DOP2018000008A - Inhibidores del receptor del factor estimulador de colonias 1 (csf-1r) - Google Patents
Inhibidores del receptor del factor estimulador de colonias 1 (csf-1r)Info
- Publication number
- DOP2018000008A DOP2018000008A DO2018000008A DO2018000008A DOP2018000008A DO P2018000008 A DOP2018000008 A DO P2018000008A DO 2018000008 A DO2018000008 A DO 2018000008A DO 2018000008 A DO2018000008 A DO 2018000008A DO P2018000008 A DOP2018000008 A DO P2018000008A
- Authority
- DO
- Dominican Republic
- Prior art keywords
- csf
- inhibitors
- colonia
- stimulator factor
- factor receiver
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 241001398967 Colonia Species 0.000 title 1
- 101000916644 Homo sapiens Macrophage colony-stimulating factor 1 receptor Proteins 0.000 abstract 2
- 102100028198 Macrophage colony-stimulating factor 1 receptor Human genes 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
-
- 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
-
- 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
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
Compuestos de fórmulas que son útiles como inhibidores del receptor del factor estimulador de colonias 1 (CSF-1R) (inhibidores de CSF 1R).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562194619P | 2015-07-20 | 2015-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
DOP2018000008A true DOP2018000008A (es) | 2018-05-15 |
Family
ID=56551024
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DO2018000008A DOP2018000008A (es) | 2015-07-20 | 2018-01-09 | Inhibidores del receptor del factor estimulador de colonias 1 (csf-1r) |
Country Status (27)
Country | Link |
---|---|
US (3) | US11274108B2 (es) |
EP (1) | EP3325471A1 (es) |
JP (3) | JP6898914B2 (es) |
KR (1) | KR102665765B1 (es) |
CN (1) | CN107922396B (es) |
AR (1) | AR105392A1 (es) |
AU (3) | AU2016297558B2 (es) |
BR (1) | BR112018001017B1 (es) |
CA (2) | CA2993018A1 (es) |
CL (1) | CL2018000140A1 (es) |
CO (1) | CO2018001621A2 (es) |
CR (1) | CR20180109A (es) |
DO (1) | DOP2018000008A (es) |
EC (1) | ECSP18012103A (es) |
GT (1) | GT201800020A (es) |
IL (3) | IL305843B1 (es) |
MA (1) | MA42023B2 (es) |
MX (2) | MX2018000880A (es) |
MY (1) | MY186368A (es) |
PE (1) | PE20180573A1 (es) |
PH (1) | PH12018500140A1 (es) |
RU (1) | RU2748884C2 (es) |
SG (1) | SG10201912699RA (es) |
TN (1) | TN2018000020A1 (es) |
TW (1) | TWI734693B (es) |
WO (1) | WO2017015267A1 (es) |
ZA (1) | ZA201800082B (es) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9056852B2 (en) | 2011-03-28 | 2015-06-16 | Mei Pharma, Inc. | (Alpha-substituted aralkylamino and heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, pharmaceutical compositions thereof, and their use in treating proliferative diseases |
EP3630118A4 (en) | 2017-05-23 | 2021-03-31 | MEI Pharma, Inc. | POLYTHERAPY |
EP3661509A4 (en) | 2017-08-04 | 2021-01-13 | Skyhawk Therapeutics, Inc. | METHODS AND COMPOSITIONS FOR MODULATING THE SPLICE |
CN111212643A (zh) | 2017-08-14 | 2020-05-29 | 梅制药公司 | 联合疗法 |
JP2022521467A (ja) | 2019-02-05 | 2022-04-08 | スカイホーク・セラピューティクス・インコーポレーテッド | スプライシングを調節するための方法および組成物 |
