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Ruo Xu

Showing results (71-80 of 84) with videos related to

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Molecular Plant-Microbe Interactions : MPMI|May 5, 2015
Broadly Conserved Fungal Effector BEC1019 Suppresses Host Cell Death and Enhances Pathogen Virulence in Powdery Mildew of Barley (Hordeum vulgare L.)Ehren Whigham, Shan Qi, Divya Mistry, et al.
Journal of Medicinal Chemistry|October 27, 2015
Discovery of a Novel, Potent Spirocyclic Series of γ-Secretase InhibitorsZhiqiang Zhao, Dmitri A Pissarnitski, Hubert B Josien, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2007
Discovery of 2,4,6-trisubstituted N-arylsulfonyl piperidines as gamma-secretase inhibitorsHongmei Li, Theodros Asberom, Thomas A Bara, et al.
Bioorganic & Medicinal Chemistry|January 31, 2006
Bicyclic[4.1.0]heptanes as phenyl replacements for melanin concentrating hormone receptor antagonistsRuo Xu, Shengjian Li, Jaroslava Paruchova, et al.
ACS Central Science|July 6, 2018
Lipid-Protein Interactions Are Unique Fingerprints for Membrane ProteinsValentina Corradi, Eduardo Mendez-Villuendas, Helgi I Ingólfsson, et al.
Bioorganic & Medicinal Chemistry Letters|February 26, 2004
SAR development of polycyclic guanine derivatives targeted to the discovery of a selective PDE5 inhibitor for treatment of erectile dysfunctionDmitri A Pissarnitski, Theodros Asberom, Craig D Boyle, et al.
European Journal of Medicinal Chemistry|August 26, 2016
Substituted 4-morpholine N-arylsulfonamides as γ-secretase inhibitorsZhiqiang Zhao, Dmitri A Pissarnitski, Hubert B Josien, et al.
Journal of Medicinal Chemistry|March 31, 2006
Discovery of orally efficacious melanin-concentrating hormone receptor-1 antagonists as antiobesity agents. Synthesis, SAR, and biological evaluation of bicyclo[3.1.0]hexyl ureasMark D McBriar, Henry Guzik, Sherry Shapiro, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2002
Design and synthesis of xanthine analogues as potent and selective PDE5 inhibitorsYuguang Wang, Samuel Chackalamannil, Zhiyong Hu, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of SCH 900229, a Potent Presenilin 1 Selective γ-Secretase Inhibitor for the Treatment of Alzheimer's DiseaseWen-Lian Wu, Martin Domalski, Duane A Burnett, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Molecular Plant-Microbe Interactions : MPMI|May 5, 2015
Broadly Conserved Fungal Effector BEC1019 Suppresses Host Cell Death and Enhances Pathogen Virulence in Powdery Mildew of Barley (Hordeum vulgare L.)Ehren Whigham, Shan Qi, Divya Mistry, et al.
Journal of Medicinal Chemistry|October 27, 2015
Discovery of a Novel, Potent Spirocyclic Series of γ-Secretase InhibitorsZhiqiang Zhao, Dmitri A Pissarnitski, Hubert B Josien, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2007
Discovery of 2,4,6-trisubstituted N-arylsulfonyl piperidines as gamma-secretase inhibitorsHongmei Li, Theodros Asberom, Thomas A Bara, et al.
Bioorganic & Medicinal Chemistry|January 31, 2006
Bicyclic[4.1.0]heptanes as phenyl replacements for melanin concentrating hormone receptor antagonistsRuo Xu, Shengjian Li, Jaroslava Paruchova, et al.
ACS Central Science|July 6, 2018
Lipid-Protein Interactions Are Unique Fingerprints for Membrane ProteinsValentina Corradi, Eduardo Mendez-Villuendas, Helgi I Ingólfsson, et al.
Bioorganic & Medicinal Chemistry Letters|February 26, 2004
SAR development of polycyclic guanine derivatives targeted to the discovery of a selective PDE5 inhibitor for treatment of erectile dysfunctionDmitri A Pissarnitski, Theodros Asberom, Craig D Boyle, et al.
European Journal of Medicinal Chemistry|August 26, 2016
Substituted 4-morpholine N-arylsulfonamides as γ-secretase inhibitorsZhiqiang Zhao, Dmitri A Pissarnitski, Hubert B Josien, et al.
Journal of Medicinal Chemistry|March 31, 2006
Discovery of orally efficacious melanin-concentrating hormone receptor-1 antagonists as antiobesity agents. Synthesis, SAR, and biological evaluation of bicyclo[3.1.0]hexyl ureasMark D McBriar, Henry Guzik, Sherry Shapiro, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2002
Design and synthesis of xanthine analogues as potent and selective PDE5 inhibitorsYuguang Wang, Samuel Chackalamannil, Zhiyong Hu, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of SCH 900229, a Potent Presenilin 1 Selective γ-Secretase Inhibitor for the Treatment of Alzheimer's DiseaseWen-Lian Wu, Martin Domalski, Duane A Burnett, et al.
Pageof 9