GT200400133AA - PIRROLO DERIVATIVES [3,4-C] PIRAZOL, ASSETS AS QUINASE INHIBITORS, PROCESS FOR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM. (FRACTIONARY APPLICATION NO. 1, DERIVED FROM THE PATENT NO. PI-2004-0133). - Google Patents
PIRROLO DERIVATIVES [3,4-C] PIRAZOL, ASSETS AS QUINASE INHIBITORS, PROCESS FOR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM. (FRACTIONARY APPLICATION NO. 1, DERIVED FROM THE PATENT NO. PI-2004-0133).Info
- Publication number
- GT200400133AA GT200400133AA GT200400133AK GT200400133K GT200400133AA GT 200400133A A GT200400133A A GT 200400133AA GT 200400133A K GT200400133A K GT 200400133AK GT 200400133 K GT200400133 K GT 200400133K GT 200400133A A GT200400133A A GT 200400133AA
- Authority
- GT
- Guatemala
- Prior art keywords
- fractionary
- pirazol
- assets
- understand
- derived
- Prior art date
Links
Classifications
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- 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
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
Abstract
LA PRESENTE INVENCION SE REFIERE A COMPUESTOS DE LA FORMULA GENERAL I EN LA QUE R,X,R1,R2, SON GRUPOS FUNCIONALES DESCRITOS EN EL EXPEDIENTE. ESTOS COMPUESTOS SON INHIBIDORES DE QUINASA POR LO QUE SON DE UTILIDAD EN PATOLOGIAS DE HIPERPROLIFERACION CELULAR TALES COMO EL CANCER.THE PRESENT INVENTION REFERS TO COMPOUNDS OF GENERAL FORMULA I IN WHICH R, X, R1, R2, ARE FUNCTIONAL GROUPS DESCRIBED IN THE RECORD. THESE COMPOUNDS ARE QUINASE INHIBITORS FOR WHICH THEY ARE USEFUL IN CELLULAR HYPERPROLIFERATION PATHOLOGIES SUCH AS CANCER.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48581403P | 2003-07-09 | 2003-07-09 |
Publications (1)
Publication Number | Publication Date |
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GT200400133AA true GT200400133AA (en) | 2007-07-10 |
Family
ID=34062099
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200400133AK GT200400133AA (en) | 2003-07-09 | 2004-07-09 | PIRROLO DERIVATIVES [3,4-C] PIRAZOL, ASSETS AS QUINASE INHIBITORS, PROCESS FOR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM. (FRACTIONARY APPLICATION NO. 1, DERIVED FROM THE PATENT NO. PI-2004-0133). |
GT200400133A GT200400133A (en) | 2003-07-09 | 2004-07-09 | PIRROLO DERIVATIVES [3,4-C] PIRAZOL ASSETS AS QUINASE INHIBITORS, PROCESS FOR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200400133A GT200400133A (en) | 2003-07-09 | 2004-07-09 | PIRROLO DERIVATIVES [3,4-C] PIRAZOL ASSETS AS QUINASE INHIBITORS, PROCESS FOR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM |
Country Status (42)
Families Citing this family (30)
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DE60143041D1 (en) * | 2000-08-10 | 2010-10-21 | Pfizer Italia Srl | Bicyclic pyrazoles are effective as kinase inhibitors, processes for their preparation, and pharmaceutical compositions containing them |
AU2004276341B2 (en) * | 2003-09-23 | 2011-04-14 | Vertex Pharmaceuticals Incorporated | Pyrazolopyrrole derivatives as protein kinase inhibitors |
JP2007514759A (en) * | 2003-12-19 | 2007-06-07 | タケダ サン ディエゴ インコーポレイテッド | Kinase inhibitor |
WO2005105788A1 (en) * | 2004-04-23 | 2005-11-10 | Takeda San Diego, Inc. | Indole derivatives and use thereof as kinase inhibitors |
WO2006023931A2 (en) * | 2004-08-18 | 2006-03-02 | Takeda San Diego, Inc. | Kinase inhibitors |
US7713973B2 (en) | 2004-10-15 | 2010-05-11 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
ES2365245T3 (en) * | 2005-01-10 | 2011-09-27 | Pfizer, Inc. | PIRROLOPIRAZOLES, POWERFUL INHIBITORS OF QUINASAS. |
US8119655B2 (en) * | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
TW200808311A (en) | 2006-03-30 | 2008-02-16 | Nerviano Medical Sciences Srl | Use of a kinase inhibitor for the treatment of particular resistant tumors |
WO2008017465A1 (en) * | 2006-08-10 | 2008-02-14 | F. Hoffmann-La Roche Ag | Bicyclic lactam derivatives, their manufacture and use as pharmaceutical agents |
GEP20135728B (en) | 2006-10-09 | 2013-01-25 | Takeda Pharmaceuticals Co | Kinase inhibitors |
