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D M Floyd

Showing results (11-20 of 26) with videos related to

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The Journal of Organic Chemistry|September 22, 1972
11,15-Epiprostaglandin E 2 and its enantiomer. Biological activity and synthesisE J Corey, S Terashima, P W Ramwell, et al.
Journal of Medicinal Chemistry|February 1, 1991
Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agentsK S Atwal, B N Swanson, S E Unger, et al.
Journal of Medicinal Chemistry|May 1, 1990
Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridinesK S Atwal, G C Rovnyak, J Schwartz, et al.
Journal - Association of Official Analytical Chemists|March 1, 1981
Extraction of light filth from tea: collaborative studyF F Lim, J Barnett, A Bright, et al.
The Journal of Antimicrobial Chemotherapy|December 1, 1981
Monobactams: isolation and structure determinationW L Parker, C M Cimarusti, D M Floyd, et al.
Journal of Medicinal Chemistry|February 4, 1994
The discovery of sulfonamide endothelin antagonists and the development of the orally active ETA antagonist 5-(dimethylamino)-N-(3,4-dimethyl-5-isoxazolyl)-1-naphthalenesulf onamideP D Stein, J T Hunt, D M Floyd, et al.
Bioorganic & Medicinal Chemistry|July 1, 1993
Structure-activity studies of endothelin leading to novel peptide ETA antagonistsJ T Hunt, V G Lee, D McMullen, et al.
Journal of Medicinal Chemistry|April 14, 1995
Discovery and structure-activity relationships of sulfonamide ETA-selective antagonistsP D Stein, D M Floyd, S Bisaha, et al.
Journal of Medicinal Chemistry|February 21, 1992
Benzazepinone calcium channel blockers. 4. Structure-activity overview and intracellular binding siteS D Kimball, D M Floyd, J Das, et al.
Journal of Medicinal Chemistry|July 10, 1992
Benzazepinone calcium channel blockers. 5. Effects on antihypertensive activity associated with N1 and aromatic substituentsJ Das, D M Floyd, S D Kimball, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
The Journal of Organic Chemistry|September 22, 1972
11,15-Epiprostaglandin E 2 and its enantiomer. Biological activity and synthesisE J Corey, S Terashima, P W Ramwell, et al.
Journal of Medicinal Chemistry|February 1, 1991
Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agentsK S Atwal, B N Swanson, S E Unger, et al.
Journal of Medicinal Chemistry|May 1, 1990
Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridinesK S Atwal, G C Rovnyak, J Schwartz, et al.
Journal - Association of Official Analytical Chemists|March 1, 1981
Extraction of light filth from tea: collaborative studyF F Lim, J Barnett, A Bright, et al.
The Journal of Antimicrobial Chemotherapy|December 1, 1981
Monobactams: isolation and structure determinationW L Parker, C M Cimarusti, D M Floyd, et al.
Journal of Medicinal Chemistry|February 4, 1994
The discovery of sulfonamide endothelin antagonists and the development of the orally active ETA antagonist 5-(dimethylamino)-N-(3,4-dimethyl-5-isoxazolyl)-1-naphthalenesulf onamideP D Stein, J T Hunt, D M Floyd, et al.
Bioorganic & Medicinal Chemistry|July 1, 1993
Structure-activity studies of endothelin leading to novel peptide ETA antagonistsJ T Hunt, V G Lee, D McMullen, et al.
Journal of Medicinal Chemistry|April 14, 1995
Discovery and structure-activity relationships of sulfonamide ETA-selective antagonistsP D Stein, D M Floyd, S Bisaha, et al.
Journal of Medicinal Chemistry|February 21, 1992
Benzazepinone calcium channel blockers. 4. Structure-activity overview and intracellular binding siteS D Kimball, D M Floyd, J Das, et al.
Journal of Medicinal Chemistry|July 10, 1992
Benzazepinone calcium channel blockers. 5. Effects on antihypertensive activity associated with N1 and aromatic substituentsJ Das, D M Floyd, S D Kimball, et al.
Pageof 3