Patents
Patents for C07D 457 - Heterocyclic compounds containing indolo [4, 3-f, g] quinoline ring systems, e.g. derivatives of ergoline, of the formula: , e.g. lysergic acid (836)
03/2015
03/03/2015US8969374 Iso-ergoline derivatives
02/2015
02/03/2015US8946420 Neuromodulatory compounds
11/2014
11/25/2014US8895743 Methysergide derivatives
10/2014
10/14/2014US8859579 Compostions and methods for preventing and/or treating disorders associated with cephalic pain
09/2014
09/09/2014US8829021 Treatment of pediatric tumors
07/2014
07/31/2014WO2014114664A1 Process for producing 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid and complexes thereof
07/10/2014US20140194435 Novel substituted indolo 4,3 fg quinolines useful for treating migraine
07/03/2014WO2014070971A3 Somatostatin-dopamine chimeric analogs
07/01/2014US8765760 [1,2,4] triazol [1,5-a] pyrazines useful as inhibitors of phosphodiesterases
06/2014
06/26/2014WO2014100354A1 Novel methysergide derivatives
06/26/2014US20140179706 Fluoroergoline derivatives and uses thereof
05/2014
05/28/2014CN103827113A 新型氟麦角碱类似物 The new fluorine ergot alkaloids like
05/22/2014WO2014078857A1 Ergoline derivatives as dopamine receptor modulators
04/2014
04/30/2014EP2723735A1 Novel fluoroergoline analogs
04/03/2014US20140094483 Novel iso-ergoline derivatives
02/2014
02/27/2014US20140058108 Lisuride, Terguride and Derivatives Thereof for Use in the Prophylaxis and/or Treatment of Fibrotic Changes
02/06/2014US20140039188 Novel iso-ergoline derivatives
12/2013
12/26/2013US20130345253 Novel cabergoline derivatives
10/2013
10/15/2013CA2608702C Ergoline derivatives and their use as chemokine receptor ligands
06/2013
06/27/2013US20130165469 Novel neuromodulatory compounds
06/20/2013US20130158064 Novel iso-ergoline derivatives
06/19/2013CN103159756A Novel preparation method for nicergoline
05/2013
05/29/2013DE102010060382B4 Analysenverfahren zur Isolierung von Mykotoxinen mit einer Ergolin-Grundstruktur, insbesondere von Ergotalkaloiden Analysis method for the isolation of mycotoxins with a basic ergoline structure, in particular of ergot alkaloids
12/2012
12/27/2012WO2012177962A1 Novel fluoroergoline analogs
12/27/2012CA2838991A1 Novel fluoroergoline analogs
12/25/2012US8338445 Crystal form of cabergoline
12/04/2012US8324386 Somatostatin-dopamine chimeric analogs
11/2012
11/14/2012CN102775402A Intermediate for preparation of dihydrolysergic acid and its preparation method
10/2012
10/24/2012CN102134239B Method of extracting high-purity lysergol from Ipomoea herderacea
10/10/2012CN102718761A Preparation method for nicergoline
07/2012
07/25/2012EP2084158B1 Process for the preparation of crystal forms of cabergoline via novel stable solvates of cabergoline
07/18/2012CN102596950A Deuterated compounds for electronic applications
05/2012
05/15/2012US8178651 Somatostatin-dopamine chimeric analogs
03/2012
03/22/2012WO2012001308A9 Method for synthesizing ergoline alkaloids from indolic bicyclic compounds by double cyclization, resulting materials, and intermediate materials
03/20/2012CA2363067C Compounds and methods to inhibit or augment an inflammatory response
01/2012
01/05/2012WO2012001308A1 Method for synthesizing ergoline alkaloids from indolic bicyclic compounds by double cyclization, resulting materials, and intermediate materials
11/2011
11/16/2011EP2386565A2 Compounds and methods to inhibit or augment an inflammatory response
09/2011
09/20/2011CA2565440C Preparation of cabergoline form i from a solvate of cabergoline and ethylbenzene
09/14/2011CN101781296B Method for producing nicergoline
08/2011
08/02/2011CA2449634C Somatostatin-dopamine chimeric analogs
07/2011
07/27/2011CN102134239A Method of extracting high-purity lysergol from Ipomoea herderacea
07/20/2011EP2344488A1 Methods and kits for the determining the presence or absence of ergot alkaloids
06/2011
06/09/2011US20110137035 Preparation of microbiologically produced ergot alkaloids
05/2011
05/26/2011US20110124600 Use of Dopamine partial agonists for treament of the restless leg syndrome and corresponding pharmaceutical preparation
05/19/2011WO2011059463A1 Deuterated compounds for electronic applications
05/10/2011US7939665 reacting 6-(2-propenyl)-ergoline-8 beta -carboxylic acid with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide in a halogenated solvent or anisole; prolactin inhibitors; industrial scale, cost-effective synthetic method; treating Parkinson's disease, Restless Legs Syndrome
04/2011
04/27/2011EP2313405A1 Preparation of microbiologically produced ergot alkaloids
03/2011
03/16/2011EP2294067A1 Preparation of n-6 demethylated, 9-10-dihydrolysergic acid alkyl esters
03/08/2011CA2376703C Method for preparing lysergic acid
12/2010
12/28/2010US7858791 high yield, milder reaction conditions and a shorter reaction time; easier purification by normal phase chromatography if needed; cabergoline is a dopamine agonist, a drug for treating Parkinson's disease
12/22/2010CN101184754B Ergoline derivatives and their use as chemokine receptor ligands
07/2010
07/21/2010CN101781296A Method for producing nicergoline
07/15/2010US20100179304 Somatostatin-Dopamine Chimeric analogs
06/2010
