 (sv) 2003-08-18 2003-08-18 Astrazeneca Ab Novel Compounds
SE0303180D0 (sv) * 2003-11-26 2003-11-26 Astrazeneca Ab Novel compounds
ES2304010T3 (es) 2004-03-11 2008-09-01 Actelion Pharmaceuticals Ltd. Derivados de tetrahidropiridoindol.
CN101084190B (zh) 2004-12-27 2011-01-26 埃科特莱茵药品有限公司 作为crth2受体拮抗剂的2,3,4,9-四氢-1h-咔唑衍生物
GB0500604D0 (en) * 2005-01-13 2005-02-16 Astrazeneca Ab Novel process
DOP2006000016A (es) * 2005-01-26 2006-07-31 Aventis Pharma Inc 2-fenil-indoles como antagonistas del receptor de la prostaglandina d2.
DK1871374T3 (da) 2005-04-21 2011-12-05 Merck Serono Sa 2,3-substituerede pyrazinsulfonamider som CRTH2-inhibitorer
MX2007014256A (es) 2005-05-24 2008-03-26 Serono Lab Derivados espiro triciclicos como moduladores crth2.
EP1911759A4 (en) 2005-07-22 2010-07-21 Shionogi & Co AZAINDOL DERIVATIVE ANTAGONISTIC EFFECT ON PGD2 RECEPTOR
EP2397476A3 (en) 2005-07-22 2011-12-28 Shionogi & Co., Ltd. Indole derivative having PGD2 receptor antagonist activity
EP1939175B1 (en) 2005-09-27 2017-03-01 Shionogi&Co., Ltd. Sulfonamide derivative having pgd2 receptor antagonistic activity
CA2622000C (en) * 2005-09-30 2014-01-21 Argenta Discovery Limited Quinolines and their therapeutic use
US7741360B2 (en) 2006-05-26 2010-06-22 Astrazeneca Ab Bi-aryl or aryl-heteroaryl substituted indoles
PL2037967T3 (pl) 2006-06-16 2017-07-31 The Trustees Of The University Of Pennsylvania Antagoniści receptora prostaglandyny D2 w leczeniu łysienia androgenowego
EP2046740B1 (en) * 2006-07-22 2012-05-23 Oxagen Limited Compounds having crth2 antagonist activity
CA2658986C (en) 2006-08-07 2014-11-25 Actelion Pharmaceuticals Ltd (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetic acid derivatives
GB0702456D0 (en) 2007-02-08 2007-03-21 Astrazeneca Ab New combination
CN101772489B (zh) * 2007-06-21 2013-02-20 艾克提麦斯医药品有限公司 一种crth2拮抗剂的胺盐
EP2327693B9 (en) 2007-12-14 2012-10-24 Pulmagen Therapeutics (Asthma) Limited Indoles and their therapeutic use
US7750027B2 (en) * 2008-01-18 2010-07-06 Oxagen Limited Compounds having CRTH2 antagonist activity
US20110312945A1 (en) * 2008-10-01 2011-12-22 James Jia Crth2 modulators
AU2010212970A1 (en) 2009-02-12 2011-08-18 Merck Serono S.A. Phenoxy acetic acid derivatives
BR112012000353B1 (pt) * 2009-07-06 2020-06-02 Astrazeneca Ab Composto de fórmula markush, uso do composto, processos de reação com agente de acetilação e processo para preparação de um composto
GB0913345D0 (en) 2009-07-31 2009-09-16 Astrazeneca Ab New combination 802
WO2011061527A1 (en) 2009-11-17 2011-05-26 Astrazeneca Ab Combinations comprising a glucocorticoid receptor modulator for the treatment of respiratory diseases
US9032565B2 (en) 2009-12-16 2015-05-19 Kohler Co. Touchless faucet assembly and method of operation
WO2011073662A1 (en) 2009-12-17 2011-06-23 Astrazeneca Ab Combination of a benzoxazinone and a further agent for treating respiratory diseases
BR112012024114B1 (pt) 2010-03-22 2021-02-09 Idorsia Pharmaceuticals Ltd Compostos derivados de 3-(heteroarilamino)-1,2,3,4-tetrahidro-9h-carbazol, uso dos mesmos, e, composição farmacêutica
GB201021979D0 (en) 2010-12-23 2011-02-02 Astrazeneca Ab New compound
GB201021992D0 (en) 2010-12-23 2011-02-02 Astrazeneca Ab Compound
JP5964945B2 (ja) 2011-04-14 2016-08-03 アクテリオン ファーマシューティカルズ リミテッドＡｃｔｅｌｉｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｌｔｄ ７−（ヘテロアリ−ル−アミノ）−６，７，８，９−テトラヒドロピリド［１，２−ａ］インド−ル酢酸誘導体及びプロスタグランジンＤ２受容体調節剤としてのそれらの使用
