MA39688B1 - Composés hétéroaryle pour le traitement de maladies ophtalmiques - Google Patents

Composés hétéroaryle pour le traitement de maladies ophtalmiques

Info

Publication number
MA39688B1
MA39688B1 MA39688A MA39688A MA39688B1 MA 39688 B1 MA39688 B1 MA 39688B1 MA 39688 A MA39688 A MA 39688A MA 39688 A MA39688 A MA 39688A MA 39688 B1 MA39688 B1 MA 39688B1
Authority
MA
Morocco
Prior art keywords
rbp4
treatment
img
ophthalmic diseases
heteroaryl compounds
Prior art date
Application number
MA39688A
Other languages
English (en)
Other versions
MA39688A (fr
Inventor
Shigekazu Sasaki
Yoshihiro Banno
Masahiro Kamaura
Kazuaki Takami
Koichiro Fukuda
Original Assignee
Takeda Pharmaceuticals Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Takeda Pharmaceuticals Co filed Critical Takeda Pharmaceuticals Co
Publication of MA39688A publication Critical patent/MA39688A/fr
Publication of MA39688B1 publication Critical patent/MA39688B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C07D231/20—One oxygen atom attached in position 3 or 5
    • C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/46—Sulfur atoms
    • 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
    • A61K31/415—1,2-Diazoles
    • 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
    • A61K31/42—Oxazoles
    • A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
    • 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
    • A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/65—One oxygen atom attached in position 3 or 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/70—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/34—One oxygen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/36—One oxygen atom
    • C07D263/38—One oxygen atom attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Genetics & Genomics (AREA)
  • Ophthalmology & Optometry (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Wood Science & Technology (AREA)
  • Molecular Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Plant Pathology (AREA)
  • Physics & Mathematics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Microbiology (AREA)
  • Toxicology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

L'invention porte sur un composé hétérocyclique ayant une action abaissant la rbp4 supérieure et utile comme médicament pour la prophylaxie ou le traitement d'une maladie ou d'un symptôme médié par une augmentation de rbp4 ou de rétinol fourni par rbp4. Composé représenté par la formule (i): <img file="imga0001.Tif" frnum="0001" he="46" id="ia01" img-content="chem" img-format="tif" inline="no" orientation="portrait" pgnum="0001" wi="113"/> dans laquelle chaque symbole est tel que défini dans la description, ou un sel de celui-ci a une action abaissant la rbp4 supérieure, et est utile comme médicament pour la prophylaxie ou le traitement d'une maladie ou d'un symptôme à médiation par une augmentation de rbp4 ou de rétinol fourni par rbp4.
MA39688A 2014-10-24 2015-10-22 Composés hétéroaryle pour le traitement de maladies ophtalmiques MA39688B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2014217770 2014-10-24
PCT/JP2015/079782 WO2016063933A1 (fr) 2014-10-24 2015-10-22 Composé hétérocyclique

Publications (2)

Publication Number Publication Date
MA39688A MA39688A (fr) 2017-08-30
MA39688B1 true MA39688B1 (fr) 2021-02-26

Family

ID=55760964

Family Applications (2)

Application Number Title Priority Date Filing Date
MA39688A MA39688B1 (fr) 2014-10-24 2015-10-22 Composés hétéroaryle pour le traitement de maladies ophtalmiques
MA053568A MA53568A (fr) 2014-10-24 2015-10-22 Médicaments pour le traitement de maladies ophtalmiques

Family Applications After (1)

Application Number Title Priority Date Filing Date
MA053568A MA53568A (fr) 2014-10-24 2015-10-22 Médicaments pour le traitement de maladies ophtalmiques

Country Status (38)

