AR099379A1 - Compuestos tricíclicos como agentes antineoplásicos - Google Patents
Compuestos tricíclicos como agentes antineoplásicosInfo
- Publication number
- AR099379A1 AR099379A1 ARP140104912A ARP140104912A AR099379A1 AR 099379 A1 AR099379 A1 AR 099379A1 AR P140104912 A ARP140104912 A AR P140104912A AR P140104912 A ARP140104912 A AR P140104912A AR 099379 A1 AR099379 A1 AR 099379A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- cycloalkyl
- hydrogen
- heteroaryl
- Prior art date
Links
Classifications
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- 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
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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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/495—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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
-
- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Peptides Or Proteins (AREA)
- Steroid Compounds (AREA)
Abstract
Compuestos tricíclicos, composiciones aceptables desde el punto de vista farmacéutico que comprenden compuestos de la presente y métodos para usar esas composiciones en el tratamiento de diversos trastornos. Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1) en donde: A es heterociclo opcionalmente sustituido o heteroarilo opcionalmente sustituido, en donde los sustituyentes son uno o más R; R es independientemente uno o más hidrógeno, halógeno, haloalquilo, hidroxialquilo, CN, CF₃, CH₂F, CHF₂, C₁₋₆ alquilo opcionalmente sustituido, C₁₋₆ alcoxi opcionalmente sustituido, C₃₋₆ cicloalquilo opcionalmente sustituido, heterociclo opcionalmente sustituido, -OR⁴, -CONR³R⁴, -NR³R⁴, NR³R⁴C₁₋₆ alquil-, -NR⁶OCOR³, -NR⁶COR³, NR⁶COR³C₁₋₆ alquil-, -NR⁶CO₂R³, NR⁶CO₂R³C₁₋₆ alquil-, -NR⁶CONR³R⁴, -SO₂NR³R⁴, SO₂C₁₋₆ alquil-, -NR⁶SO₂NR³R⁴, -NR⁶SO₂R⁴ o NR⁶SO₂R⁴C₁₋₆ alquil-; X e Y se seleccionan independientemente de hidrógeno, C₁₋₆ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido o heterociclo opcionalmente sustituido; Z es hidrógeno, halógeno, -OH, C₁₋₆ alquilo, C₁₋₆ alcoxi, -NR³R⁴, -CONR³R⁴, -OCONR³R⁴, -NR⁶OCOR³, -NR⁶CONR³R⁴, -NR⁶SO₂NR³R⁴ o -NR⁶SO₂R⁴; R¹ es, independientemente en cada caso, uno o más hidrógeno, halógeno, -CN, -OR⁴, -NR³R⁴, -CONR³R⁴, -COOH, -OCONR³R⁴, -NR⁶OCOR³, -NR⁶CONR³R⁴, -NR⁶SO₂NR³R⁴, -NR⁶SO₂R⁴, C₁₋₆ alquilo opcionalmente sustituido, C₂₋₆ alquenilo opcionalmente sustituido, C₂₋₆ alquinilo opcionalmente sustituido, C₁₋₆ alcoxi opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, C₃₋₈ cicloalquil-C₁₋₆ alquilo opcionalmente sustituido, C₃₋₈ cicloalquil-CO- opcionalmente sustituido, C₃₋₈ cicloalquil-SO₂- opcionalmente sustituido, aril-C₁₋₆ alcoxi opcionalmente sustituido, C₃₋₈ cicloalquil-C₁₋₆ alcoxi opcionalmente sustituido, heterociclil-CO- opcionalmente sustituido, heterociclilo opcionalmente sustituido, C₁₋₆ alquil-SO₂- opcionalmente sustituido, C₁₋₆ alquilo-NR⁶SO₂- opcionalmente sustituido, heterociclo-NR⁶SO₂- opcionalmente sustituido, C₁₋₆ alquil-NR⁶SO₂- opcionalmente sustituido o heterociclo-NR⁶SO₂- opcionalmente sustituido; R² es hidrógeno, halógeno, -CN, OH, -CONR³R⁴, -NR⁶COOR⁴, -NR⁶CONR³R⁴, -NR⁶COR⁴, -NR⁶SO₂R⁵, -SO₂NR³R⁴, -NR⁶SO₂NR³R⁴, C₁₋₆ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, C₁₋₆ alcoxi opcionalmente sustituido, arilo opcionalmente sustituido, C₁₋₆ alquil-SO₂- opcionalmente sustituido, aril-SO₂ opcionalmente