EP3920928A4 (en) | 2019-02-06 | 2022-09-28 | Skyhawk Therapeutics, Inc. | METHODS AND COMPOSITIONS FOR MODULATION OF SPLICING |
EP3950063A4 (en) * | 2019-03-29 | 2022-11-30 | Kowa Company, Ltd. | NEW AZAINDOLE DERIVATIVE |
IL299989A (en) | 2020-07-20 | 2023-03-01 | Nido Biosciences Inc | Indole compounds as androgen receptor modulators |
TW202220988A (zh) * | 2020-09-21 | 2022-06-01 | 大陸商和記黃埔醫藥(上海)有限公司 | 雜芳環類化合物及其用途 |
WO2022140528A1 (en) | 2020-12-23 | 2022-06-30 | Genzyme Corporation | Deuterated colony stimulating factor-1 receptor (csf-1r) inhibitors |
EP4267573A1 (en) * | 2020-12-23 | 2023-11-01 | Genzyme Corporation | Deuterated colony stimulating factor-1 receptor (csf-1r) inhibitors |
WO2023249989A1 (en) | 2022-06-22 | 2023-12-28 | Genzyme Corporation | Solid forms of deuterated colony stimulating factor-1 receptor (csf-1r) inhibitors |
Family Cites Families (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4612323A (en) * | 1983-06-27 | 1986-09-16 | Sumitomo Chemical Company, Limited | Insecticidal and acaricidal derivatives of 1-benzylbenzimidazole |
JPS61151176A (ja) * | 1984-12-24 | 1986-07-09 | Sumitomo Chem Co Ltd | ベンズイミダゾール誘導体およびそれを有効成分とする殺虫、殺ダニ剤 |
US5187159A (en) * | 1991-10-07 | 1993-02-16 | Merck & Co., Inc. | Angiotensin II antagonists incorporating a substituted 1,3-benzodioxole or 1,3-benzodithiole |
AU4348593A (en) * | 1992-06-25 | 1994-01-24 | Zeneca Limited | Chromanderivatives as angiotensin ii antagonists |
FR2693197B1 (fr) * | 1992-07-03 | 1994-09-23 | Synthelabo | Nouveaux dérivés de quinoléine, leur procédé de préparation et leur application thérapeutique. |
ATE177101T1 (de) * | 1992-12-17 | 1999-03-15 | Pfizer | Pyrrolopyrimidine als crf antagonisten |
ZA939516B (en) | 1992-12-22 | 1994-06-06 | Smithkline Beecham Corp | Endothelin receptor antagonists |
JPH09202774A (ja) * | 1996-01-25 | 1997-08-05 | Green Cross Corp:The | 2−アリールキノリン類およびその製造方法 |
JPH101471A (ja) * | 1996-06-13 | 1998-01-06 | Green Cross Corp:The | N−[(キノリン−2−イル)フェニル]スルホンアミド類の結晶およびその製造方法 |
WO1998008514A1 (fr) * | 1996-08-30 | 1998-03-05 | Yoshitomi Pharmaceutical Industries, Ltd. | Compositions destinees au traitement preventif ou curatif de la degenerescence du tissu musculaire |
BR9810456A (pt) * | 1997-06-27 | 2001-09-25 | Fujisawa Pharmaceutical Co | Composto de sulfonamida, método para sua obtenção e seu uso farmacêutico |
US6143743A (en) | 1997-07-03 | 2000-11-07 | Dupont Pharmaceuticals Company | Imidazopyrimidines and imidazopyridines for the treatment of neurological disorders |
US6130333A (en) * | 1998-11-27 | 2000-10-10 | Monsanto Company | Bicyclic imidazolyl derivatives as phosphodiesterase inhibitors, pharmaceutical compositions and method of use |
EP1262475A4 (en) * | 2000-03-09 | 2005-01-05 | Ono Pharmaceutical Co | INDOIND DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE |
US7135495B2 (en) * | 2000-03-09 | 2006-11-14 | Ono Pharmaceutical Co., Ltd. | Indole derivatives |
PA8535601A1 (es) | 2000-12-21 | 2002-11-28 | Pfizer | Derivados benzimidazol y piridilimidazol como ligandos para gabaa |
