PE20080935A1 - THERAPY USING CYTOKINE INHIBITORS - Google Patents
THERAPY USING CYTOKINE INHIBITORSInfo
- Publication number
- PE20080935A1 PE20080935A1 PE2007000714A PE2007000714A PE20080935A1 PE 20080935 A1 PE20080935 A1 PE 20080935A1 PE 2007000714 A PE2007000714 A PE 2007000714A PE 2007000714 A PE2007000714 A PE 2007000714A PE 20080935 A1 PE20080935 A1 PE 20080935A1
- Authority
- PE
- Peru
- Prior art keywords
- ter
- tolil
- butil
- members
- saturated
- Prior art date
Links
- 102000004127 Cytokines Human genes 0.000 title abstract 2
- 108090000695 Cytokines Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- 238000002560 therapeutic procedure Methods 0.000 title 1
- -1 INDAZOLYL Chemical class 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000001363 autoimmune Effects 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000001721 carbon Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- 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
- 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
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
SE REFIERE A UN METODO PARA TRATAR UN TRASTORNO POR UNA O MAS CITOCINAS QUE COMPRENDE EN ADMINISTRAR UN COMPUESTO DE FORMULAS: IA, IB, IC, II, III y IV; ENTRE OTROS; SOLOS O EN COMBINACION; EN DONDE G ES UN CARBOCICLILO(C3-C10), HETEROCICLILO MONOCICLILO DE 5 A 8 MIEMBROS O HETEROCICLILO BICICLICO DE 8 A 11 MIEMBROS; X ES C(O), C(S) O CH2; Ar ES DIOXIDO DE INDAZOLILO, INDOLILO, IMIDAZOLILO, PIRAZOLILO, ENTRE OTROS; L ES UN ENLACE COVALENTE O UNA CADENA DE CARBONO(C1-C10) SATURADA O NO SATURADA; Q ES H, CICLOALQUILO, ARILO, ALCOXI DE C1-C6, ENTRE OTROS. SON SELECCIONADOS: (5-TER-BUTIL-2-p-TOLIL-2H-PIRAZOL-3-IL)-AMIDA DEL ACIDO 1H-INDAZOL-3-CARBOXILICO, 3-TER-BUTIL-5-FENIL-1-p-TOLIL-1,6-DIHIDRO-IMIDAZO[4,5-c]PIRAZOL, N-(5-TER-BUTIL-3-METANSULFONILAMINO-2-METOXI-FENIL)-2-[4-(2-MORFOLIN-4-IL-PIRIMIDIN-4-ILOXI)-NALTALEN-1-IL]-2-OXO-ACETAMIDA. TAMBIEN SE FERIERE A UNA COMPOSICION FARMACEUTICA. SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES AUTOINMUNES, INFLAMATORIAS, CARDIOVASCULARES Y CANCERREFERS TO A METHOD TO TREAT A DISORDER DUE TO ONE OR MORE CYTOKINES THAT INCLUDES ADMINISTERING A COMPOUND OF FORMULAS: IA, IB, IC, II, III and IV; AMONG OTHERS; ALONE OR IN COMBINATION; WHERE G IS A CARBOCYCLYL (C3-C10), HETEROCYCLYL MONOCYCLYL OF 5 TO 8 MEMBERS OR BICYCLE HETEROCYCLE OF 8 TO 11 MEMBERS; X IS C (O), C (S) O CH2; Ar IS DIOXIDE OF INDAZOLYL, INDOLYL, IMIDAZOLYL, PYRAZOLIL, AMONG OTHERS; L IS A COVALENT LINK OR A SATURATED OR NON-SATURATED CARBON (C1-C10) CHAIN; Q IS H, CYCLOALKYL, ARYL, C1-C6 ALCOXY, AMONG OTHERS. THEY ARE SELECTED: (5-TER-BUTIL-2-p-TOLIL-2H-PIRAZOL-3-IL) -AMIDE OF 1H-INDAZOL-3-CARBOXYL ACID, 3-TER-BUTIL-5-FENIL-1-p- TOLIL-1,6-DIHYDRO-IMIDAZO [4,5-c] PYRAZOLE, N- (5-TER-BUTYL-3-METANSULPHONYLAMINO-2-METHYL-PHENYL) -2- [4- (2-MORFOLIN-4- IL-PYRIMIDIN-4-ILOXI) -NALTALEN-1-IL] -2-OXO-ACETAMIDE. IT ALSO CONFIRMS A PHARMACEUTICAL COMPOSITION. BEING USEFUL IN THE TREATMENT OF AUTOIMMUNE, INFLAMMATORY, CARDIOVASCULAR AND CANCER DISEASES
