SMAP200900041A - Sali e forme cristalline di 2-metil-2-[4-(3-metil-2-osso-8-chinolin-3-il-2,3-diidro-imidazo[4,5-c]chinolin-1il)-fenil]-propionitrile - Google Patents

Sali e forme cristalline di 2-metil-2-[4-(3-metil-2-osso-8-chinolin-3-il-2,3-diidro-imidazo[4,5-c]chinolin-1il)-fenil]-propionitrile

Info

Publication number: SMAP200900041A
Authority: SM; San Marino
Prior art keywords: quinolin; methyl; salts; crystalline forms; propionitrile
Prior art date: 2006-11-20

Application number

SM200900041T

Other languages

English (en)

Other versions

SMP200900041B (it

Inventor

Frank Stowasser

Markus Banziger

Sudhakar Devidasrao Garad

Original Assignee

Novartis Ag

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.)

2006-11-20

Filing date

2009-05-28

Publication date

2009-07-14

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39345299&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SMAP200900041(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2009-05-28 Application filed by Novartis Ag filed Critical Novartis Ag

2009-07-14 Publication of SMAP200900041A publication Critical patent/SMAP200900041A/it

2009-09-07 Publication of SMP200900041B publication Critical patent/SMP200900041B/it

Links

150000003839 salts Chemical class 0.000 title abstract 3
JOGKUKXHTYWRGZ-UHFFFAOYSA-N dactolisib Chemical compound O=C1N(C)C2=CN=C3C=CC(C=4C=C5C=CC=CC5=NC=4)=CC3=C2N1C1=CC=C(C(C)(C)C#N)C=C1 JOGKUKXHTYWRGZ-UHFFFAOYSA-N 0.000 title abstract 2
241001465754 Metazoa Species 0.000 abstract 2
238000002405 diagnostic procedure Methods 0.000 abstract 2
150000004677 hydrates Chemical class 0.000 abstract 2
238000002360 preparation method Methods 0.000 abstract 2
239000012453 solvate Substances 0.000 abstract 2
230000001225 therapeutic effect Effects 0.000 abstract 2
238000000034 method Methods 0.000 abstract 1
239000008194 pharmaceutical composition Substances 0.000 abstract 1
239000000825 pharmaceutical preparation Substances 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/29—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings
- C07C309/30—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings of six-membered aromatic rings substituted by alkyl groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Dermatology (AREA)
Oncology (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Endocrinology (AREA)
Reproductive Health (AREA)
Hematology (AREA)
Urology & Nephrology (AREA)
Epidemiology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

SM200900041T 2006-11-20 2009-05-28 Sali e forme cristalline di 2-metil-2-[4-(3-metil-2-osso-8-chinolin-3-il-2,3-diidro-imidazo[4,5-c]chinolin-1il)-fenil]-propionitrile SMP200900041B (it)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US86648306P	2006-11-20	2006-11-20
PCT/US2007/084893 WO2008064093A2 (en)	2006-11-20	2007-11-16	Salts and crystal forms of 2-methyl-2-[4-(3-methyl-2-oxo-8-quinolin-3-yl-2,3-dihydro-imidazo[4,5-c]quinolin-1-yl)-phenyl]-propionitrile

Publications (2)

Publication Number	Publication Date
SMAP200900041A true SMAP200900041A (it)	2009-07-14
SMP200900041B SMP200900041B (it)	2009-09-07

Family

ID=39345299

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SM200900041T SMP200900041B (it)	2006-11-20	2009-05-28	Sali e forme cristalline di 2-metil-2-[4-(3-metil-2-osso-8-chinolin-3-il-2,3-diidro-imidazo[4,5-c]chinolin-1il)-fenil]-propionitrile

Country Status (35)

