DE2951135A1 (en) | 1979-12-19 | 1981-06-25 | Hoechst Ag, 6230 Frankfurt | SULFONYL UREAS, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICAL PREPARATIONS BASED ON THESE COMPOUNDS AND THEIR USE |
US4617307A (en) | 1984-06-20 | 1986-10-14 | Ciba-Geigy Corporation | Substituted imidazo[1,5-A]pyridine derivatives as aromatase inhibitors |
US4889861A (en) | 1982-12-21 | 1989-12-26 | Ciba-Geigy Corp. | Substituted imidazo[1,5-a]pyridine derivatives and other substituted bicyclic derivatives and their use as aromatase inhibitors |
DE3347565A1 (en) | 1983-12-30 | 1985-07-11 | Thomae Gmbh Dr K | NEW PHENYL ACETIC DERIVATIVES, MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF |
JPS6354321A (en) | 1985-03-27 | 1988-03-08 | Ajinomoto Co Inc | Blood sugar lowering agent |
US5120712A (en) | 1986-05-05 | 1992-06-09 | The General Hospital Corporation | Insulinotropic hormone |
US5118666A (en) | 1986-05-05 | 1992-06-02 | The General Hospital Corporation | Insulinotropic hormone |
JP3262329B2 (en) | 1990-01-24 | 2002-03-04 | アイ. バックレイ,ダグラス | GLP-1 analog useful for the treatment of diabetes |
AU654331B2 (en) | 1991-03-30 | 1994-11-03 | Kissei Pharmaceutical Co. Ltd. | Succinic acid compounds |
US5155100A (en) | 1991-05-01 | 1992-10-13 | Ciba-Geigy Corporation | Phosphono/biaryl substituted dipeptide derivatives |
RU2086544C1 (en) | 1991-06-13 | 1997-08-10 | Хоффманн-Ля Рош АГ | Benzenesulfonamide derivatives of pyrimidine or their salts, pharmaceutical composition for treatment of diseases associated with endothelin activity |
DE10075006I2 (en) | 1991-06-21 | 2004-01-08 | Boehringer Ingelheim Pharma | Use of (S) (+) - 2-ethoxy-4- [N- [1- (2-piperidino-phenyl) -3-methyl-1-butyl [aminocarbonylmethyl] benzoic acid for the manufacture of a long-term antidiabetic. |
DE69217762T2 (en) | 1991-07-30 | 1997-10-09 | Ajinomoto Kk | Crystals of N- (Trans-4-isopropylcyclohexylcarbonyl) -D-phenylalanine and process for their preparation |
EP0618803A4 (en) | 1991-12-19 | 1995-03-22 | Southwest Found Biomed Res | Cetp inhibitor polypeptide, antibodies against the synthetic polypeptide and prophylactic and therapeutic anti-atherosclerosis treatments. |
DK0712389T3 (en)* | 1993-08-02 | 2001-06-05 | Commw Scient Ind Res Org | Therapeutic compound - fatty acid conjugates |
IL111785A0 (en) | 1993-12-03 | 1995-01-24 | Ferring Bv | Dp-iv inhibitors and pharmaceutical compositions containing them |
US5705483A (en) | 1993-12-09 | 1998-01-06 | Eli Lilly And Company | Glucagon-like insulinotropic peptides, compositions and methods |
US5512549A (en) | 1994-10-18 | 1996-04-30 | Eli Lilly And Company | Glucagon-like insulinotropic peptide analogs, compositions, and methods of use |
TW313568B (en) | 1994-12-20 | 1997-08-21 | Hoffmann La Roche | |
DE122010000020I1 (en) | 1996-04-25 | 2010-07-08 | Prosidion Ltd | Method for lowering the blood glucose level in mammals |
TW492957B (en) | 1996-11-07 | 2002-07-01 | Novartis Ag | N-substituted 2-cyanopyrrolidnes |