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81226806P | 2006-06-09 | 2006-06-09 | |
| US83307806P | 2006-07-24 | 2006-07-24 | |
| US83527006P | 2006-08-03 | 2006-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20080935A1 true PE20080935A1 (en) | 2008-08-02 |
Family
ID=38832677
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007000714A PE20080935A1 (en) | 2006-06-09 | 2007-06-08 | THERAPY USING CYTOKINE INHIBITORS |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP2035005A4 (en) |
| AR (1) | AR061273A1 (en) |
| AU (1) | AU2007257959A1 (en) |
| CA (1) | CA2691214A1 (en) |
| CL (1) | CL2007001670A1 (en) |
| PE (1) | PE20080935A1 (en) |
| TW (1) | TW200814998A (en) |
| WO (1) | WO2007146712A2 (en) |
Families Citing this family (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1986633B1 (en) | 2006-02-10 | 2014-07-30 | Summit Corporation Plc | Treatment of duchenne muscular dystrophy |
| US7989459B2 (en) | 2006-02-17 | 2011-08-02 | Pharmacopeia, Llc | Purinones and 1H-imidazopyridinones as PKC-theta inhibitors |
| US7915268B2 (en) | 2006-10-04 | 2011-03-29 | Wyeth Llc | 8-substituted 2-(benzimidazolyl)purine derivatives for immunosuppression |
| US7902187B2 (en) | 2006-10-04 | 2011-03-08 | Wyeth Llc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
| AR063142A1 (en) | 2006-10-04 | 2008-12-30 | Pharmacopeia Inc | DERIVATIVES OF 2- (BENCIMIDAZOLIL) PURINE AND PURINONES 6-USEFUL SUBSTITUTES AS IMMUNOSUPPRESSORS, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| US8563573B2 (en) | 2007-11-02 | 2013-10-22 | Vertex Pharmaceuticals Incorporated | Azaindole derivatives as CFTR modulators |
| US7902248B2 (en) | 2006-12-14 | 2011-03-08 | Hoffmann-La Roche Inc. | Oxime glucokinase activators |
| US8440832B2 (en) * | 2007-07-13 | 2013-05-14 | Board Of Regents, The University Of Texas System | Heterocyclic modulators of cannabinoid receptors |
| LT2170396T (en) | 2007-08-03 | 2017-03-10 | Summit (Oxford) Limited | Drug combinations for the treatment of duchenne muscular dystrophy |
| US8304413B2 (en) | 2008-06-03 | 2012-11-06 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
| WO2010053861A2 (en) * | 2008-11-07 | 2010-05-14 | H. Lundbeck A/S | Biologically active amides |
| WO2010141932A1 (en) | 2009-06-05 | 2010-12-09 | Link Medicine Corporation | Aminopyrrolidinone derivatives and uses thereof |
| US20110117055A1 (en) * | 2009-11-19 | 2011-05-19 | Macdonald James E | Methods of Treating Hepatitis C Virus with Oxoacetamide Compounds |
| ES2550033T3 (en) * | 2009-12-23 | 2015-11-04 | Ratiopharm Gmbh | Ticagrelor solid pharmaceutical dosage form |
| US8802868B2 (en) | 2010-03-25 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of (R)-1(2,2-difluorobenzo[D][1,3]dioxo1-5-yl)-N-(1-(2,3-dihydroxypropyl-6-fluoro-2-(1-hydroxy-2-methylpropan2-yl)-1H-Indol-5-yl)-Cyclopropanecarboxamide |
| SG10201502484SA (en) | 2010-03-30 | 2015-05-28 | Verseon Corp | Multisubstituted aromatic compounds as inhibitors of thrombin |