WO2013088109A1 (en) 2011-12-16 2013-06-20 Oxagen Limited Combination of crth2 antagonist and a proton pump inhibitor for the treatment of eosinophilic esophagitis
CA2867901A1 (en) 2012-03-21 2013-09-26 The Trustees Of The University Of Pennsylvania Compositions and methods for regulating hair growth
WO2014055595A1 (en) * 2012-10-05 2014-04-10 Merck Sharp & Dohme Corp. Indoline compounds as aldosterone synthase inhibitiors related applications
WO2014145051A1 (en) 2013-03-15 2014-09-18 Jiazhong Zhang Heterocyclic compounds and uses thereof
US20140303121A1 (en) 2013-03-15 2014-10-09 Plexxikon Inc. Heterocyclic compounds and uses thereof
WO2014190199A1 (en) * 2013-05-24 2014-11-27 The California Institute For Biomedical Research Compounds for treatment of drug resistant and persistent tuberculosis
TWI649321B (zh) 2014-03-17 2019-02-01 瑞士商愛杜西亞製藥有限公司 氮雜吲哚乙酸衍生物及彼等作為前列腺素ｄ２受體調節劑之用途
WO2015140701A1 (en) 2014-03-18 2015-09-24 Actelion Pharmaceuticals Ltd Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators
GB201407820D0 (en) 2014-05-02 2014-06-18 Atopix Therapeutics Ltd Polymorphic form
GB201407807D0 (en) 2014-05-02 2014-06-18 Atopix Therapeutics Ltd Polymorphic form
JP6770522B2 (ja) 2015-02-13 2020-10-14 アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル 全身性エリテマトーデスを予防し、及び／又は、治療するためのｐｔｇｄｒ−１及び／又はｐｔｇｄｒ−２アンタゴニスト
HK1256553A1 (zh) 2015-07-30 2019-09-27 The Trustees Of The University Of Pennsylvania 用於检测pgd2对毛发生长抑制的易感性的人dp-2基因的单核苷酸多态性等位基因
AU2016323262B2 (en) 2015-09-15 2020-11-19 Idorsia Pharmaceuticals Ltd Crystalline forms
US10717735B2 (en) 2017-10-13 2020-07-21 Plexxikon Inc. Solid forms of a compound for modulating kinases
US12493355B2 (en) 2022-04-14 2025-12-09 Kohler Co. Touchless plumbing control system

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE790679A (fr) 1971-11-03 1973-04-27 Ici Ltd Derives de l'indole
JPH0615542B2 (ja) 1986-07-22 1994-03-02 吉富製薬株式会社 ピラゾロピリジン化合物
US5095031A (en) 1990-08-20 1992-03-10 Abbott Laboratories Indole derivatives which inhibit leukotriene biosynthesis
WO1993005020A1 (en) 1991-09-06 1993-03-18 Merck & Co., Inc. Indoles as inhibitors of hiv reverse transcriptase
FR2692574B1 (fr) 1992-06-23 1995-06-23 Sanofi Elf Derives hydroxy-4 benzenethio, leur preparation ainsi que leur utilisation pour la preparation de derives aminoalkoxybenzenesulfonyles.
AU6254294A (en) 1993-02-24 1994-09-14 Merck & Co., Inc. Inhibitors of hiv reverse transcriptase
US5486525A (en) * 1993-12-16 1996-01-23 Abbott Laboratories Platelet activating factor antagonists: imidazopyridine indoles
US5567711A (en) 1995-04-19 1996-10-22 Abbott Laboratories Indole-3-carbonyl and indole-3-sulfonyl derivatives as platelet activating factor antagonists
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
PL194689B1 (pl) 1996-02-13 2007-06-29 Astrazeneca Uk Ltd Pochodne chinazoliny, ich kompozycje farmaceutyczne oraz ich zastosowania
EP0885198B1 (en) 1996-03-05 2001-12-19 AstraZeneca AB 4-anilinoquinazoline derivatives
TW472045B (en) 1996-09-25 2002-01-11 Astra Ab Protein kinase C inhibitor compounds, method for their preparation, pharmaceutical composition thereof and intermediate used for their preparation
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
ZA987554B (en) 1997-08-21 2000-02-21 American Home Prod Methods for the solid phase synthesis of substituted indole compounds.
