J C Lancelot - JoVE Visualize

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Farmaco (Societa Chimica Italiana : 1989)|March 1, 1997

Synthesis and pharmacological activities of some 2,3,4,5-tetrahydro[1,5]benzo[f]thiazepinesC Saturnino, P Saturnino, G De Martino, et al.

Bioorganic & Medicinal Chemistry Letters|March 7, 2001

First tricyclic oximino derivatives as 5-HT3 ligandsI Baglin, C Daveu, J C Lancelot, et al.

Allergie Et Immunologie|November 1, 1988

[Potential interest in powerful and specific ligands for the histamine H3 receptor]J M Arrang, M Garbarg, J C Lancelot, et al.

Nature|May 14, 1987

Highly potent and selective ligands for histamine H3-receptorsJ M Arrang, M Garbarg, J C Lancelot, et al.

Metal-Based Drugs|May 14, 2008

In Vivo Nitric Oxide Synthase Inhibitors Can Be Deprived of This Activity: Unexpected Influence of the Tetrachloroplatinate(II) Counteranion. Crystal Structures of Bis(S-Methyl-Isothiouronium)-N,N'-Bis(3-Guanidinopropyl)Piperazinium and Hexamidinium Tetrachloroplatinates(II) SaltsG Morgant, B Viossat, M Roch-Arveiller, et al.

International Archives of Allergy and Applied Immunology|January 1, 1989

The third histamine receptor. Highly potent and selective ligandsJ M Arrang, M Garbarg, J C Lancelot, et al.

European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|November 22, 1997

In vivo inhibition of nitric oxide synthase by bisisothiouronium and bisguanidinium saltsM Roch-Arveiller, C Regnault, J P Giroud, et al.

Investigative Radiology|September 1, 1988

Highly potent and selective ligands for a new class H3 of histamine receptorJ M Arrang, M Garbarg, J C Lancelot, et al.

Anti-Cancer Drug Design|July 20, 2000

Biological properties of 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles: a new class of potent antitumour drugsV Moinet-Hedin, T Tabka, L Poulain, et al.

Mutation Research|March 17, 1997

Mutagenicity of nitro- and amino-substituted carbazoles in Salmonella typhimurium. III. Methylated derivatives of 9H-carbazoleV André, C Boissart, F Sichel, et al.

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Showing results (11-20 of 24) with videos related to

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Farmaco (Societa Chimica Italiana : 1989)|March 1, 1997

Synthesis and pharmacological activities of some 2,3,4,5-tetrahydro[1,5]benzo[f]thiazepinesC Saturnino, P Saturnino, G De Martino, et al.

Bioorganic & Medicinal Chemistry Letters|March 7, 2001

First tricyclic oximino derivatives as 5-HT3 ligandsI Baglin, C Daveu, J C Lancelot, et al.

Allergie Et Immunologie|November 1, 1988

[Potential interest in powerful and specific ligands for the histamine H3 receptor]J M Arrang, M Garbarg, J C Lancelot, et al.

Nature|May 14, 1987

Highly potent and selective ligands for histamine H3-receptorsJ M Arrang, M Garbarg, J C Lancelot, et al.

Metal-Based Drugs|May 14, 2008

In Vivo Nitric Oxide Synthase Inhibitors Can Be Deprived of This Activity: Unexpected Influence of the Tetrachloroplatinate(II) Counteranion. Crystal Structures of Bis(S-Methyl-Isothiouronium)-N,N'-Bis(3-Guanidinopropyl)Piperazinium and Hexamidinium Tetrachloroplatinates(II) SaltsG Morgant, B Viossat, M Roch-Arveiller, et al.

International Archives of Allergy and Applied Immunology|January 1, 1989

The third histamine receptor. Highly potent and selective ligandsJ M Arrang, M Garbarg, J C Lancelot, et al.

European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|November 22, 1997

In vivo inhibition of nitric oxide synthase by bisisothiouronium and bisguanidinium saltsM Roch-Arveiller, C Regnault, J P Giroud, et al.

Investigative Radiology|September 1, 1988

Highly potent and selective ligands for a new class H3 of histamine receptorJ M Arrang, M Garbarg, J C Lancelot, et al.

Anti-Cancer Drug Design|July 20, 2000

Biological properties of 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles: a new class of potent antitumour drugsV Moinet-Hedin, T Tabka, L Poulain, et al.

Mutation Research|March 17, 1997

Mutagenicity of nitro- and amino-substituted carbazoles in Salmonella typhimurium. III. Methylated derivatives of 9H-carbazoleV André, C Boissart, F Sichel, et al.

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