US7030150B2 (en) * | 2001-05-11 | 2006-04-18 | Trimeris, Inc. | Benzimidazole compounds and antiviral uses thereof |
DE60318198T2 (de) | 2002-05-02 | 2008-12-04 | Merck & Co., Inc. | Tyrosinkinase-hemmer |
US20060235222A1 (en) * | 2003-01-22 | 2006-10-19 | Eli Lilly And Company | Indole-derivative modulators of steroid hormone nuclear receptors |
DE10342503A1 (de) * | 2003-09-12 | 2005-04-14 | Merck Patent Gmbh | Benzyl-Benzimidazolylderivate |
CN101906106A (zh) | 2003-09-18 | 2010-12-08 | 康福玛医药公司 | 作为hsp90-抑制剂的新的杂环化合物 |
US20060025383A1 (en) * | 2004-02-03 | 2006-02-02 | Neil Wishart | Aminobenzoxazoles as therapeutic agents |
WO2006009755A2 (en) | 2004-06-17 | 2006-01-26 | Plexxikon, Inc. | Azaindoles modulating c-kit activity and uses therefor |
US7361764B2 (en) * | 2004-07-27 | 2008-04-22 | Sgx Pharmaceuticals, Inc. | Pyrrolo-pyridine kinase modulators |
AU2005280739B2 (en) | 2004-09-03 | 2010-11-11 | Yuhan Corporation | Pyrrolo[3,2-c]pyridine derivatives and processes for the preparation thereof |
TWI278682B (en) | 2004-11-23 | 2007-04-11 | Ind Tech Res Inst | Fiber optic interferometric position sensor and measuring method thereof |
CN101193867A (zh) | 2004-12-01 | 2008-06-04 | Osi医药有限公司 | N取代的苯并咪唑基c-Kit抑制剂和苯并咪唑组合库 |
FR2883286B1 (fr) | 2005-03-16 | 2008-10-03 | Sanofi Aventis Sa | NOUVEAUX DERIVES D'IMIDAZO[1,5-a]PYRIDINES, INHIBITEURS DE FGFs, LEUR PROCEDE DE PREPARATION ET LES COMPOSITIONS PHARMACEUTIQUES LES CONTENANT |
EP1885723A2 (en) | 2005-05-17 | 2008-02-13 | Plexxikon, Inc. | Pyrrolo[2,3-b]pyridine derivatives as protein kinase inhibitors |
WO2007002433A1 (en) | 2005-06-22 | 2007-01-04 | Plexxikon, Inc. | Pyrrolo [2, 3-b] pyridine derivatives as protein kinase inhibitors |
EP2251341A1 (en) * | 2005-07-14 | 2010-11-17 | Astellas Pharma Inc. | Heterocyclic Janus kinase 3 inhibitors |
NL2000613C2 (nl) * | 2006-05-11 | 2007-11-20 | Pfizer Prod Inc | Triazoolpyrazinederivaten. |
PE20080403A1 (es) | 2006-07-14 | 2008-04-25 | Amgen Inc | Derivados heterociclicos fusionados y metodos de uso |
SI2081937T1 (sl) | 2006-10-23 | 2012-11-30 | Sgx Pharmaceuticals Inc | Triazolopiridazinski modulatorji proteinskih kinaz |
BRPI0717317A2 (pt) | 2006-10-23 | 2013-10-22 | Sgx Pharmaceuticals Inc | Modularoes da proteína cinase triazalopiridazina |
WO2008064219A1 (en) * | 2006-11-22 | 2008-05-29 | Johnson Controls Technology Company | Multichannel evaporator with flow mixing manifold |
WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
EP2094701A2 (en) | 2006-12-21 | 2009-09-02 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
WO2008130951A1 (en) * | 2007-04-17 | 2008-10-30 | Bristol-Myers Squibb Company | Fused heterocyclic 11-beta-hydroxysteroid dehydrogenase type i inhibitors |
EP2178563A2 (en) | 2007-07-06 | 2010-04-28 | OSI Pharmaceuticals, Inc. | Combination anti-cancer therapy comprising an inhibitor of both mtorc1 and mtorc2 |
US8119658B2 (en) | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
BRPI0820342A2 (pt) | 2007-11-07 | 2015-05-26 | Foldrx Pharmaceuticals Inc | Modulação de tráfego de proteína |
