Author

George McGarry

Observed names: G. MCGARRY, G. McGarry

Institution: Merck & Co., Inc., Rahway, NJ, USA (United States)

Observed institution: Merck & Co., Inc., Rahway, NJ, USA (United States)

OpenAlex ID: A5085886489

Discovery and SAR of Org 24598—A Selective Glycine Uptake Inhibitor

2001 · Angus Brown, Ian Carlyle, et al. · Bioorganic & Medicinal Chemistry Letters · 95

Design and optimization of a series of novel 2-cyano-pyrimidines as cathepsin K inhibitors

2010 · Zoran Rankovic, Jiaqiang Cai, et al. · Bioorganic & Medicinal Chemistry Letters · 25

Optimisation of 2-cyano-pyrimidine inhibitors of cathepsin K: Improving selectivity over hERG

2010 · Zoran Rankovic, Jiaqiang Cai, et al. · Bioorganic & Medicinal Chemistry Letters · 12

2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitors

2010 · Jiaqiang Cai, D. Jonathan Bennett, et al. · Bioorganic & Medicinal Chemistry Letters · 12

Antiarrhythmic activity of 17.beta.-aminoestratrienes. Comparison of 3-ols and 3-acetates with the corresponding 3-(3-amino-2-hydroxypropyl) ethers

1986 · J. K. Campbell, R. T. Logan, et al. · Journal of Medicinal Chemistry · 12

Alkylated steroids. Part 3. The 21-alkylation of 20-oxopregnanes and synthesis of a novel anti-inflammatory 16α,17α,21-trimethyl steroid (Org 6216)

1981 · James Cairns, Robert T. Logan, et al. · Journal of the Chemical Society Perkin Transactions 1 · 7

Alkylated steroids. Part 2. 16α,17α-Dimethylpregnanes functionalised in ring C

1978 · James Cairns, Colin L. Hewett, et al. · Journal of the Chemical Society Perkin Transactions 1 · 3

Alkylated steroids. Part 1. 16α-Substituted 17α-methylpregnanes

1976 · James Cairns, Colin L. Hewett, et al. · Journal of the Chemical Society Perkin Transactions 1 · 3

ChemInform Abstract: Discovery and SAR of Org 24598 — A Selective Glycine Uptake Inhibitor.

2001 · Angus Brown, Ian Carlyle, et al. · ChemInform

ChemInform Abstract: Antiarrhythmic Activity of 17β‐Aminoestratrienes. Comparison of 3‐Ols and 3‐Acetates with the Corresponding 3‐(3‐Amino‐2‐hydroxypropyl) Ethers.

1986 · J. K. CAMPBELL, R. T. LOGAN, et al. · ChemInform

ChemInform Abstract: ALKYLATED STEROIDS. PART 3. THE 21‐ALKYLATION OF 20‐OXOPREGNANES AND SYNTHESIS OF A NOVEL ANTIINFLAMMATORY 16α,17α,21‐TRIMETHYL STEROID (ORG 6216)

1981 · J. CAIRNS, R. T. LOGAN, et al. · ChemInform

ChemInform Abstract: ALKYLATED STEROIDS. PART 2. 16α,17α‐DIMETHYLPREGNANES FUNCTIONALIZED IN RING C

1979 · J. CAIRNS, C. L. HEWETT, et al. · ChemInform

ChemInform Abstract: ALKYLATED STEROIDS. PART 1. 16α‐SUBSTITUTED 17α‐METHYLPREGNANES

1976 · J. CAIRNS, C. L. HEWETT, et al. · ChemInform

Works count: 13

Citation count: 169

H-index: 6

I10-index: 5