AP2369A - Carbonylamino pyrrolopyrazoles, potent kinase inhibitors. - Google Patents

Carbonylamino pyrrolopyrazoles, potent kinase inhibitors.

Info

Publication number: AP2369A
Authority: AP; ARIPO
Prior art keywords: pyrrolopyrazoles; carbonylamino; kinase inhibitors; potent kinase; potent
Prior art date: 2005-12-21

Application number

AP2008004506A

Other languages

English (en)

Other versions

AP2008004506A0 (en

Inventor

Liming Dong

Chuangxing Guo

Yufeng Hong

Original Assignee

Pfizer Prod Inc

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.)

2005-12-21

Filing date

2006-12-12

Publication date

2012-02-29

2006-12-12 Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc

2008-06-30 Publication of AP2008004506A0 publication Critical patent/AP2008004506A0/xx

2012-02-29 Application granted granted Critical

2012-02-29 Publication of AP2369A publication Critical patent/AP2369A/xx

Links

XPBFIMLMVNXIIB-UHFFFAOYSA-N 3-isocyanatopyrrolo[3,2-c]pyrazole Chemical class N1=CC=C2N=NC(N=C=O)=C21 XPBFIMLMVNXIIB-UHFFFAOYSA-N 0.000 title 1
229940043355 kinase inhibitor Drugs 0.000 title 1
239000003757 phosphotransferase inhibitor Substances 0.000 title 1
230000003389 potentiating effect Effects 0.000 title 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
- 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
- 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
- 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

Landscapes

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

AP2008004506A 2005-12-21 2006-12-12 Carbonylamino pyrrolopyrazoles, potent kinase inhibitors. AP2369A (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US75334905P	2005-12-21	2005-12-21
US86493206P	2006-11-08	2006-11-08
PCT/IB2006/003646 WO2007072153A2 (fr)	2005-12-21	2006-12-12	Carbonylaminopyrrolopyrazoles, inhibiteurs puissants de kinase

Publications (2)

Publication Number	Publication Date
AP2008004506A0 AP2008004506A0 (en)	2008-06-30
AP2369A true AP2369A (en)	2012-02-29

Family

ID=38189022

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AP2008004506A AP2369A (en)	2005-12-21	2006-12-12	Carbonylamino pyrrolopyrazoles, potent kinase inhibitors.

Country Status (26)

