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Bioorganic & Medicinal Chemistry
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August 4, 2009
Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl-D-aspartate receptors
Cara A Mosley, Scott J Myers, Ernest E Murray, et al.
ACS Medicinal Chemistry Letters
|
May 26, 2018
Discovery of <i>N</i>-Alkyl Piperazine Side Chain Based CXCR4 Antagonists with Improved Drug-like Properties
Yesim A Tahirovic, Valarie M Truax, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
January 20, 2018
Synthesis and SAR of 1,2,3,4-Tetrahydroisoquinoline-Based CXCR4 Antagonists
Robert J Wilson, Edgars Jecs, Eric J Miller, et al.
Journal of Medicinal Chemistry
|
July 28, 2018
Design, Synthesis, and Pharmacological Evaluation of Second-Generation Tetrahydroisoquinoline-Based CXCR4 Antagonists with Favorable ADME Properties
Huy H Nguyen, Michelle B Kim, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
February 20, 2018
Synthesis of Novel Tetrahydroisoquinoline CXCR4 Antagonists with Rigidified Side-Chains
Edgars Jecs, Eric J Miller, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
October 22, 2021
Amino-Heterocycle Tetrahydroisoquinoline CXCR4 Antagonists with Improved ADME Profiles via Late-Stage Buchwald Couplings
Huy H Nguyen, Yesim A Tahirovic, Valarie M Truax, et al.
Journal of Medicinal Chemistry
|
September 20, 2008
Enantiomeric propanolamines as selective N-methyl-D-aspartate 2B receptor antagonists
Yesim A Tahirovic, Matthew Geballe, Ewa Gruszecka-Kowalik, et al.
Journal of Medicinal Chemistry
|
January 20, 2018
Discovery of Tetrahydroisoquinoline-Containing CXCR4 Antagonists with Improved in Vitro ADMET Properties
Eric J Miller, Edgars Jecs, Valarie M Truax, et al.
Journal of Medicinal Chemistry
|
February 18, 2022
Synthesis and Evaluation of Novel Tetrahydronaphthyridine CXCR4 Antagonists with Improved Drug-like Profiles
Edgars Jecs, Yesim A Tahirovic, Robert J Wilson, et al.
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Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Bioorganic & Medicinal Chemistry
|
August 4, 2009
Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl-D-aspartate receptors
Cara A Mosley, Scott J Myers, Ernest E Murray, et al.
ACS Medicinal Chemistry Letters
|
May 26, 2018
Discovery of <i>N</i>-Alkyl Piperazine Side Chain Based CXCR4 Antagonists with Improved Drug-like Properties
Yesim A Tahirovic, Valarie M Truax, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
January 20, 2018
Synthesis and SAR of 1,2,3,4-Tetrahydroisoquinoline-Based CXCR4 Antagonists
Robert J Wilson, Edgars Jecs, Eric J Miller, et al.
Journal of Medicinal Chemistry
|
July 28, 2018
Design, Synthesis, and Pharmacological Evaluation of Second-Generation Tetrahydroisoquinoline-Based CXCR4 Antagonists with Favorable ADME Properties
Huy H Nguyen, Michelle B Kim, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
February 20, 2018
Synthesis of Novel Tetrahydroisoquinoline CXCR4 Antagonists with Rigidified Side-Chains
Edgars Jecs, Eric J Miller, Robert J Wilson, et al.
ACS Medicinal Chemistry Letters
|
October 22, 2021
Amino-Heterocycle Tetrahydroisoquinoline CXCR4 Antagonists with Improved ADME Profiles via Late-Stage Buchwald Couplings
Huy H Nguyen, Yesim A Tahirovic, Valarie M Truax, et al.
Journal of Medicinal Chemistry
|
September 20, 2008
Enantiomeric propanolamines as selective N-methyl-D-aspartate 2B receptor antagonists
Yesim A Tahirovic, Matthew Geballe, Ewa Gruszecka-Kowalik, et al.
Journal of Medicinal Chemistry
|
January 20, 2018
Discovery of Tetrahydroisoquinoline-Containing CXCR4 Antagonists with Improved in Vitro ADMET Properties
Eric J Miller, Edgars Jecs, Valarie M Truax, et al.
Journal of Medicinal Chemistry
|
February 18, 2022
Synthesis and Evaluation of Novel Tetrahydronaphthyridine CXCR4 Antagonists with Improved Drug-like Profiles
Edgars Jecs, Yesim A Tahirovic, Robert J Wilson, et al.
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