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In Situ Measurement of Solvent-Mediated Phase Transformations During Dissolution Testing
In Situ Measurement of Solvent-Mediated Phase Transformations During Dissolution Testing
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In Situ Measurement of Solvent-Mediated Phase Transformations During Dissolution Testing

Aaltonen, Jaakko ; Heinänen, Paula ; Peltonen, Leena ; Kortejärvi, Hanna ; Tanninen, Veli Pekka ; Christiansen, Leena ; Hirvonen, Jouni ; Yliruusi, Jouko ; Rantanen, Jukka

Journal of pharmaceutical sciences, 2006-12, Vol.95 (12), p.2730-2737 [Periódico revisado por pares]

Hoboken: Elsevier Inc

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2
Route of administration and sex differences in the pharmacokinetics of aspirin, administered as its lysine salt
Route of administration and sex differences in the pharmacokinetics of aspirin, administered as its lysine salt
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Route of administration and sex differences in the pharmacokinetics of aspirin, administered as its lysine salt

AARONS, L ; HOPKINS, K ; ROWLAND, M ; BROSSEL, S ; THIERCELIN, J.-F

Pharmaceutical research, 1989-08, Vol.6 (8), p.660-666 [Periódico revisado por pares]

New York, NY: Springer

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3
An Improved Synthesis of the Antiulcer Drug Ranitidine from N-[2-[[[5-(hydroxymethyl)-2-furanyl]-methyl]-thio]-ethyl]-N′-methyl-2-nitro-1,1-ethenediamine
An Improved Synthesis of the Antiulcer Drug Ranitidine from N-[2-[[[5-(hydroxymethyl)-2-furanyl]-methyl]-thio]-ethyl]-N′-methyl-2-nitro-1,1-ethenediamine
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An Improved Synthesis of the Antiulcer Drug Ranitidine from N-[2-[[[5-(hydroxymethyl)-2-furanyl]-methyl]-thio]-ethyl]-N′-methyl-2-nitro-1,1-ethenediamine

Aasen, Arne Jørgeb ; Skramstad, Jan

Archiv der Pharmazie (Weinheim), 1998-06, Vol.331 (6), p.228-229 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag GmbH

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4
Role of Guanylyl Cyclase Activation via Thiamine in Suppressing Chemically-induced Writhing in Mouse
Role of Guanylyl Cyclase Activation via Thiamine in Suppressing Chemically-induced Writhing in Mouse
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Role of Guanylyl Cyclase Activation via Thiamine in Suppressing Chemically-induced Writhing in Mouse

Abacioğlu, Nurettin ; Demir, Sema ; Çakici, İclal ; Tunçtan, Bahar ; Kanzik, İlker

Arzneimittel-Forschung, 2000-06, Vol.50 (6), p.554-558

Aulendorf (Germany): Editio Cantor Verlag

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5
Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activities of Morphine and Mepyramine in Mice
Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activities of Morphine and Mepyramine in Mice
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Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activities of Morphine and Mepyramine in Mice

ABACIOGLU, Nurettin ; ÖZMEN, Rüya ; CAKICI, Iclal ; TUNCTAN, Bahar ; KANZIK, Ilker

Arzneimittel-Forschung, 2001-01, Vol.51 (12), p.977-983

Aulendorf (Germany): Editio Cantor Verlag

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6
The Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activity of Pyridoxine in Mouse
The Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activity of Pyridoxine in Mouse
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The Role of L-Arginine/Nitric Oxide Pathway in the Antinociceptive Activity of Pyridoxine in Mouse

Abacioğlu, Nurettin ; Tunçtan, Bahar ; Çakici, İiclal ; Akbulut, Esen ; Uludağ, Orhan ; Kanzik, İlker

Arzneimittel-Forschung, 2001-10, Vol.51 (10), p.832-838

Aulendorf (Germany): Editio Cantor Verlag

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7
Synthesis of active nitroguaiacol ether derivatives of streptomycin
Synthesis of active nitroguaiacol ether derivatives of streptomycin
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Synthesis of active nitroguaiacol ether derivatives of streptomycin

ABAD, J. P ; AMILS, R

Antimicrobial Agents and Chemotherapy, 1990-10, Vol.34 (10), p.1908-1914 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

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8
5-Substituted 2-Bromoindolo[3,2-b]quinoxalines. A Class of Potential Antitumor Agents with cdc25 Phosphatase Inhibitory Properties
5-Substituted 2-Bromoindolo[3,2-b]quinoxalines. A Class of Potential Antitumor Agents with cdc25 Phosphatase Inhibitory Properties
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5-Substituted 2-Bromoindolo[3,2-b]quinoxalines. A Class of Potential Antitumor Agents with cdc25 Phosphatase Inhibitory Properties

Abadi, Ashraf H.

Archiv der Pharmazie (Weinheim), 1998-11, Vol.331 (11), p.352-358 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag GmbH

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9
Phenylpiperazinylmethylheterocycle Derivatives: Synthesis and Dopamine Receptor Binding Profiles
Phenylpiperazinylmethylheterocycle Derivatives: Synthesis and Dopamine Receptor Binding Profiles
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Phenylpiperazinylmethylheterocycle Derivatives: Synthesis and Dopamine Receptor Binding Profiles

Abadi, Ashraf H.

Archiv der Pharmazie (Weinheim), 2004-07, Vol.337 (7), p.383-390 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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10
Synthesis and Evaluation of Novel 7-Trifluoromethyl-4-(4-substituted anilino)quinolines as Antiparasitic and Antineoplastic Agents
Synthesis and Evaluation of Novel 7-Trifluoromethyl-4-(4-substituted anilino)quinolines as Antiparasitic and Antineoplastic Agents
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Synthesis and Evaluation of Novel 7-Trifluoromethyl-4-(4-substituted anilino)quinolines as Antiparasitic and Antineoplastic Agents

Abadi, Ashraf H. ; Brun, Reto

Arzneimittel-Forschung, 2003-01, Vol.53 (9), p.655-663

Aulendorf (Germany): Editio Cantor Verlag

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