sustituido, heteroarilo opcionalmente sustituido o heterociclo opcionalmente sustituido; R³ es hidrógeno, C₁₋₆ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, C₂₋₆ alquenilo opcionalmente sustituido, C₂₋₆ alquinilo opcionalmente sustituido, ciano-C₁₋₆ alquilo, hidroxi-C₁₋₆ alquilo, arilo opcionalmente sustituido, aril-C₁₋₆ alquilo opcionalmente sustituido, ariloxi-C₁₋₆ alquilo opcionalmente sustituido, C₁₋₆ alquil-SO₂- opcionalmente sustituido, heterociclilo opcionalmente sustituido, heterociclil-C₁₋₆ alquilo opcionalmente sustituido, heteroarilo opcionalmente sustituido o heteroaril-C₁₋₆ alquilo opcionalmente sustituido; R⁴ es hidrógeno, C₁₋₆ alquilo opcionalmente sustituido o C₃₋₈ cicloalquilo opcionalmente sustituido; o R³ y R⁴ pueden tomarse junto con el átomo de nitrógeno al que están unidos para formar un C₄₋₈ heteroarilo opcionalmente sustituido o un anillo C₄₋₈ heterocíclico; R⁵ es hidrógeno, C₁₋₆ alquilo opcionalmente sustituido, C₃₋₈ cicloalquilo opcionalmente sustituido, C₂₋₆ alquenilo opcionalmente sustituido, C₂₋₆ alquinilo opcionalmente sustituido, ciano-C₁₋₆ alquilo, hidroxi-C₁₋₆ alquilo, arilo opcionalmente sustituido, aril-C₁₋₆ alquilo opcionalmente sustituido, ariloxi-C₁₋₆ alquilo opcionalmente sustituido, C₁₋₆ alquil-SO₂- opcionalmente sustituido, heterociclilo opcionalmente sustituido, heterociclil-C₁₋₆ alquilo opcionalmente sustituido, heteroarilo opcionalmente sustituido o heteroaril-C₁₋₆ alquilo opcionalmente sustituido; R⁶ es hidrógeno o C₁₋₆ alquilo opcionalmente sustituido; R⁷ es hidrógeno, C₁₋₆ alquilo opcionalmente sustituido, -OR⁴, CN o halógeno; y/o una sal, un tautómero o un estereoisómero de aquel aceptables desde el punto de vista farmacéutico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361920500P | 2013-12-24 | 2013-12-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR099379A1 true AR099379A1 (es) | 2016-07-20 |
Family
ID=52293305
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP140104912A AR099379A1 (es) | 2013-12-24 | 2014-12-23 | Compuestos tricíclicos como agentes antineoplásicos |
| ARP210103062A AR123996A2 (es) | 2013-12-24 | 2021-11-03 | Compuestos tricíclicos novedosos como agentes antineoplásicos |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP210103062A AR123996A2 (es) | 2013-12-24 | 2021-11-03 | Compuestos tricíclicos novedosos como agentes antineoplásicos |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US20160318928A1 (es) |
| EP (2) | EP3087071B1 (es) |
| JP (2) | JP6466456B2 (es) |
| KR (1) | KR102457145B1 (es) |
| CN (2) | CN106029663B (es) |
| AR (2) | AR099379A1 (es) |
| AU (1) | AU2014369982B2 (es) |
| BR (1) | BR112016013744B1 (es) |
| CA (1) | CA2934953C (es) |
| CL (1) | CL2016001629A1 (es) |
| CY (2) | CY1121076T1 (es) |
| DK (2) | DK3087071T3 (es) |
| EA (2) | EA032469B1 (es) |
| ES (2) | ES2698998T3 (es) |
| HR (2) | HRP20181849T1 (es) |
| HU (2) | HUE041719T2 (es) |
| IL (1) | IL246359B (es) |
| LT (2) | LT3466949T (es) |
| MA (1) | MA39211B1 (es) |
| MX (1) | MX369491B (es) |
| MY (1) | MY176489A (es) |
| NZ (1) | NZ722326A (es) |
| PE (1) | PE20160844A1 (es) |
| PH (1) | PH12016500953A1 (es) |
| PL (2) | PL3466949T3 (es) |
| PT (2) | PT3466949T (es) |
| RS (2) | RS58014B1 (es) |
| SG (1) | SG11201605097SA (es) |
| SI (2) | SI3087071T1 (es) |
| SM (2) | SMT201800643T1 (es) |
| TN (1) | TN2016000238A1 (es) |
| TW (2) | TWI726544B (es) |
| UY (1) | UY35916A (es) |