WO2009143018A2 (en) * | 2008-05-19 | 2009-11-26 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
BRPI1013545A2 (pt) | 2009-04-22 | 2019-09-24 | Janssen Phamaceutica N V | azetidinil diamidas como inibidores de monoacilglicerol lipase |
CA2798080C (en) * | 2010-05-17 | 2020-08-25 | Incozen Therapeutics Pvt. Ltd. | 3,5-disubstitued-3h-imidazo[4,5-b]pyridine and 3,5- disubstitued -3h-[1,2,3]triazolo[4,5-b] pyridine compounds as modulators of protein kinases |
WO2011156632A2 (en) * | 2010-06-09 | 2011-12-15 | Georgetown University | Compositions and methods of treatment for tumors in the nervous system |
RU2013127637A (ru) | 2010-11-24 | 2014-12-27 | Аллерган, Инк. | Индольные производные в качестве модуляторов рецепторов s1p |
WO2012107500A1 (en) | 2011-02-10 | 2012-08-16 | Novartis Ag | [1, 2, 4] triazolo [4, 3 -b] pyridazine compounds as inhibitors of the c-met tyrosine kinase |
US8748435B2 (en) | 2011-04-01 | 2014-06-10 | Novartis Ag | Pyrazolo pyrimidine derivatives |
EP2714688B1 (en) * | 2011-05-26 | 2016-02-24 | Daiichi Sankyo Company, Limited | Heterocyclic compounds as protein kinase inhibitors |
ES2624984T3 (es) | 2011-07-15 | 2017-07-18 | Viiv Healthcare Uk Limited | Derivados de ácido 2-(pirrolo[2,3-b]piridin-5-il)-2-(t-butoxi)-acético como inhibidores de la replicación del VIH para el tratamiento del SIDA |
CA2851155C (en) | 2011-10-14 | 2021-02-23 | Ambit Biosciences Corporation | Heterocyclic compounds and methods of use thereof |
EP2775841B1 (en) * | 2011-11-03 | 2017-09-13 | Merck Sharp & Dohme Corp. | QUINOLINE CARBOXAMIDE AND QUINOLINE CARBONITRILE DERIVATIVES AS mGluR2-NEGATIVE ALLOSTERIC MODULATORS, COMPOSITIONS, AND THEIR USE |
WO2013116182A1 (en) * | 2012-01-31 | 2013-08-08 | Boehringer Ingelheim International Gmbh | Heterocyclic compounds as inhibitors of leukotriene production |
US9358235B2 (en) * | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
EA026412B1 (ru) | 2012-03-30 | 2017-04-28 | Ризен Фармасьютикалз Са | НОВЫЕ СОЕДИНЕНИЯ 3,5-ДИЗАМЕЩЕННОГО-3H-ИМИДАЗО[4,5-b]ПИРИДИНА И 3,5-ДИЗАМЕЩЕННОГО-3H-[1,2,3]ТРИАЗОЛО[4,5-b]ПИРИДИНА КАК МОДУЛЯТОРЫ c-MET ПРОТЕИНКИНАЗ |
WO2014081820A1 (en) * | 2012-11-20 | 2014-05-30 | Discoverybiomed, Inc. | Small molecule cftr correctors |
US9067914B1 (en) * | 2013-12-10 | 2015-06-30 | Genzyme Corporation | Tropomyosin-related kinase (TRK) inhibitors |
CN105980387B (zh) | 2013-12-30 | 2019-04-19 | 阵列生物制药公司 | 丝氨酸/苏氨酸激酶抑制剂 |
CR20160512A (es) * | 2014-05-01 | 2016-12-21 | Novartis Ag | Compuestos y composiciones como agonistas del receptor tipo toll 7 |
-
2016
- 2016-07-19 MX MX2018000880A patent/MX2018000880A/es unknown
- 2016-07-19 CR CR20180109A patent/CR20180109A/es unknown
- 2016-07-19 BR BR112018001017-0A patent/BR112018001017B1/pt active IP Right Grant
- 2016-07-19 US US15/745,223 patent/US11274108B2/en active Active
- 2016-07-19 RU RU2018106060A patent/RU2748884C2/ru active
- 2016-07-19 KR KR1020187004799A patent/KR102665765B1/ko active IP Right Grant
- 2016-07-19 MA MA42023A patent/MA42023B2/fr unknown
- 2016-07-19 MY MYPI2017705168A patent/MY186368A/en unknown