| RU2569678C2 (en) | 2010-04-22 | 2015-11-27 | Вертекс Фармасьютикалз Инкорпорейтед | Method for producing cycloalkylcarboxamido-indole compounds |
| AR081331A1 (en) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | AMINO- PYRIMIDINES COMPOSITIONS OF THE SAME AND METHODS FOR THE USE OF THE SAME |
| AR081626A1 (en) | 2010-04-23 | 2012-10-10 | Cytokinetics Inc | AMINO-PYRIDAZINIC COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE OF THE SAME TO TREAT CARDIAC AND SKELETIC MUSCULAR DISORDERS |
| WO2011133920A1 (en) | 2010-04-23 | 2011-10-27 | Cytokinetics, Inc. | Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use |
| US8759380B2 (en) | 2011-04-22 | 2014-06-24 | Cytokinetics, Inc. | Certain heterocycles, compositions thereof, and methods for their use |
| US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
| GB2515942A (en) | 2011-10-21 | 2015-01-07 | Abbvie Inc | Combination treatment (e.g. with ABT-072 or ABT-333) of DAAs for use in treating HCV |
| US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| PT107894A (en) | 2011-10-21 | 2014-10-31 | Abbvie Inc | METHODS FOR THE TREATMENT OF HCV COMPREHENDING AT LEAST TWO ANTIVIRAL AGENTS OF DIRECT ACTIVITY, RIBAVIRIN, BUT NOT INTERFERED. |
| AR092742A1 (en) | 2012-10-02 | 2015-04-29 | Intermune Inc | ANTIFIBROTIC PYRIDINONES |
| ES2702182T3 (en) | 2013-03-15 | 2019-02-27 | Verseon Corp | Aromatic compounds multisubstituted as serine protease inhibitors |
| KR102373700B1 (en) | 2014-04-02 | 2022-03-11 | 인터뮨, 인크. | Anti-fibrotic pyridinones |
| PT3131582T (en) | 2014-04-15 | 2018-10-08 | Vertex Pharma | Pharmaceutical compositions for the treatment of cystic fibrosis transmembrane conductance regulator mediated diseases |
| BR112017004704A2 (en) | 2014-09-17 | 2018-01-23 | Verseon Corp | compound, pharmaceutical composition, and method for treating a disease or disorder in an individual |
| WO2016094688A1 (en) | 2014-12-10 | 2016-06-16 | Massachusetts Institute Of Technology | Fused 1,3-azole derivatives useful for the treatment of proliferative diseases |
| SG11201706411YA (en) | 2015-02-27 | 2017-09-28 | Verseon Corp | Substituted pyrazole compounds as serine protease inhibitors |
| US10576086B2 (en) | 2015-06-12 | 2020-03-03 | University Of Greenwich | Triazine derivatives as interferon-gamma inhibitors |
| EP3365340B1 (en) | 2015-10-19 | 2022-08-10 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| HUE060680T2 (en) | 2015-11-19 | 2023-04-28 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| JP6448867B2 (en) | 2015-12-15 | 2019-01-09 | アストラゼネカ・アクチエボラーグAstrazeneca Aktiebolag | Isoindole compounds |
| EP3394033B1 (en) | 2015-12-22 | 2020-11-25 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| EP3416950A1 (en) | 2016-02-16 | 2018-12-26 | Massachusetts Institute of Technology | Max binders as myc modulators and uses thereof |
| US11192914B2 (en) | 2016-04-28 | 2021-12-07 | Emory University | Alkyne containing nucleotide and nucleoside therapeutic compositions and uses related thereto |
