IL192657A - Theophenic history as 1edg / 1p1s receptor agonists - Google Patents

Theophenic history as 1edg / 1p1s receptor agonists

Info

Publication number
IL192657A
IL192657A IL192657A IL19265708A IL192657A IL 192657 A IL192657 A IL 192657A IL 192657 A IL192657 A IL 192657A IL 19265708 A IL19265708 A IL 19265708A IL 192657 A IL192657 A IL 192657A
Authority
IL
Israel
Prior art keywords
receptor agonists
thiophene derivatives
edg1 receptor
edg1
thiophene
Prior art date
Application number
IL192657A
Other languages
English (en)
Hebrew (he)
Other versions
IL192657A0 (en
Original Assignee
Actelion Pharmaceuticals 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37908151&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IL192657(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd
Publication of IL192657A0 publication Critical patent/IL192657A0/en
Publication of IL192657A publication Critical patent/IL192657A/en

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    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • C07D413/04Heterocyclic 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

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  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Diabetes (AREA)
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  • Physical Education & Sports Medicine (AREA)
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  • Orthopedic Medicine & Surgery (AREA)
  • Pulmonology (AREA)
  • Oncology (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Communicable Diseases (AREA)
  • Obesity (AREA)
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IL192657A 2006-01-11 2008-07-07 Theophenic history as 1edg / 1p1s receptor agonists IL192657A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IB2006050103 2006-01-11
PCT/IB2007/050070 WO2007080542A1 (en) 2006-01-11 2007-01-10 Novel thiophene derivatives as s1p1/edg1 receptor agonists

Publications (2)

Publication Number Publication Date
IL192657A0 IL192657A0 (en) 2009-02-11
IL192657A true IL192657A (en) 2015-09-24

Family

ID=37908151

Family Applications (1)

Application Number Title Priority Date Filing Date
IL192657A IL192657A (en) 2006-01-11 2008-07-07 Theophenic history as 1edg / 1p1s receptor agonists

Country Status (17)

Country Link
US (1) US8003800B2 (enExample)
EP (1) EP1976512B1 (enExample)
JP (1) JP5114430B2 (enExample)
KR (1) KR101382710B1 (enExample)
CN (1) CN101370496B (enExample)
AR (1) AR058956A1 (enExample)
AU (1) AU2007204121B2 (enExample)
BR (1) BRPI0706476A2 (enExample)
CA (1) CA2635047C (enExample)
ES (1) ES2553345T3 (enExample)
IL (1) IL192657A (enExample)
MY (1) MY154909A (enExample)
NO (1) NO20083462L (enExample)
NZ (1) NZ570258A (enExample)
RU (1) RU2437877C2 (enExample)
TW (1) TWI404706B (enExample)
WO (1) WO2007080542A1 (enExample)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20080092385A (ko) 2006-01-24 2008-10-15 액테리온 파마슈티칼 리미티드 신규한 피리딘 유도체
PL2069336T3 (pl) * 2006-09-07 2013-05-31 Idorsia Pharmaceuticals Ltd Pochodne pirydyn-4-ylu jako środki immunomodulujące
TWI408139B (zh) * 2006-09-07 2013-09-11 Actelion Pharmaceuticals Ltd 新穎噻吩衍生物
AU2007292992B2 (en) * 2006-09-08 2013-01-10 Actelion Pharmaceuticals Ltd Pyridin-3-yl derivatives as immunomodulating agents
MX2009006304A (es) 2006-12-15 2009-06-23 Abbott Lab Nuevos compuestos de oxadiazol.
SI2125797T1 (sl) * 2007-03-16 2014-03-31 Actelion Pharmaceuticals Ltd. Derivati amino-piridina kot agonisti receptorja s1p1/edg1
PE20090305A1 (es) * 2007-05-22 2009-03-15 Wyeth Corp Proceso mejorado para la elaboracion de hidrazidas
ES2361463T3 (es) * 2007-08-17 2011-06-17 Actelion Pharmaceuticals Ltd. Derivados de piridina como moduladores del receptor s1p1/edg1.
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