ATE383424T1 (en) | 1997-12-24 | 2008-01-15 | Takeda Pharmaceutical | POLYPEPTIDES, THEIR PRODUCTION AND USE |
WO1999043357A1 (en)* | 1998-02-25 | 1999-09-02 | Micrologix Biotech Inc. | Indolicidin and cationic peptides conjugated with polymers |
GT199900147A (en) | 1998-09-17 | 1999-09-06 | | 1, 2, 3, 4- TETRAHIDROQUINOLINAS 2-SUBSTITUTED 4-AMINO SUBSTITUTED. |
US6197786B1 (en) | 1998-09-17 | 2001-03-06 | Pfizer Inc | 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines |
CO5150173A1 (en) | 1998-12-10 | 2002-04-29 | Novartis Ag | COMPOUNDS N- (REPLACED GLYCLE) -2-DIPEPTIDYL-IV PEPTIDASE INHIBITING CYANOPIRROLIDINS (DPP-IV) WHICH ARE EFFECTIVE IN THE TREATMENT OF CONDITIONS MEDIATED BY DPP-IV INHIBITION |
US6723752B2 (en) | 1999-09-23 | 2004-04-20 | Pharmacia Corporation | (R)-chiral halogenated substituted n-benzyl-n-phenyl aminoalcohol compounds useful for inhibiting cholesteryl ester transfer protein activity |
US7635751B2 (en) | 2000-03-23 | 2009-12-22 | Takada Pharmaceutical Company Limited | Peptides having ligand activities on APJ that is an orphan G protein-coupled receptor, and use thereof |
KR20020089437A (en) | 2000-04-12 | 2002-11-29 | 노파르티스 아게 | Combination of organic compounds |
JP2004537984A (en) | 2001-04-19 | 2004-12-24 | ザ スクリップス リサーチ インスティテュート | Methods and compositions for producing orthogonal tRNA-aminoacyl tRNA synthetase pairs |
CA2466034C (en) | 2001-11-08 | 2012-12-18 | Protein Design Labs, Inc. | Stable aqueous pharmaceutical formulations of daclizumab antibodies |
AU2003232941A1 (en) | 2002-06-07 | 2003-12-22 | Glaxo Group Limited | N-mercaptoacyl phenyalanine derivatives, process for their preparation, and pharmaceutical compositions containing them |
JP4533139B2 (en) | 2002-08-07 | 2010-09-01 | ノバルティス アーゲー | Organic compounds as treatments for aldosterone-mediated conditions |
CA2505752A1 (en) | 2002-11-18 | 2004-06-03 | Novartis Ag | Imidazo[1,5a]pyridine derivatives and methods for treating aldosterone mediated diseases |
EP1626981A4 (en)* | 2003-03-04 | 2006-11-22 | Biorexis Pharmaceutical Corp | Dipeptidyl-peptidase protected proteins |
ATE433984T1 (en) | 2004-03-26 | 2009-07-15 | Lilly Co Eli | COMPOUNDS AND METHODS FOR TREATING DYSLIPIDEMIA |
UA90269C2 (en) | 2004-04-02 | 2010-04-26 | Мицубиси Танабе Фарма Корпорейшн | Tetrahydroquinoline derivatives and a process for preparing the same |
JP5179174B2 (en) | 2004-05-28 | 2013-04-10 | ノバルティス ファーマ アーゲー | Tetrahydro-imidazo [1,5-A] pyridine derivatives as aldosterone synthase inhibitors |
US20080076794A1 (en) | 2004-05-28 | 2008-03-27 | Peter Herold | Heterocyclic Compounds And Their Use As Aldosterone Synthase Inhibitors |
TW200611898A (en) | 2004-05-28 | 2006-04-16 | Speedel Experimenta Ag | Organic compounds |
AR049711A1 (en) | 2004-07-09 | 2006-08-30 | Speedel Experimenta Ag | HETEROCICLIC COMPOUNDS CONDENSED AS INHIBITORS OF ALDOSTERONE SINTASA; PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OR PREVENTION OF DISEASES RELATED TO HYPERALDOSTERISM AND EXCESSIVE CORTISO RELEASE |