Country	Link
US (2)	US8436177B2 (it)
EP (2)	EP2364981A1 (it)
JP (2)	JP5562033B2 (it)
KR (3)	KR20140091718A (it)
CN (5)	CN106045993A (it)
AR (1)	AR064256A1 (it)
AU (1)	AU2007323820B2 (it)
BR (1)	BRPI0719112A2 (it)
CA (1)	CA2669199C (it)
CL (1)	CL2007003316A1 (it)
CO (1)	CO6382134A2 (it)
CR (1)	CR10757A (it)
DO (1)	DOP2009000116A (it)
EA (1)	EA015677B1 (it)
EC (1)	ECSP099340A (it)
GE (1)	GEP20125436B (it)
GT (1)	GT200900133A (it)
HR (1)	HRP20140627T1 (it)
IL (2)	IL198467A (it)
JO (1)	JO2903B1 (it)
MA (1)	MA30967B1 (it)
MX (1)	MX2009005360A (it)
MY (1)	MY150216A (it)
NI (1)	NI200900091A (it)
NO (1)	NO20092227L (it)
NZ (1)	NZ576357A (it)
PE (2)	PE20120083A1 (it)
PH (1)	PH12013502100A1 (it)
RS (1)	RS53335B (it)
SM (1)	SMP200900041B (it)
TN (1)	TN2009000191A1 (it)
TW (2)	TW201402567A (it)
UA (1)	UA98473C2 (it)
UY (1)	UY30728A1 (it)
WO (1)	WO2008064093A2 (it)

