Search Results - "Patel, Dinesh V"
-
1
Actinonin, a Naturally Occurring Antibacterial Agent, Is a Potent Deformylase Inhibitor
Published in Biochemistry (Easton) (15-02-2000)“…Peptide deformylase (PDF) is essential in prokaryotes and absent in mammalian cells, thus making it an attractive target for the discovery of novel…”
Get full text
Journal Article -
2
Approaches to Combinatorial Synthesis of Heterocycles: A Solid-Phase Synthesis of 1,4-Dihydropyridines
Published in Journal of organic chemistry (09-02-1996)“…N-Immobilized enamino esters 2 derived from amine-functionalized PAL or Rink polystyrene resins react with preformed 2-arylidene β-keto esters or directly with…”
Get full text
Journal Article -
3
N-Alkyl Urea Hydroxamic Acids as a New Class of Peptide Deformylase Inhibitors with Antibacterial Activity
Published in Antimicrobial Agents and Chemotherapy (01-09-2002)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
Get full text
Journal Article -
4
Pharmacokinetics and Pharmacodynamics of AR9281, an Inhibitor of Soluble Epoxide Hydrolase, in Single- and Multiple-Dose Studies in Healthy Human Subjects
Published in Journal of clinical pharmacology (01-03-2012)“…AR9281, a potent and selective inhibitor of soluble epoxide hydrolase (s-EH), is in clinical development targeting hypertension and type 2 diabetes. The…”
Get full text
Journal Article -
5
Selective Solid Phase Synthesis of Ureas and Hydantoins from Common Phenyl Carbamate Intermediates
Published in Journal of organic chemistry (03-10-1997)“…An efficient method for selective, solid phase synthesis of unsymmetrical ureas and hydantoins from a common phenyl carbamate dipeptide intermediate is…”
Get full text
Journal Article -
6
alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin
Published in Journal of medicinal chemistry (01-10-1995)“…The design and application of alpha-hydroxy phosphonates, a new class of transition state analogs, toward the discovery of novel and potent inhibitors of the…”
Get full text
Journal Article -
7
N- and C-terminal modifications of negamycin
Published in Bioorganic & medicinal chemistry letters (21-07-2003)“…Negamycin 1 is a bactericidal antibiotic with activity against Gram-negative bacteria, and served as a template in an antibiotic discovery program. An…”
Get full text
Journal Article -
8
1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia
Published in Bioorganic & medicinal chemistry letters (01-02-2011)“…1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) attenuated the enhanced glucose excursion following an intraperitoneal glucose tolerance test and…”
Get full text
Journal Article -
9
Rational Design and Combinatorial Evaluation of Enzyme Inhibitor Scaffolds: Identification of Novel Inhibitors of Matrix Metalloproteinases
Published in Journal of medicinal chemistry (18-06-1998)“…The discovery of a novel series of heterocyclic matrix metalloproteinase (MMPs) inhibitors is described. Published crystal structures of peptidyl hydroxamates…”
Get full text
Journal Article -
10
Discovery and Characterization of a Potent Interleukin-6 Binding Peptide with Neutralizing Activity In Vivo
Published in PloS one (10-11-2015)“…Interleukin-6 (IL-6) is an important member of the cytokine superfamily, exerting pleiotropic actions on many physiological processes. Over-production of IL-6…”
Get full text
Journal Article -
11
Conformationally restricted analogs of deoxynegamycin
Published in Bioorganic & medicinal chemistry letters (21-06-2004)“…Methods were developed to synthesize a number of conformationally restricted β-amino acids. Incorporation of these β-amino acids into deoxynegamycin template…”
Get full text
Journal Article -
12
Farnesyl Diphosphate-Based Inhibitors of Ras Farnesyl Protein Transferase
Published in Journal of medicinal chemistry (01-07-1995)“…The rational design, synthesis, and biological activity of farnesyl diphosphate (FPP)-based inhibitors of the enzyme Ras farnesyl protein transferase (FPT) is…”
Get full text
Journal Article -
13
Non-urea functionality as the primary pharmacophore in soluble epoxide hydrolase inhibitors
Published in Bioorganic & medicinal chemistry letters (15-02-2009)“…Inhibition of soluble epoxide hydrolase (sEH) has been proposed as a promising new pharmaceutical target for diseases involving hypertension and vascular…”
Get full text
Journal Article -
14
Activated ketone based inhibitors of human renin
Published in Journal of medicinal chemistry (20-08-1993)“…Application of the concept of activated ketones to the design of novel and potent transition-state analog inhibitors of the aspartyl protease renin is…”
Get full text
Journal Article -
15
Design and synthesis of thiazole-5-hydroxamic acids as novel histone deacetylase inhibitors
Published in Bioorganic & medicinal chemistry letters (01-11-2007)“…The synthesis, histone deacetylase (HDAC) inhibitory activity and the antiproliferative activity of thiazole-5-hydroxamic acids 6– 9 are described. We have…”
Get full text
Journal Article -
16
Conformational Constraint in Oxazolidinone Antibacterials. Synthesis and Structure−Activity Studies of (Azabicyclo[3.1.0]hexylphenyl)oxazolidinones
Published in Journal of medicinal chemistry (28-07-2005)“…The oxazolidinones are a new class of synthetic antibacterials effective against a broad range of pathogenic Gram-positive bacteria, including…”
Get full text
Journal Article -
17
Novel oxazolidinone–quinolone hybrid antimicrobials
Published in Bioorganic & medicinal chemistry letters (01-12-2003)“…Antimicrobial compounds incorporating oxazolidinone and quinolone pharmacophore substructures have been synthesized and evaluated. Representative analogues 2,…”
Get full text
Journal Article -
18
Mercaptoamide-based non-hydroxamic acid type histone deacetylase inhibitors
Published in Bioorganic & medicinal chemistry letters (15-04-2005)“…The synthesis and histone deacetylase (HDAC) inhibitory activity of mercaptoamides 2 and 3 is described. Inhibitors of histone deacetylases (HDAC) are emerging…”
Get full text
Journal Article -
19
A New and Efficient Solid Phase Synthesis of Hydroxamic Acids
Published in Journal of organic chemistry (17-10-1997)Get full text
Journal Article -
20
Synthesis and structure–activity studies of antibacterial oxazolidinones containing dihydrothiopyran or dihydrothiazine C-rings
Published in Bioorganic & medicinal chemistry letters (01-07-2006)“…A new series of oxazolidinone analogs bearing unsaturated sulfur-containing C-rings is described. New synthetic approaches to the dihydrothiazine ring system…”
Get full text
Journal Article