Balwinder S. Bhatti - Concepedia

Author

Balwinder S. Bhatti

Also Known As

B. Bhatti, B. S. BHATTI, B. S. Bhatti, B.S. Bhatti, B.S. Bhatti,, Balwinder Bhatti, Balwinder S. Bhatti, Bhatti, B., Bhatti, B.S.

Publications

343

Citations

H-Index

Concepts

All Affiliations

Reynolds American (United States)University of Kentucky Wake Forest University

About

Balwinder S. Bhatti is an author at Reynolds American (United States) specializing in biochemistry, pharmacology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	8	8	152
2	Medicine	6	6	114
3	Natural Sciences	6	6	113
4	Biomolecular Engineering	3	3	49
5	Engineering	2	2	38

Balwinder S. Bhatti

Publications

335

Citations

H-Index

Page 1

	Year	Citations
The Neuroprotective Effect of 2-(3-Pyridyl)-1-azabicyclo[3.2.2]nonane (TC-1698), a Novel α7 Ligand, Is Prevented through Angiotensin II Activation of a Tyrosine Phosphatase Mario B. Marrero, Roger L. Papke, Balwinder S. Bhatti, Journal of Pharmacology and Experimental Therapeutics	2004	56
Characterization of the glucuronide conjugate of cotinine: a previously unidentified major metabolite of nicotine in smokers' urine William S. Caldwell, Justin Greene, Gary D. Byrd, Chemical Research in Toxicology	1992	55
The Heterocyclic Substituted Pyridine Derivative (±)-2-(-3-pyridinyl)-1-Azabicyclo[2.2.2]octane (RJR-2429): A Selective Ligand at Nicotinic Acetylcholine Receptors Merouane Bencherif, Jeffrey D. Schmitt, Balwinder S. Bhatti, Journal of Pharmacology and Experimental Therapeutics	1998	47
Discovery of 3-(5-Chloro-2-furoyl)-3,7-diazabicyclo[3.3.0]octane (TC-6683, AZD1446), a Novel Highly Selective α4β2 Nicotinic Acetylcholine Receptor Agonist for the Treatment of Cognitive Disorders Anatoly Mazurov, Lan Miao, Balwinder S. Bhatti, Journal of Medicinal Chemistry Psychotropic MedicationPeptide SciencePharmacotherapyCognitive DisordersPharmaceutical Chemistry	2012	33
New Oligospirostanosides and Oligofurostanosides from Asparagus adscendens Roots Sandeep Sharma, Ramesh Chand, Balwinder S. Bhatti, Planta Medica Food ChemistryBiosynthesisAsparanin CBiochemistryMedicine	1982	27
Synthesis of α-d-galactopyranosyl-linked oligosaccharides containing the α-Gal → β-Gal → GlcNAc sequence employing methyl-2,3,4,6-tetra-O-(4-methoxybenzyl)-1-thio- β-d-galactopyranoside as an efficient glycosyl donor Gurijala V. Reddy, Rakesh K. Jain, Balwinder S. Bhatti, Carbohydrate Research BiosynthesisBioorganic ChemistryEngineeringBiochemistryNatural Sciences	1994	23
Synthesis of 2-(Pyridin-3-yl)-1-azabicyclo[3.2.2]nonane, 2-(Pyridin-3-yl)-1-azabicyclo[2.2.2]octane, and 2-(Pyridin-3-yl)-1-azabicyclo[3.2.1]octane, a Class of Potent Nicotinic Acetylcholine Receptor–Ligands Balwinder S. Bhatti, Jon‐Paul Strachan, Scott R. Breining, The Journal of Organic Chemistry Combinatorial ChemistryMedicinal ChemistryRing Opening/aminocyclization SequenceHeterocyclicAlpha7 Receptor Subtype	2008	18
A novel enantioselective synthesis of (S)-(?)- and (R)-(+)-nornicotine via alkylation of a chiral 2-hydroxy-3-pinanone ketimine template Jason H. Swango, Balwinder S. Bhatti, M. M. Qureshi, Chirality EngineeringOrganic ChemistryChemistryStereoselective SynthesisNovel Enantioselective Synthesis	1999	15
Structure–Activity Studies of 7-Heteroaryl-3-azabicyclo[3.3.1]non-6-enes: A Novel Class of Highly Potent Nicotinic Receptor Ligands Scott R. Breining, Matt S. Melvin, Balwinder S. Bhatti, Journal of Medicinal Chemistry	2012	15
Diazaspirocyclic compounds as selective ligands for the α4β2 nicotinic acetylcholine receptor Jon‐Paul Strachan, Jarrett J. Farias, Jenny Zhang, Bioorganic & Medicinal Chemistry Letters BiochemistryMedicineNatural SciencesSelective LigandsNicotine	2012	13

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