PL2134685T3 - Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 - Google Patents
Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1Info
- Publication number
- PL2134685T3 PL2134685T3 PL08745934T PL08745934T PL2134685T3 PL 2134685 T3 PL2134685 T3 PL 2134685T3 PL 08745934 T PL08745934 T PL 08745934T PL 08745934 T PL08745934 T PL 08745934T PL 2134685 T3 PL2134685 T3 PL 2134685T3
- Authority
- PL
- Poland
- Prior art keywords
- nonsubstituted
- mcl
- inhibitors
- indole derivatives
- indole
- Prior art date
Links
- 101001056180 Homo sapiens Induced myeloid leukemia cell differentiation protein Mcl-1 Proteins 0.000 title 1
- 102100026539 Induced myeloid leukemia cell differentiation protein Mcl-1 Human genes 0.000 title 1
- 229940054051 antipsychotic indole derivative Drugs 0.000 title 1
- 150000002475 indoles Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91204907P | 2007-04-16 | 2007-04-16 | |
| US94968307P | 2007-07-13 | 2007-07-13 | |
| PCT/US2008/060427 WO2008130970A1 (en) | 2007-04-16 | 2008-04-16 | 7-nonsubstituted indole mcl-1 inhibitors |
| EP08745934.3A EP2134685B1 (en) | 2007-04-16 | 2008-04-16 | 7-nonsubstituted indole derivatives as mcl-1 inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2134685T3 true PL2134685T3 (pl) | 2016-02-29 |
Family
ID=39683700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL08745934T PL2134685T3 (pl) | 2007-04-16 | 2008-04-16 | Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7981888B2 (pl) |
| EP (1) | EP2134685B1 (pl) |
| JP (2) | JP5496876B2 (pl) |
| CN (1) | CN101711235A (pl) |
| CA (2) | CA2682354C (pl) |
| DK (1) | DK2134685T3 (pl) |
| ES (1) | ES2550753T3 (pl) |
| MX (1) | MX2009011210A (pl) |
| PL (1) | PL2134685T3 (pl) |
| PT (1) | PT2134685E (pl) |
| WO (1) | WO2008130970A1 (pl) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2009011211A (es) * | 2007-04-16 | 2009-10-30 | Abbott Lab | Indoles sustituidos en la posicion 7 inhibidores de mci-1. |
| EP2373629B1 (en) * | 2008-12-08 | 2013-04-10 | Boehringer Ingelheim International Gmbh | Compounds for treating cancer |
| CN102325531B (zh) | 2008-12-19 | 2014-04-02 | 健泰科生物技术公司 | 化合物和使用方法 |
| CA2747170C (en) * | 2008-12-19 | 2017-07-18 | Abbott Laboratories | Tetrahydroisoquinoline derivatives and their uses to treat cancers and autoimmune disorders |
| US20130035304A1 (en) | 2010-01-29 | 2013-02-07 | Walensky Loren D | Small molecules for the modulation of mcl-1 and methods of modulating cell death, cell division, cell differentiation and methods of treating disorders |
| EP2487159A1 (en) | 2011-02-11 | 2012-08-15 | MSD Oss B.V. | RorgammaT inhibitors |
| EP2567698B1 (en) * | 2011-09-07 | 2014-02-12 | Rheinische Friedrich-Wilhelms-Universität Bonn | GPR 17 agonists and screening assay |
| US8940737B2 (en) | 2011-10-14 | 2015-01-27 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| WO2013142281A1 (en) * | 2012-03-20 | 2013-09-26 | Dana Farber Cancer Institute, Inc. | Inhibition of mcl-1 and/or bfl-1/a1 |
| WO2014026327A1 (en) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | 4-heteroaryl substituted benzoic acid compounds as rorgammat inhibitors and uses thereof |
| WO2014026330A1 (en) * | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | 3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF |
