TN2010000137A1 - Spiropyrrolidines and their use against hcv and hiv infection - Google Patents
Spiropyrrolidines and their use against hcv and hiv infectionInfo
- Publication number
- TN2010000137A1 TN2010000137A1 TNP2010000137A TN2010000137A TN2010000137A1 TN 2010000137 A1 TN2010000137 A1 TN 2010000137A1 TN P2010000137 A TNP2010000137 A TN P2010000137A TN 2010000137 A TN2010000137 A TN 2010000137A TN 2010000137 A1 TN2010000137 A1 TN 2010000137A1
- Authority
- TN
- Tunisia
- Prior art keywords
- spiropyrrolidines
- hiv infection
- use against
- against hcv
- hcv
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1016—Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
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)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Virology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Biophysics (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97897407P | 2007-10-10 | 2007-10-10 | |
PCT/EP2008/063460 WO2009047264A1 (fr) | 2007-10-10 | 2008-10-08 | Composés organiques et leurs utilisations |
Publications (1)
Publication Number | Publication Date |
---|---|
TN2010000137A1 true TN2010000137A1 (en) | 2011-09-26 |
Family
ID=40243948
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TNP2010000137A TN2010000137A1 (en) | 2007-10-10 | 2010-03-26 | Spiropyrrolidines and their use against hcv and hiv infection |
Country Status (20)
Country | Link |
---|---|
US (2) | US8008263B2 (fr) |
EP (1) | EP2205584A1 (fr) |
JP (1) | JP5095824B2 (fr) |
KR (2) | KR101396696B1 (fr) |
CN (2) | CN104016970A (fr) |
AR (1) | AR068756A1 (fr) |
AU (1) | AU2008309589B2 (fr) |
BR (1) | BRPI0817881A2 (fr) |
CA (1) | CA2702132A1 (fr) |
CL (1) | CL2008002995A1 (fr) |
CO (1) | CO6270317A2 (fr) |
CR (1) | CR11310A (fr) |
EA (1) | EA020951B1 (fr) |
MA (1) | MA31767B1 (fr) |
MX (1) | MX2010003916A (fr) |
PE (1) | PE20091237A1 (fr) |
TN (1) | TN2010000137A1 (fr) |
TW (1) | TW200932737A (fr) |
WO (1) | WO2009047264A1 (fr) |
ZA (1) | ZA201001585B (fr) |
Families Citing this family (40)
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NZ571826A (en) * | 2006-04-11 | 2012-01-12 | Novartis Ag | HCV/HIV inhibitors and their uses |
US8293705B2 (en) | 2007-12-21 | 2012-10-23 | Avila Therapeutics, Inc. | HCV protease inhibitors and uses thereof |
US8309685B2 (en) | 2007-12-21 | 2012-11-13 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
NZ586232A (en) | 2007-12-21 | 2012-12-21 | Avila Therapeutics Inc | HCV protease inhibitors comprising a functionalised proline derivative |
AU2008340257B2 (en) | 2007-12-21 | 2015-06-11 | Celgene Avilomics Research, Inc. | HCV protease inhibitors and uses thereof |
JP2012505897A (ja) * | 2008-10-15 | 2012-03-08 | インターミューン・インコーポレーテッド | 治療用抗ウイルス性ペプチド |
US8512690B2 (en) | 2009-04-10 | 2013-08-20 | Novartis Ag | Derivatised proline containing peptide compounds as protease inhibitors |
US20110182850A1 (en) * | 2009-04-10 | 2011-07-28 | Trixi Brandl | Organic compounds and their uses |