06/17/2010US20100152223 Crystal form of cabergoline
05/2010
05/27/2010DE102007014947B4 Stabilisierte wässrige Lösungen von Ergolinverbindungen The stabilized aqueous solutions of ergoline compounds
05/26/2010EP1720869B1 Process for the preparation of cabergoline
05/11/2010US7714132 Tetrahydropyridoindole derivatives
04/2010
04/22/2010WO2010045527A1 Methods and kits for the determining the presence or absence of ergot alkaloids
02/2010
02/23/2010US7666877 Ergoline derivatives
01/2010
01/07/2010WO2010000676A1 Preparation of microbiologically produced ergot alkaloids
01/06/2010EP2141165A1 Processing microbiologically produced ergot alkaloids
12/2009
12/23/2009EP2135869A1 Preparation of a crystalline form of cabergoline
12/15/2009US7632948 reacting 8-amino-1,2,3,4-tetrahydro-isoquinoline with chloral hydrate and hydroxylamine hydrochloride to give an N-(1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-hydroxyimino-acetamide, adding H2SO4 to provide a 2,3-dioxo-2,3,6,7,8,9-hexahydro-1H-pyrrolo[3,2-h]isoquinoline, finally reacting with butyrolactone
11/2009
11/24/2009US7622476 1-allyl-( 5R,8S,10R)-terguride; antagonistic properties to 5-HT2 receptors for the prevention of migraine-related headache, Parkinson's disease, disorders of the thrombocyte function
11/17/2009US7618979 Prostaglandin receptor antagonists; allergic rhinitis, nasal congestion and asthma; [5-[(4-chlorophenyl)thio]-4-(methylsulfonyl)-6,7,8,9-tetrahydropyrido[3,2-b]indolizin-6-yl]acetic acid
11/05/2009WO2009133097A1 Preparation of n-6 demethylated, 9-10-dihydrolysergic acid alkyl esters
11/05/2009US20090275501 Somatostatin-dopamine chimeric analogs
11/04/2009EP2113504A1 Preparation of N-6 demethylated, 9,10-dihydrolysergic acid alkyl esters
10/2009
10/22/2009US20090264456 Compostions and methods for preventing and/or treating disorders asociated with cephalic pain
10/07/2009EP1311249B1 Set of transdermal therapeutic systems
09/2009
09/24/2009WO2009071607A3 Ergoline derivatives as selective radical scavengers for neurons
08/2009
08/25/2009US7579435 Somatostatin-dopamine chimeric analogs
08/13/2009WO2008104956A3 Process for the preparation of amorphous cabergoline
08/11/2009US7572883 Somatostatin-dopamine chimeric analogs
08/05/2009EP2084158A1 Process for the preparation of crystal forms of cabergoline via novel stable solvates of cabergoline
07/2009
07/30/2009WO2008049884A8 Process for the preparation of crystal forms of cabergoline via novel stable solvates of cabergoline
07/29/2009EP2083008A1 Ergoline derivatives as selective radical scavengers for neurons
07/28/2009US7566549 Using hapten derivatives for the preparation of antigens, antibodies and reagents for use detecting lysergic acid diethylamide (LSD) in samples; hallucinogen
07/22/2009EP2079458A2 Transdermal therapeutic system with two-phase releasing profile
07/21/2009CA2478393C 1-allyl ergot alkaloid derivatives, methods for their production and their use for migraine prevention and treatment
07/15/2009CN101481405A Somatostatin-dopamine chimeric analogs
06/2009
06/11/2009WO2009071607A2 Ergoline derivatives as selective radical scavengers for neurons
06/10/2009EP2067780A1 Ergoline derivatives as selective radical scavengers for neurons
05/2009
05/27/2009EP2062914A2 Somatostatin-dopamine chimeric analogs
05/12/2009US7531551 Polymorphs of cabergoline
03/2009
03/11/2009CN101384589A Production of cabergoline and novel polymorphic form thereof
03/04/2009EP1401863B1 Somatostatin-dopamine chimeric analogs
01/2009
01/15/2009US20090018127 (6aR,9R)-9-(Pyrrolidine-1-carbonyl)-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-7-carboxylic acid phenylamide; preventing or treating disorders or diseases mediated by chemokine receptors; antiinflammatory agents treating inflammatory or autoimmune diseases; chemical preparation
12/2008
12/31/2008EP2007761A2 Production of cabergoline and novel polymorphic form thereof
11/2008
11/19/2008EP1485382B1 Process for the synthesis of pergolide
11/13/2008WO2007091039A8 Production of cabergoline and novel polymorphic form thereof
11/06/2008US20080275240 reacting 6-(2-propenyl)-ergoline-8 beta -carboxylic acid with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide in a halogenated solvent or anisole; prolactin inhibitors; industrial scale, cost-effective synthetic method; treating Parkinson's disease, Restless Legs Syndrome
11/05/2008EP1303278B1 Combination of a transdermal therapeutic system and an oral and/or parenteral preparation containing dopamine agonists for the treatment of dopaminergic disease states
11/04/2008CA2587880A1 A new and efficient process for the preparation of cabergoline and its intermediates
09/2008
09/25/2008DE102007014947A1 Stabilisierte wässrige Lösungen von Ergolinverbindungen The stabilized aqueous solutions of ergoline compounds
09/04/2008WO2008104956A2 Process for the preparation of amorphous cabergoline
08/2008
08/07/2008WO2008092881A1 New crystal form of cabergoline
08/06/2008EP1953157A1 New crystal form of cabergoline
07/2008
07/23/2008CN101228159A Solvate of cabergoline and preparations of cabergoline form i
06/2008
06/25/2008CN101208337A Preparation of cabergoline
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