| WO2014026329A1 (en) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | N-alkylated indole and indazole compounds as rorgammat inhibitors and uses thereof |
| US10093640B2 (en) | 2012-09-21 | 2018-10-09 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors |
| US10005728B2 (en) | 2013-08-28 | 2018-06-26 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
| CN106456602B (zh) * | 2014-03-27 | 2020-11-24 | 范德比尔特大学 | 取代的吲哚mcl-1抑制剂 |
| US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
| WO2016065410A1 (en) | 2014-10-29 | 2016-05-06 | The Walter And Eliza Hall Institute Of Medical Research | Use of therapeutic agents |
| US10221142B2 (en) | 2015-02-11 | 2019-03-05 | Merck Sharp & Dohme Corp. | Substituted pyrazole compounds as RORgammaT inhibitors and uses thereof |
| US10463649B2 (en) | 2015-06-08 | 2019-11-05 | Texas Tech University System | Inhibitors of Mc1-1 as drugs to overcome resistance to BRAF inhibitors and MEK inhibitors |
| CA3002853A1 (en) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Heteroaryl substituted benzoic acids as rorgammat inhibitors and uses thereof |
| US10287272B2 (en) | 2015-10-27 | 2019-05-14 | Merck Sharp & Dohme Corp. | Substituted indazole compounds as RORgammaT inhibitors and uses thereof |
| EP3368516B1 (en) | 2015-10-27 | 2020-07-15 | Merck Sharp & Dohme Corp. | SUBSTITUTED BICYCLIC PYRAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF |
| IL259051B2 (en) * | 2015-11-02 | 2024-11-01 | Carmel Haifa Univ Economic Corporation Ltd | Compounds that mimic APOPTOSIS RELATED PROTEIN IN THE TGF-BETA SIGNALING PATHWAY (ARTS), preparations containing them, methods and their uses in initiating differentiation and/or apoptosis in pre-malignant and malignant cells, and restoring their normal-like phenotype |
| EP4292662A3 (en) * | 2016-03-04 | 2024-02-21 | Vanderbilt University | Substituted indole mcl-1 inhibitors |
| MA44721B1 (fr) | 2016-04-22 | 2020-05-29 | Astrazeneca Ab 151 85 Soedertaelje | Inhibiteurs de mcl1 macrocycliques pour le traitement du cancer |
| JP7013389B2 (ja) | 2016-05-19 | 2022-01-31 | バイエル アクチェンゲゼルシャフト | 大環状インドール誘導体 |
| WO2017198341A1 (en) | 2016-05-19 | 2017-11-23 | Bayer Aktiengesellschaft | Macrocyclic indole derivatives |
| JP6910027B2 (ja) * | 2017-03-29 | 2021-07-28 | 株式会社コーセー | チロシナーゼ活性阻害剤、メラニン産生抑制剤及び美白剤 |
| EP3618831A4 (en) * | 2017-04-30 | 2021-12-01 | Development Center for Biotechnology | ANTI-CANCER FOOT MEDICINE |
| EP3710451A1 (en) | 2017-11-17 | 2020-09-23 | Bayer Aktiengesellschaft | Substituted macrocyclic indole derivatives |
| TW201932473A (zh) | 2017-11-17 | 2019-08-16 | 美商博德研究所有限公司 | 巨環吲哚衍生物 |
| WO2019096909A1 (en) | 2017-11-17 | 2019-05-23 | The Broad Institute, Inc. | Macrocyclic fluorine substituted indole derivatives as mcl-1 inhibitors, for use in the treatment of cancer |
| WO2019096905A1 (en) | 2017-11-17 | 2019-05-23 | Bayer Aktiengesellschaft | Macrocyclic chlorine substituted indole derivatives |
| US11447504B2 (en) | 2017-11-17 | 2022-09-20 | Bayer Aktiengesellschaft | Macrocyclic chlorine substituted indole derivatives |
| US20210253598A1 (en) | 2017-11-17 | 2021-08-19 | Bayer Aktiengesellschaft | Aryl annulated macrocyclic indole derivatives |
| CN112533929B (zh) * | 2018-09-30 | 2022-09-16 | 福建盛迪医药有限公司 | 吲哚类大环衍生物、其制备方法及其在医药上的应用 |
| CN110845520B (zh) * | 2018-11-22 | 2021-04-13 | 苏州亚盛药业有限公司 | 作为mcl-1抑制剂的大环吲哚 |