Country Link
US (4) US10214498B2 (fr)
EP (2) EP3848353A1 (fr)
JP (2) JP6588027B2 (fr)
KR (1) KR102490156B1 (fr)
CN (2) CN107108506B (fr)
AR (1) AR104342A1 (fr)
AU (2) AU2015336480B2 (fr)
BR (1) BR112017007138A2 (fr)
CA (1) CA2965465C (fr)
CL (1) CL2017000944A1 (fr)
CO (1) CO2017003699A2 (fr)
CR (1) CR20170160A (fr)
CY (1) CY1123842T1 (fr)
DK (1) DK3210973T3 (fr)
DO (1) DOP2017000098A (fr)
EA (1) EA033446B1 (fr)
EC (1) ECSP17026687A (fr)
ES (1) ES2848999T3 (fr)
HR (1) HRP20210320T1 (fr)
HU (1) HUE053443T2 (fr)
IL (2) IL285105B2 (fr)
LT (1) LT3210973T (fr)
MA (2) MA39688B1 (fr)
MX (2) MX2017004629A (fr)
MY (1) MY183209A (fr)
PE (1) PE20170669A1 (fr)
PH (1) PH12017500747B1 (fr)
PL (1) PL3210973T3 (fr)
PT (1) PT3210973T (fr)
RS (1) RS61504B1 (fr)
SG (1) SG11201702312UA (fr)
SI (1) SI3210973T1 (fr)
SM (1) SMT202100082T1 (fr)
TN (1) TN2017000097A1 (fr)
TW (2) TWI703131B (fr)
UA (1) UA121871C2 (fr)
WO (1) WO2016063933A1 (fr)
ZA (1) ZA201703344B (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6588027B2 (ja) 2014-10-24 2019-10-09 武田薬品工業株式会社 複素環化合物
AU2018240031B2 (en) 2017-03-20 2022-07-14 President And Fellows Of Harvard College Compounds and methods for the treatment of parasitic diseases
TWI848911B (zh) 2017-06-15 2024-07-21 美國哥倫比亞大學紐約市信託會 以三唑并吡啶治療rbp4相關疾病之方法
US11389444B2 (en) * 2017-06-15 2022-07-19 Belite Bio, Inc Methods of treating metabolic diseases with fused bicyclic pyrazoles
US12440486B2 (en) 2018-08-01 2025-10-14 The Trustees Of Columbia University In The City Of New York RBP4 antagonists for treatment and prevention of non-alcoholic fatty liver disease and gout
CN111690698A (zh) * 2020-05-19 2020-09-22 浙江工业大学 两步串联流动合成3-(苯并[d][1,3]二氧-5-氨基)丙羟肟酸的方法
CN111690695A (zh) * 2020-05-19 2020-09-22 浙江工业大学 3-苯氨基丙羟肟酸的酶促微流控在线合成方法
CN117440774A (zh) * 2021-05-21 2024-01-23 倍亮生物有限责任公司 年龄相关黄斑变性的生物标记
WO2022256301A1 (fr) * 2021-06-01 2022-12-08 Stargazer Pharmaceuticals, Inc. Méthodes et composés pour traiter des sujets atteints d'une maladie de stargardt
CN116286900B (zh) * 2022-10-28 2024-04-26 昆明理工大学 一种乙酸渗透酶A基因RkAcpa及其应用
CN116019791B (zh) * 2022-12-28 2025-12-16 浙江工业大学台州研究院 二苯醚类化合物在制备β-葡萄糖醛酸苷酶抑制剂中应用

