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Design and synthesis of potent inhibitors of cholesteryl ester transfer protein (CETP) exploiting a 1,2,3,4-tetrahydroquinoline platform

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (9), p.2456-2460

2009

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Improved Asymmetric Synthesis of 3,4-Dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)phenyl]-α-(trifluoromethyl)-1(2H)-quinolineethanol, a Potent Cholesteryl Ester Transfer Protein Inhibitor

Organic letters, 2009-07, Vol.11 (13), p.2812-2815

2009

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Solid phase synthesis of aryl ethers via the mitsunobu reaction

Tetrahedron letters, 1995-05, Vol.36 (22), p.3789-3792

1995

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Total synthesis of the cytotoxic macrocycle (+)-hitachimycin

Journal of the American Chemical Society, 1992-10, Vol.114 (21), p.8008-8022

1992

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Indinavir analogues with blocked metabolism sites as HIV protease inhibitors with improved pharmacological profiles and high potency against PI-Resistant viral strains

Bioorganic & medicinal chemistry letters, 2002-09, Vol.12 (17), p.2419-2422

2002

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HIV protease inhibitors with picomolar potency against PI-resistant HIV-1 by extension of the P3 substituent

Bioorganic & medicinal chemistry letters, 2003-08, Vol.13 (15), p.2569-2572

2003

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A combinatorial approach defines specificities of members of the caspase family and granzyme B. Functional relationships established for key mediators of apoptosis

The Journal of biological chemistry, 1997-07, Vol.272 (29), p.17907

1997

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A Combinatorial Library of Indinavir Analogues and Its In Vitro and In Vivo Studies

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (4), p.529-532

2002

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Combinatorial diversification of indinavir: in vivo mixture dosing of an HIV protease inhibitor library

Bioorganic & medicinal chemistry letters, 2000-07, Vol.10 (14), p.1527-1530

2000

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A highly efficient method for the preparation of 2-aryl substituted carbapenems exploiting a Pd(0) mediated cross-coupling reaction

Tetrahedron letters, 1990, Vol.31 (20), p.2853-2856

1990

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A Combinatorial Approach Defines Specificities of Members of the Caspase Family and Granzyme B

The Journal of biological chemistry, 1997-07, Vol.272 (29), p.17907-17911

1997

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Total synthesis of (+)-hitachimycin

Journal of organic chemistry, 1990-02, Vol.55 (4), p.1136-1138

1990

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Total synthesis of the cytotoxic macrocycle (+)-hitachimycin. [Erratum to document cited in CA117(17):171036e]

Journal of the American Chemical Society, 1993-06, Vol.115 (11), p.4947-4947

1993

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HIV protease inhibitors with picomolar potency against PI-Resistant HIV-1 by extension of the P 3 substituent

Bioorganic & medicinal chemistry letters, 2003-08, Vol.13 (15), p.2569-2572

2003

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A combinatorial approach for determining protease specificities: application to interleukin-1β converting enzyme (ICE)

Chemistry & biology, 1997, Vol.4 (2), p.149-155

1997

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Exploratory study: Evaluation of a symptom checker effectiveness for providing a diagnosis and evaluating the situation emergency compared to emergency physicians using simulated and standardized patients

PloS one, 2023-02, Vol.18 (2), p.e0277568-e0277568

2023

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Finding MeVO: Identifying Intracranial Medium-Vessel Occlusions at CT Angiography

Radiographics, 2024-11, Vol.44 (11), p.e240010

2024

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GC-MS Based Identification of the Volatile Components of Six Astragalus Species from Uzbekistan and Their Biological Activity

Plants (Basel), 2021-01, Vol.10 (1), p.124

2021

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Black and gold howler monkeys (Alouatta caraya) as sentinels of ecosystem health: patterns of zoonotic protozoa infection relative to degree of human-primate contact

American journal of primatology, 2011-01, Vol.73 (1), p.75-83

2011

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Factors Affecting Selection of TraineE for Neurointervention (FASTEN)