KR20130026410A (en) * | 2009-09-28 | 2013-03-13 | Intermune Inc | Cyclic peptide inhibitors of hepatitis c virus replication |
TW201116540A (en) * | 2009-10-01 | 2011-05-16 | Intermune Inc | Therapeutic antiviral peptides |
KR20130120481A (ko) * | 2010-10-08 | 2013-11-04 | 노파르티스 아게 | 술파미드 ns3 억제제의 비타민 e 제제 |
US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2013030750A1 (fr) | 2011-09-01 | 2013-03-07 | Lupin Limited | Composés antiviraux |
CA2862755A1 (fr) | 2012-02-10 | 2013-08-15 | Lupin Limited | Composes antiviraux avec une fraction dibenzooxaheterocycle |
CN103420991B (zh) * | 2012-05-17 | 2017-07-07 | 乳源东阳光药业有限公司 | 作为丙型肝炎抑制剂的吡咯烷衍生物及其在药物中的应用 |
TW201408669A (zh) * | 2012-08-08 | 2014-03-01 | Merck Sharp & Dohme | Hcv ns3蛋白酶抑制劑 |
TW201412709A (zh) | 2012-09-28 | 2014-04-01 | Sunshine Lake Pharma Co Ltd | 作為丙型肝炎抑制劑的螺環化合物及其在藥物中的應用 |
EA025560B1 (ru) | 2012-10-19 | 2017-01-30 | Бристол-Майерс Сквибб Компани | Ингибиторы вируса гепатита с |
EP2914613B1 (fr) | 2012-11-02 | 2017-11-22 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
US9334279B2 (en) | 2012-11-02 | 2016-05-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2014070974A1 (fr) | 2012-11-05 | 2014-05-08 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
CN103848818B (zh) | 2012-11-29 | 2017-03-15 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的并环化合物、药物组合物及它们在药物中的应用 |
CN103848819B (zh) * | 2012-11-29 | 2017-04-12 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的螺环化合物、药物组合物及它们在药物中的应用 |
CN103848821B (zh) | 2012-11-29 | 2016-10-12 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的螺环化合物、药物组合物及它们的用途 |
EP2964664B1 (fr) | 2013-03-07 | 2017-01-11 | Bristol-Myers Squibb Company | Inhibiteurs du virus de l'hépatite c |
JP6431038B2 (ja) | 2013-03-15 | 2018-11-28 | ザイムワークス インコーポレイティド | 細胞毒性及び抗有糸分裂性化合物とその使用方法 |
US11560422B2 (en) | 2013-12-27 | 2023-01-24 | Zymeworks Inc. | Sulfonamide-containing linkage systems for drug conjugates |
CA2935064C (fr) | 2013-12-27 | 2023-06-27 | Zymeworks Inc. | Conjugues var2csa-medicament |
CN104803989B (zh) | 2014-01-23 | 2017-12-22 | 广东东阳光药业有限公司 | 作为丙型肝炎抑制剂的桥环化合物及其在药物中的应用 |
PT3194421T (pt) | 2014-09-17 | 2022-02-07 | Zymeworks Inc | Compostos citotóxicos e antimitóticos e métodos de uso dos mesmos |
US11234977B2 (en) | 2017-12-20 | 2022-02-01 | Novartis Ag | Fused tricyclic pyrazolo-dihydropyrazinyl-pyridone compounds as antivirals |
MX2023005983A (es) | 2020-11-23 | 2023-08-15 | Enanta Pharm Inc | Nuevos agentes antivirales derivados de la espiropirrolidina. |
US20240051950A1 (en) * | 2020-12-22 | 2024-02-15 | The Regents Of The University Of California | Novel CYP3A4-Specific Inhibitors and Methods of Using Same |
US11970502B2 (en) | 2021-05-04 | 2024-04-30 | Enanta Pharmaceuticals, Inc. | Macrocyclic antiviral agents |
WO2023003610A1 (fr) * | 2021-07-23 | 2023-01-26 | Enanta Pharmaceuticals, Inc. | Nouveaux agents antiviraux dérivés de spiropyrrolidine |
WO2023086352A1 (fr) | 2021-11-12 | 2023-05-19 | Enanta Pharmaceuticals, Inc. | Nouveaux agents antiviraux dérivés de spiropyrrolidine |