| WO (1) | WO2015100282A1 (es) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2961747B1 (en) | 2013-02-27 | 2017-11-15 | Bristol-Myers Squibb Company | Carbazole compounds useful as bromodomain inhibitors |
| US11446309B2 (en) | 2013-11-08 | 2022-09-20 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (BET) protein inhibitors |
| CN106029663B (zh) * | 2013-12-24 | 2018-06-01 | 百时美施贵宝公司 | 作为抗癌剂的新颖三环化合物 |
| US9458156B2 (en) | 2014-12-23 | 2016-10-04 | Bristol-Myers Squibb Company | Tricyclic compounds as anticancer agents |
| US9580430B2 (en) * | 2014-02-28 | 2017-02-28 | The Regents Of The University Of Michigan | 9H-pyrimido[4,5-B]indoles and related analogs as BET bromodomain inhibitors |
| US9725449B2 (en) | 2015-05-12 | 2017-08-08 | Bristol-Myers Squibb Company | Tricyclic compounds as anticancer agents |
| EP3307740B1 (en) | 2015-05-12 | 2019-12-18 | Bristol-Myers Squibb Company | 5h-pyrido[3,2-b]indole compounds as anticancer agents |
| NZ739503A (en) * | 2015-07-16 | 2023-06-30 | Bioxcel Therapeutics Inc | A novel approach for treatment of cancer using immunomodulation |
| EP3355922A2 (en) * | 2015-10-02 | 2018-08-08 | Dana Farber Cancer Institute, Inc. | Combination therapy of bromodomain inhibitors and checkpoint blockade |
| WO2017124934A1 (zh) * | 2016-01-20 | 2017-07-27 | 宁波文达医药科技有限公司 | 作为布罗莫区结构域抑制剂的含膦咔啉衍生物 |
| EP3406612B1 (en) | 2016-01-20 | 2021-07-21 | Ningbo Wenda Pharma Technology Ltd. | Carboline derivative serving as bromodomain inhibitor |
| US20190040063A1 (en) * | 2016-02-05 | 2019-02-07 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Tricyclic compound for bromodomain-containing protein inhibitor and preparation pharmaceutical composition, and application thereof |
| KR20180116372A (ko) | 2016-03-01 | 2018-10-24 | 코어셉트 쎄라퓨틱스, 잉크. | 체크포인트 억제제를 강화시키기 위한 글루코코르티코이드 수용체 조정제의 용도 |
| US10150754B2 (en) * | 2016-04-19 | 2018-12-11 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| AU2017357329A1 (en) | 2016-11-10 | 2019-06-13 | Luoxin Pharmaceutical (Shanghai) Co., Ltd. | Nitrogenous macrocyclic compound, preparation method therefor, pharmaceutical composition and application thereof |
| CN106905347B (zh) * | 2017-04-18 | 2019-04-16 | 四川大学 | Brd4抑制剂及其在肿瘤治疗药物中的应用 |
| WO2019080941A1 (en) * | 2017-10-27 | 2019-05-02 | Jacobio-Beta Pharmaceuticals Co., Ltd. | NEW TRICYCLIC COMPOUNDS |
| SG11202012819YA (en) | 2018-06-25 | 2021-01-28 | Jacobio Pharmaceuticals Co Ltd | Tricyclic compounds |
| CN108840868B (zh) * | 2018-08-01 | 2019-10-18 | 上海山的实业有限公司 | 具有抗肿瘤活性的吲哚并吡啶酮类化合物的制备方法及应用 |
| US11234971B2 (en) | 2018-12-19 | 2022-02-01 | Corcept Therapeutics Incorporated | Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent |
| WO2020132046A1 (en) | 2018-12-19 | 2020-06-25 | Corcept Therapeutics Incorporated | Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent |
| CN113544129B (zh) * | 2019-04-04 | 2024-07-23 | 上海华汇拓医药科技有限公司 | 三环类化合物制备方法及其在医药领域的应用 |
| CN110003204B (zh) * | 2019-04-30 | 2020-08-11 | 上海勋和医药科技有限公司 | 一种bet蛋白抑制剂、其制备方法及用途 |
| US10947253B2 (en) | 2019-08-05 | 2021-03-16 | Ankh Life Sciences Limited | Fused polycyclic dimers |
| EP4039333A4 (en) | 2019-09-30 | 2024-02-14 | Kyowa Kirin Co., Ltd. | BET DEGRADATION AGENT |
| US12129265B2 (en) | 2020-07-21 | 2024-10-29 | Ankh Life Sciences Limited | Therapeutic agents and uses thereof |
| CA3206066A1 (en) * | 2021-01-22 | 2022-07-28 | Jingrui Biopharma Co., Ltd. | Tricyclic compounds as anticancer agents |
