Expression of functional TRPA1 receptor on human lung fibroblast and epithelial cells

…, S Kuruganti, S Thorat, N Khairatkar-Joshi - Journal of Receptors …, 2011 - Taylor & Francis
The transient receptor potential subfamily A member 1 (TRPA1) is a non-selective cation
channel implicated in the pathogenesis of several airway diseases like asthma and chronic …

TRPV1 antagonists: the challenges for therapeutic targeting

N Khairatkar-Joshi, A Szallasi - Trends in molecular medicine, 2009 - cell.com
The capsaicin receptor TRPV1 (transient receptor potential cation channel, subfamily V,
member 1) is a polymodal nociceptor whose expression is upregulated in several painful …

[HTML][HTML] Transient Receptor Potential Ankyrin 1 Receptor Activation In Vitro and In Vivo by Pro-tussive Agents: GRC 17536 as a Promising Anti-Tussive Therapeutic

…, I Ghosh, D Wale, V Bhosale, N Khairatkar-Joshi - PloS one, 2014 - journals.plos.org
Cough is a protective reflex action that helps clear the respiratory tract which is continuously
exposed to airborne environmental irritants. However, chronic cough presents itself as a …

[HTML][HTML] Blocking TRPA1 in respiratory disorders: does it hold a promise?

I Mukhopadhyay, A Kulkarni, N Khairatkar-Joshi - Pharmaceuticals, 2016 - mdpi.com
Transient Receptor Potential Ankyrin 1 (TRPA1) ion channel is expressed abundantly on the
C fibers that innervate almost entire respiratory tract starting from oral cavity and oropharynx…

Imidazopyridazinones as novel PDE7 inhibitors: SAR and in vivo studies in Parkinson's disease model

…, RR Sangana, GS Gudi, N Khairatkar-Joshi… - Bioorganic & medicinal …, 2012 - Elsevier
The synthesis and structure-activity relationship studies of a series of compounds from
imidazopyridazinone scaffold as PDE7 inhibitors are disclosed. Potent analogs such as …

Synthesis and pharmacological evaluation of novel N-aryl-3, 4-dihydro-1′ H-spiro [chromene-2, 4′-piperidine]-1′-carboxamides as TRPM8 antagonists

SS Chaudhari, AB Kadam, N Khairatkar-Joshi… - Bioorganic & medicinal …, 2013 - Elsevier
A novel series of N-aryl-3,4-dihydro-1′H-spiro[chromene-2,4′-piperidine]-1′-carboxamides
was identified as transient receptor potential melastatin 8 (TRPM8) channel blockers …

Discovery of benzo [d] imidazo [5, 1-b] thiazole as a new class of phosphodiesterase 10A inhibitors

…, S Jadhav, GS Gudi, N Khairatkar-Joshi… - Bioorganic & medicinal …, 2013 - Elsevier
The design, synthesis and structure activity relationship studies of a series of compounds
from benzo[d]imidazo[5,1-b]thiazole scaffold as phosphodiesterase 10A (PDE10A) inhibitors …

The TRPV3 receptor as a pain target: a therapeutic promise or just some more new biology

NK Khairatkar Joshi, N Maharaj… - The Open Drug …, 2010 - benthamopen.com
Human beings have evolved with a powerful peripheral thermo-sensory capacity to maintain
thermal homeostasis and to avoid potentially harmful stimuli. Specialized sensory neurons …

Design, Synthesis, and Pharmacological Evaluation of 5,6-Disubstituted Pyridin-2(1H)-one Derivatives as Phosphodiesterase 10A (PDE10A) Antagonists

…, S Kummari, N Khairatkar-Joshi… - Journal of Medicinal …, 2015 - ACS Publications
We report the design and synthesis of novel 5,6-diarylated pyridin-2(1H)-one derivatives as
pharmacophoric PDE10A inhibitors. This highly potent molecular scaffold was developed …

Discovery of 2-((2-chloro-6-fluorophenyl) amino)-N-(3-fluoro-5-(trifluoromethyl) phenyl)-1-methyl-7, 8-dihydro-1H-[1, 4] dioxino [2′, 3′: 3, 4] benzo [1, 2-d] imidazole …

…, MYA Mahat, GS Gudi, N Khairatkar-Joshi… - Bioorganic & medicinal …, 2016 - Elsevier
The discovery and SAR of potent, selective dioxane-fused tricyclic benz[d]imidazole derivatives
as mPGES-1 inhibitor are herein described. Various amide modifications in this series …