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Journal of Medicinal Chemistry
|
March 4, 1994
1-((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo [2.2.1]-heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperaz ine (L-368,899): an orally bioavailable, non-peptide oxytocin antagonist with potential utility for managing preterm labor
P D Williams, P S Anderson, R G Ball, et al.
Bioorganic & Medicinal Chemistry
|
September 1, 1994
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation
P D Williams, R G Ball, B V Clineschmidt, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 28, 1999
Imidazole-containing diarylether and diarylsulfone inhibitors of farnesyl-protein transferase
C J Dinsmore, T M Williams, T J O'Neill, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 18, 1999
Non-thiol 3-aminomethylbenzamide inhibitors of farnesyl-protein transferase
T M Ciccarone, S C MacTough, T M Williams, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 19, 2001
Evaluation of amino acid-based linkers in potent macrocyclic inhibitors of farnesyl-protein transferase
D C Beshore, I M Bell, C J Dinsmore, et al.
Journal of Medicinal Chemistry
|
August 25, 2001
Design and biological activity of (S)-4-(5-([1-(3-chlorobenzyl)-2-oxopyrrolidin-3-ylamino]methyl)imidazol-1-ylmethyl)benzonitrile, a 3-aminopyrrolidinone farnesyltransferase inhibitor with excellent cell potency
I M Bell, S N Gallicchio, M Abrams, et al.
Page
of 2
Search research articles
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Journal of Medicinal Chemistry
|
March 4, 1994
1-((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo [2.2.1]-heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperaz ine (L-368,899): an orally bioavailable, non-peptide oxytocin antagonist with potential utility for managing preterm labor
P D Williams, P S Anderson, R G Ball, et al.
Bioorganic & Medicinal Chemistry
|
September 1, 1994
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation
P D Williams, R G Ball, B V Clineschmidt, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 28, 1999
Imidazole-containing diarylether and diarylsulfone inhibitors of farnesyl-protein transferase
C J Dinsmore, T M Williams, T J O'Neill, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 18, 1999
Non-thiol 3-aminomethylbenzamide inhibitors of farnesyl-protein transferase
T M Ciccarone, S C MacTough, T M Williams, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 19, 2001
Evaluation of amino acid-based linkers in potent macrocyclic inhibitors of farnesyl-protein transferase
D C Beshore, I M Bell, C J Dinsmore, et al.
Journal of Medicinal Chemistry
|
August 25, 2001
Design and biological activity of (S)-4-(5-([1-(3-chlorobenzyl)-2-oxopyrrolidin-3-ylamino]methyl)imidazol-1-ylmethyl)benzonitrile, a 3-aminopyrrolidinone farnesyltransferase inhibitor with excellent cell potency
I M Bell, S N Gallicchio, M Abrams, et al.
Page
of 2