Indrapal Singh Aidhen

Affiliations: 
1995- IIT Madras 
Area:
Synthetic carbohydrate chemistry, synthesis of biologically/medicinally important compounds
Website:
http://chem.iitm.ac.in/faculty/indrapal/
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"Indrapal Singh Aidhen"
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Publications

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Maji NC, Rastogi P, Krishnasamy A, et al. (2022) Storage and Temperature Stability of Emulsified Biodiesel-Diesel Blends. Acs Omega. 7: 44762-44771
Yadav A, Shah N, Tiwari PK, et al. (2020) Novel Chemical Scaffolds to Inhibit the Neutral Amino Acid Transporter BAT1 (SLC6A19), a Potential Target to Treat Metabolic Diseases. Frontiers in Pharmacology. 11: 140
Sudarshan K, Boda AK, Dogra S, et al. (2018) Discovery of an isocoumarin analogue that modulates neuronal functions via neurotrophin receptor TrkB. Bioorganic & Medicinal Chemistry Letters
Borkar SR, Aidhen IS. (2017) Stereoselective total synthesis of Oxylipin from open chain gluco-configured building block. Carbohydrate Research. 443: 23-28
Ramanan M, Sinha S, Sudarshan K, et al. (2016) Inhibition of the enzymes in the leukotriene and prostaglandin pathways in inflammation by 3-aryl isocoumarins. European Journal of Medicinal Chemistry. 124: 428-434
Aidhen IS, Mukkamala R, Weidner C, et al. (2015) A common building block for the syntheses of amorfrutin and cajaninstilbene acid libraries toward efficient binding with peroxisome proliferator-activated receptors Organic Letters. 17: 194-197
Swain J, Mohapatra M, Borkar SR, et al. (2013) Study of aqueous phase aggregation of FTY720 (fingolimod hydrochloride) and its effect on DMPC liposomes using fluorescent molecular probes. Physical Chemistry Chemical Physics : Pccp. 15: 17962-70
Borkar SR, Manjunath BN, Balasubramaniam S, et al. (2012) Convenient synthesis of D- and L-xylo-1,2,3,4-alkane tetrols from a D-gluco-configured common building block. Carbohydrate Research. 358: 23-30
Senthilmurugan A, Aidhen IS. (2012) Convenient strategies for the synthesis of 1,4-phenylene spaced sugars. Carbohydrate Research. 347: 55-63
Mahalingam SM, Aidhen IS. (2006) Propargyl bromide as an excellent alpha-bromoacetone equivalent: convenient and new route to alpha-aroylacetones. The Journal of Organic Chemistry. 71: 349-51
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