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3625970A (en) 1968-04-17 1971-12-07 Cutter Lab 1-(disubstituted phenyl or benzyl)-1h-indazol-3-yloxyacetic acid
US5239080A (en) 1989-02-08 1993-08-24 Takeda Chemical Industries, Ltd. Oxazole compounds and their use as antidiabetic and bone-reduction inhibitory agents
EP0440183A1 (fr) * 1990-02-01 1991-08-07 Takeda Chemical Industries, Ltd. Composés à base d'oxazol, procédé pour leur préparation et leur utilisation
US6057338A (en) 1997-04-04 2000-05-02 Merck & Co., Inc. Somatostatin agonists
US6025372A (en) 1997-04-04 2000-02-15 Merck & Co., Inc. Somatostatin agonists
AU1285499A (en) 1997-10-30 1999-05-24 Merck & Co., Inc. Somatostatin agonists
AR035016A1 (es) 1999-08-25 2004-04-14 Takeda Chemical Industries Ltd Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima.
AU7556800A (en) 1999-10-07 2001-05-10 Tadeka Chemical Industries, Ltd. Amine derivatives
CA2390923A1 (fr) 1999-11-10 2001-05-31 Takeda Chemical Industries, Ltd. Composes heterocycliques n a 5 elements a activite hypoglycemique et hypolipidemique
GB0020351D0 (en) 2000-08-17 2000-10-04 Catalyst Biomedica Ltd Treatment of hyperproliferative diseases
DE10149568A1 (de) 2001-10-08 2003-04-24 Consequence Gmbh Verfahren zur Sequenzanalyse von Polypeptiden
WO2003042204A1 (fr) 2001-10-19 2003-05-22 Takeda Chemical Industries, Ltd. Derive d'amine
US20040214788A1 (en) 2003-03-11 2004-10-28 Raj Madhwa H.G. Treatment of prostate cancer
TW200505902A (en) 2003-03-20 2005-02-16 Schering Corp Cannabinoid receptor ligands
EP1658273B1 (fr) 2003-08-20 2007-01-03 Eli Lilly And Company Composes, procedes et preparations destines a l'apport oral d'un compose peptidique de type glucagon (glp-1) ou d'un peptide agoniste du recepteur 4 de melanocortine (mc4)
EP1692521A1 (fr) 2003-12-11 2006-08-23 Beth Israel Deaconess Medical Center, Inc. Utilisation de la proteine rbp 4 dans le traitement de la sensibilite/resistance insulinique, du diabete , et de l'obesite
US7838561B2 (en) 2004-06-14 2010-11-23 Wisconsin Alumni Research Foundation Method for preventing or treating cardiac hypertrophy
KR100862930B1 (ko) 2004-06-23 2008-10-13 시리온 테라퓨틱스, 인크. 레티닐 유도체를 사용하여 안 증상을 치료하기 위한 방법및 조성물
US20080033053A1 (en) 2004-07-22 2008-02-07 Wolfgang Curt D Cross-Reference To Related Applications
WO2006042252A2 (fr) 2004-10-08 2006-04-20 Potentia Pharmeceuticals, Inc. Proteines regulatrices du complement viral pour troubles de la vue
AU2007260872A1 (en) 2006-06-22 2007-12-27 Sirion Therapeutics, Inc Methods and compositions for treating ophthalmic conditions via modulation of megalin activity
CA2691003A1 (fr) 2007-06-26 2008-12-31 Lexicon Pharmaceuticals, Inc. Procedes de traitement de maladies et de troubles vehicules par la serotonine
US8093291B2 (en) 2007-06-26 2012-01-10 Lexicon Pharmaceuticals, Inc. Methods of using and compositions comprising tryptophan hydroxylase inhibitors
KR20100097098A (ko) * 2007-09-27 2010-09-02 리비젼 쎄러퓨틱스, 인크. 레티놀 관련 질환을 치료하기 위한 방법 및 화합물
US7973079B2 (en) 2007-09-27 2011-07-05 Revision Therapeutics, Inc. Methods and compounds for treating retinol-related diseases
EP2202223B1 (fr) 2007-10-18 2017-01-25 Takeda Pharmaceutical Company Limited Composé hétérocyclique en tant qu'agent diminuant les rpb4 sanguines
US8541388B2 (en) 2008-05-22 2013-09-24 Isis Pharmaceuticals, Inc. Methods for modulating expression of RBP4
BRPI0913291A2 (pt) 2008-05-30 2019-01-15 Takeda Pharmaceuticals Co composto, pró-droga, medicamento, métodos para diminuir a proteína 4 ou tratamento de diabete em um mamífero, e, uso do composto
CA2758587A1 (fr) 2009-04-13 2010-10-21 Irm Llc Compositions et procedes pour moduler la liaison du retinol a la proteine 4 de liaison au retinol (rbp4)
JP5706337B2 (ja) * 2009-04-16 2015-04-22 武田薬品工業株式会社 (とりわけ)糖尿病の予防または治療に有用なn−アシル−n’−フェニルピペラジンの誘導体
US20130012591A1 (en) 2009-10-28 2013-01-10 Revision Therapeutics, Inc. Prophylaxis of skin cancer with retinamides
JP5848712B2 (ja) 2009-12-11 2016-01-27 ノノ インコーポレイテッド 虚血性疾患および他の疾患を治療するための薬剤および方法
SG10201502484SA (en) 2010-03-30 2015-05-28 Verseon Corp Multisubstituted aromatic compounds as inhibitors of thrombin
WO2012071369A2 (fr) 2010-11-24 2012-05-31 The Trustees Of Columbia University In The City Of New York Antagoniste rbp4 non rétinoïde pour le traitement de la dégénérescence maculaire liée à l'âge et de la maladie de stargardt
TR201906779T4 (tr) 2011-05-12 2019-05-21 Proteostasis Therapeutics Inc Proteostaz regülatörleri.
GB201205679D0 (en) 2012-03-30 2012-05-16 Dyson Technology Ltd A hand held appliance
WO2013166041A1 (fr) 2012-05-01 2013-11-07 The Trustees Of Columbia University In The City Of New York Ligands de la transthyrétine pouvant inhiber l'interaction de rbp4-ttr dépendante du rétinol pour le traitement de la dégénérescence maculaire liée à l'âge, de la maladie de stargardt et d'autres maladies de la rétine caractérisées par une accumulation excessive de lipofuscine
US9580400B2 (en) 2013-02-26 2017-02-28 Northeastern University Cannabinergic nitrate esters and related analogs
WO2014160409A1 (fr) 2013-03-14 2014-10-02 The Trustees Of Columbia University In The City Of New York Antagonistes de rbp4 pour le traitement de la dégénérescence maculaire liée à l'âge et de la maladie de stargardt
WO2014153643A1 (fr) 2013-03-26 2014-10-02 The University Of British Columbia Compositions et procédés d'utilisation associés dans le traitement de l'aniridie
JP2017508798A (ja) 2014-03-07 2017-03-30 ザ ジョンズ ホプキンス ユニバーシティ ヒストンリジン特異的デメチラーゼ(lsd1)およびヒストンデアセチラーゼ(hdac)の阻害剤
JP6588027B2 (ja) * 2014-10-24 2019-10-09 武田薬品工業株式会社 複素環化合物
TWI676618B (zh) 2014-10-24 2019-11-11 美商必治妥美雅史谷比公司 三環化合物
MX393057B (es) 2014-10-24 2025-03-24 Bristol Myers Squibb Co Compuestos de indol carboxamida útiles como inhibidores de cinasas.
WO2016172631A2 (fr) 2015-04-24 2016-10-27 President And Fellows Of Harvard College Inhibiteurs sélectifs de substrats d'enzyme dégradant l'insuline (ide) et utilisations associées
US10189797B2 (en) 2015-12-30 2019-01-29 Duke University Chemical modulators of immune checkpoints and therapeutic use

