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Journal of the American Academy of Dermatology
|
October 1, 1993
Complement polymorphism in herpes gestationis: association with C4 null allele
J K Shornick, C M Artlett, R E Jenkins, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2009
The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore
Brian A Johns, Jason G Weatherhead, Scott H Allen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2009
1,3,4-Oxadiazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 2: SAR of the C5 position
Brian A Johns, Jason G Weatherhead, Scott H Allen, et al.
The Journal of Biological Chemistry
|
October 28, 1994
Potent and selective inhibition of human nitric oxide synthases. Inhibition by non-amino acid isothioureas
E P Garvey, J A Oplinger, G J Tanoury, et al.
Antimicrobial Agents and Chemotherapy
|
September 16, 2015
VT-1161 Protects Immunosuppressed Mice from Rhizopus arrhizus var. arrhizus Infection
Teclegiorgis Gebremariam, Nathan P Wiederhold, Annette W Fothergill, et al.
Antimicrobial Agents and Chemotherapy
|
August 7, 2019
Impact of the Major Candida glabrata Triazole Resistance Determinants on the Activity of the Novel Investigational Tetrazoles VT-1598 and VT-1161
Andrew T Nishimoto, Sarah G Whaley, Nathan P Wiederhold, et al.
Antimicrobial Agents and Chemotherapy
|
June 28, 2017
Prophylactic Treatment with VT-1161 Protects Immunosuppressed Mice from Rhizopus arrhizus var. arrhizus Infection
Teclegiorgis Gebremariam, Sondus Alkhazraji, Lin Lin, et al.
The Journal of Biological Chemistry
|
October 28, 1994
Potent and selective inhibition of human nitric oxide synthases. Selective inhibition of neuronal nitric oxide synthase by S-methyl-L-thiocitrulline and S-ethyl-L-thiocitrulline
E S Furfine, M F Harmon, J E Paith, et al.
Antimicrobial Agents and Chemotherapy
|
May 11, 2016
The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme
Andrew G S Warrilow, Josie E Parker, Claire L Price, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 19, 2012
Naphthyridinone (NTD) integrase inhibitors: N1 protio and methyl combination substituent effects with C3 amide groups
Brian A Johns, Takashi Kawasuji, Jason G Weatherhead, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 122) with videos related to
Sort By:
Page
of 13
Journal of the American Academy of Dermatology
|
October 1, 1993
Complement polymorphism in herpes gestationis: association with C4 null allele
J K Shornick, C M Artlett, R E Jenkins, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2009
The use of oxadiazole and triazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 1: Establishing the pharmacophore
Brian A Johns, Jason G Weatherhead, Scott H Allen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 17, 2009
1,3,4-Oxadiazole substituted naphthyridines as HIV-1 integrase inhibitors. Part 2: SAR of the C5 position
Brian A Johns, Jason G Weatherhead, Scott H Allen, et al.
The Journal of Biological Chemistry
|
October 28, 1994
Potent and selective inhibition of human nitric oxide synthases. Inhibition by non-amino acid isothioureas
E P Garvey, J A Oplinger, G J Tanoury, et al.
Antimicrobial Agents and Chemotherapy
|
September 16, 2015
VT-1161 Protects Immunosuppressed Mice from Rhizopus arrhizus var. arrhizus Infection
Teclegiorgis Gebremariam, Nathan P Wiederhold, Annette W Fothergill, et al.
Antimicrobial Agents and Chemotherapy
|
August 7, 2019
Impact of the Major Candida glabrata Triazole Resistance Determinants on the Activity of the Novel Investigational Tetrazoles VT-1598 and VT-1161
Andrew T Nishimoto, Sarah G Whaley, Nathan P Wiederhold, et al.
Antimicrobial Agents and Chemotherapy
|
June 28, 2017
Prophylactic Treatment with VT-1161 Protects Immunosuppressed Mice from Rhizopus arrhizus var. arrhizus Infection
Teclegiorgis Gebremariam, Sondus Alkhazraji, Lin Lin, et al.
The Journal of Biological Chemistry
|
October 28, 1994
Potent and selective inhibition of human nitric oxide synthases. Selective inhibition of neuronal nitric oxide synthase by S-methyl-L-thiocitrulline and S-ethyl-L-thiocitrulline
E S Furfine, M F Harmon, J E Paith, et al.
Antimicrobial Agents and Chemotherapy
|
May 11, 2016
The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme
Andrew G S Warrilow, Josie E Parker, Claire L Price, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 19, 2012
Naphthyridinone (NTD) integrase inhibitors: N1 protio and methyl combination substituent effects with C3 amide groups
Brian A Johns, Takashi Kawasuji, Jason G Weatherhead, et al.
Page
of 13