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Science (New York, N.Y.)
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January 19, 2019
The importance of synthetic chemistry in the pharmaceutical industry
Kevin R Campos, Paul J Coleman, Juan C Alvarez, et al.
Bioconjugate Chemistry
|
July 30, 2016
Novel Phosphate Modified Cathepsin B Linkers: Improving Aqueous Solubility and Enhancing Payload Scope of ADCs
Jeffrey C Kern, Deborah Dooney, Rena Zhang, et al.
Bioconjugate Chemistry
|
March 19, 2013
Endosomolytic bioreducible poly(amido amine disulfide) polymer conjugates for the in vivo systemic delivery of siRNA therapeutics
Rubina Giare Parmar, Marina Busuek, Eileen S Walsh, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 13, 2014
Adenosine analogue inhibitors of S-adenosylhomocysteine hydrolase
Antonella Converso, Timothy Hartingh, Mark E Fraley, et al.
The Journal of Organic Chemistry
|
October 30, 2019
Multiple Synthetic Routes to the Mini-Protein Omomyc and Coiled-Coil Domain Truncations
Zachary Z Brown, Claudio Mapelli, Iman Farasat, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of Oxazolobenzimidazoles as Positive Allosteric Modulators for the mGluR2 Receptor
Robert M Garbaccio, Edward J Brnardic, Mark E Fraley, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2016
Discovery of 5-aryl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-ones as positive allosteric modulators of metabotropic glutamate subtype-2 (mGlu2) receptors with efficacy in a preclinical model of psychosis
Mark E Layton, Alexander J Reif, Timothy J Hartingh, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2007
Kinesin spindle protein (KSP) inhibitors. Part V: discovery of 2-propylamino-2,4-diaryl-2,5-dihydropyrroles as potent, water-soluble KSP inhibitors, and modulation of their basicity by beta-fluorination to overcome cellular efflux by P-glycoprotein
Christopher D Cox, Michael J Breslin, David B Whitman, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 23, 2010
3-Aryl-5-phenoxymethyl-1,3-oxazolidin-2-ones as positive allosteric modulators of mGluR2 for the treatment of schizophrenia: Hit-to-lead efforts
Edward J Brnardic, Mark E Fraley, Robert M Garbaccio, et al.
ACS Medicinal Chemistry Letters
|
March 18, 2016
Optimization of Novel Aza-benzimidazolone mGluR2 PAMs with Respect to LLE and PK Properties and Mitigation of CYP TDI
Joseph E Pero, Michael A Rossi, Michael J Kelly, et al.
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Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Science (New York, N.Y.)
|
January 19, 2019
The importance of synthetic chemistry in the pharmaceutical industry
Kevin R Campos, Paul J Coleman, Juan C Alvarez, et al.
Bioconjugate Chemistry
|
July 30, 2016
Novel Phosphate Modified Cathepsin B Linkers: Improving Aqueous Solubility and Enhancing Payload Scope of ADCs
Jeffrey C Kern, Deborah Dooney, Rena Zhang, et al.
Bioconjugate Chemistry
|
March 19, 2013
Endosomolytic bioreducible poly(amido amine disulfide) polymer conjugates for the in vivo systemic delivery of siRNA therapeutics
Rubina Giare Parmar, Marina Busuek, Eileen S Walsh, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 13, 2014
Adenosine analogue inhibitors of S-adenosylhomocysteine hydrolase
Antonella Converso, Timothy Hartingh, Mark E Fraley, et al.
The Journal of Organic Chemistry
|
October 30, 2019
Multiple Synthetic Routes to the Mini-Protein Omomyc and Coiled-Coil Domain Truncations
Zachary Z Brown, Claudio Mapelli, Iman Farasat, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of Oxazolobenzimidazoles as Positive Allosteric Modulators for the mGluR2 Receptor
Robert M Garbaccio, Edward J Brnardic, Mark E Fraley, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2016
Discovery of 5-aryl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-ones as positive allosteric modulators of metabotropic glutamate subtype-2 (mGlu2) receptors with efficacy in a preclinical model of psychosis
Mark E Layton, Alexander J Reif, Timothy J Hartingh, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 31, 2007
Kinesin spindle protein (KSP) inhibitors. Part V: discovery of 2-propylamino-2,4-diaryl-2,5-dihydropyrroles as potent, water-soluble KSP inhibitors, and modulation of their basicity by beta-fluorination to overcome cellular efflux by P-glycoprotein
Christopher D Cox, Michael J Breslin, David B Whitman, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 23, 2010
3-Aryl-5-phenoxymethyl-1,3-oxazolidin-2-ones as positive allosteric modulators of mGluR2 for the treatment of schizophrenia: Hit-to-lead efforts
Edward J Brnardic, Mark E Fraley, Robert M Garbaccio, et al.
ACS Medicinal Chemistry Letters
|
March 18, 2016
Optimization of Novel Aza-benzimidazolone mGluR2 PAMs with Respect to LLE and PK Properties and Mitigation of CYP TDI
Joseph E Pero, Michael A Rossi, Michael J Kelly, et al.
Page
of 4