M
Malkeet Singh Bahia
Researcher at Punjabi University
Publications - 29
Citations - 589
Malkeet Singh Bahia is an academic researcher from Punjabi University. The author has contributed to research in topics: Docking (molecular) & Pharmacophore. The author has an hindex of 12, co-authored 28 publications receiving 468 citations.
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Journal ArticleDOI
Purinergic receptor P2X₇: a novel target for anti-inflammatory therapy.
Nisha Mehta,Maninder Kaur,Manjinder Singh,Sukhvir Chand,Bhawna Vyas,Pragati Silakari,Malkeet Singh Bahia,Om Silakari +7 more
TL;DR: Various aspects of P2X₇ receptors are explored including therapeutic potential, and recent discoveries and developments of P 2X⁇ receptor antagonists to serve as novel therapeutic agents to combat various inflammatory conditions.
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Thiazolidine-2,4-dione derivatives: programmed chemical weapons for key protein targets of various pathological conditions.
TL;DR: Thiazolidine-2,4-dione is an extensively explored heterocyclic nucleus for designing of novel agents implicated for a wide variety of pathophysiological conditions, that is, diabetes, diabetic complications, cancer, arthritis, inflammation, microbial infection, and melanoma, and the structure based SAR of TZD derivatives for various protein targets would serve as a benchmark for the alteration of existing ligands to design new ones with better binding interactions.
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Benzimidazole derivatives: search for GI-friendly anti-inflammatory analgesic agents
Monika Gaba,Punam Gaba,Deepika Uppal,Neelima Dhingra,Malkeet Singh Bahia,Om Silakari,Chander Mohan +6 more
TL;DR: In this paper, the synthesis and biological evaluation of N-1-(phenylsulfonyl)-2-methylamino-substituted-1H-benzimidazole derivatives with lower GI toxicity was described.
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Interleukin-1 receptor associated kinase inhibitors: potential therapeutic agents for inflammatory- and immune-related disorders.
TL;DR: IRAK-4 has been evaluated as an indispensable element of IL-Rs and TLR pathways that can regulate the abnormal levels of cytokines, and therefore could be employed to manage immune- and inflammation-related disorders.
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Inhibitors of microsomal prostaglandin E2 synthase-1 enzyme as emerging anti-inflammatory candidates.
TL;DR: Microsomal prostaglandin E2 synthase‐1 (mPGES‐1), a downstream PG synthase, specifically catalyzes the biosynthesis of COX‐2‐derived PGE2 from PGH2, and describes itself as a valuable therapeutic target for the treatment of acute and chronic inflammatory disease conditions.