WO2023086350A1 (fr) | 2021-11-12 | 2023-05-19 | Enanta Pharmaceuticals, Inc. | Agents antiviraux contenant des alcynes |
US11919910B2 (en) | 2021-11-12 | 2024-03-05 | Enanta Pharmaceuticals, Inc. | Spiropyrrolidine derived antiviral agents |
US11993600B2 (en) | 2021-12-08 | 2024-05-28 | Enanta Pharmaceuticals, Inc. | Saturated spirocyclics as antiviral agents |
Family Cites Families (41)
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US7244721B2 (en) * | 2000-07-21 | 2007-07-17 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
BR0112540A (pt) * | 2000-07-21 | 2003-06-24 | Schering Corp | Peptìdios como inibidores da ns-3-serina protease do vìrus da hepatite c |
SV2003000617A (es) * | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
PE20030857A1 (es) | 2002-01-23 | 2003-10-25 | Schering Corp | Compuestos como inhibidores de la proteasa serina ns3 del virus de la hepatitis c |
US7309717B2 (en) * | 2003-06-17 | 2007-12-18 | Schering Corporation | Process and intermediates for the preparation of (1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3,1,0]hexane-2-carboxylates or salts thereof |
EP1664090A2 (fr) * | 2003-08-26 | 2006-06-07 | Schering Corporation | Nouveaux inhibiteurs peptidomimetiques de la serine protease ns3 du virus de l'hepatite c |
TWI359147B (en) * | 2003-09-05 | 2012-03-01 | Vertex Pharma | Inhibitors of serine proteases, particularly hcv n |
US20050119189A1 (en) * | 2003-09-18 | 2005-06-02 | Cottrell Kevin M. | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
PT1677827E (pt) * | 2003-10-27 | 2009-03-13 | Vertex Pharma | Associações para o tratamento do vhc |
RU2006124594A (ru) * | 2003-12-11 | 2008-01-27 | Шеринг Корпорейшн (US) | Ингибиторы сериновой протеазы ns3/ns4а вируса гепатита с |
AU2005212257A1 (en) * | 2004-02-04 | 2005-08-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases, particularly HCV NS3-NS4A protease |
US7635694B2 (en) * | 2004-02-27 | 2009-12-22 | Schering Corporation | Cyclobutenedione-containing compounds as inhibitors of hepatitis C virus NS3 serine protease |
RU2006134005A (ru) * | 2004-02-27 | 2008-04-10 | Шеринг Корпорейшн (US) | Новые соединения, действующие как ингибиторы сериновой протеазы ns3 вируса гепатита с |
CA2557304C (fr) * | 2004-02-27 | 2013-08-06 | Schering Corporation | Nouveaux cetoamides a p4 cycliques en tant qu'inhibiteurs de la ns3 serine protease du virus de l'hepatite c |
JP4745327B2 (ja) * | 2004-02-27 | 2011-08-10 | シェーリング コーポレイション | C型肝炎ウイルスns3プロテアーゼのインヒビター |
CA2557495C (fr) * | 2004-02-27 | 2014-04-15 | Schering Corporation | Composes soufres en tant qu'inhibiteurs de la protease serine ns3 du virus de l'hepatite c |
JP2007525512A (ja) * | 2004-02-27 | 2007-09-06 | シェーリング コーポレイション | C型肝炎ウイルスns3セリンプロテアーゼのインヒビターとしての3,4−(シクロペンチル)−縮合プロリン化合物 |
AR049635A1 (es) * | 2004-05-06 | 2006-08-23 | Schering Corp | (1r,2s,5s)-n-((1s)-3-amino-1-(ciclobutilmetil)-2,3-dioxopropil)-3-((2s)-2-((((1,1-dimetiletil)amino)carbonil)amino)-3,3-dimetil-1-oxobutil)-6,6-dimetil-3-azabiciclo(3.1.0)hexan-2-carboxamida como inhibidor de la ns3/ns4a serina proteasa del virus de la hepatitis c |