Country	Link
US (1)	US7884117B2 (fr)
EP (1)	EP1979356B1 (fr)
JP (1)	JP4635089B2 (fr)
KR (1)	KR101029167B1 (fr)
AP (1)	AP2369A (fr)
AU (1)	AU2006327866B2 (fr)
BR (1)	BRPI0620354A2 (fr)
CA (1)	CA2634381C (fr)
CR (1)	CR10094A (fr)
CU (1)	CU23751B7 (fr)
DK (1)	DK1979356T3 (fr)
EA (1)	EA015513B1 (fr)
EC (1)	ECSP088558A (fr)
ES (1)	ES2435405T3 (fr)
GE (1)	GEP20104974B (fr)
HR (1)	HRP20130976T1 (fr)
IL (1)	IL191776A (fr)
MA (1)	MA30076B1 (fr)
ME (1)	ME00006B (fr)
MY (1)	MY151455A (fr)
NO (1)	NO20082482L (fr)
NZ (1)	NZ568692A (fr)
PL (1)	PL1979356T3 (fr)
PT (1)	PT1979356E (fr)
RS (2)	RS20080281A (fr)
WO (1)	WO2007072153A2 (fr)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
PL385265A1 (pl) *	2008-05-23	2009-12-07	Zakłady Farmaceutyczne POLPHARMA Spółka Akcyjna	Sposób wytwarzania solifenacyny i/lub jej soli o wysokiej czystości farmaceutycznej
SG171914A1 (en)	2008-12-02	2011-07-28	Chiralgen Ltd	Method for the synthesis of phosphorus atom modified nucleic acids
EP2451461A4 (fr)	2009-07-06	2013-05-29	Ontorii Inc	Nouveaux précurseurs d'acide nucléique et leurs méthodes d'utilisation
EP2937345B1 (fr)	2009-12-29	2018-03-21	Dana-Farber Cancer Institute, Inc.	Inhibiteurs de la kinase raf de type ii
DK2620428T3 (da) *	2010-09-24	2019-07-01	Wave Life Sciences Ltd	Asymmetrisk hjælpegruppe
WO2012065935A1 (fr)	2010-11-17	2012-05-24	F. Hoffmann-La Roche Ag	Méthodes de traitement de tumeurs
US8771682B2 (en)	2011-04-26	2014-07-08	Technische Universtität Dresden	Methods and compositions for reducing interleukin-4 or interleukin-13 signaling
US9605019B2 (en)	2011-07-19	2017-03-28	Wave Life Sciences Ltd.	Methods for the synthesis of functionalized nucleic acids
WO2013074986A1 (fr)	2011-11-17	2013-05-23	Dana-Farber Cancer Institute, Inc.	Inhibiteurs de la kinase c-jun-n-terminale (jnk)
KR20140135198A (ko)	2012-03-16	2014-11-25	에프. 호프만-라 로슈 아게	Pak1 억제제로 흑색종을 치료하는 방법
DK2872485T3 (da)	2012-07-13	2021-03-08	Wave Life Sciences Ltd	Asymmetrisk hjælpegruppe
JP6246121B2 (ja)	2012-07-13	2017-12-13	株式会社新日本科学	キラル核酸アジュバント
CN112007045B (zh)	2012-07-13	2026-01-06	波涛生命科学有限公司	手性控制
US10112927B2 (en)	2012-10-18	2018-10-30	Dana-Farber Cancer Institute, Inc.	Inhibitors of cyclin-dependent kinase 7 (CDK7)
US10000483B2 (en)	2012-10-19	2018-06-19	Dana-Farber Cancer Institute, Inc.	Bone marrow on X chromosome kinase (BMX) inhibitors and uses thereof
US9758522B2 (en)	2012-10-19	2017-09-12	Dana-Farber Cancer Institute, Inc.	Hydrophobically tagged small molecules as inducers of protein degradation
WO2015058140A1 (fr)	2013-10-18	2015-04-23	Dana-Farber Cancer Institute, Inc.	Inhibiteurs polycycliques de kinase cycline-dépendante 7 (cdk7)
WO2015058126A1 (fr)	2013-10-18	2015-04-23	Syros Pharmaceuticals, Inc.	Composés hétéroaromatiques utiles dans le traitement de maladies prolifératives
WO2015108048A1 (fr)	2014-01-15	2015-07-23	株式会社新日本科学	Adjuvant d'acide nucléique chiral ayant un effet antitumoral et agent antitumoral
