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G Rihs

Showing results (1-10 of 11) with videos related to

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Helvetica Chimica Acta|March 10, 1972
[Crystal structure of 3 -acetoxy-17 -iodo- 5 -androstenes]H C Mez, G Rihs
Acta Crystallographica. Section C, Crystal Structure Communications|May 18, 2000
Sodium mycophenolateG Rihs, C Papageorgiou, S Pfeffer
Journal of Medicinal Chemistry|July 1, 1983
Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. 2. Mode of action and X-ray structure of 1-[[p-[2-(crotonylamino)ethyl]phenyl]sulfonyl]-3-cyclohexyl-2-iminoimidazolidineE H Schweizer, F Märki, G Rihs
Archiv Der Pharmazie|July 1, 1996
Sulfogriseofulvin derivatives. synthesis by [4 + 2]cycloaddition, structure, properties, crystal structure analysis, and antifungal activity of spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxidesM Friedrich, W Meichle, H Bernhard, et al.
Journal of Medicinal Chemistry|May 14, 1993
Aromatase inhibitors: synthesis, biological activity, and binding mode of azole-type compoundsP Furet, C Batzl, A Bhatnagar, et al.
Inorganic Chemistry|April 17, 2001
Synthesis, structural characterization, and conformational bias in solution of a sterically congested pyrophosphite: experimental and computational evidence for restricted rotation about an sp3-sp3 P-O single bondA D DeBellis, S D Pastor, G Rihs, et al.
The Journal of Antibiotics|June 1, 1988
Synthesis and biological activity of 2-lactonyl penemsH G Capraro, E Francotte, B Kohler, et al.
Journal of Medicinal Chemistry|April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinaseU Trinks, E Buchdunger, P Furet, et al.
Journal of Medicinal Chemistry|July 21, 1995
5-Methyl-6-phenyl-1,3,5,6-tetrahydro-3,6-methano-1,5-benzodiazocine-2,4-dione (BA 41899): representative of a novel class of purely calcium-sensitizing agentsP Herold, J W Herzig, P Wenk, et al.
Journal of Medicinal Chemistry|November 23, 2000
Chiral resolution, pharmacological characterization, and receptor docking of the noncompetitive mGlu1 receptor antagonist (+/-)-2-hydroxyimino- 1a, 2-dihydro-1H-7-oxacyclopropa[b]naphthalene-7a-carboxylic acid ethyl esterD Ott, P Floersheim, W Inderbitzin, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Helvetica Chimica Acta|March 10, 1972
[Crystal structure of 3 -acetoxy-17 -iodo- 5 -androstenes]H C Mez, G Rihs
Acta Crystallographica. Section C, Crystal Structure Communications|May 18, 2000
Sodium mycophenolateG Rihs, C Papageorgiou, S Pfeffer
Journal of Medicinal Chemistry|July 1, 1983
Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. 2. Mode of action and X-ray structure of 1-[[p-[2-(crotonylamino)ethyl]phenyl]sulfonyl]-3-cyclohexyl-2-iminoimidazolidineE H Schweizer, F Märki, G Rihs
Archiv Der Pharmazie|July 1, 1996
Sulfogriseofulvin derivatives. synthesis by [4 + 2]cycloaddition, structure, properties, crystal structure analysis, and antifungal activity of spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxidesM Friedrich, W Meichle, H Bernhard, et al.
Journal of Medicinal Chemistry|May 14, 1993
Aromatase inhibitors: synthesis, biological activity, and binding mode of azole-type compoundsP Furet, C Batzl, A Bhatnagar, et al.
Inorganic Chemistry|April 17, 2001
Synthesis, structural characterization, and conformational bias in solution of a sterically congested pyrophosphite: experimental and computational evidence for restricted rotation about an sp3-sp3 P-O single bondA D DeBellis, S D Pastor, G Rihs, et al.
The Journal of Antibiotics|June 1, 1988
Synthesis and biological activity of 2-lactonyl penemsH G Capraro, E Francotte, B Kohler, et al.
Journal of Medicinal Chemistry|April 1, 1994
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinaseU Trinks, E Buchdunger, P Furet, et al.
Journal of Medicinal Chemistry|July 21, 1995
5-Methyl-6-phenyl-1,3,5,6-tetrahydro-3,6-methano-1,5-benzodiazocine-2,4-dione (BA 41899): representative of a novel class of purely calcium-sensitizing agentsP Herold, J W Herzig, P Wenk, et al.
Journal of Medicinal Chemistry|November 23, 2000
Chiral resolution, pharmacological characterization, and receptor docking of the noncompetitive mGlu1 receptor antagonist (+/-)-2-hydroxyimino- 1a, 2-dihydro-1H-7-oxacyclopropa[b]naphthalene-7a-carboxylic acid ethyl esterD Ott, P Floersheim, W Inderbitzin, et al.
Pageof 2