Heather J. Finlay - Concepedia

Author

Heather J. Finlay

Bristol-Myers Squibb (United States)ORCID

Also Known As

Finlay, H.J., Finlay, Heather J., H J Finlay, H. FINLAY, H. Finlay, H. J. FINLAY, H.J. Finlay, Heather Finlay, Heather J. Finlay

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Bristol-Myers Squibb (United States)Dartmouth College Bristol-Myers Squibb (Germany)Canadian Forest Service Biocon (India)

About

Heather J. Finlay is an author at Bristol-Myers Squibb (United States) specializing in pharmacology, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	13	738
2	Biochemistry	9	9	578
3	Natural Sciences	8	8	327
4	Engineering	2	2	50
5	Public Health	1	1	22

Heather J. Finlay

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Novel triterpenoids suppress inducible nitric oxide synthase (iNOS) and inducible cyclooxygenase (COX-2) in mouse macrophages. Nanjoo Suh, Tadashi Honda, Heather J. Finlay, PubMed InflammationInducible CyclooxygenaseCox-2 MrnaAnti-inflammatoryBiochemistry	1998	326
Synthetic Oleanane and Ursane Triterpenoids with Modified Rings A and C: A Series of Highly Active Inhibitors of Nitric Oxide Production in Mouse Macrophages Tadashi Honda, BarbieAnn V. Rounds, Lothar Bore, Journal of Medicinal Chemistry	2000	235
Novel Synthetic Oleanane and Ursane Triterpenoids with Various Enone Functionalities in Ring A as Inhibitors of Nitric Oxide Production in Mouse Macrophages Tadashi Honda, Gordon W. Gribble, Nanjoo Suh, Journal of Medicinal Chemistry	2000	116
New enone derivatives of oleanolic acid and ursolic acid as inhibitors of nitric oxide production in mouse macrophages Tadashi Honda, Heather J. Finlay, Gordon W. Gribble, Bioorganic & Medicinal Chemistry Letters Bioorganic ChemistryPharmaceutical ChemistryRedox BiologyOxidative StressInflammation	1997	90
Pyrrolidine amides of pyrazolodihydropyrimidines as potent and selective KV1.5 blockers John Lloyd, Heather J. Finlay, Wayne Vacarro, Bioorganic & Medicinal Chemistry Letters Combinatorial ChemistryMedicinal ChemistryNatural SciencesMedicineOrganic Chemistry	2010	89
Dihydropyrazolopyrimidines containing benzimidazoles as KV1.5 potassium channel antagonists John Lloyd, Heather J. Finlay, Karnail S. Atwal, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyMedicinePharmacological AgentPharmacotherapyPharmacology	2009	43
Novel A-ring cleaved analogs of oleanolic and ursolic acids which affect growth regulation in NRP.152 prostate cells Heather J. Finlay, Tadashi Honda, Gordon W. Gribble, Bioorganic & Medicinal Chemistry Letters Nrp.152 Prostate CellsMedicinal ChemistryUrologyDerivativesBiochemistry	1997	37
In Vitro and In Vivo Evaluation of a Small-Molecule APJ (Apelin Receptor) Agonist, BMS-986224, as a Potential Treatment for Heart Failure Peter S. Gargalovic, Pancras C. Wong, Joelle M. Onorato, Circulation Heart Failure	2021	37
Benzopyran sulfonamides as KV1.5 potassium channel blockers John Lloyd, Karnail S. Atwal, Heather J. Finlay, Bioorganic & Medicinal Chemistry Letters HeterocyclicMedicineIon ChannelsOrganic ChemistryPharmacology	2007	32
Expedient synthesis of unsaturated amide alkaloids from <i>Piper</i> spp: Exploring the scope of recent methodology George M. Strunz, Heather J. Finlay Canadian Journal of Chemistry EngineeringUnsaturated Amide AlkaloidsOrganic ChemistryChemistryAlkaloid Piperstachine	1996	28

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