MX347619B - Polimorfos y sales de 6-(1h-indol-4-il)-4-(5-{[4-(1-metiletil)-1-p iperazinil] metil}-1,3-oxazol-2-il)-1h-indazol como inhibidores de pi3k para usarse por ejemplo en el tratamiento de trastornos respiratorios. - Google Patents
Polimorfos y sales de 6-(1h-indol-4-il)-4-(5-{[4-(1-metiletil)-1-p iperazinil] metil}-1,3-oxazol-2-il)-1h-indazol como inhibidores de pi3k para usarse por ejemplo en el tratamiento de trastornos respiratorios.Info
- Publication number
- MX347619B MX347619B MX2013004783A MX2013004783A MX347619B MX 347619 B MX347619 B MX 347619B MX 2013004783 A MX2013004783 A MX 2013004783A MX 2013004783 A MX2013004783 A MX 2013004783A MX 347619 B MX347619 B MX 347619B
- Authority
- MX
- Mexico
- Prior art keywords
- polymorphs
- salts
- perazinyl
- oxazol
- indazole
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 2
- MCIDWGZGWVSZMK-UHFFFAOYSA-N 2-[6-(1h-indol-4-yl)-1h-indazol-4-yl]-5-[(4-propan-2-ylpiperazin-1-yl)methyl]-1,3-oxazole Chemical class C1CN(C(C)C)CCN1CC1=CN=C(C=2C=3C=NNC=3C=C(C=2)C=2C=3C=CNC=3C=CC=2)O1 MCIDWGZGWVSZMK-UHFFFAOYSA-N 0.000 title 1
- 239000012828 PI3K inhibitor Substances 0.000 title 1
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 title 1
- 208000023504 respiratory system disease Diseases 0.000 title 1
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 abstract 1
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
Classifications
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- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
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- 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
- A61K31/41—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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
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- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- Health & Medical Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
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- General Health & Medical Sciences (AREA)
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- Epidemiology (AREA)
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- Dermatology (AREA)
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Abstract
La presente invención está dirigida a un polimorfo de un compuesto de la fórmula (II) y sales y polimorfos de las mismas, que son inhibidores de la actividad de la PI3 cinasa.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1018124.6A GB201018124D0 (en) | 2010-10-27 | 2010-10-27 | Polymorphs and salts |
PCT/EP2011/068604 WO2012055846A1 (en) | 2010-10-27 | 2011-10-25 | Polymorphs and salts of 6-(1h-indol-4-yl)-4-(5- { [4-(1-methylethyl)-1-pi perazinyl] methyl} -1,3-oxazol-2-yl)-1h-indazole as pi3k inhibitors for use in the treatment of e.g. respiratory disorders |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2013004783A MX2013004783A (es) | 2013-06-03 |
MX347619B true MX347619B (es) | 2017-05-04 |
Family
ID=43365584
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2013004783A MX347619B (es) | 2010-10-27 | 2011-10-25 | Polimorfos y sales de 6-(1h-indol-4-il)-4-(5-{[4-(1-metiletil)-1-p iperazinil] metil}-1,3-oxazol-2-il)-1h-indazol como inhibidores de pi3k para usarse por ejemplo en el tratamiento de trastornos respiratorios. |
Country Status (26)
Country | Link |
---|---|
US (1) | US8993576B2 (es) |
EP (2) | EP2632921B1 (es) |
JP (1) | JP5894603B2 (es) |
KR (1) | KR101774026B1 (es) |
CN (1) | CN103270037B (es) |
AU (1) | AU2011322649B2 (es) |
BR (1) | BR112013010126B1 (es) |
CA (1) | CA2814436C (es) |
CY (1) | CY1121248T1 (es) |
DK (1) | DK2632921T3 (es) |
EA (1) | EA022872B1 (es) |
ES (1) | ES2703716T3 (es) |
GB (1) | GB201018124D0 (es) |
HR (1) | HRP20182059T1 (es) |
HU (1) | HUE042754T2 (es) |
IL (1) | IL225704A (es) |
LT (1) | LT2632921T (es) |
MX (1) | MX347619B (es) |
PL (1) | PL2632921T3 (es) |
PT (1) | PT2632921T (es) |
RS (1) | RS58072B1 (es) |
SG (1) | SG189179A1 (es) |
SI (1) | SI2632921T1 (es) |
TR (1) | TR201819939T4 (es) |
WO (1) | WO2012055846A1 (es) |
ZA (1) | ZA201302480B (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5508400B2 (ja) | 2008-06-05 | 2014-05-28 | グラクソ グループ リミテッド | Pi3キナーゼの阻害剤としてのベンズピラゾール誘導体 |
ATE552255T1 (de) | 2008-06-05 | 2012-04-15 | Glaxo Group Ltd | 4-aminoindazole |
JP5502076B2 (ja) | 2008-06-05 | 2014-05-28 | グラクソ グループ リミテッド | 新規化合物 |
WO2010102958A1 (en) | 2009-03-09 | 2010-09-16 | Glaxo Group Limited | 4-oxadiazol-2 -yl- indazoles as inhibitors of p13 kinases |
PL2424864T3 (pl) | 2009-04-30 | 2015-05-29 | Glaxo Group Ltd | Podstawione oksazolami indazole jako inhibitory kinazy pi3 |
JP5876051B2 (ja) * | 2010-09-08 | 2016-03-02 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体 |
GB201018124D0 (en) | 2010-10-27 | 2010-12-08 | Glaxo Group Ltd | Polymorphs and salts |
KR102226489B1 (ko) * | 2012-07-27 | 2021-03-11 | 사토 파머슈티컬 가부시키가이샤 | 디플루오로메틸렌 화합물 |
EA035391B1 (ru) | 2012-11-08 | 2020-06-05 | Ризен Фармасьютикалз Са | Фармацевтические композиции, содержащие ингибитор pde4 и ингибитор pi3-дельта или двойной ингибитор pi3-дельта-гамма киназы |
WO2015055690A1 (en) | 2013-10-17 | 2015-04-23 | Glaxosmithkline Intellectual Property Development Limited | Pi3k inhibitor for treatment of respiratory disease |
WO2015055691A1 (en) | 2013-10-17 | 2015-04-23 | Glaxosmithkline Intellectual Property Development Limited | Pi3k inhibitor for treatment of respiratory disease |
GB201509492D0 (en) * | 2015-06-02 | 2015-07-15 | Glaxosmithkline Ip Dev Ltd | Novel processes |
JP7549306B2 (ja) | 2016-07-22 | 2024-09-11 | 株式会社リピドームラボ | 新規リン脂質およびその利用ならびにリン脂質分離測定法の開発 |
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