| CN114127079A (zh) | 2019-05-17 | 2022-03-01 | 布罗德研究所有限公司 | 制备大环吲哚的方法 |
| WO2021092061A1 (en) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Combination treatment for senescence-associated diseases |
| WO2021092053A1 (en) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Mcl-1 inhibitor macrocycle compounds for use in clinical management of conditions caused or mediated by senescent cells and for treating cancer |
| US20230021562A1 (en) | 2019-11-21 | 2023-01-26 | Janssen Pharmaceutica Nv | Macrocylic indole derivatives mcl-1 inhibitors |
| KR20220103985A (ko) | 2019-11-21 | 2022-07-25 | 얀센 파마슈티카 엔.브이. | Mcl-1 억제제로서의 거대환식 술포닐 유도체 |
| JPWO2021107125A1 (pl) | 2019-11-29 | 2021-06-03 | ||
| CN115335384B (zh) * | 2020-03-30 | 2024-10-22 | 江苏恒瑞医药股份有限公司 | 一种吲哚类大环衍生物的结晶形式及其制备方法 |
| MX2022015005A (es) | 2020-05-29 | 2023-01-04 | Janssen Pharmaceutica Nv | Derivados de 7-pirazol-5-il-indol macrociclicos como inhibidores de mcl-1. |
| BR112022025674A2 (pt) | 2020-06-19 | 2023-01-17 | Janssen Pharmaceutica Nv | Derivados de 7-(pirazol-5-il)-indol macrocíclico n-ligado como inibidores de mcl-1 |
| WO2022261310A1 (en) | 2021-06-11 | 2022-12-15 | Gilead Sciences, Inc. | Combination mcl-1 inhibitors with anti-body drug conjugates |
| US11957693B2 (en) | 2021-06-11 | 2024-04-16 | Gilead Sciences, Inc. | Combination MCL-1 inhibitors with anti-cancer agents |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3632805A (en) | 1967-12-08 | 1972-01-04 | Sumitomo Chemical Co | Process for producing 1-aminoalkyl-benzodiazepine derivatives |
| FR2187318B1 (pl) | 1972-06-08 | 1975-06-20 | Delalande Sa | |
| US4994477A (en) * | 1988-03-24 | 1991-02-19 | Abbott Laboratories | Heterocyclic renin inhibitors |
| ES2208935T3 (es) * | 1996-08-01 | 2004-06-16 | Merckle Gmbh | Acidos acil-pirrol-dicarboxilicos y acidos acil-indol-dicarboxilicos, asi como sus derivados como inhibidores de la fosfolipasa a2 citosolica. |
| GB9716657D0 (en) * | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
| DE69929720T2 (de) | 1998-11-27 | 2006-09-21 | Mitsubishi Chemical Corp. | Verfahren zur Herstellung von Maleinsäureanhydrid |
| GB9902452D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902455D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB0000626D0 (en) | 2000-01-13 | 2000-03-01 | Zeneca Ltd | Chemical compounds |
| KR20030036917A (ko) * | 2000-10-10 | 2003-05-09 | 스미스클라인 비참 코포레이션 | 치환된 인돌, 이를 함유하는 약제학적 조성물, 및 이의PPAR-γ결합제로서의 용도 |
| DE10153346A1 (de) | 2001-10-29 | 2004-04-22 | Grünenthal GmbH | Substituierte Indole |
| US7053071B2 (en) | 2001-11-30 | 2006-05-30 | The Burnham Institute | Induction of apoptosis in cancer cells |
| JP2005519915A (ja) * | 2002-01-18 | 2005-07-07 | セレテック・リミテッド・ライアビリティ・カンパニー | Edg受容体に関連する症状の処置方法 |
| WO2003091214A1 (en) * | 2002-04-23 | 2003-11-06 | Aventis Pharmaceuticals Inc. | 3-substituted amino-1h-indole-2-carboxylic acid and 3-substituted amino-benzo |
| ES2502490T3 (es) * | 2003-02-26 | 2014-10-03 | Sugen, Inc. | Compuestos aminoheteroarílicos como inhibidores de proteín quinasas |
| US7141600B2 (en) * | 2003-04-15 | 2006-11-28 | The Regents Of The University Of California | Small molecule inhibition of a PDZ-domain interaction |
| SE0302035D0 (sv) * | 2003-07-09 | 2003-07-09 | Biolipox Ab | New compound |
| US7268159B2 (en) * | 2003-09-25 | 2007-09-11 | Wyeth | Substituted indoles |
