CY1107281T1 - Παραγωγα τροπανιου υποκατεστημενα με ιδιδαζοπυριδινη με ενεργοτητα ανταγωνιστη ccr5 υποδοχεα για τη θεραπεια hiv και φλεγμονης - Google Patents
Παραγωγα τροπανιου υποκατεστημενα με ιδιδαζοπυριδινη με ενεργοτητα ανταγωνιστη ccr5 υποδοχεα για τη θεραπεια hiv και φλεγμονηςInfo
- Publication number
- CY1107281T1 CY1107281T1 CY20081100178T CY081100178T CY1107281T1 CY 1107281 T1 CY1107281 T1 CY 1107281T1 CY 20081100178 T CY20081100178 T CY 20081100178T CY 081100178 T CY081100178 T CY 081100178T CY 1107281 T1 CY1107281 T1 CY 1107281T1
- Authority
- CY
- Cyprus
- Prior art keywords
- hiv
- tropani
- ididazopyridine
- antagonist activity
- ccr5 antagonist
- Prior art date
Links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
- A61K31/41—Heterocyclic 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
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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Abstract
Η παρούσα εφεύρεση εξασφαλίζει ενώσεις του τύπου (Ι) όπου R1 και R2 είναι όπως ορίστηκαν ανωτέρω. Οι ενώσεις της παρούσας εφεύρεσης είναι διαμορφωτές, ειδικότερα ανταγωνιστές, της ενεργότητας των υποδοχέων των CCR5 χημοκινών. Οι διαμορφωτές του CCR5 υποδοχέα μπορούν να είναι χρήσιμοι στην θεραπεία διαφόρων φλεγμονωδών ασθενειών και καταστάσεων, και στη θεραπεία της μόλυνσης από ΗIV και γενετικά συναφών ρετροϊών.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0323236.0A GB0323236D0 (en) | 2003-10-03 | 2003-10-03 | Chemical compounds |
GB0325020A GB0325020D0 (en) | 2003-10-27 | 2003-10-27 | Chemical compounds |
GB0418566A GB0418566D0 (en) | 2004-08-19 | 2004-08-19 | Tropane derivatives |
EP04769496A EP1682545B1 (en) | 2003-10-03 | 2004-09-28 | Imidazopyridine substituted tropane derivatives with ccr5 receptor antagonist activity for the treatment of hiv and inflammation |
Publications (1)
Publication Number | Publication Date |
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CY1107281T1 true CY1107281T1 (el) | 2012-11-21 |
Family
ID=34426592
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CY20081100178T CY1107281T1 (el) | 2003-10-03 | 2008-02-14 | Παραγωγα τροπανιου υποκατεστημενα με ιδιδαζοπυριδινη με ενεργοτητα ανταγωνιστη ccr5 υποδοχεα για τη θεραπεια hiv και φλεγμονης |
Country Status (35)
Country | Link |
---|---|
US (2) | US7309790B2 (el) |
EP (1) | EP1682545B1 (el) |
JP (1) | JP4874107B2 (el) |
KR (1) | KR100777885B1 (el) |
AP (1) | AP2174A (el) |
AR (1) | AR045856A1 (el) |
AT (1) | ATE380813T1 (el) |
AU (1) | AU2004278158B2 (el) |
BR (1) | BRPI0414862A (el) |
CA (1) | CA2540834C (el) |
CY (1) | CY1107281T1 (el) |
DE (1) | DE602004010708T2 (el) |
DK (1) | DK1682545T3 (el) |
EA (1) | EA009941B1 (el) |
EC (1) | ECSP066475A (el) |
ES (1) | ES2295924T3 (el) |
GE (1) | GEP20084417B (el) |
HN (1) | HN2004000383A (el) |
HR (1) | HRP20080052T3 (el) |
IL (1) | IL174208A0 (el) |
MA (1) | MA28080A1 (el) |
MX (1) | MXPA06003749A (el) |
MY (1) | MY137609A (el) |
NO (1) | NO20061978L (el) |
NZ (1) | NZ545837A (el) |
OA (1) | OA13266A (el) |
PA (1) | PA8614301A1 (el) |
PE (1) | PE20050961A1 (el) |
PL (1) | PL1682545T3 (el) |
PT (1) | PT1682545E (el) |
RS (1) | RS20060198A (el) |
SI (1) | SI1682545T1 (el) |
TW (1) | TWI280244B (el) |
UY (1) | UY28546A1 (el) |