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JP5789252B2 (ja)	2009-05-07	2015-10-07	インテリカイン，エルエルシー	複素環式化合物およびその使用
AU2010255727B2 (en)	2009-06-04	2013-02-28	Novartis Ag	1H-imidazo[4,5-c]quinolinone derivatives
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AR088218A1 (es)	2011-07-19	2014-05-21	Infinity Pharmaceuticals Inc	Compuestos heterociclicos utiles como inhibidores de pi3k
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US9499561B2 (en)	2012-04-10	2016-11-22	Shanghai Yingli Pharmaceutical Co., Ltd.	Fused pyrimidine compound, and preparation method, intermediate, composition, and uses thereof
US8828998B2 (en)	2012-06-25	2014-09-09	Infinity Pharmaceuticals, Inc.	Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
AU2013203714B2 (en)	2012-10-18	2015-12-03	Signal Pharmaceuticals, Llc	Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
AU2013337717B2 (en)	2012-11-01	2018-10-25	Infinity Pharmaceuticals, Inc.	Treatment of cancers using PI3 kinase isoform modulators
US9481667B2 (en)	2013-03-15	2016-11-01	Infinity Pharmaceuticals, Inc.	Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
MA38522A1 (fr) *	2013-03-21	2017-10-31	Novartis Ag	Thérapie de combinaison comprenant un inhibiteur de b-raf et un second inhibiteur.
CN105377299B (zh)	2013-04-17	2018-06-12	西格诺药品有限公司	用于治疗前列腺癌的包含二氢吡嗪并-吡嗪化合物和雄激素受体拮抗剂的组合疗法
WO2014172436A1 (en)	2013-04-17	2014-10-23	Signal Pharmaceuticals, Llc	Combination therapy comprising a tor kinase inhibitor and a 5-substituted quinazolinone compound for treating cancer
CA2908742C (en)	2013-04-17	2021-06-01	Signal Pharmaceuticals, Llc	Combination therapy comprising a tor kinase inhibitor and a cytidine analog for treating cancer
US9505764B2 (en)	2013-04-17	2016-11-29	Signal Pharmaceuticals, Llc	Treatment of cancer with dihydropyrazino-pyrazines
US9630966B2 (en)	2013-04-17	2017-04-25	Signal Pharmaceuticals, Llc	Treatment of cancer with dihydropyrazino-pyrazines
CA2909579A1 (en)	2013-04-17	2014-10-23	Signal Pharmaceuticals, Llc	Combination therapy comprising a tor kinase inhibitor and n-(3-(5-fluoro-2-(4-(2-methoxyethoxy)phenylamino)pyrimidin-4-ylamino)phenyl)acrylamide for treating cancer
CA2909629C (en)	2013-04-17	2022-12-13	Signal Pharmaceuticals, Llc	Pharmaceutical formulations, processes, solid forms and methods of use relating to 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one
NZ629486A (en)	2013-05-29	2017-11-24	Signal Pharm Llc	Pharmaceutical compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino [2,3-b]pyrazin-2(1h)-one, a solid form thereof and methods of their use
EP3053926B1 (en)	2013-09-30	2018-08-08	Shanghai Yingli Pharmaceutical Co. Ltd.	Fused pyrimidine compound, intermediate, preparation method therefor, and composition and application thereof
US9751888B2 (en)	2013-10-04	2017-09-05	Infinity Pharmaceuticals, Inc.	Heterocyclic compounds and uses thereof
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CN104557872B (zh)	2013-10-16	2017-05-24	上海璎黎药业有限公司	稠合杂环化合物、其制备方法、药物组合物和用途
MX382033B (es)	2014-03-19	2025-03-13	Infinity Pharmaceuticals Inc	Compuestos heterocíclicos para utilizarlos en el tratamiento de trastornos mediados por pi3k-gamma.
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2007
- 2007-11-16 KR KR1020147014039A patent/KR20140091718A/ko not_active Ceased
- 2007-11-16 CN CN201610405653.7A patent/CN106045993A/zh active Pending
- 2007-11-16 HR HRP20140627TT patent/HRP20140627T1/hr unknown
- 2007-11-16 NZ NZ576357A patent/NZ576357A/en not_active IP Right Cessation
- 2007-11-16 EP EP10176298A patent/EP2364981A1/en not_active Withdrawn
- 2007-11-16 UA UAA200905006A patent/UA98473C2/ru unknown
- 2007-11-16 GE GEAP200711260A patent/GEP20125436B/en unknown
- 2007-11-16 CA CA2669199A patent/CA2669199C/en not_active Expired - Fee Related
- 2007-11-16 KR KR1020097010203A patent/KR20090080530A/ko not_active Ceased
- 2007-11-16 MX MX2009005360A patent/MX2009005360A/es active IP Right Grant
- 2007-11-16 US US12/514,976 patent/US8436177B2/en not_active Expired - Fee Related
- 2007-11-16 CN CN2012102686473A patent/CN102993202A/zh active Pending
- 2007-11-16 AU AU2007323820A patent/AU2007323820B2/en not_active Ceased
- 2007-11-16 CN CN201910073048.8A patent/CN109970735A/zh active Pending
- 2007-11-16 BR BRPI0719112-0A patent/BRPI0719112A2/pt not_active IP Right Cessation
- 2007-11-16 AR ARP070105114A patent/AR064256A1/es unknown
- 2007-11-16 JP JP2009537381A patent/JP5562033B2/ja not_active Expired - Fee Related
- 2007-11-16 EA EA200900638A patent/EA015677B1/ru not_active IP Right Cessation
- 2007-11-16 WO PCT/US2007/084893 patent/WO2008064093A2/en not_active Ceased
- 2007-11-16 RS RS20140278A patent/RS53335B/sr unknown
- 2007-11-16 CN CNA2007800420773A patent/CN101541793A/zh active Pending
- 2007-11-16 KR KR1020147029446A patent/KR20140129396A/ko not_active Ceased
- 2007-11-16 MY MYPI20091920A patent/MY150216A/en unknown
- 2007-11-16 CN CN2011103337901A patent/CN102336752A/zh active Pending
- 2007-11-16 EP EP07864492.9A patent/EP2094700B1/en active Active
- 2007-11-19 CL CL200703316A patent/CL2007003316A1/es unknown
- 2007-11-19 TW TW102134663A patent/TW201402567A/zh unknown
- 2007-11-19 PE PE2011001508A patent/PE20120083A1/es not_active Application Discontinuation
- 2007-11-19 TW TW096143742A patent/TWI417292B/zh not_active IP Right Cessation
- 2007-11-19 PE PE2007001607A patent/PE20081780A1/es not_active Application Discontinuation
- 2007-11-19 JO JO2007482A patent/JO2903B1/en active
- 2007-11-20 UY UY30728A patent/UY30728A1/es not_active Application Discontinuation
2009
- 2009-04-29 CR CR10757A patent/CR10757A/es unknown
- 2009-04-30 IL IL198467A patent/IL198467A/en not_active IP Right Cessation
- 2009-05-15 TN TNP2009000191A patent/TN2009000191A1/fr unknown
- 2009-05-18 GT GT200900133A patent/GT200900133A/es unknown
- 2009-05-18 CO CO09050683A patent/CO6382134A2/es active IP Right Grant
- 2009-05-18 EC EC2009009340A patent/ECSP099340A/es unknown
- 2009-05-18 NI NI200900091A patent/NI200900091A/es unknown
- 2009-05-19 DO DO2009000116A patent/DOP2009000116A/es unknown
- 2009-05-28 SM SM200900041T patent/SMP200900041B/it unknown
- 2009-06-03 MA MA31947A patent/MA30967B1/fr unknown
- 2009-06-09 NO NO20092227A patent/NO20092227L/no not_active Application Discontinuation
2012
- 2012-05-17 IL IL219877A patent/IL219877A0/en unknown
2013
- 2013-04-04 US US13/856,458 patent/US20130289064A1/en not_active Abandoned
- 2013-05-13 JP JP2013101604A patent/JP2013173788A/ja active Pending
- 2013-10-10 PH PH12013502100A patent/PH12013502100A1/en unknown