Also Published As

Publication number Publication date
KR20170067791A (ko) 2017-06-16
MA39688A (fr) 2017-08-30
SMT202100082T1 (it) 2021-03-15
SG11201702312UA (en) 2017-05-30
ES2848999T3 (es) 2021-08-13
TN2017000097A1 (en) 2018-07-04
MA53568A (fr) 2022-02-23
CR20170160A (es) 2017-06-15
US20210340114A1 (en) 2021-11-04
CO2017003699A2 (es) 2017-07-28
US10214498B2 (en) 2019-02-26
DOP2017000098A (es) 2017-07-15
IL285105A (en) 2021-08-31
RS61504B1 (sr) 2021-03-31
AU2020204426A1 (en) 2020-07-23
EP3210973B1 (fr) 2020-12-02
TWI749661B (zh) 2021-12-11
IL285105B (en) 2022-11-01
US20200157062A1 (en) 2020-05-21
CL2017000944A1 (es) 2018-01-12
JP6995094B2 (ja) 2022-02-21
US20180237404A1 (en) 2018-08-23
IL251695B (en) 2021-08-31
AU2015336480A2 (en) 2017-06-01
BR112017007138A2 (pt) 2017-12-26
PH12017500747A1 (en) 2017-10-30
PL3210973T3 (pl) 2021-06-28
CN107108506B (zh) 2022-06-21
US10544111B2 (en) 2020-01-28
PH12017500747B1 (en) 2017-10-30
IL285105B2 (en) 2023-03-01
CN107108506A (zh) 2017-08-29
US10975043B2 (en) 2021-04-13
MY183209A (en) 2021-02-18
EP3210973A1 (fr) 2017-08-30
JPWO2016063933A1 (ja) 2017-08-03
UA121871C2 (uk) 2020-08-10
JP2020007347A (ja) 2020-01-16
CY1123842T1 (el) 2022-05-27
MX2021001188A (es) 2021-04-19
EP3210973A4 (fr) 2018-04-25
WO2016063933A1 (fr) 2016-04-28
TW202042805A (zh) 2020-12-01
AR104342A1 (es) 2017-07-12
ECSP17026687A (es) 2017-09-29
PT3210973T (pt) 2021-02-12
IL251695A0 (en) 2017-06-29
TW201714876A (zh) 2017-05-01
EA201790912A1 (ru) 2017-09-29
ZA201703344B (en) 2018-08-29
AU2015336480A1 (en) 2017-05-25
EP3848353A1 (fr) 2021-07-14
AU2020204426B2 (en) 2022-02-03
CA2965465C (fr) 2023-08-01
EA033446B1 (ru) 2019-10-31
SI3210973T1 (sl) 2021-04-30
US20190119225A1 (en) 2019-04-25
PE20170669A1 (es) 2017-06-06
AU2015336480B2 (en) 2020-04-02
KR102490156B1 (ko) 2023-01-18
TWI703131B (zh) 2020-09-01
JP6588027B2 (ja) 2019-10-09
DK3210973T3 (da) 2021-02-08
MX2017004629A (es) 2017-06-30
HUE053443T2 (hu) 2021-06-28
HRP20210320T1 (hr) 2021-04-30
LT3210973T (lt) 2021-03-25
CA2965465A1 (fr) 2016-04-28
CN115197160A (zh) 2022-10-18