EP3095461A4 (fr)	2014-01-15	2017-08-23	Shin Nippon Biomedical Laboratories, Ltd.	Adjuvant d'acide nucléique chiral possédant une activité d'induction d'immunité, et activateur d'induction d'immunité
US10322173B2 (en)	2014-01-15	2019-06-18	Shin Nippon Biomedical Laboratories, Ltd.	Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent
KR102423317B1 (ko)	2014-01-16	2022-07-22	웨이브 라이프 사이언시스 리미티드	키랄 디자인
WO2015164604A1 (fr)	2014-04-23	2015-10-29	Dana-Farber Cancer Institute, Inc.	Inhibiteurs de janus kinase marqués de manière hydrophobe et utilisations associées
US10017477B2 (en)	2014-04-23	2018-07-10	Dana-Farber Cancer Institute, Inc.	Janus kinase inhibitors and uses thereof
JP6690543B2 (ja)	2014-10-31	2020-04-28	宇部興産株式会社	置換ジヒドロピロロピラゾール化合物
AU2015371251B2 (en) *	2014-12-23	2020-06-11	Dana-Farber Cancer Institute, Inc.	Inhibitors of cyclin-dependent kinase 7 (CDK7)
CN107427521B (zh)	2015-03-27	2021-08-03	达纳-法伯癌症研究所股份有限公司	细胞周期蛋白依赖性激酶的抑制剂
EP3307728A4 (fr)	2015-06-12	2019-07-17	Dana Farber Cancer Institute, Inc.	Thérapie d'association utilisant des inhibiteurs de transcription et des inhibiteurs de kinases
US10273252B2 (en)	2015-06-15	2019-04-30	Ube Industries, Ltd.	Substituted dihydropyrrolopyrazole derivative
JP7028766B2 (ja)	2015-09-09	2022-03-02	ダナ－ファーバーキャンサーインスティテュート，インコーポレイテッド	サイクリン依存性キナーゼの阻害剤
WO2017144546A1 (fr)	2016-02-23	2017-08-31	INSERM (Institut National de la Santé et de la Recherche Médicale)	Méthodes et compositions pharmaceutiques pour le traitement d'un carcinome de rhinopharyngite
JP7590185B2 (ja)	2018-06-25	2024-11-26	ダナ－ファーバーキャンサーインスティテュート，インコーポレイテッド	Ｔａｉｒｅファミリーキナーゼインヒビターおよびそれらの使用
WO2020100944A1 (fr)	2018-11-14	2020-05-22	宇部興産株式会社	Dérivé de dihydropyrrolopyrazole
WO2020140098A1 (fr) *	2018-12-28	2020-07-02	Dana-Farber Cancer Institute, Inc.	Inhibiteurs de la kinase dépendante des cyclines 7 et leurs utilisations
EP3956446A1 (fr)	2019-04-17	2022-02-23	INSERM (Institut National de la Santé et de la Recherche Médicale)	Procédés et compositions de traitement de troubles dépendants de il-1beta mediés par inflamasome nlrp3
CN114981298B (zh)	2019-12-12	2024-08-20	听治疗有限责任公司	用于预防和治疗听力损失的组合物和方法
WO2021198511A1 (fr)	2020-04-03	2021-10-07	INSERM (Institut National de la Santé et de la Recherche Médicale)	Méthodes et compositions pour le traitement d'une infection par sars-cov-2
WO2022008597A1 (fr)	2020-07-08	2022-01-13	INSERM (Institut National de la Santé et de la Recherche Médicale)	Méthodes et composition pharmaceutique pour le traitement de maladies infectieuses
WO2024261302A1 (fr)	2023-06-22	2024-12-26	Institut National de la Santé et de la Recherche Médicale	Inhibiteurs de nlrp3, inhibiteurs de pak1/2 et/ou inhibiteurs de caspase 1 pour le traitement de maladies monogéniques liées au rac2
WO2025078334A1 (fr)	2023-10-09	2025-04-17	Institut National de la Santé et de la Recherche Médicale	Combinaison d'inhibiteurs de pak1 et d'inhibiteurs de clk pour prévenir la résistance à la chimiothérapie chez des patients souffrant de leucémie myéloïde aiguë