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Publication number	Publication date
US8436177B2 (en)	2013-05-07
TW201402567A (zh)	2014-01-16
BRPI0719112A2 (pt)	2013-12-10
ECSP099340A (es)	2009-06-30
DOP2009000116A (es)	2009-05-31
HRP20140627T1 (hr)	2014-09-26
GT200900133A (es)	2010-05-21
EA200900638A1 (ru)	2009-12-30
JO2903B1 (en)	2015-09-15
CN109970735A (zh)	2019-07-05
MX2009005360A (es)	2009-06-05
CO6382134A2 (es)	2012-02-15
JP5562033B2 (ja)	2014-07-30
CN102993202A (zh)	2013-03-27
KR20090080530A (ko)	2009-07-24
PH12013502100A1 (en)	2015-09-21
CL2007003316A1 (es)	2008-06-27
PE20120083A1 (es)	2012-03-01
EP2094700B1 (en)	2014-04-02
JP2013173788A (ja)	2013-09-05
GEP20125436B (en)	2012-03-26
KR20140091718A (ko)	2014-07-22
US20100168153A1 (en)	2010-07-01
AU2007323820B2 (en)	2012-02-23
HK1132739A1 (en)	2010-03-05
UA98473C2 (ru)	2012-05-25
AU2007323820A1 (en)	2008-05-29
WO2008064093A3 (en)	2008-08-14
PE20081780A1 (es)	2009-01-01
CN102336752A (zh)	2012-02-01
IL198467A0 (en)	2010-02-17
KR20140129396A (ko)	2014-11-06
TW200827356A (en)	2008-07-01
JP2010510240A (ja)	2010-04-02
US20130289064A1 (en)	2013-10-31
TWI417292B (zh)	2013-12-01
MY150216A (en)	2013-12-13
IL219877A0 (en)	2012-06-28
CR10757A (es)	2009-06-11
EA015677B1 (ru)	2011-10-31
NO20092227L (no)	2009-08-17
UY30728A1 (es)	2008-07-03
CA2669199C (en)	2015-12-29
MA30967B1 (fr)	2009-12-01
IL198467A (en)	2014-11-30
RS53335B (sr)	2014-10-31
NZ576357A (en)	2011-01-28
EP2364981A1 (en)	2011-09-14
CN101541793A (zh)	2009-09-23
CA2669199A1 (en)	2008-05-29
EP2094700A2 (en)	2009-09-02
CN106045993A (zh)	2016-10-26
SMP200900041B (it)	2009-09-07
NI200900091A (es)	2010-02-17
AR064256A1 (es)	2009-03-25
WO2008064093A2 (en)	2008-05-29
TN2009000191A1 (en)	2010-10-18

