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Bioorganic & Medicinal Chemistry Letters
|
March 19, 2015
trans-(3S,4S)-Disubstituted pyrrolidines as inhibitors of the human aspartyl protease renin. Part I: prime site exploration using an amino linker
Edwige Lorthiois, Frederic Cumin, Claus Ehrhardt, et al.
Bioorganic & Medicinal Chemistry
|
September 12, 2007
Is adamantane a suitable substituent to pre-organize the acid orientation in E-selectin antagonists?
Alexander Titz, John Patton, André M Alker, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Novel immunomodulator FTY720 is phosphorylated in rats and humans to form a single stereoisomer. Identification, chemical proof, and biological characterization of the biologically active species and its enantiomer
Rainer Albert, Klaus Hinterding, Volker Brinkmann, et al.
Angewandte Chemie (International Ed. in English)
|
May 2, 2018
Novel Amide-Based Molecular Knots: Complete Enantiomeric Separation, Chiroptical Properties, and Absolute Configuration
Fritz Vögtle, Annette Hünten, Erik Vogel, et al.
Journal of Medicinal Chemistry
|
February 22, 2013
The discovery of novel potent trans-3,4-disubstituted pyrrolidine inhibitors of the human aspartic protease renin from in silico three-dimensional (3D) pharmacophore searches
Edwige Lorthiois, Werner Breitenstein, Frederic Cumin, et al.
Journal of Medicinal Chemistry
|
April 2, 2004
Orally bioavailable competitive CCR5 antagonists
Gebhard Thoma, François Nuninger, Marc Schaefer, et al.
Journal of Medicinal Chemistry
|
March 9, 2010
Conformational refinement of hydroxamate-based histone deacetylase inhibitors and exploration of 3-piperidin-3-ylindole analogues of dacinostat (LAQ824)
Young Shin Cho, Lewis Whitehead, Jianke Li, et al.
Journal of Medicinal Chemistry
|
January 31, 2013
A novel class of oral direct renin inhibitors: highly potent 3,5-disubstituted piperidines bearing a tricyclic p3-p1 pharmacophore
Nils Ostermann, Simon Ruedisser, Claus Ehrhardt, et al.
Journal of Medicinal Chemistry
|
June 24, 2010
Spirotetrahydro beta-carbolines (spiroindolones): a new class of potent and orally efficacious compounds for the treatment of malaria
Bryan K S Yeung, Bin Zou, Matthias Rottmann, et al.
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of 2
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Showing results (11-20 of 19) with videos related to
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You have reached the last page of results.
This site can display upto 19 results.
Bioorganic & Medicinal Chemistry Letters
|
March 19, 2015
trans-(3S,4S)-Disubstituted pyrrolidines as inhibitors of the human aspartyl protease renin. Part I: prime site exploration using an amino linker
Edwige Lorthiois, Frederic Cumin, Claus Ehrhardt, et al.
Bioorganic & Medicinal Chemistry
|
September 12, 2007
Is adamantane a suitable substituent to pre-organize the acid orientation in E-selectin antagonists?
Alexander Titz, John Patton, André M Alker, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Novel immunomodulator FTY720 is phosphorylated in rats and humans to form a single stereoisomer. Identification, chemical proof, and biological characterization of the biologically active species and its enantiomer
Rainer Albert, Klaus Hinterding, Volker Brinkmann, et al.
Angewandte Chemie (International Ed. in English)
|
May 2, 2018
Novel Amide-Based Molecular Knots: Complete Enantiomeric Separation, Chiroptical Properties, and Absolute Configuration
Fritz Vögtle, Annette Hünten, Erik Vogel, et al.
Journal of Medicinal Chemistry
|
February 22, 2013
The discovery of novel potent trans-3,4-disubstituted pyrrolidine inhibitors of the human aspartic protease renin from in silico three-dimensional (3D) pharmacophore searches
Edwige Lorthiois, Werner Breitenstein, Frederic Cumin, et al.
Journal of Medicinal Chemistry
|
April 2, 2004
Orally bioavailable competitive CCR5 antagonists
Gebhard Thoma, François Nuninger, Marc Schaefer, et al.
Journal of Medicinal Chemistry
|
March 9, 2010
Conformational refinement of hydroxamate-based histone deacetylase inhibitors and exploration of 3-piperidin-3-ylindole analogues of dacinostat (LAQ824)
Young Shin Cho, Lewis Whitehead, Jianke Li, et al.
Journal of Medicinal Chemistry
|
January 31, 2013
A novel class of oral direct renin inhibitors: highly potent 3,5-disubstituted piperidines bearing a tricyclic p3-p1 pharmacophore
Nils Ostermann, Simon Ruedisser, Claus Ehrhardt, et al.
Journal of Medicinal Chemistry
|
June 24, 2010
Spirotetrahydro beta-carbolines (spiroindolones): a new class of potent and orally efficacious compounds for the treatment of malaria
Bryan K S Yeung, Bin Zou, Matthias Rottmann, et al.
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of 2