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H. Lundbeck A/s(1259)
专利信息
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[专利权人] 包含 'H. Lundbeck A/s'
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1259
条记录, 当前第2/126页。
公开号
公开日
申请号
申请日
1.
US8598213B2
2013/12/3
专利标题
:Positive allosteric modulators of nicotinic acetylcholine receptor
专利权人
:
H. Lundbeck A/s
;
The present invention relates to compounds useful in therapy to compositions comprising said compounds and to methods of treating diseases comprising administration of said compounds. The compounds referred to are positive allosteric modulators (PAMs) of the nicotinic acetylcholine alpha7 receptor.
2.
EP2398785B1
2013/11/27
专利标题
:Purification of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]-piperazine
专利权人
:
H. Lundbeck A/s
;
3.
AU2012283208A1
2013/11/21
专利标题
:Positive allosteric modulators of nicotinic acetylcholine receptor
专利权人
:
H. Lundbeck A/s
;
The present invention relates to compounds of formula (I) useful in therapy to compositions comprising said compounds and to methods of treating diseases comprising administration of said compounds. The compounds referred to are positive allosteric modulators (PAMs) of the nicotinic acetylcholine α7 receptor.
4.
US8580963B2
2013/11/12
US13/287391
2011/11/2
专利标题
:Method for the manufacturing of naltrexone
专利权人
:
H. Lundbeck A/s
;
The present invention relates to an improved process for producing naltrexone[17-(cyclopropylmethyl)-45alpha-epoxy-314-dihydroxy-morphinan-6-one] from noroxymorphone[45-alpha-epoxy-314-dihydroxy-morphinan-6-one] by alkylation with a cyclopropylmethyl halide.
5.
WO2013164383A1
2013/11/7
WO2013EP59104
2013/5/2
专利标题
:Method for the manufacturing of naltrexone
专利权人
:
H. Lundbeck A/s
;
The present invention relates to a new process for producing naltrexone [17-(cyclopropylmethyl)-45α-epoxy-314-dihydroxy-morphinan-6-one] from noroxymorphone [45- α-epoxy-314-dihydroxy-morphinan-6-one] by alkylation with a cyclopropylmethyl halide.
6.
BG66372B1
2013/10/31
专利标题
:Process for the preparation of racemic citalopram and/or s- or r-citalopram by separation of a mixture of r- and s-citalopram
专利权人
:
H. Lundbeck A/s
;
The invention relates to a process for the preparation of racemic citalopram free base or an acid addition salt thereof and/or R- or S-citalopram as the free base of an acid addition salt thereof by separation of a mixture of R- and S-citalopram with more than 50% of one of the enantiomers into a fraction consisting of racemic citalopram and/or a fraction of S-citalopram or R-citalopram characterised in that (i) citalopram is precipitated from a solvent as the free base or as an acid addition sa...
7.
NZ600365A
2013/10/25
NZ20100600365
2010/12/15
专利标题
:Heteroaromatic aryl triazole derivatives as pde10a enzyme inhibitors
专利权人
:
H. Lundbeck A/s
;
600416 Disclosed are 5-bicycloheteroarylalkyl-3-phenyl-124-triazole derivatives as represented by the general formula (I) wherein: HET-1 is a heteroaromatic group of formula II containing from 2 to 4 nitrogen atoms and which is preferably selected from [124]triazolo[15-a]pyridine [124]triazolo[15-a]pyrimidine or [124]triazolo[15-a]pyrazine and which may be optionally substituted; Q is phenyl optionally substituted with one to five substituents or a monocyclic 5-membered or 6-membered heteroaroma...
8.
EP2635586A1
2013/9/11
EP20110785301
2011/11/4
专利标题
:Method for the manufacturing of naltrexone
专利权人
:
H. Lundbeck A/s
;
9.
NZ600416A
2013/8/30
NZ20100600416
2010/12/15
专利标题
:2-arylimidazole derivatives as pde10a enzyme inhibitors
专利权人
:
H. Lundbeck A/s
;
600416 Disclosed are 4-bicycloheteroarylalkyl-2-phenyl-imidazole derivatives as represented by the general formula (I) wherein: HET-1 is a heteroaromatic group of formula II containing from 2 to 4 nitrogen atoms and which is preferably selected from [124]triazolo[15-a]pyrazine or [124]triazolo[15-a]pyridine and which may be optionally substituted; Q is phenyl optionally substituted with one to five substituents or a monocyclic 5-membered or 6-membered heteroaromatic group containing 1 or 2 heter...
10.
US20130217776A1
2013/8/22
US13/552699
2012/7/19
专利标题
:Combination of a serotonin reuptake inhibitor and agomelatine
专利权人
:
H. Lundbeck A/s
;
The present invention relates to the use of a combination of agomelatine and a serotonin reuptake inhibitor (SRIs) or any other compound which causes an elevation in the level of extracellular serotonin for the treatment of depression and other affective disorders.
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