TWI389688B (zh) * | 2004-06-08 | 2013-03-21 | Vertex Pharma | Vx-950之形態與調配物及其製備方法與用途 |
WO2006026352A1 (fr) * | 2004-08-27 | 2006-03-09 | Schering Corporation | Composes d'acylsulfonamide inhibiteurs de la serine protease ns3 du virus de l'hepatite c |
US7250441B2 (en) * | 2004-09-23 | 2007-07-31 | Wyeth | Carbazole and cyclopentaindole derivatives to treat infection with Hepatitis C virus |
EP1804821A4 (fr) * | 2004-10-01 | 2009-07-15 | Vertex Pharma | Inhibition de la protease ns3-ns4a du vhc |
MY141025A (en) * | 2004-10-29 | 2010-02-25 | Vertex Pharma | Dose forms |
US20070004635A1 (en) * | 2005-06-02 | 2007-01-04 | Schering Corporation | Method of treating interferon non-responders using HCV protease inhibitor |
EP1891089B1 (fr) * | 2005-06-02 | 2014-11-05 | Merck Sharp & Dohme Corp. | Inhibiteurs de protease du VHC en combinaison avec des aliments |
US20060276404A1 (en) * | 2005-06-02 | 2006-12-07 | Anima Ghosal | Medicaments and methods combining a HCV protease inhibitor and an AKR competitor |
WO2006130626A2 (fr) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Procede de modulation de l'activite de la protease du vhc au moyen d'un nouvel inhibiteur de la protease du vhc aux fins de la reduction de la duree du traitement |
WO2006130687A2 (fr) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Taux de concentration foie/plasma pour le dosage de l'inhibiteur de protease du virus de l'hepatite c |
US7608592B2 (en) * | 2005-06-30 | 2009-10-27 | Virobay, Inc. | HCV inhibitors |
JP2009505966A (ja) * | 2005-08-02 | 2009-02-12 | バーテックス ファーマシューティカルズ インコーポレイテッド | セリンプロテアーゼのインヒビター |
AR055395A1 (es) * | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
WO2007120595A2 (fr) * | 2006-04-11 | 2007-10-25 | Novartis Ag | Composés organiques et leurs utilisations |
AU2007238252A1 (en) * | 2006-04-11 | 2007-10-25 | Novartis Ag | HCV inhibitors comprising beta amino acids and their uses |
KR20080104366A (ko) * | 2006-04-11 | 2008-12-02 | 노파르티스 아게 | Hcv 억제제 |
NZ571826A (en) * | 2006-04-11 | 2012-01-12 | Novartis Ag | HCV/HIV inhibitors and their uses |
WO2008059367A1 (fr) | 2006-11-14 | 2008-05-22 | Pfizer Products Inc. | Promédicaments de sulopénème |
CL2008000018A1 (es) | 2007-01-04 | 2008-08-01 | Prosidion Ltd | Compuestos derivados de heterociclos de nitrogeno y oxigeno, agonistas de gpcr; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de la obesidad, diabetes, sindrome metabolico, hiperlipidemia, toleranci |
CL2008000017A1 (es) | 2007-01-04 | 2008-08-01 | Prosidion Ltd | Compuestos derivados de heterociclos de nitrogeno y oxigeno, agonistas de gpcr; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento de la obesidad, diabetes, sindrome metabolico, hiperlipidemia, toleranci |
JP5591706B2 (ja) | 2007-10-10 | 2014-09-17 | アムジエン・インコーポレーテツド | 置換ビフェニルgpr40調節因子 |
TW200924778A (en) | 2007-10-10 | 2009-06-16 | Takeda Pharmaceutical | Amide compound |