JP2010505961A (en) * | 2006-10-09 | 2010-02-25 | タケダ サン ディエゴ インコーポレイテッド | Kinase inhibitor |
BRPI0717998A2 (en) * | 2006-11-03 | 2013-12-03 | Nerviano Medical Sciences Srl | METHOD FOR ADMINISTERING AN ANTITUMOR COMPOUND. |
CL2009001158A1 (en) * | 2008-05-15 | 2009-10-23 | Nerviano Medical Sciences Srl | Compounds derived from carboxylic acids, such as 5,6-dihiro-4h-pyrrolo [3,4-c] pyrazole, furo [3,2-c] pyrazole, thieno [2,3-c] pyrazole, 4,5 , 6,7-tetrahydropyrazole [4,3-c] pyridine and indazole; pharmaceutical composition; and its use in the treatment of cell proliferative disorders associated with altered protein kinase activity, such as cancer. |
US20100022553A1 (en) * | 2008-07-24 | 2010-01-28 | Nerviano Medical Sciences S.R.L. | Therapeutic Combination Comprising an Aurora Kinase Inhibitor and Imatinib |
CN102105148B (en) * | 2008-07-24 | 2013-04-10 | 内尔维阿诺医学科学有限公司 | Therapeutic combination comprising an AURORA kinase inhibitor and antiproliferative agents |
JP5518062B2 (en) * | 2008-07-24 | 2014-06-11 | ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ | A therapeutic combination comprising an aurora kinase inhibitor and an antineoplastic agent |
KR101741168B1 (en) | 2008-12-22 | 2017-05-29 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | Combination of aurora kinase inhibitors and anti-cd20 antibodies |
MX356401B (en) | 2011-12-12 | 2018-05-21 | Dr Reddys Laboratories Ltd | Substituted pyrazolo[1,5-a] pyridine as tropomyosin receptor kinase (trk) inhibitors. |
CN104072498B (en) * | 2013-03-26 | 2016-12-28 | 沈阳药科大学 | (R) synthetic method of N [5 (2 methoxyl group 2 phenyl acetyl) 1,4,5,6 nafoxidines also [3,4 c] pyrazoles 3 base] 4 (4 methyl piperazine 1 base) Benzoylamide |
JP6525474B2 (en) | 2013-12-06 | 2019-06-05 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | Combination of Aurora kinase inhibitor and anti-CD30 antibody |
EP3157921A1 (en) | 2014-06-23 | 2017-04-26 | Dr. Reddy's Laboratories Ltd. | Substituted imidazo[1,2-a]pyridine compounds useful for the treatment of pain |
KR102588426B1 (en) * | 2015-06-15 | 2023-10-13 | 유비이 가부시키가이샤 | Substituted dihydropyrrolopyrazole derivatives |
CN107337674B (en) * | 2016-04-29 | 2019-09-20 | 江苏吉贝尔药业股份有限公司 | For the oxinane amine derivative of DPP-IV inhibitor, its pharmaceutical composition and preparation and purposes |
US11874276B2 (en) | 2018-04-05 | 2024-01-16 | Dana-Farber Cancer Institute, Inc. | STING levels as a biomarker for cancer immunotherapy |
US20220305048A1 (en) | 2019-08-26 | 2022-09-29 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
CN113563346A (en) * | 2021-08-19 | 2021-10-29 | 守恒(厦门)医疗科技有限公司 | Pyrrole [3,4-c ] pyrazole diamide derivatives and application thereof in antitumor drugs |
WO2023196959A1 (en) | 2022-04-07 | 2023-10-12 | Eli Lilly And Company | Process for making a kras g12c inhibitor |
WO2023196887A1 (en) | 2022-04-08 | 2023-10-12 | Eli Lilly And Company | Method of treatment including kras g12c inhibitors and aurora a inhibitors |
US20240108618A1 (en) | 2022-06-30 | 2024-04-04 | Eli Lilly And Company | Kras g12c inhibitor dosing regimens |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
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FR2717380B1 (en) * | 1994-03-15 | 1996-04-26 | Oreal | Cosmetic compositions containing a synergistic blend of conditioning polymers. |
GB9911053D0 (en) | 1999-05-12 | 1999-07-14 | Pharmacia & Upjohn Spa | 4,5,6,7-tetrahydroindazole derivatives process for their preparation and their use as antitumour agents |
DE19932144A1 (en) * | 1999-07-09 | 2001-01-11 | Basf Ag | Microcapsule preparations and washing and cleaning agents containing microcapsules |
US6387900B1 (en) | 1999-08-12 | 2002-05-14 | Pharmacia & Upjohn S.P.A. | 3(5)-ureido-pyrazole derivatives process for their preparation and their use as antitumor agents |
SK1812002A3 (en) | 1999-08-12 | 2003-02-04 | Pharmacia Italia Spa | 3(5)-Amino-pyrazole derivatives, process for their preparation and their use as antitumor agents |