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2002012242A2 (fr) *	2000-08-10	2002-02-14	Pharmacia Italia S.P.A.	Bicyclo-pyrazoles actifs en tant qu'inhibiteurs de kinase, leur procede de preparation et compositions pharmaceutiques les contenant
WO2004056827A2 (fr) *	2002-12-19	2004-07-08	Pharmacia Italia Spa	Derives de pyrrolo-pyrazoles substitues constituant des inhibiteurs de kinases
WO2005030776A1 (fr) *	2003-09-23	2005-04-07	Vertex Pharmaceuticals Incorporated	Derives de pyrazolopyrrole utilises en tant qu'inhibiteurs de proteines kinases

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1527074A1 (fr)	2002-07-25	2005-05-04	Pharmacia Italia S.p.A.	Bicyclo-pyrazoles actifs inhibiteurs de kinase, procede de preparation et compositions pharmaceutiques contenant ceux-ci
GB0229526D0 (en)	2002-12-19	2003-01-22	Astrazeneca Ab	Chemical compounds
KR100919343B1 (ko)	2005-01-10	2009-09-25	화이자 인코포레이티드	키네이스 억제제로서 피롤로피라졸

2006
- 2006-12-12 JP JP2008546667A patent/JP4635089B2/ja not_active Expired - Fee Related
- 2006-12-12 PT PT68317312T patent/PT1979356E/pt unknown
- 2006-12-12 EA EA200801291A patent/EA015513B1/ru not_active IP Right Cessation
- 2006-12-12 MY MYPI20082267 patent/MY151455A/en unknown
- 2006-12-12 AP AP2008004506A patent/AP2369A/xx active
- 2006-12-12 CA CA2634381A patent/CA2634381C/fr not_active Expired - Fee Related
- 2006-12-12 ES ES06831731T patent/ES2435405T3/es active Active
- 2006-12-12 GE GEAP200610777A patent/GEP20104974B/en unknown
- 2006-12-12 US US12/158,241 patent/US7884117B2/en not_active Expired - Fee Related
- 2006-12-12 RS RSP-2008/0281A patent/RS20080281A/sr unknown
- 2006-12-12 HR HRP20130976TT patent/HRP20130976T1/hr unknown
- 2006-12-12 BR BRPI0620354-0A patent/BRPI0620354A2/pt not_active IP Right Cessation
- 2006-12-12 ME MEP-2008-8A patent/ME00006B/fr unknown
- 2006-12-12 WO PCT/IB2006/003646 patent/WO2007072153A2/fr not_active Ceased
- 2006-12-12 RS RS20130498A patent/RS53029B/sr unknown
- 2006-12-12 PL PL06831731T patent/PL1979356T3/pl unknown
- 2006-12-12 AU AU2006327866A patent/AU2006327866B2/en not_active Ceased
- 2006-12-12 KR KR1020087014963A patent/KR101029167B1/ko not_active Expired - Fee Related
- 2006-12-12 DK DK06831731.2T patent/DK1979356T3/da active
- 2006-12-12 EP EP06831731.2A patent/EP1979356B1/fr active Active
- 2006-12-12 NZ NZ568692A patent/NZ568692A/en not_active IP Right Cessation
2008
- 2008-05-27 IL IL191776A patent/IL191776A/en not_active IP Right Cessation
- 2008-06-02 NO NO20082482A patent/NO20082482L/no not_active Application Discontinuation
- 2008-06-18 EC EC2008008558A patent/ECSP088558A/es unknown
- 2008-06-19 CU CU20080115A patent/CU23751B7/es active IP Right Grant
- 2008-06-20 MA MA31060A patent/MA30076B1/fr unknown
- 2008-06-20 CR CR10094A patent/CR10094A/es unknown

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2002012242A2 (fr) *	2000-08-10	2002-02-14	Pharmacia Italia S.P.A.	Bicyclo-pyrazoles actifs en tant qu'inhibiteurs de kinase, leur procede de preparation et compositions pharmaceutiques les contenant
WO2004056827A2 (fr) *	2002-12-19	2004-07-08	Pharmacia Italia Spa	Derives de pyrrolo-pyrazoles substitues constituant des inhibiteurs de kinases
WO2005030776A1 (fr) *	2003-09-23	2005-04-07	Vertex Pharmaceuticals Incorporated	Derives de pyrazolopyrrole utilises en tant qu'inhibiteurs de proteines kinases

