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Kim Andersen

Showing results (11-20 of 19) with videos related to

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Bioorganic & Medicinal Chemistry|July 25, 2003
Synthesis and biological evaluation of novel carbon-11-labelled analogues of citalopram as potential radioligands for the serotonin transporterJacob Madsen, Pinelopi Merachtsaki, Padideh Davoodpour, et al.
Bioorganic & Medicinal Chemistry Letters|April 6, 2002
Solid-phase synthesis and pharmacological evaluation of analogues of PhTX-12-A potent and selective nicotinic acetylcholine receptor antagonistKristian Strømgaard, Ian R Mellor, Kim Andersen, et al.
Nuclear Medicine and Biology|March 19, 2004
New alpha(1)-adrenoceptor antagonists derived from the antipsychotic sertindole - carbon-11 labelling and pet examination of brain uptake in the cynomolgus monkeyThomas Balle, Christer Halldin, Linus Andersen, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
N-Heteroaryl glycinamides and glycinamines as potent NPY5 antagonistsLingyun Wu, Kai Lu, Mahesh Desai, et al.
Bioorganic & Medicinal Chemistry Letters|July 1, 2004
The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitorsGarrick Smith, Thomas Ruhland, Gitte Mikkelsen, et al.
Bioorganic & Medicinal Chemistry Letters|September 20, 2011
5-(2'-Pyridyl)-2-aminothiazoles: alkyl amino sulfonamides and sulfamides as potent NPY(5) antagonistsMathivanan Packiarajan, Heather Coate, Mahesh Desai, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
Discovery of Lu AA33810: a highly selective and potent NPY5 antagonist with in vivo efficacy in a model of mood disorderMathivanan Packiarajan, Mohammad R Marzabadi, Mahesh Desai, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists Part 1. The discovery of arylacetamides as viable replacements for the dihydropyrimidinone moiety of an HTS hitYu Jiang, Chien-An Chen, Kai Lu, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists part 2: A hybrid strategy combining key fragments of HTS hitsChien-An Chen, Yu Jiang, Kai Lu, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Bioorganic & Medicinal Chemistry|July 25, 2003
Synthesis and biological evaluation of novel carbon-11-labelled analogues of citalopram as potential radioligands for the serotonin transporterJacob Madsen, Pinelopi Merachtsaki, Padideh Davoodpour, et al.
Bioorganic & Medicinal Chemistry Letters|April 6, 2002
Solid-phase synthesis and pharmacological evaluation of analogues of PhTX-12-A potent and selective nicotinic acetylcholine receptor antagonistKristian Strømgaard, Ian R Mellor, Kim Andersen, et al.
Nuclear Medicine and Biology|March 19, 2004
New alpha(1)-adrenoceptor antagonists derived from the antipsychotic sertindole - carbon-11 labelling and pet examination of brain uptake in the cynomolgus monkeyThomas Balle, Christer Halldin, Linus Andersen, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
N-Heteroaryl glycinamides and glycinamines as potent NPY5 antagonistsLingyun Wu, Kai Lu, Mahesh Desai, et al.
Bioorganic & Medicinal Chemistry Letters|July 1, 2004
The synthesis and SAR of 2-arylsulfanyl-phenyl piperazinyl acetic acids as glyT-1 inhibitorsGarrick Smith, Thomas Ruhland, Gitte Mikkelsen, et al.
Bioorganic & Medicinal Chemistry Letters|September 20, 2011
5-(2'-Pyridyl)-2-aminothiazoles: alkyl amino sulfonamides and sulfamides as potent NPY(5) antagonistsMathivanan Packiarajan, Heather Coate, Mahesh Desai, et al.
Bioorganic & Medicinal Chemistry Letters|July 26, 2011
Discovery of Lu AA33810: a highly selective and potent NPY5 antagonist with in vivo efficacy in a model of mood disorderMathivanan Packiarajan, Mohammad R Marzabadi, Mahesh Desai, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists Part 1. The discovery of arylacetamides as viable replacements for the dihydropyrimidinone moiety of an HTS hitYu Jiang, Chien-An Chen, Kai Lu, et al.
Journal of Medicinal Chemistry|August 3, 2007
Synthesis and SAR investigations for novel melanin-concentrating hormone 1 receptor (MCH1) antagonists part 2: A hybrid strategy combining key fragments of HTS hitsChien-An Chen, Yu Jiang, Kai Lu, et al.
Pageof 2