WO (1) | WO2005033107A1 (el) |
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CN105348203B (zh) | 2005-06-08 | 2018-09-18 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
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JP2009528295A (ja) | 2006-02-24 | 2009-08-06 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Jak経路の阻害のための組成物および方法 |
MX2008012936A (es) * | 2006-04-05 | 2008-10-15 | Schering Corp | Formulaciones farmaceuticas: sales de 8-[{1-(3,5-bis-(trifluoromet il)fenil)-etoxi} metil]-8-fenil-1,7-diaza-espiro[4,5]decan-2-ona y metodos de tratamiento usando las mismas. |
US20080108586A1 (en) * | 2006-09-06 | 2008-05-08 | Incyte Corporation | Combination therapy for human immunodeficiency virus infection |
DK2089369T3 (da) | 2006-10-19 | 2011-05-09 | Rigel Pharmaceuticals Inc | 2,4-pyrimidindiaminderivater som hæmmere af JAK-kinaser til behandling af autoimmune sygdomme |
EP2120938A4 (en) * | 2006-12-20 | 2010-12-08 | Merck Sharp & Dohme | IMIDAZOPYRIDINE ANALOGUE AS CB2 RECEPTOR MODULATORS FOR THE TREATMENT OF PAIN, RESPIRATORY AND NON-RESPIRATORY DISEASES |
AR065802A1 (es) * | 2007-03-22 | 2009-07-01 | Schering Corp | Formulaciones de comprimidos que contienen sales de 8- [( 1- ( 3,5- bis- (trifluorometil) fenil) -etoxi ) - metil) -8- fenil -1, 7- diaza- spiro [ 4,5] decan -2- ona y comprimidos elaborados a partir de estas |
MX2010004493A (es) * | 2007-10-25 | 2010-06-11 | Exelixis Inc | Compuestos de tropano. |
PT2265607T (pt) | 2008-02-15 | 2017-03-08 | Rigel Pharmaceuticals Inc | Compostos de pirimidina-2-amina e sua utilização como inibidores de jak cinases |
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AU2009238590A1 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
JP2010043063A (ja) | 2008-05-09 | 2010-02-25 | Agency For Science Technology & Research | 川崎病の診断及び治療 |
ES2609640T3 (es) | 2009-08-14 | 2017-04-21 | Opko Health, Inc | Formulaciones intravenosas de rolapitant |
BR112012024522A2 (pt) | 2010-04-02 | 2017-08-08 | Phivco 1 Llc | combinação, uso de uma combinação, composição farmacêutica, forma de dosagem única , kit, e, método para tratar um distúrbio |
WO2012061428A2 (en) | 2010-11-01 | 2012-05-10 | Portola Pharmaceuticals, Inc. | Nicotinamides as jak kinase modulators |
US20140271680A1 (en) | 2011-08-12 | 2014-09-18 | Universite Paris-Est Creteil Val De Marne | Methods and pharmaceutical compositions for treatment of pulmonary hypertension |
EP2782579B1 (en) | 2011-11-23 | 2019-01-02 | Portola Pharmaceuticals, Inc. | Pyrazine kinase inhibitors |
US9676756B2 (en) | 2012-10-08 | 2017-06-13 | Portola Pharmaceuticals, Inc. | Substituted pyrimidinyl kinase inhibitors |
PL3049378T3 (pl) * | 2013-09-25 | 2019-06-28 | SpecGx LLC | Wytwarzanie radiojodowanego 3-fluoropropylo-nor-beta-CIT |
GB201321748D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
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US6855724B2 (en) * | 2002-04-08 | 2005-02-15 | Agouron Pharmaceuticals, Inc. | Tropane derivatives useful in therapy |
RS51550B (en) | 2002-04-08 | 2011-06-30 | Pfizer Inc. | KAO DERIVATIVES KAO MODULATORS CCR5 |
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2004
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