ZA9811672B (en) 1997-12-19 2000-06-19 Lilly Co Eli Hypoglycemic imidazoline compounds.
US6916841B2 (en) 1998-02-25 2005-07-12 Genetics Institute, Llc Inhibitors of phospholipase enzymes
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
WO2000078761A1 (en) 1999-06-23 2000-12-28 Sepracor, Inc. Indolyl-benzimidazole antibacterials, and methods of use thereof
AU7962200A (en) 1999-10-29 2001-05-14 Wakunaga Pharmaceutical Co., Ltd Novel indole derivatives and drugs containing the same as the active ingredient
MXPA02006338A (es) 1999-12-24 2002-12-13 Aventis Pharma Ltd Azaindoles.
EP1289952A1 (en) 2000-05-31 2003-03-12 AstraZeneca AB Indole derivatives with vascular damaging activity
WO2002008213A1 (en) 2000-07-07 2002-01-31 Angiogene Pharmaceuticals Limited Colchinol derivatives as angiogenesis inhibitors
CN1255391C (zh) 2000-07-07 2006-05-10 安吉奥金尼药品有限公司 作为血管破坏剂的colchinol衍生物
US6878522B2 (en) * 2000-07-07 2005-04-12 Baiyong Li Methods for the identification of compounds useful for the treatment of disease states mediated by prostaglandin D2
JP4595182B2 (ja) * 2000-09-07 2010-12-08 ソニー株式会社 情報記録装置、情報再生装置、情報記録方法、情報再生方法、および情報記録媒体、並びにプログラム提供媒体
TWI317634B (en) 2001-12-13 2009-12-01 Nat Health Research Institutes Aroyl indoles compounds
EP1501826B1 (en) 2002-02-01 2006-09-27 F. Hoffman-la Roche AG Substituted indoles as alpha-1 agonists
SE0200356D0 (sv) 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
SE0200411D0 (sv) 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
US7534897B2 (en) 2002-05-16 2009-05-19 Shionogi & Co., Ltd. Indole arylsulfonaimide compounds exhibiting PGD 2 receptor antagonism
SE0201635D0 (sv) * 2002-05-30 2002-05-30 Astrazeneca Ab Novel compounds
TW200307542A (en) 2002-05-30 2003-12-16 Astrazeneca Ab Novel compounds
SE0202241D0 (sv) 2002-07-17 2002-07-17 Astrazeneca Ab Novel Compounds
SE0202463D0 (sv) 2002-08-14 2002-08-14 Astrazeneca Ab Novel compounds
SE0301569D0 (sv) * 2003-05-27 2003-05-27 Astrazeneca Ab Novel compounds
SE0302232D0 (sv) 2003-08-18 2003-08-18 Astrazeneca Ab Novel Compounds
EP1675826A1 (en) 2003-10-14 2006-07-05 Oxagen Limited Compounds having crth2 antagonist activity
SE0303180D0 (sv) 2003-11-26 2003-11-26 Astrazeneca Ab Novel compounds
GB0500604D0 (en) * 2005-01-13 2005-02-16 Astrazeneca Ab Novel process
GB2422831A (en) 2005-02-04 2006-08-09 Oxagen Ltd Pyrrolopyridines and their use in the treatment of diseases mediated by PGD2 at the CRTH2 receptor
US7741360B2 (en) 2006-05-26 2010-06-22 Astrazeneca Ab Bi-aryl or aryl-heteroaryl substituted indoles
MX2008015501A (es) 2006-06-08 2009-02-18 Neurokey As Uso de agonistas del receptor de canabinoide como farmacos inductores de hipotermia para el tratamiento de isquemia.
JP5237938B2 (ja) 2006-06-28 2013-07-17 サノフイ 新規なｃｘｃｒ２阻害剤

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