UA100527C2 (en) | 2007-10-10 | 2013-01-10 | Астразенека Аб | Benzothiazoles as ghrelin receptor modulators |
-
2008
- 2008-10-08 CN CN201410273335.0A patent/CN104016970A/zh active Pending
- 2008-10-08 MX MX2010003916A patent/MX2010003916A/es active IP Right Grant
- 2008-10-08 CA CA2702132A patent/CA2702132A1/fr not_active Abandoned
- 2008-10-08 JP JP2010528385A patent/JP5095824B2/ja not_active Expired - Fee Related
- 2008-10-08 AR ARP080104396A patent/AR068756A1/es not_active Application Discontinuation
- 2008-10-08 AU AU2008309589A patent/AU2008309589B2/en not_active Ceased
- 2008-10-08 WO PCT/EP2008/063460 patent/WO2009047264A1/fr active Application Filing
- 2008-10-08 EP EP08805142A patent/EP2205584A1/fr not_active Withdrawn
- 2008-10-08 BR BRPI0817881 patent/BRPI0817881A2/pt not_active IP Right Cessation
- 2008-10-08 KR KR1020127015695A patent/KR101396696B1/ko not_active IP Right Cessation
- 2008-10-08 CN CN200880110944.7A patent/CN101868452B/zh not_active Expired - Fee Related
- 2008-10-08 KR KR1020107007789A patent/KR101218882B1/ko not_active IP Right Cessation
- 2008-10-08 EA EA201000556A patent/EA020951B1/ru not_active IP Right Cessation
- 2008-10-09 CL CL2008002995A patent/CL2008002995A1/es unknown
- 2008-10-09 TW TW097139071A patent/TW200932737A/zh unknown
- 2008-10-09 PE PE2008001744A patent/PE20091237A1/es not_active Application Discontinuation
- 2008-10-10 US US12/249,186 patent/US8008263B2/en not_active Expired - Fee Related
-
2010
- 2010-03-04 ZA ZA2010/01585A patent/ZA201001585B/en unknown
- 2010-03-11 CR CR11310A patent/CR11310A/es not_active Application Discontinuation
- 2010-03-26 TN TNP2010000137A patent/TN2010000137A1/fr unknown
- 2010-04-08 MA MA32757A patent/MA31767B1/fr unknown
- 2010-04-30 CO CO10051497A patent/CO6270317A2/es not_active Application Discontinuation
-
2011
- 2011-07-19 US US13/185,683 patent/US8222425B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
KR101396696B1 (ko) | 2014-05-16 |
CO6270317A2 (es) | 2011-04-20 |
AU2008309589B2 (en) | 2012-07-05 |
CL2008002995A1 (es) | 2009-06-26 |
AR068756A1 (es) | 2009-12-02 |
US8222425B2 (en) | 2012-07-17 |
CR11310A (es) | 2010-05-06 |
JP2011500528A (ja) | 2011-01-06 |
KR101218882B1 (ko) | 2013-01-07 |
MX2010003916A (es) | 2010-05-05 |
CN104016970A (zh) | 2014-09-03 |
EA201000556A1 (ru) | 2010-10-29 |
ZA201001585B (en) | 2010-12-29 |
JP5095824B2 (ja) | 2012-12-12 |
CN101868452A (zh) | 2010-10-20 |
BRPI0817881A2 (pt) | 2015-03-31 |
MA31767B1 (fr) | 2010-10-01 |
AU2008309589A1 (en) | 2009-04-16 |
WO2009047264A1 (fr) | 2009-04-16 |
KR20120094049A (ko) | 2012-08-23 |
CA2702132A1 (fr) | 2009-04-16 |
TW200932737A (en) | 2009-08-01 |
US8008263B2 (en) | 2011-08-30 |
PE20091237A1 (es) | 2009-09-14 |
US20110275819A1 (en) | 2011-11-10 |
US20090137495A1 (en) | 2009-05-28 |
CN101868452B (zh) | 2014-08-06 |
EA020951B1 (ru) | 2015-03-31 |
KR20100051749A (ko) | 2010-05-17 |
EP2205584A1 (fr) | 2010-07-14 |
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