- 2016-07-19 EP EP16744651.7A patent/EP3325471A1/en active Pending
- 2016-07-19 CA CA2993018A patent/CA2993018A1/en active Pending
- 2016-07-19 WO PCT/US2016/042917 patent/WO2017015267A1/en active Application Filing
- 2016-07-19 CN CN201680042348.4A patent/CN107922396B/zh active Active
- 2016-07-19 JP JP2018502627A patent/JP6898914B2/ja active Active
- 2016-07-19 AR ARP160102184A patent/AR105392A1/es unknown
- 2016-07-19 IL IL305843A patent/IL305843B1/en unknown
- 2016-07-19 AU AU2016297558A patent/AU2016297558B2/en active Active
- 2016-07-19 CA CA3217238A patent/CA3217238A1/en active Pending
- 2016-07-19 TN TNP/2018/000020A patent/TN2018000020A1/en unknown
- 2016-07-19 IL IL276292A patent/IL276292B2/en unknown
- 2016-07-19 SG SG10201912699RA patent/SG10201912699RA/en unknown
- 2016-07-19 PE PE2018000091A patent/PE20180573A1/es unknown
- 2016-07-20 TW TW105122945A patent/TWI734693B/zh active
-
2018
- 2018-01-05 ZA ZA2018/00082A patent/ZA201800082B/en unknown
- 2018-01-09 DO DO2018000008A patent/DOP2018000008A/es unknown
- 2018-01-15 GT GT201800020A patent/GT201800020A/es unknown
- 2018-01-17 IL IL256964A patent/IL256964B/en unknown
- 2018-01-17 PH PH12018500140A patent/PH12018500140A1/en unknown
- 2018-01-17 CL CL2018000140A patent/CL2018000140A1/es unknown
- 2018-01-19 MX MX2021015102A patent/MX2021015102A/es unknown
- 2018-02-19 EC ECIEPI201812103A patent/ECSP18012103A/es unknown
- 2018-02-20 CO CONC2018/0001621A patent/CO2018001621A2/es unknown
-
2021
- 2021-04-13 JP JP2021067423A patent/JP7401482B2/ja active Active
- 2021-06-18 AU AU2021204116A patent/AU2021204116B2/en active Active
-
2022
- 2022-02-09 US US17/668,209 patent/US20220396588A1/en not_active Abandoned
-
2023
- 2023-02-21 AU AU2023201013A patent/AU2023201013A1/en active Pending
- 2023-12-05 JP JP2023205068A patent/JP2024028845A/ja active Pending
-
2024
- 2024-01-04 US US18/404,409 patent/US20240217991A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DOP2018000008A (es) | Inhibidores del receptor del factor estimulador de colonias 1 (csf-1r) | |
MX2018006148A (es) | Inhibidores de cxcr2. | |
PH12017501042A1 (en) | Anti-cd38 antibodies for treatment of acute myeloid leukemia | |
MX2020001278A (es) | Sintesis de compuestos de carbamoilpiridona policiclica. | |
PH12016501192A1 (en) | Tetrahydropyridopyrazines modulators of gpr6 | |
BR112017012272A2 (pt) | derivados de 2-anilinopirimidina como moduladores de egfr | |
MX2016014765A (es) | Incremento del rendimiento utilizando soforolipidos. | |
ECSP16074207A (es) | Pirazinas moduladoras de gpr6 | |
MX2019008375A (es) | Tiobenzoimidazol como fungicidas. | |
MX2019002017A (es) | Derivados de sofosbuvir para el tratamiento de la hepatitis c. | |
EA201692246A1 (ru) | Способ получения 2,6-диметилбензохинона | |
MX2016010268A (es) | Pirimidinimidazolaminas como modulares de actividad de cinasa. | |
GB2564185A (en) | Process for the preparation of derivatives of benzodioxole | |
IN2014MU00069A (es) | ||
UA104379U (uk) | Біс(оксифеніленімінометилен)дифеноли з перфторованими моно- та біфеніленовими центральними фрагментами як прекурсори для синтезу бензоксазинів |