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Chemmedchem
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May 19, 2015
A Phytochemical-Halogenated Quinoline Combination Therapy Strategy for the Treatment of Pathogenic Bacteria
Yasmeen Abouelhassan, Aaron T Garrison, Fang Bai, et al.
Journal of Medicinal Chemistry
|
April 12, 2018
An Efficient Buchwald-Hartwig/Reductive Cyclization for the Scaffold Diversification of Halogenated Phenazines: Potent Antibacterial Targeting, Biofilm Eradication, and Prodrug Exploration
Aaron T Garrison, Yasmeen Abouelhassan, Dimitris Kallifidas, et al.
Angewandte Chemie (International Ed. in English)
|
October 21, 2015
Halogenated Phenazines that Potently Eradicate Biofilms, MRSA Persister Cells in Non-Biofilm Cultures, and Mycobacterium tuberculosis
Aaron T Garrison, Yasmeen Abouelhassan, Dimitris Kallifidas, et al.
Journal of Medicinal Chemistry
|
December 21, 1992
Bioisosteric replacement of the alpha-amino carboxylic acid functionality in 2-amino-5-phosphonopentanoic acid yields unique 3,4-diamino-3-cyclobutene-1,2-dione containing NMDA antagonists
W A Kinney, N E Lee, D T Garrison, et al.
Journal of Medicinal Chemistry
|
March 29, 2016
Structure-Activity Relationships of a Diverse Class of Halogenated Phenazines That Targets Persistent, Antibiotic-Tolerant Bacterial Biofilms and Mycobacterium tuberculosis
Aaron T Garrison, Yasmeen Abouelhassan, Verrill M Norwood, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 20, 2003
2-(Anilinomethyl)imidazolines as alpha1 adrenergic receptor agonists: alpha1a subtype selective 2'-heteroaryl compounds
Jason D Speake, Frank Navas, Michael J Bishop, et al.
Journal of Medicinal Chemistry
|
February 11, 1998
Design and synthesis of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)-ethyl]phosphonic acid (EAA-090), a potent N-methyl-D-aspartate antagonist, via the use of 3-cyclobutene-1,2-dione as an achiral alpha-amino acid bioisostere
W A Kinney, M Abou-Gharbia, D T Garrison, et al.
Journal of Medicinal Chemistry
|
May 17, 2002
2-(Anilinomethyl)imidazolines as alpha1 adrenergic receptor agonists: the discovery of alpha1a subtype selective 2'-alkylsulfonyl-substituted analogues
Stephen J Hodson, Michael J Bishop, Jason D Speake, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 7, 2002
Alpha(1)-adrenoceptor activation: a comparison of 4-(anilinomethyl)imidazoles and 4-(phenoxymethyl)imidazoles to related 2-imidazolines
Stephen J Hodson, Eric C Bigham, Deanna T Garrison, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2002
2-(anilinomethyl)imidazolines as alpha1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series
Frank Navas, Michael J Bishop, Deanna T Garrison, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
Chemmedchem
|
May 19, 2015
A Phytochemical-Halogenated Quinoline Combination Therapy Strategy for the Treatment of Pathogenic Bacteria
Yasmeen Abouelhassan, Aaron T Garrison, Fang Bai, et al.
Journal of Medicinal Chemistry
|
April 12, 2018
An Efficient Buchwald-Hartwig/Reductive Cyclization for the Scaffold Diversification of Halogenated Phenazines: Potent Antibacterial Targeting, Biofilm Eradication, and Prodrug Exploration
Aaron T Garrison, Yasmeen Abouelhassan, Dimitris Kallifidas, et al.
Angewandte Chemie (International Ed. in English)
|
October 21, 2015
Halogenated Phenazines that Potently Eradicate Biofilms, MRSA Persister Cells in Non-Biofilm Cultures, and Mycobacterium tuberculosis
Aaron T Garrison, Yasmeen Abouelhassan, Dimitris Kallifidas, et al.
Journal of Medicinal Chemistry
|
December 21, 1992
Bioisosteric replacement of the alpha-amino carboxylic acid functionality in 2-amino-5-phosphonopentanoic acid yields unique 3,4-diamino-3-cyclobutene-1,2-dione containing NMDA antagonists
W A Kinney, N E Lee, D T Garrison, et al.
Journal of Medicinal Chemistry
|
March 29, 2016
Structure-Activity Relationships of a Diverse Class of Halogenated Phenazines That Targets Persistent, Antibiotic-Tolerant Bacterial Biofilms and Mycobacterium tuberculosis
Aaron T Garrison, Yasmeen Abouelhassan, Verrill M Norwood, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 20, 2003
2-(Anilinomethyl)imidazolines as alpha1 adrenergic receptor agonists: alpha1a subtype selective 2'-heteroaryl compounds
Jason D Speake, Frank Navas, Michael J Bishop, et al.
Journal of Medicinal Chemistry
|
February 11, 1998
Design and synthesis of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)-ethyl]phosphonic acid (EAA-090), a potent N-methyl-D-aspartate antagonist, via the use of 3-cyclobutene-1,2-dione as an achiral alpha-amino acid bioisostere
W A Kinney, M Abou-Gharbia, D T Garrison, et al.
Journal of Medicinal Chemistry
|
May 17, 2002
2-(Anilinomethyl)imidazolines as alpha1 adrenergic receptor agonists: the discovery of alpha1a subtype selective 2'-alkylsulfonyl-substituted analogues
Stephen J Hodson, Michael J Bishop, Jason D Speake, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 7, 2002
Alpha(1)-adrenoceptor activation: a comparison of 4-(anilinomethyl)imidazoles and 4-(phenoxymethyl)imidazoles to related 2-imidazolines
Stephen J Hodson, Eric C Bigham, Deanna T Garrison, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2002
2-(anilinomethyl)imidazolines as alpha1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series
Frank Navas, Michael J Bishop, Deanna T Garrison, et al.
Page
of 6