| WO2017192961A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| TW201808902A (en) | 2016-05-26 | 2018-03-16 | 美商英塞特公司 | Heterocyclic compounds as immunomodulators |
| AU2017277478B2 (en) * | 2016-06-08 | 2023-03-16 | Support-Venture Gmbh | Pharmaceutical combinations for treating cancer |
| MD3472167T2 (en) | 2016-06-20 | 2023-02-28 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| WO2018013789A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| US20180057486A1 (en) | 2016-08-29 | 2018-03-01 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| HUE054548T2 (en) | 2016-12-20 | 2021-09-28 | Astrazeneca Ab | Aminotriazolopyridine compounds and their use in the treatment of cancer |
| MA47123A (en) | 2016-12-22 | 2021-03-17 | Incyte Corp | BENZOOXAZOLE DERIVATIVES AS MMUNOMODULATORS |
| EP3558989B1 (en) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
| EP3558973B1 (en) | 2016-12-22 | 2021-09-15 | Incyte Corporation | Pyridine derivatives as immunomodulators |
| PE20200005A1 (en) | 2016-12-22 | 2020-01-06 | Incyte Corp | DERIVATIVES OF TETRAHYDRO IMIDAZO [4,5-C] PYRIDINE AS INDUCTORS OF INTERNALIZATION PD-L1 |
| EP3558963B1 (en) | 2016-12-22 | 2022-03-23 | Incyte Corporation | Bicyclic heteroaromatic compounds as immunomodulators |
| MX389668B (en) * | 2017-05-15 | 2025-03-20 | Recurium Ip Holdings Llc | Analgesic compounds |
| WO2018229155A1 (en) | 2017-06-14 | 2018-12-20 | Astrazeneca Ab | 2,3-dihydroisoindole-1-carboxamides useful as ror-gamma modulators |
| CN107474043A (en) * | 2017-09-13 | 2017-12-15 | 厦门稀土材料研究所 | Nicotinic acid derivatives and their preparation methods and uses |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| PT3691620T (en) | 2017-10-05 | 2022-10-06 | Fulcrum Therapeutics Inc | P38 kinase inhibitors reduce dux4 and downstream gene expression for the treatment of fshd |
| US11667651B2 (en) | 2017-12-22 | 2023-06-06 | Hibercell, Inc. | Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors |
| PL4212529T3 (en) | 2018-03-30 | 2025-07-07 | Incyte Corporation | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
| HRP20230306T1 (en) | 2018-05-11 | 2023-05-12 | Incyte Corporation | TETRAHYDRO-IMIDAZO[4,5-C]PYRIDINE DERIVATIVES AS PD-L1 IMMUNOMODULATORS |
| BR112020024879A2 (en) | 2018-06-07 | 2021-03-09 | Idorsia Pharmaceuticals Ltd | COMPOUND, PHARMACEUTICAL COMPOSITION, USE OF A COMPOUND, AND, METHOD |
| WO2020056191A1 (en) * | 2018-09-13 | 2020-03-19 | Eirion Therapeutics, Inc. | Uses of plasminogen activator inhibitor 1 (pai-1) inhibitors |
| AU2019387367A1 (en) | 2018-11-30 | 2021-06-10 | Nuvation Bio Inc. | Diarylhydantoin compounds and methods of use thereof |
| US11034669B2 (en) | 2018-11-30 | 2021-06-15 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN111825605B (en) * | 2019-04-19 | 2023-03-31 | 中国科学院上海药物研究所 | Aryl ketone amide compound and preparation method and application thereof |
| TW202112767A (en) | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors |
| AR119162A1 (en) | 2019-06-18 | 2021-12-01 | Idorsia Pharmaceuticals Ltd | PYRIDIN-3-YL DERIVATIVES |