Interventional neuroradiology, 2024-02, p.15910199241232726

2024

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Design, Synthesis, and Biological Evaluation of (2R,αS)-3,4-Dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl]-α-(trifluoromethyl)-1(2H)-quinolineethanol as Potent and Orally Active Cholesteryl Ester Transfer Protein Inhibitor

Journal of medicinal chemistry, 2009-03, Vol.52 (6), p.1768-1772

2009

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4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable stearoyl-CoA desaturase-1 (SCD1) inhibitors: part 2. Pyridazine-based analogs

Bioorganic & medicinal chemistry letters, 2014-03, Vol.24 (5), p.1437-1441

2014

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Reduction of sternal infection by application of topical vancomycin

The Journal of thoracic and cardiovascular surgery, 1989-10, Vol.98 (4), p.618-622

1989

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Progress toward the total synthesis of (+)-hitachimycin (stubomycin)

Rano, Thomas Anthony

1989

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Design and synthesis of potent inhibitors of cholesteryl ester transfer protein (CETP) exploiting a 1,2,3,4-tetrahydroquinoline platform

Improved Asymmetric Synthesis of 3,4-Dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)phenyl]-α-(trifluoromethyl)-1(2H)-quinolineethanol, a Potent Cholesteryl Ester Transfer Protein Inhibitor

Solid phase synthesis of aryl ethers via the mitsunobu reaction

Total synthesis of the cytotoxic macrocycle (+)-hitachimycin

Indinavir analogues with blocked metabolism sites as HIV protease inhibitors with improved pharmacological profiles and high potency against PI-Resistant viral strains

HIV protease inhibitors with picomolar potency against PI-resistant HIV-1 by extension of the P3 substituent

A combinatorial approach defines specificities of members of the caspase family and granzyme B. Functional relationships established for key mediators of apoptosis

A Combinatorial Library of Indinavir Analogues and Its In Vitro and In Vivo Studies

Combinatorial diversification of indinavir: in vivo mixture dosing of an HIV protease inhibitor library

A highly efficient method for the preparation of 2-aryl substituted carbapenems exploiting a Pd(0) mediated cross-coupling reaction

A Combinatorial Approach Defines Specificities of Members of the Caspase Family and Granzyme B

Total synthesis of (+)-hitachimycin

Total synthesis of the cytotoxic macrocycle (+)-hitachimycin. [Erratum to document cited in CA117(17):171036e]

HIV protease inhibitors with picomolar potency against PI-Resistant HIV-1 by extension of the P 3 substituent

A combinatorial approach for determining protease specificities: application to interleukin-1β converting enzyme (ICE)

Exploratory study: Evaluation of a symptom checker effectiveness for providing a diagnosis and evaluating the situation emergency compared to emergency physicians using simulated and standardized patients

Finding MeVO: Identifying Intracranial Medium-Vessel Occlusions at CT Angiography

GC-MS Based Identification of the Volatile Components of Six Astragalus Species from Uzbekistan and Their Biological Activity

Development of 'Core Outcome Sets' for Meningioma in Clinical Studies (The COSMIC Project): protocol for two systematic literature reviews, eDelphi surveys and online consensus meetings

Black and gold howler monkeys (Alouatta caraya) as sentinels of ecosystem health: patterns of zoonotic protozoa infection relative to degree of human-primate contact

Factors Affecting Selection of TraineE for Neurointervention (FASTEN)

Design, Synthesis, and Biological Evaluation of (2R,αS)-3,4-Dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl]-α-(trifluoromethyl)-1(2H)-quinolineethanol as Potent and Orally Active Cholesteryl Ester Transfer Protein Inhibitor

4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable stearoyl-CoA desaturase-1 (SCD1) inhibitors: part 2. Pyridazine-based analogs

Reduction of sternal infection by application of topical vancomycin

Progress toward the total synthesis of (+)-hitachimycin (stubomycin)

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