Similar Documents

Publication Publication Date Title
MA39688A (fr) Composés hétéroaryle pour le traitement de maladies ophtalmiques
MA45940B1 (fr) Composé hétérocyclique
MA39246A1 (fr) Composé hétérocyclique fusionné
MA47368B1 (fr) N-[4-fluoro-5-[[(2s,4s)-2-méthyl-4-[(5-méthyl-1,2,4-oxadiazol-3-yl)méthoxy]-1-pipéridyl]méthyl]thiazol-2-yl]acétamide utilisés en tant qu&#39;inhibiteur d&#39;oga
MA35623B1 (fr) Composés de 1-arylcarbonyl-4-oxypipéridine utiles pour le traitement de maladies neurodégénératives
EA201892207A1 (ru) Индолкарбоксамидные соединения
MA46337A (fr) Composé de pyridine
MA39247A1 (fr) 2-(4-guanidinophenyl)-2-oxo-ethyle substitues inhibiteurs d&#39;enteropeptidase utiles pour le traitement ou la prevention, par ex. L&#39;obesite, le diabete sucre, les troubles de l&#39;alimentation, l&#39;hyperlipidemie, l&#39;hypertension, l&#39;insuffisance cardiaque
MA42795A (fr) Composés thérapeutiques utiles pour le traitement prophylactique ou thérapeutique d&#39;une infection par le virus du vih
MA52948B1 (fr) Composés
MA52063B1 (fr) Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu&#39;inhibiteurs de la kallicréine plasmatique
MA56553B1 (fr) Tétrahydropyranyl-amino-pyrrolopyrimidinone pour une utilisation dans un procédé de traitement d&#39;un trouble médié par btk
EA201790271A1 (ru) Ингибиторы гликозидазы
EP4276095A3 (fr) Procédés de préparation d&#39;inhibiteurs ask1
JOP20200230B1 (ar) ناهضات ppar (مستقبل ناشر بيروكسيزوم منشط)، ومركبات، ومكونات أدوية، وطرق استعمالها
MA39898B1 (fr) Composés 4-amino-imidazoquinoline
MA38323B1 (fr) Dérivés pyrimidone et leur utilisation dans le traitement, l&#39;amélioration ou la prévention d&#39;une maladie virale
MA38078A1 (fr) Dérivé de pyridine
EA201692433A1 (ru) Соединения ppar для применения при лечении фиброзных заболеваний
MX2019010085A (es) Inhibidores de la glicosidasa de sulfoximina.
TN2017000158A1 (en) Carbazole derivatives
MA41431A (fr) Prévention ou traitement de maladie de goutte ou d&#39;acide urique
PE20180204A1 (es) Procedimiento para la preparacion de 2-4-[2-([2-(4-(clorofenil)-1,3-tiazol-4-il]metilsulfanil)-3,5-diciano-6-(pirrolidin-1-il)piridina-4-il]fenoxietil-l-alanil-l-alaninato-monohidrocloruro
MA41975B1 (fr) Derives d&#39;aminohydrothiazine fusionnee contenant du tetrahydrofurane utiles dans le traitement de la maladie d&#39;alzheimer
EP3463372A4 (fr) Composés bicycliques fusionnés pour le traitement d&#39;une maladie