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Journal of Medicinal Chemistry
|
June 21, 1996
Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: significance of the "aromatic" nature of the novel ester-type coumarin for strong inhibitory activity
L Pochet, C Doucet, M Schynts, et al.
Journal De Pharmacie De Belgique
|
July 1, 1997
Pharmacomodulation of torasemide led to original diuretic, neuroprotective, anticonvulsant and antithrombotic drugs
B Masereel, J M Dogné, J Damas, et al.
Journal of Medicinal Chemistry
|
July 27, 2001
Original 2-alkylamino-6-halogenoquinazolin-4(3H)-ones and K(ATP) channel activity
F Somers, R Ouedraogo, M H Antoine, et al.
Bioorganic & Medicinal Chemistry
|
September 11, 1999
Preparation and pharmacological evaluation of the R- and S-enantiomers of 3-(2-butylamino)-4H- and 3-(3-methyl-2-butylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxide, two tissue selective ATP-sensitive potassium channel openers
S Khelili, P de Tullio, P Lebrun, et al.
Journal of Medicinal Chemistry
|
February 16, 1996
3-and 4-substituted 4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides as potassium channel openers: synthesis, pharmacological evaluation, and structure-activity relationships
P de Tullio, B Pirotte, P Lebrun, et al.
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Search research articles
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Showing results (81-90 of 85) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 85 results.
Journal of Medicinal Chemistry
|
June 21, 1996
Esters and amides of 6-(chloromethyl)-2-oxo-2H-1-benzopyran-3-carboxylic acid as inhibitors of alpha-chymotrypsin: significance of the "aromatic" nature of the novel ester-type coumarin for strong inhibitory activity
L Pochet, C Doucet, M Schynts, et al.
Journal De Pharmacie De Belgique
|
July 1, 1997
Pharmacomodulation of torasemide led to original diuretic, neuroprotective, anticonvulsant and antithrombotic drugs
B Masereel, J M Dogné, J Damas, et al.
Journal of Medicinal Chemistry
|
July 27, 2001
Original 2-alkylamino-6-halogenoquinazolin-4(3H)-ones and K(ATP) channel activity
F Somers, R Ouedraogo, M H Antoine, et al.
Bioorganic & Medicinal Chemistry
|
September 11, 1999
Preparation and pharmacological evaluation of the R- and S-enantiomers of 3-(2-butylamino)-4H- and 3-(3-methyl-2-butylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxide, two tissue selective ATP-sensitive potassium channel openers
S Khelili, P de Tullio, P Lebrun, et al.
Journal of Medicinal Chemistry
|
February 16, 1996
3-and 4-substituted 4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxides as potassium channel openers: synthesis, pharmacological evaluation, and structure-activity relationships
P de Tullio, B Pirotte, P Lebrun, et al.
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of 9