Publication	Publication Date	Title
SMAP200900041A (it)	2009-07-14	Sali e forme cristalline di 2-metil-2-[4-(3-metil-2-osso-8-chinolin-3-il-2,3-diidro-imidazo[4,5-c]chinolin-1il)-fenil]-propionitrile
EA201101243A1 (ru)	2012-04-30	3h-имидазо[4,5-c]пиридин-6-карбоксамиды в качестве противовоспалительных средств
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BRPI0513750A (pt)	2008-05-13	2-fenilamino-benzamidas-5-substituìdas como inibidoras de mek
TW200606162A (en)	2006-02-16	Pyrazolopyridine derivatives
BR112012023139A2 (pt)	2018-06-26	composição farmacêutica para a prevenção ou o tratamento de doença do fígado gordo não alcóolico e o método para a prevenção ou tratamento de doença do fígado gordo não alcóolico usando a mesma.
TW200508207A (en)	2005-03-01	New benzimidazole derivatives
NZ610467A (en)	2015-01-30	Pharmaceutical compositions of imidazoquinoline derivative compounds
UY31588A1 (es)	2009-08-03	Derivados de imidazo[1,2-a]piridin-2-carboxamidas, su preparacion y su aplicacion en terapéutica
CY1112638T1 (el)	2016-02-10	Χρηση των παραγωγων ινδολιου ως ενεργοποιητες νurr-1 για την θεραπεια νοσου ραrκινsον
PT1869038E (pt)	2009-10-06	Compostos de 5,6,7,8-tetra-hidro-imidazo[1,2-a]piridin-2- ilamina substituída e sua utilização para produzir fármacos
BRPI0517689A (pt)	2008-10-14	compostos orgánicos
DK1730144T3 (da)	2009-10-12	Substituerede 1,4,8-triazaspiro[4.5]decan-2-on-forbindelser
UY31593A1 (es)	2009-08-03	Derivados de 2-heteroaroil-imidazo[1,2-a]piridina, su preparacion y su aplicacion en terapéutica
WO2002059109A3 (en)	2002-09-19	Naphthostyril derivatives and their use as inhibitors of cyclin- dependent kinases
WO2007056184A3 (en)	2007-07-05	Azaindole compounds and use thereof as phospholipase-a2 inhibitors
UY31586A1 (es)	2009-08-03	Derivados de n-fenil-imidazo[1,2-a]piridin-2-carboxamidas, su preparacion y su aplicacion en terapéutica
SE0300907D0 (sv)	2003-03-31	Novel compounds
SE0300906D0 (sv)	2003-03-31	Novel compounds
NO20072091L (no)	2007-06-01	Forbindelser, sammensetninger som inneholder dem, fremstilling derav og anvendelse derav III
TH101185A (th)	2010-04-30	เกลือโมโนโทซิลเลต (Monotosylate salt) รูปผลึกของ 2-เมทธิล-2-[4-(3-เมทธิล-2-ออกโซ-8-ควิโนลิน-3-อิล-2,3-ไดไฮโดร-อิมิดาโซ[4,5-c]ควิโนลิน- 1อิล)-ฟีนิล]-โพรพิโอไนไตรล์(2-methyl-2-[4-(3-methyl-2-oxo-8-quinolin-3-yl-2,3-dihydro-imidazo[4,5-c]quinolin-1-yl]-phenyl]-propionitrile)
CL2012003552A1 (es)	2013-04-12	Compuestos derivados de n-(8-metil-1-fenil-8-azabiciclo[3.2.1]oct-2-il)benzamida; procedimiento de preparacion; composicion farmaceutica; y su uso para el tratamiento o la profilaxis de las psicosis, el dolor, esquizofrenia, entre otros.