| AU2022227673A1 (en) * | 2021-02-25 | 2023-08-17 | Impact Biomedicines, Inc. | Use of a bet inhibitor alone or in combination with fedratinib or ruxolitinib for treating a hematological malignancy such as myelofibrosis |
| CN117881659A (zh) * | 2021-05-06 | 2024-04-12 | 拉结尔治疗有限公司 | 结晶咔唑衍生物 |
| WO2024099441A1 (en) * | 2022-11-11 | 2024-05-16 | Jingrui Biopharma (Shandong) Co., Ltd. | Bromodomain and extra-terminal (bet) protein degrader |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0623125A1 (en) * | 1992-01-15 | 1994-11-09 | E.I. Du Pont De Nemours And Company | Bridged heterocyclic fungicides |
| WO2005039569A1 (en) | 2003-10-18 | 2005-05-06 | Bayer Healthcare Ag | 5-substituted 2-(phenylmethyl) thio-4-phenyl-4h-1,2,4-triazole derivatives and related compounds as gaba-agonists for the treatment of urinary incontinence and related diseases |
| WO2005051318A2 (en) * | 2003-11-24 | 2005-06-09 | Viropharma Incorporated | Compounds, compositions and methods for treatment and prophylaxis of hepatitis c viral infections and associated diseases |
| TWI309240B (en) | 2004-09-17 | 2009-05-01 | Hoffmann La Roche | Anti-ox40l antibodies |
| WO2006105021A2 (en) | 2005-03-25 | 2006-10-05 | Tolerrx, Inc. | Gitr binding molecules and uses therefor |
| GB0507298D0 (en) | 2005-04-11 | 2005-05-18 | Novartis Ag | Organic compounds |
| BR122020016659B8 (pt) | 2005-05-10 | 2021-07-27 | Incyte Holdings Corp | moduladores de 2,3-dioxigenase de indolamina e métodos de modulação de atividade de inibição e de imunossupressão |
| EP2982379A1 (en) | 2005-07-01 | 2016-02-10 | E. R. Squibb & Sons, L.L.C. | Human monoclonal antibodies to programmed death ligand 1 (pd-l1) |
| JP5294874B2 (ja) | 2005-12-20 | 2013-09-18 | インサイト・コーポレイション | インドールアミン２，３−ジオキシゲナーゼのモジュレーターとしてのｎ−ヒドロキシアミジノヘテロ環 |
| US7696166B2 (en) | 2006-03-28 | 2010-04-13 | Albany Molecular Research, Inc. | Use of cyclosporin alkyne/alkene analogues for preventing or treating viral-induced disorders |
| ES2444574T3 (es) | 2006-09-19 | 2014-02-25 | Incyte Corporation | N-hidroxiamidinoheterociclos como moduladores de la indolamina 2,3-dioxigenasa |
| CL2007002650A1 (es) | 2006-09-19 | 2008-02-08 | Incyte Corp | Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras. |
| UY30892A1 (es) | 2007-02-07 | 2008-09-02 | Smithkline Beckman Corp | Inhibidores de la actividad akt |
| EP1987839A1 (en) | 2007-04-30 | 2008-11-05 | I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale | Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease |
| CA2693677C (en) | 2007-07-12 | 2018-02-13 | Tolerx, Inc. | Combination therapies employing gitr binding molecules |
| EP2044949A1 (en) | 2007-10-05 | 2009-04-08 | Immutep | Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response |
| JP5583592B2 (ja) | 2007-11-30 | 2014-09-03 | ニューリンク ジェネティクス コーポレイション | Ｉｄｏ阻害剤 |
| FR2927330B1 (fr) | 2008-02-07 | 2010-02-19 | Sanofi Aventis | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii |
| AR072999A1 (es) | 2008-08-11 | 2010-10-06 | Medarex Inc | Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos |
| PT2376535T (pt) | 2008-12-09 | 2017-06-23 | Hoffmann La Roche | Anticorpos anti-pd-l1 e a sua utilização para a melhoria do funcionamento das células t |
| CN102325752B (zh) * | 2008-12-19 | 2015-02-04 | 百时美施贵宝公司 | 咔唑和咔啉激酶抑制剂 |
| US8709424B2 (en) | 2009-09-03 | 2014-04-29 | Merck Sharp & Dohme Corp. | Anti-GITR antibodies |
