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Weighted ensemble: Recent mathematical developments

The Journal of chemical physics, 2023-01, Vol.158 (1), p.014108-014108

2023

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Percolation of Hard Disks

Journal of applied probability, 2014-03, Vol.51 (1), p.235-246

Aristoff, D.

2014

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Layering in crumpled sheets

Europhysics letters, 2010-09, Vol.91 (5), p.56003

2010

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Percolation of Hard Disks

Journal of applied probability, 2014-03, Vol.51 (1), p.235-246

Aristoff, D.

2014

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The Parallel Replica Method for Simulating Long Trajectories of Markov Chains

Applied mathematics research express, 2014-01, Vol.2, p.332-352

2014

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Rifamycins – Obstacles and opportunities

Tuberculosis (Edinburgh, Scotland), 2010-03, Vol.90 (2), p.94-118

2010

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Data-driven variance reduction in weighted ensemble simulations

Biophysical journal, 2024-02, Vol.123 (3), p.423a-423a

2024

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Unbiased Trajectory-Based Estimation of Stationary Distributions and Splitting Probabilities

Biophysical journal, 2021-02, Vol.120 (3), p.177a-177a

2021

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Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIV Protease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class

Journal of medicinal chemistry, 1998-08, Vol.41 (18), p.3467-3476

1998

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Oxazolidinones: a new class of antibacterials

Current Opinion in Pharmacology, 2001-10, Vol.1 (5), p.470-476

2001

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Nonnucleoside Reverse Transcriptase Inhibitors that Potently and Specifically Block Human Immunodeficiency Virus Type 1 Replication

Proceedings of the National Academy of Sciences - PNAS, 1991-10, Vol.88 (19), p.8806-8810

1991

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Synthesis and biological evaluation of benzazepine oxazolidinone antibacterials

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (23), p.4197-4200

2003

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Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

The Journal of biological chemistry, 1993-03, Vol.268 (9), p.6119-6124

1993

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The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

Biochemical pharmacology, 1996-03, Vol.51 (6), p.743-750

1996

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The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

The Journal of biological chemistry, 1993-07, Vol.268 (20), p.14875-14880

1993

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Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Biochemistry (Easton), 1993-07, Vol.32 (26), p.6548-6554

1993

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Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Journal of medicinal chemistry, 1996-11, Vol.39 (23), p.4630-4642

1996

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Synthesis of CBI-PDE-I-dimer, the benzannelated analog of CC-1065

Journal of organic chemistry, 1992-11, Vol.57 (23), p.6234-6239

1992

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U-90152, a potent inhibitor of human immunodeficiency virus type 1 replication

Antimicrobial Agents and Chemotherapy, 1993-05, Vol.37 (5), p.1127-1131

1993

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Synthesis and biochemical evaluation of the CBI-PDE-I-dimer, a benzannelated analog of (+)-CC-1065 that also produces delayed toxicity in mice

Journal of medicinal chemistry, 1993-07, Vol.36 (14), p.1956-1963

1993

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Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

Biochemical pharmacology, 1994-06, Vol.47 (11), p.2017-2028

1994

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Interstrand DNA cross-linking with dimers of the spirocyclopropyl alkylating moiety of CC-1065

Journal of the American Chemical Society, 1989-08, Vol.111 (16), p.6428-6429

1989

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Viscous Hydraulic Jumps

Physics of fluids (1994), 2004-09, Vol.16 (9), p.S4-S4

2004

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Weighted ensemble: Recent mathematical developments

Percolation of Hard Disks

Layering in crumpled sheets

Percolation of Hard Disks

The Parallel Replica Method for Simulating Long Trajectories of Markov Chains

Rifamycins – Obstacles and opportunities

Data-driven variance reduction in weighted ensemble simulations

Unbiased Trajectory-Based Estimation of Stationary Distributions and Splitting Probabilities

Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIV Protease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class

Oxazolidinones: a new class of antibacterials

Nonnucleoside Reverse Transcriptase Inhibitors that Potently and Specifically Block Human Immunodeficiency Virus Type 1 Replication

Synthesis and biological evaluation of benzazepine oxazolidinone antibacterials

Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E

Antibacterial Oxazolidinones Possessing a Novel C-5 Side Chain. (5R)-trans-3-[3-Fluoro-4- (1-oxotetrahydrothiopyran-4-yl)phenyl]-2- oxooxazolidine-5-carboxylic Acid Amide (PF-00422602), a New Lead Compound

The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase

The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase

Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E

Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Synthesis of CBI-PDE-I-dimer, the benzannelated analog of CC-1065

U-90152, a potent inhibitor of human immunodeficiency virus type 1 replication

Structure-Based Design of Nonpeptidic HIV Protease Inhibitors: The Sulfonamide-Substituted Cyclooctylpyranones

Synthesis and biochemical evaluation of the CBI-PDE-I-dimer, a benzannelated analog of (+)-CC-1065 that also produces delayed toxicity in mice

Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E

Interstrand DNA cross-linking with dimers of the spirocyclopropyl alkylating moiety of CC-1065

Viscous Hydraulic Jumps

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