TW200716105A (en) | 2005-05-31 | 2007-05-01 | Speedel Experimenta Ag | Imidazole compounds |
TW200716636A (en) | 2005-05-31 | 2007-05-01 | Speedel Experimenta Ag | Heterocyclic spiro-compounds |
TW200716634A (en) | 2005-05-31 | 2007-05-01 | Speedel Experimenta Ag | Heterocyclic spiro-compounds |
GT200600381A (en) | 2005-08-25 | 2007-03-28 | | ORGANIC COMPOUNDS |
US8673848B2 (en)* | 2012-01-27 | 2014-03-18 | Novartis Ag | Synthetic apelin mimetics for the treatment of heart failure |
TW200804378A (en) | 2005-12-09 | 2008-01-16 | Speedel Experimenta Ag | Organic compounds |
TW200738261A (en) | 2005-12-20 | 2007-10-16 | Bristol Myers Squibb Co | Stable protein formulations |
US20090156875A1 (en) | 2006-04-04 | 2009-06-18 | Takafumi Tomioka | Methane separation method, methane separation apparatus, and methane utilization system |
TW200808812A (en) | 2006-04-12 | 2008-02-16 | Speedel Experimenta Ag | Imidazo compounds |
TW200808813A (en) | 2006-04-12 | 2008-02-16 | Speedel Experimenta Ag | Imidazo compounds |
MX2008014284A (en) | 2006-05-10 | 2008-11-18 | Novartis Ag | Bicyclic derivatives as cetp inhibitors. |
EP1886695A1 (en) | 2006-06-27 | 2008-02-13 | Speedel Experimenta AG | Pharmaceutical combination of an aldosterone synthase inhibitor and a glucocorticoid receptor antagonist or a cortisol synthesis inhibitor or a corticotropin releasing factor antagonist |
WO2008009435A1 (en) | 2006-07-20 | 2008-01-24 | Novartis Ag | Amino-piperidine derivatives as cetp inhibitors |
KR20090055595A (en) | 2006-08-25 | 2009-06-02 | 노파르티스 아게 | Fusion imidazole derivatives for the treatment of disorders mediated by aldosterone synthase and / or 11-beta-hydroxylase and / or aromatase |
US7834164B2 (en)* | 2006-10-25 | 2010-11-16 | Amgen Inc. | DNA encoding OSK1 toxin peptide analogs and vectors and cells for combinant expression |
JP2010513558A (en) | 2006-12-18 | 2010-04-30 | ノバルティス アーゲー | 4-imidazolyl-1,2,3,4-tetrahydroquinoline derivatives and their use as aldosterone / 11-beta-hydroxylase inhibitors |
BRPI0721290A2 (en) | 2006-12-18 | 2014-03-25 | Novartis Ag | ORGANIC COMPOUNDS |
EA200900811A1 (en) | 2006-12-18 | 2009-12-30 | Новартис Аг | IMIDAZOLES AS ANALYSTERONSYNTASE INHIBITORS |
ES2354008T3 (en) | 2007-03-29 | 2011-03-09 | Novartis Ag | SPIROHETEROCYCLIC COMPOUNDS. |
TWI448284B (en) | 2007-04-24 | 2014-08-11 | Theravance Inc | Dual-acting antihypertensive agents |
JP2010538071A (en) | 2007-09-07 | 2010-12-09 | セラヴァンス, インコーポレーテッド | Dual acting antihypertensive |
AU2008324243B2 (en) | 2007-11-05 | 2012-03-08 | Novartis Ag | 4-benzylamino-1-carboxyacyl-piperidine derivatives as CETP inhibitors useful for the treatment of diseases such as hyperlipidemia or arteriosclerosis |
AU2008333272B2 (en) | 2007-12-03 | 2012-03-29 | Novartis Ag | 1,2-disubstituted-4-benzylamino-pyrrolidine derivatives as CETP inhibitors useful for the treatment of diseases such as hyperli pidemia or arteriosclerosis |