DE60143041D1 (en) | 2000-08-10 | 2010-10-21 | Pfizer Italia Srl | Bicyclic pyrazoles are effective as kinase inhibitors, processes for their preparation, and pharmaceutical compositions containing them |
FR2815032B1 (en) | 2000-10-10 | 2003-08-08 | Pf Medicament | NOVEL AMINOPHENYL PIPERAZINE OR AMINO PHENYL PIPERIDE DERIVATIVES PRENYL TRANSFERASE PROTEIN INHIBITORS AND PREPARATIONS THEREOF |
MXPA03004644A (en) | 2000-11-27 | 2003-09-05 | Pharmacia Italia Spa | Phenylacetamido- pyrazole derivatives and their use as antitumor agents. |
MXPA03006478A (en) | 2001-01-26 | 2003-09-22 | Pharmacia Italia Spa | Chromane derivatives, process for their preparation and their use as antitumor agents. |
ES2380054T3 (en) | 2001-09-26 | 2012-05-08 | Pfizer Italia S.R.L. | Active aminoindazole derivatives such as kinase inhibitors, preparation procedures, and pharmaceutical compositions containing them |
BR0312924A (en) | 2002-07-25 | 2005-07-12 | Pharmacia Italia Spa | Active bicyclo-pyrazoles as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them |
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2004
- 2004-07-01 US US10/882,493 patent/US7141568B2/en active Active
- 2004-07-08 RS YUP-2006/0004A patent/RS20060004A/en unknown
- 2004-07-08 AU AU2004255347A patent/AU2004255347B2/en not_active Ceased
- 2004-07-08 GE GEAP20049209A patent/GEP20084395B/en unknown
- 2004-07-08 NZ NZ544514A patent/NZ544514A/en not_active IP Right Cessation
- 2004-07-08 EA EA200600209A patent/EA009462B1/en not_active IP Right Cessation
- 2004-07-08 CA CA2531759A patent/CA2531759C/en not_active Expired - Fee Related
- 2004-07-08 SI SI200431502T patent/SI1644376T1/en unknown
- 2004-07-08 ES ES04763132T patent/ES2349780T3/en active Active
- 2004-07-08 PL PL04763132T patent/PL1644376T3/en unknown
- 2004-07-08 KR KR1020067000310A patent/KR101075711B1/en active IP Right Grant
- 2004-07-08 CN CNB2004800195930A patent/CN100564380C/en not_active Expired - Fee Related
- 2004-07-08 DK DK04763132.0T patent/DK1644376T3/en active
- 2004-07-08 TW TW093120474A patent/TWI343382B/en not_active IP Right Cessation
- 2004-07-08 PT PT04763132T patent/PT1644376E/en unknown
- 2004-07-08 MX MXPA06000362A patent/MXPA06000362A/en active IP Right Grant
- 2004-07-08 JP JP2006518148A patent/JP4728232B2/en not_active Expired - Fee Related
- 2004-07-08 ME MEP-519/08A patent/MEP51908A/en unknown
- 2004-07-08 EP EP04763132A patent/EP1644376B1/en active Active
- 2004-07-08 AT AT04763132T patent/ATE480540T1/en active
- 2004-07-08 WO PCT/EP2004/007515 patent/WO2005005427A1/en active Search and Examination
- 2004-07-08 AP AP2006003480A patent/AP2214A/en active
- 2004-07-08 RS RS20060004A patent/RS52155B/en unknown
- 2004-07-08 PE PE2004000657A patent/PE20050325A1/en not_active Application Discontinuation
- 2004-07-08 BR BRPI0411868A patent/BRPI0411868B8/en not_active IP Right Cessation
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- 2004-07-09 HN HN2004000232A patent/HN2004000232A/en unknown
- 2004-07-09 GT GT200400133AK patent/GT200400133AA/en unknown
- 2004-07-09 GT GT200400133A patent/GT200400133A/en unknown
- 2004-07-09 MY MYPI20042753A patent/MY139072A/en unknown
- 2004-07-09 PA PA20048606201A patent/PA8606201A1/en unknown
- 2004-07-12 AR ARP040102447A patent/AR050045A1/en active IP Right Grant
- 2004-08-07 UA UAA200601248A patent/UA81682C2/en unknown
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2005
- 2005-12-22 IS IS8192A patent/IS2843B/en unknown
- 2005-12-22 EC EC2005006246A patent/ECSP056246A/en unknown
- 2005-12-29 IL IL172923A patent/IL172923A/en active IP Right Grant
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2006
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- 2006-01-09 TN TNP2006000009A patent/TNSN06009A1/en unknown
- 2006-01-09 MA MA28721A patent/MA28064A1/en unknown
- 2006-08-11 US US11/503,256 patent/US7582628B2/en active Active
- 2006-09-15 HK HK06110252.6A patent/HK1089769A1/en not_active IP Right Cessation
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2010
- 2010-10-18 CY CY20101100924T patent/CY1110832T1/en unknown
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