Also Published As

Publication number	Publication date
ECSP088558A (es)	2008-07-30
NZ568692A (en)	2011-07-29
WO2007072153A2 (fr)	2007-06-28
HK1128290A1 (en)	2009-10-23
JP2009520805A (ja)	2009-05-28
CA2634381A1 (fr)	2007-06-28
EA015513B1 (ru)	2011-08-30
AU2006327866B2 (en)	2012-06-14
CU20080115A7 (es)	2010-08-30
MEP0808A (xx)	2010-02-10
JP4635089B2 (ja)	2011-02-16
WO2007072153A8 (fr)	2008-08-14
IL191776A (en)	2013-03-24
IL191776A0 (en)	2008-12-29
US7884117B2 (en)	2011-02-08
CU23751B7 (es)	2012-01-31
CA2634381C (fr)	2011-03-08
RS53029B (sr)	2014-04-30
ME00006B (fr)	2010-02-10
MA30076B1 (fr)	2008-12-01
AU2006327866A1 (en)	2007-06-28
EA200801291A1 (ru)	2008-12-30
GEP20104974B (en)	2010-04-26
DK1979356T3 (da)	2013-11-18
AP2008004506A0 (en)	2008-06-30
US20090318440A1 (en)	2009-12-24
ES2435405T3 (es)	2013-12-19
HRP20130976T1 (hr)	2013-11-22
WO2007072153A3 (fr)	2007-10-25
NO20082482L (no)	2008-07-02
EP1979356B1 (fr)	2013-09-18
KR101029167B1 (ko)	2011-04-12
PL1979356T3 (pl)	2014-01-31
CR10094A (es)	2008-08-01
EP1979356A2 (fr)	2008-10-15
MY151455A (en)	2014-05-30
PT1979356E (pt)	2013-11-21
KR20080080567A (ko)	2008-09-04
RS20080281A (sr)	2009-09-08
BRPI0620354A2 (pt)	2011-11-08

Publication	Publication Date	Title
IL191776A0 (en)	2008-12-29	Carbonylamino pyrrolopyrazoles, potent kinase inhibitors
ZA200705628B (en)	2008-11-26	Pyrrolopyrazoles, potent kinase inhibitors
EG25264A (en)	2011-11-30	Biphenyl-n-(4-pyridyl) methylsulfonamides.
AP2402A (en)	2012-04-30	Amine derivatives.
IL190078A0 (en)	2008-08-07	Kinase inhibitors
EG25271A (en)	2011-12-04	Fungicidal combinations.
GB2424882B (en)	2008-08-06	Selective kinase inhibitors
SI2270008T1 (sl)	2013-01-31	8-heteroaril-3-alkil-1,3-dihidro-imidazo(4,5-c)kinolin-2-oni kot inhibitorji PI-3 kinaz
IL192033A0 (en)	2008-12-29	Arylpropionamide, arylacrylamide, arylpropynamide, or arylmethylurea analogs as factor xia inhibitors
AP2006003659A0 (en)	2006-06-30	Azabenzofuran substituted thioureas, inhibitors ofviral replication
AP2281A (en)	2011-10-31	Novel compounds.
ZA200805028B (en)	2009-12-30	Arylpropionamide, arylacrylamide, arylpropynamide, or arylmethylurea analogs as factor Xla inhibitors
PL1943243T3 (pl)	2011-05-31	Inhibitory kinazy
AP2337A (en)	2011-12-14	Motilide compounds.
AP2006003791A0 (en)	2006-10-31	1-Heterocyclyl-1,5-dihydro-pyridoÄ3,2-BÜindol-2-ones
ZA200804667B (en)	2010-05-26	Carbonylamino pyrrolopyrazoles, potent kinase inhibitors
NL1031384A1 (nl)	2006-09-20	Gesubstitueerde aryl-1,4-pyrazinederivaten.
GB0505823D0 (en)	2005-04-27	Boardmate, boardmate adjustable
GB0504761D0 (en)	2005-04-13	Alfatie, Coliawel, Omaatie
ITRM20050033U1 (it)	2006-09-16	Semicabina per fumatori.
ITTO20050072U1 (it)	2006-12-01	Armadio-espositore, particolarmente per tabaccherie
ZA200803287B (en)	2009-10-28	Kinase inhibitors
IL189985A0 (en)	2008-08-07	Kinase inhibitors
CY2449B1 (en)	2005-06-03	Multiple srengthened carton.
PL378279A1 (pl)	2007-06-11	Układ do osuszania gazów zwłaszcza dla komór klimatycznych