| ITMI20040874A1 (it) * | 2004-04-30 | 2004-07-30 | Ist Naz Stud Cura Dei Tumori | Derivati indolici ed azaindolici con azione antitumorale |
| CN101006054A (zh) * | 2004-06-18 | 2007-07-25 | 比奥里波克斯公司 | 用于炎症治疗的吲哚 |
| JP2008502672A (ja) * | 2004-06-18 | 2008-01-31 | バイオリポックス エービー | 炎症の治療に有用なインドール類 |
| ATE405549T1 (de) * | 2004-06-18 | 2008-09-15 | Biolipox Ab | Zur behandlung von entzündungen geeignete indole |
| WO2006041961A1 (en) | 2004-10-05 | 2006-04-20 | GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTHAND HUMAN SERVICES | Arylthioindole tubulin polymerization inhibitors and methods of treating or preventing cancer using same |
| FR2878849B1 (fr) * | 2004-12-06 | 2008-09-12 | Aventis Pharma Sa | Indoles substitues, compositions les contenant, procede de fabrication et utilisation |
| US20100197687A1 (en) * | 2005-01-19 | 2010-08-05 | Benjamin Pelcman | Indoles Useful in the Treatment of Inflammation |
| EA200701504A1 (ru) * | 2005-01-19 | 2008-02-28 | Биолипокс Аб | Индолы, пригодные для лечения воспалений |
| EP1904047B1 (en) * | 2005-07-07 | 2013-01-02 | Abbott Laboratories | Apoptosis promoters |
| PE20080767A1 (es) * | 2006-08-31 | 2008-08-08 | Smithkline Beecham Corp | Derivados de acido 1-indol-2-carboxilico como moduladores de ppar |
| MX2009011211A (es) | 2007-04-16 | 2009-10-30 | Abbott Lab | Indoles sustituidos en la posicion 7 inhibidores de mci-1. |
| CN102325531B (zh) | 2008-12-19 | 2014-04-02 | 健泰科生物技术公司 | 化合物和使用方法 |
| CA2747170C (en) | 2008-12-19 | 2017-07-18 | Abbott Laboratories | Tetrahydroisoquinoline derivatives and their uses to treat cancers and autoimmune disorders |
-
2008
- 2008-04-16 PL PL08745934T patent/PL2134685T3/pl unknown
- 2008-04-16 CA CA2682354A patent/CA2682354C/en active Active
- 2008-04-16 EP EP08745934.3A patent/EP2134685B1/en active Active
- 2008-04-16 ES ES08745934.3T patent/ES2550753T3/es active Active
- 2008-04-16 JP JP2010504205A patent/JP5496876B2/ja not_active Expired - Fee Related
- 2008-04-16 PT PT87459343T patent/PT2134685E/pt unknown
- 2008-04-16 CN CN200880020451A patent/CN101711235A/zh active Pending
- 2008-04-16 CA CA2951295A patent/CA2951295C/en active Active
- 2008-04-16 DK DK08745934.3T patent/DK2134685T3/en active
- 2008-04-16 WO PCT/US2008/060427 patent/WO2008130970A1/en not_active Ceased
- 2008-04-16 US US12/104,319 patent/US7981888B2/en active Active
- 2008-04-16 MX MX2009011210A patent/MX2009011210A/es active IP Right Grant
-
2011
- 2011-04-15 US US13/088,206 patent/US8853209B2/en active Active
-
2014
- 2014-03-04 JP JP2014041214A patent/JP5895011B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP5895011B2 (ja) | 2016-03-30 |
| JP2014129396A (ja) | 2014-07-10 |
| ES2550753T3 (es) | 2015-11-12 |
| EP2134685B1 (en) | 2015-09-02 |
| US20110263599A1 (en) | 2011-10-27 |
| JP5496876B2 (ja) | 2014-05-21 |
| CA2951295A1 (en) | 2008-10-30 |
| MX2009011210A (es) | 2009-10-30 |
| US20090124616A1 (en) | 2009-05-14 |
| CA2951295C (en) | 2020-04-28 |
| PT2134685E (pt) | 2015-11-25 |
| CN101711235A (zh) | 2010-05-19 |
| US8853209B2 (en) | 2014-10-07 |
| DK2134685T3 (en) | 2015-12-07 |
| EP2134685A1 (en) | 2009-12-23 |
| US7981888B2 (en) | 2011-07-19 |
| JP2010524955A (ja) | 2010-07-22 |
| CA2682354A1 (en) | 2008-10-30 |
| CA2682354C (en) | 2016-12-13 |
| WO2008130970A1 (en) | 2008-10-30 |
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