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Susan E. Knudson
Observed names:
Knudson Susan,
Knudson, Susan E.,
S. E. Knudson,
Susan Knudson
Institution:
Colorado State University
Observed institution:
Colorado State University
OpenAlex ID:
A5020102166
Novel Trisubstituted Benzimidazoles, Targeting Mtb FtsZ, as a New Class of Antitubercular Agents
2010
·
Kunal Kumar
, Divya Awasthi
, et al.
·
Journal of Medicinal Chemistry
·
171
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: Novel antibacterial agents against Mycobacterium tuberculosis
2010
·
Xiaokai Li
, Nina Liu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
108
Slow-Onset Inhibition of the FabI Enoyl Reductase from Francisella tularensis : Residence Time and in Vivo Activity
2009
·
Hao Lu
, Kathleen England
, et al.
·
ACS Chemical Biology
·
108
SAR Studies on Trisubstituted Benzimidazoles as Inhibitors of Mtb FtsZ for the Development of Novel Antitubercular Agents
2013
·
Divya Awasthi
, Kunal Kumar
, et al.
·
Journal of Medicinal Chemistry
·
78
Synthesis and in vitro antimycobacterial activity of B-ring modified diaryl ether InhA inhibitors
2008
·
Christopher W. am Ende
, Susan E. Knudson
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
75
Rational Design of Broad Spectrum Antibacterial Activity Based on a Clinically Relevant Enoyl-Acyl Carrier Protein (ACP) Reductase Inhibitor
2014
·
Johannes Schiebel
, Andrew Chang
, et al.
·
Journal of Biological Chemistry
·
67
Thermal and Photoinduced Copper-Promoted C–Se Bond Formation: Synthesis of 2-Alkyl-1,2-benzisoselenazol-3(2H)-ones and Evaluation against Mycobacterium tuberculosis
2017
·
Sandeep Thanna
, Christopher M. Goins
, et al.
·
The Journal of Organic Chemistry
·
64
Design, synthesis and evaluation of novel 2,5,6-trisubstituted benzimidazoles targeting FtsZ as antitubercular agents
2014
·
Bora Park
, Divya Awasthi
, et al.
·
Bioorganic & Medicinal Chemistry
·
63
Evaluating the Contribution of Transition-State Destabilization to Changes in the Residence Time of Triazole-Based InhA Inhibitors
2017
·
Lauren A. Spagnuolo
, Sandra Eltschkner
, et al.
·
Journal of the American Chemical Society
·
62
Time‐Dependent Diaryl Ether Inhibitors of InhA: Structure–Activity Relationship Studies of Enzyme Inhibition, Antibacterial Activity, and in vivo Efficacy
2014
·
Pan Pan
, Susan E. Knudson
, et al.
·
ChemMedChem
·
58
Synthesis and evaluation of new 2-aminothiophenes against Mycobacterium tuberculosis
2016
·
Sandeep Thanna
, Susan E. Knudson
, et al.
·
Organic & Biomolecular Chemistry
·
50
Benzimidazole-based antibacterial agents against Francisella tularensis
2013
·
Kunal Kumar
, Divya Awasthi
, et al.
·
Bioorganic & Medicinal Chemistry
·
47
CoA Adducts of 4-Oxo-4-phenylbut-2-enoates: Inhibitors of MenB from the M. tuberculosis Menaquinone Biosynthesis Pathway
2011
·
Xiaokai Li
, Nina Liu
, et al.
·
ACS Medicinal Chemistry Letters
·
41
Thiolactomycin-Based Inhibitors of Bacterial β-Ketoacyl-ACP Synthases with in Vivo Activity
2016
·
Gopal R. Bommineni
, Kanishk Kapilashrami
, et al.
·
Journal of Medicinal Chemistry
·
40
In vitro–in vivo activity relationship of substituted benzimidazole cell division inhibitors with activity against Mycobacterium tuberculosis
2014
·
Susan E. Knudson
, Kunal Kumar
, et al.
·
Tuberculosis
·
27
Substituted diphenyl ethers as a broad-spectrum platform for the development of chemotherapeutics for the treatment of tularaemia
2009
·
K. England
, C. am Ende
, et al.
·
Journal of Antimicrobial Chemotherapy
·
27
The Putative Secreted Serine Protease Chp-7 Is Required for Full Virulence and Induction of a Nonhost Hypersensitive Response by Clavibacter michiganensis subsp. sepedonicus
2009
·
Riitta Nissinen
, Yunjian Xia
, et al.
·
Molecular Plant-Microbe Interactions
·
25
Discovery, synthesis, and biological evaluation of piperidinol analogs with anti-tuberculosis activity
2009
·
Dianqing Sun
, Michael S. Scherman
, et al.
·
Bioorganic & Medicinal Chemistry
·
24
Cell division inhibitors with efficacy equivalent to isoniazid in the acute murineMycobacterium tuberculosisinfection model
2015
·
Susan E. Knudson
, Divya Awasthi
, et al.
·
Journal of Antimicrobial Chemotherapy
·
23
PDF
A Trisubstituted Benzimidazole Cell Division Inhibitor with Efficacy against Mycobacterium tuberculosis
2014
·
Susan E. Knudson
, Divya Awasthi
, et al.
·
PLoS ONE
·
20
PDF
Substituted Diphenyl Ethers as a Novel Chemotherapeutic Platform against Burkholderia pseudomallei
2013
·
Jason E. Cummings
, Adam J. Beaupre
, et al.
·
Antimicrobial Agents and Chemotherapy
·
14
Structure–activity relationship studies on 2,5,6-trisubstituted benzimidazoles targeting Mtb -FtsZ as antitubercular agents
2020
·
Krupanandan Haranahalli
, Simon Tong
, et al.
·
RSC Medicinal Chemistry
·
11
Formulation studies of InhA inhibitors and combination therapy to improve efficacy against Mycobacterium tuberculosis
2016
·
Susan E. Knudson
, Jason E. Cummings
, et al.
·
Tuberculosis
·
5
CCDC 1546403: Experimental Crystal Structure Determination
2017
·
Thanna, Sandeep
, Goins, Christopher M.
, et al.
·
The Cambridge Structural Database
Cover Picture: Time‐Dependent Diaryl Ether Inhibitors of InhA: Structure–Activity Relationship Studies of Enzyme Inhibition, Antibacterial Activity, and in vivo Efficacy (ChemMedChem 4/2014)
2014
·
Pan Pan
, Susan E. Knudson
, et al.
·
ChemMedChem
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Works count:
28
Citation count:
1,208
H-index:
20
I10-index:
22
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