| WO2021030162A1 (en) | 2019-08-09 | 2021-02-18 | Incyte Corporation | Salts of a pd-1/pd-l1 inhibitor |
| IL291471B2 (en) | 2019-09-30 | 2025-04-01 | Incyte Corp | Pyrido[3,2-d]pyrimidine compounds as immunomodulators |
| CN114845709B (en) * | 2019-11-05 | 2024-10-01 | 德米拉公司 | MRGPRX2 antagonists for the treatment of inflammatory disorders |
| CR20220237A (en) | 2019-11-11 | 2022-08-05 | Incyte Corp | SALTS AND CRYSTALLINE FORMS OF A PD-1/PD-L1 INHIBITOR |
| PH12022551379A1 (en) | 2019-12-06 | 2023-05-03 | Vertex Pharma | Substituted tetrahydrofurans as modulators of sodium channels |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| WO2022099075A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Crystalline form of a pd-1/pd-l1 inhibitor |
| AR124001A1 (en) | 2020-11-06 | 2023-02-01 | Incyte Corp | PROCESS FOR MANUFACTURING A PD-1 / PD-L1 INHIBITOR AND SALTS AND CRYSTALLINE FORMS THEREOF |
| CN113209112B (en) * | 2021-02-06 | 2021-12-24 | 广州市朝利良生物科技有限公司 | Novel coronavirus resistant medicine based on ACE2 and S protein binding target and application thereof |
| DK4347031T3 (en) | 2021-06-04 | 2025-12-01 | Vertex Pharma | N-(HYDROXYALKYL-(HETERO)ARYL)-TETRAHYDROFURAN-CARBOXAMIDES AS MODULATORS OF SODIUM CHANNELS |
| WO2023154519A1 (en) | 2022-02-14 | 2023-08-17 | Accent Therapeutics, Inc. | Inhibitors of rna helicase dhx9 and uses thereof |
| WO2024059220A2 (en) * | 2022-09-15 | 2024-03-21 | Vanderbilt University | 6,5 southwestern core compounds as mglu5 negative allosteric modulators and methods of making and using the same |
| CN118496159B (en) * | 2024-07-18 | 2024-09-24 | 广州医科大学附属市八医院 | Application of compound in preparation of medicine with liver fibrosis preventing and/or treating effect |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004530690A (en) * | 2001-05-16 | 2004-10-07 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | Diaryl urea derivatives useful as anti-inflammatory drugs |
| WO2005023761A2 (en) * | 2003-09-11 | 2005-03-17 | Kemia, Inc. | Cytokine inhibitors |
-
2007
- 2007-06-06 EP EP07798190A patent/EP2035005A4/en not_active Withdrawn
- 2007-06-06 AU AU2007257959A patent/AU2007257959A1/en not_active Abandoned
- 2007-06-06 WO PCT/US2007/070547 patent/WO2007146712A2/en not_active Ceased
- 2007-06-06 CA CA2691214A patent/CA2691214A1/en not_active Abandoned
- 2007-06-08 AR ARP070102483A patent/AR061273A1/en unknown
- 2007-06-08 TW TW096120764A patent/TW200814998A/en unknown
- 2007-06-08 PE PE2007000714A patent/PE20080935A1/en not_active Application Discontinuation
- 2007-06-08 CL CL2007001670A patent/CL2007001670A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR061273A1 (en) | 2008-08-13 |
| CA2691214A1 (en) | 2007-12-21 |
| WO2007146712A3 (en) | 2008-11-27 |
| AU2007257959A1 (en) | 2007-12-21 |
| EP2035005A2 (en) | 2009-03-18 |
| WO2007146712A2 (en) | 2007-12-21 |
| EP2035005A4 (en) | 2011-07-06 |
| CL2007001670A1 (en) | 2008-01-18 |
| TW200814998A (en) | 2008-04-01 |
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