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ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of SCH 900271, a Potent Nicotinic Acid Receptor Agonist for the Treatment of Dyslipidemia
Anandan Palani, Ashwin U Rao, Xiao Chen, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
Discovery of MK-8318, a Potent and Selective CRTh2 Receptor Antagonist for the Treatment of Asthma
Xianhai Huang, Jason Brubaker, Wei Zhou, et al.
Journal of Medicinal Chemistry
|
June 26, 2024
Discovery of MK-1084: An Orally Bioavailable and Low-Dose KRAS<sup>G12C</sup> Inhibitor
Xiaoshen Ma, David L Sloman, Ruchia Duggal, et al.
Journal of Medicinal Chemistry
|
April 9, 2026
From KRAS<sup><i>G12D</i></sup> to Pan-KRAS Inhibitors─A Journey Enabled by Synthetic Innovation and Structure-Based Drug Design
Xiaoshen Ma, David L Sloman, Timothy J Henderson, et al.
Journal of Medicinal Chemistry
|
November 22, 2011
Cyclic hydroxyamidines as amide isosteres: discovery of oxadiazolines and oxadiazines as potent and highly efficacious γ-secretase modulators in vivo
Zhong-Yue Sun, Theodros Asberom, Thomas Bara, et al.
Journal of Medicinal Chemistry
|
December 21, 2021
Development of ProTx-II Analogues as Highly Selective Peptide Blockers of Na<sub>v</sub>1.7 for the Treatment of Pain
Gregory L Adams, Parul S Pall, Steven M Grauer, et al.
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Showing results (51-60 of 56) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 56 results.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of SCH 900271, a Potent Nicotinic Acid Receptor Agonist for the Treatment of Dyslipidemia
Anandan Palani, Ashwin U Rao, Xiao Chen, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
Discovery of MK-8318, a Potent and Selective CRTh2 Receptor Antagonist for the Treatment of Asthma
Xianhai Huang, Jason Brubaker, Wei Zhou, et al.
Journal of Medicinal Chemistry
|
June 26, 2024
Discovery of MK-1084: An Orally Bioavailable and Low-Dose KRAS<sup>G12C</sup> Inhibitor
Xiaoshen Ma, David L Sloman, Ruchia Duggal, et al.
Journal of Medicinal Chemistry
|
April 9, 2026
From KRAS<sup><i>G12D</i></sup> to Pan-KRAS Inhibitors─A Journey Enabled by Synthetic Innovation and Structure-Based Drug Design
Xiaoshen Ma, David L Sloman, Timothy J Henderson, et al.
Journal of Medicinal Chemistry
|
November 22, 2011
Cyclic hydroxyamidines as amide isosteres: discovery of oxadiazolines and oxadiazines as potent and highly efficacious γ-secretase modulators in vivo
Zhong-Yue Sun, Theodros Asberom, Thomas Bara, et al.
Journal of Medicinal Chemistry
|
December 21, 2021
Development of ProTx-II Analogues as Highly Selective Peptide Blockers of Na<sub>v</sub>1.7 for the Treatment of Pain
Gregory L Adams, Parul S Pall, Steven M Grauer, et al.
Page
of 6