JP2011518884A (en) | 2008-04-29 | 2011-06-30 | セラヴァンス, インコーポレーテッド | Dual active antihypertensive |
AR072297A1 (en) | 2008-06-27 | 2010-08-18 | Novartis Ag | DERIVATIVES OF INDOL-2-IL-PIRIDIN-3-ILO, PHARMACEUTICAL COMPOSITION THAT INCLUDES THEM AND ITS USE IN MEDICINES FOR THE TREATMENT OF DISEASES MEDIATED BY THE SYNTHESIS ALDOSTERONE. |
MX2011000847A (en)* | 2008-08-06 | 2011-02-25 | Novo Nordisk Healthcare Ag | Conjugated proteins with prolonged in vivo efficacy. |
KR101316159B1 (en) | 2008-10-24 | 2013-10-15 | 아이알엠 엘엘씨 | Biosynthetically generated pyrroline-carboxy-lysine and site specific protein modifications via chemical derivatization of pyrroline-carboxy-lysine and pyrrolysine residues |
US20120028888A1 (en)* | 2008-11-04 | 2012-02-02 | Jay Janz | Apj receptor compounds |
RS53275B (en) | 2009-05-15 | 2014-08-29 | Novartis Ag | Aryl pyridine as aldosterone synthase inhibitors |
MA33364B1 (en) | 2009-05-28 | 2012-06-01 | Novartis Ag | SUBSTITUTED AMINOBUTYRIC DERIVATIVES AS NEPRILYSIN INHIBITORS |
EP2594557B1 (en) | 2009-05-28 | 2016-08-10 | Novartis AG | Substituted aminopropionic derivatives as neprilysin inhibitors |
US9345661B2 (en) | 2009-07-31 | 2016-05-24 | Genentech, Inc. | Subcutaneous anti-HER2 antibody formulations and uses thereof |
JO2967B1 (en) | 2009-11-20 | 2016-03-15 | نوفارتس ايه جي | Substituted carbamoylmethylamino acetic acid derivatives as novel NEP inhibitors |
PL2525834T3 (en)* | 2010-01-22 | 2020-10-19 | Novo Nordisk Health Care Ag | Growth hormones with prolonged in-vivo efficacy |
TW201138808A (en) | 2010-05-03 | 2011-11-16 | Bristol Myers Squibb Co | Serum albumin binding molecules |
BR112012028707A2 (en) | 2010-05-13 | 2019-09-24 | Univ Indiana Res & Tech Corp | glucagon compound of the peptide superfamily exhibiting g receptor activity with coupled protein, prodrug, dimer or multimer, pharmaceutical composition comprising it and method of administration thereof. |
PL2683360T3 (en) | 2011-03-11 | 2016-09-30 | | Pegylated apelin and uses thereof |
US20150011466A1 (en)* | 2012-01-09 | 2015-01-08 | Anchor Therapeutics, Inc. | APJ Receptor Compounds |
US20160067347A1 (en) | 2012-12-20 | 2016-03-10 | Amgen Inc. | Apj receptor agonists and uses thereof |
ES2708957T3 (en) | 2013-03-14 | 2019-04-12 | Regeneron Pharma | Appeline fusion proteins and uses thereof |
CN105705167A (en)* | 2013-07-25 | 2016-06-22 | 诺华股份有限公司 | Bioconjugates of synthetic APELIN polypeptides |
EP3024845A1 (en)* | 2013-07-25 | 2016-06-01 | Novartis AG | Cyclic polypeptides for the treatment of heart failure |
AU2015274574B2 (en) | 2014-06-10 | 2019-10-10 | Amgen Inc. | Apelin polypeptides |
US10588980B2 (en)* | 2014-06-23 | 2020-03-17 | Novartis Ag | Fatty acids and their use in conjugation to biomolecules |
EP3237435B1 (en) | 2014-12-23 | 2023-05-24 | INSERM - Institut National de la Santé et de la Recherche Médicale | Metabolically stable apelin analogs in the treatment of disease mediated by the apelin receptor |