| EP2493862B1 (en) | 2009-10-28 | 2016-10-05 | Newlink Genetics Corporation | Imidazole derivatives as ido inhibitors |
| PL2510010T3 (pl) | 2009-12-10 | 2016-05-31 | Hoffmann La Roche | Przeciwciała wiążące zewnątrzkomórkową domenę 4 ludzkiego CSF1R i ich zastosowanie |
| CA2791103A1 (en) | 2010-02-26 | 2011-09-01 | Boehringer Ingelheim International Gmbh | 4 - [cycloalkyloxy (hetero) arylamino] thieno [2,3-d] pyrimidines having mnk1/ mnk2 inhibiting activity for pharmaceutical compositions |
| MA34062B1 (fr) | 2010-03-04 | 2013-03-05 | Macrogenics Inc | Anticorps réagissant avec b7-h3, fragments immunologiquement actifs associés et utilisations associées |
| CN102918060B (zh) | 2010-03-05 | 2016-04-06 | 霍夫曼-拉罗奇有限公司 | 抗人csf-1r抗体及其用途 |
| RU2617966C2 (ru) | 2010-03-05 | 2017-04-28 | Ф.Хоффманн-Ля Рош Аг | Антитела против csf-1r человека и их применение |
| TWI503323B (zh) * | 2010-03-29 | 2015-10-11 | Oncotherapy Science Inc | 三環化合物以及含此化合物之ｐｂｋ抑制劑 |
| EP3943154A1 (en) | 2010-05-04 | 2022-01-26 | Five Prime Therapeutics, Inc. | Antibodies that bind csf1r |
| US8933072B2 (en) | 2010-06-16 | 2015-01-13 | Vitae Pharmaceuticals, Inc. | Substituted 5-,6- and 7-membered heterocycles, medicaments containing such compounds, and their use |
| KR101527300B1 (ko) | 2010-09-09 | 2015-06-09 | 화이자 인코포레이티드 | 4-1ｂｂ 결합 분자 |
| RS53768B1 (en) * | 2010-12-16 | 2015-06-30 | F. Hoffmann-La Roche Ag. | TRICYCLIC PI3K INHIBITORS AND USE PROCEDURES |
| US8580399B2 (en) * | 2011-04-08 | 2013-11-12 | Universal Display Corporation | Substituted oligoazacarbazoles for light emitting diodes |
| NO2694640T3 (es) | 2011-04-15 | 2018-03-17 | ||
| RS57324B1 (sr) | 2011-04-20 | 2018-08-31 | Medimmune Llc | Antitela i drugi molekuli koji vezuju b7-h1 i pd-1 |
| KR20140068883A (ko) * | 2011-09-28 | 2014-06-09 | 이데미쓰 고산 가부시키가이샤 | 유기 전계 발광 소자용 재료 및 이를 사용한 유기 전계 발광 소자 |
| HUE051954T2 (hu) | 2011-11-28 | 2021-03-29 | Merck Patent Gmbh | ANTI-PD-L1 ellenanyagok és alkalmazásaik |
| JP6242804B2 (ja) | 2011-12-15 | 2017-12-06 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ヒトｃｓｆ−１ｒに対する抗体及びその使用 |
| KR20140127855A (ko) | 2012-02-06 | 2014-11-04 | 제넨테크, 인크. | Csf1r 억제제를 사용하는 조성물 및 방법 |
| AR090263A1 (es) | 2012-03-08 | 2014-10-29 | Hoffmann La Roche | Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma |
| JP2015517490A (ja) | 2012-05-11 | 2015-06-22 | ファイブ プライム セラピューティックス インコーポレイテッド | コロニー刺激因子１受容体（ｃｓｆ１ｒ）を結合させる抗体を用いて状態を治療する方法 |
| UY34887A (es) | 2012-07-02 | 2013-12-31 | Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware | Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos |
| US20140079699A1 (en) | 2012-08-31 | 2014-03-20 | Five Prime Therapeutics, Inc. | Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r) |
| UA115576C2 (uk) * | 2012-12-06 | 2017-11-27 | Байєр Фарма Акцієнгезелльшафт | Похідні бензимідазолу як антагоністи ер4 |
| US9492460B2 (en) * | 2013-02-27 | 2016-11-15 | Bristol-Myers Squibb Company | Carbazole compounds useful as bromodomain inhibitors |
| EP2961747B1 (en) * | 2013-02-27 | 2017-11-15 | Bristol-Myers Squibb Company | Carbazole compounds useful as bromodomain inhibitors |
| WO2014164596A1 (en) * | 2013-03-11 | 2014-10-09 | The Regents Of The University Of Michigan | Bet bromodomain inhibitors and therapeutic methods using the same |
| CN106029663B (zh) * | 2013-12-24 | 2018-06-01 | 百时美施贵宝公司 | 作为抗癌剂的新颖三环化合物 |
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