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The Journal of Physical Chemistry. A
|
September 24, 2011
QTAIM application in drug development: prediction of relative stability of drug polymorphs from experimental crystal structures
Yuriy A Abramov
Molecular Pharmaceutics
|
April 17, 2015
Major Source of Error in QSPR Prediction of Intrinsic Thermodynamic Solubility of Drugs: Solid vs Nonsolid State Contributions?
Yuriy A Abramov
The Journal of Pharmacy and Pharmacology
|
April 17, 2015
Low solubility in drug development: de-convoluting the relative importance of solvation and crystal packing
Robert Docherty, Klimentina Pencheva, Yuriy A Abramov
Journal of Chemical Information and Modeling
|
February 28, 2022
Emerging Landscape of Computational Modeling in Pharmaceutical Development
Yuriy A Abramov, Guangxu Sun, Qun Zeng
Journal of Computer-Aided Molecular Design
|
October 12, 2012
Close intramolecular sulfur-oxygen contacts: modified force field parameters for improved conformation generation
Dmitry Lupyan, Yuriy A Abramov, Woody Sherman
Journal of Pharmaceutical Sciences
|
July 24, 2012
Rational coformer or solvent selection for pharmaceutical cocrystallization or desolvation
Yuriy A Abramov, Christoph Loschen, Andreas Klamt
ACS Central Science
|
August 5, 2017
New Tricks of the Trade for Crystal Structure Refinement
Jinjin Li, Yuriy A Abramov, Michael F Doherty
Fly
|
August 20, 2016
Trans-inactivation: Repression in a wrong place
Aleksei S Shatskikh, Yuriy A Abramov, Sergey A Lavrov
Chemical Science
|
June 24, 2026
Exploring celecoxib polymorph landscape using AIMNet2 machine learning interatomic potential
Peikun Zheng, Yuriy A Abramov, Changquan Calvin Sun, et al.
Molecular Pharmaceutics
|
January 14, 2020
Guiding Lead Optimization for Solubility Improvement with Physics-Based Modeling
Yuriy A Abramov, Guangxu Sun, Qiao Zeng, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
The Journal of Physical Chemistry. A
|
September 24, 2011
QTAIM application in drug development: prediction of relative stability of drug polymorphs from experimental crystal structures
Yuriy A Abramov
Molecular Pharmaceutics
|
April 17, 2015
Major Source of Error in QSPR Prediction of Intrinsic Thermodynamic Solubility of Drugs: Solid vs Nonsolid State Contributions?
Yuriy A Abramov
The Journal of Pharmacy and Pharmacology
|
April 17, 2015
Low solubility in drug development: de-convoluting the relative importance of solvation and crystal packing
Robert Docherty, Klimentina Pencheva, Yuriy A Abramov
Journal of Chemical Information and Modeling
|
February 28, 2022
Emerging Landscape of Computational Modeling in Pharmaceutical Development
Yuriy A Abramov, Guangxu Sun, Qun Zeng
Journal of Computer-Aided Molecular Design
|
October 12, 2012
Close intramolecular sulfur-oxygen contacts: modified force field parameters for improved conformation generation
Dmitry Lupyan, Yuriy A Abramov, Woody Sherman
Journal of Pharmaceutical Sciences
|
July 24, 2012
Rational coformer or solvent selection for pharmaceutical cocrystallization or desolvation
Yuriy A Abramov, Christoph Loschen, Andreas Klamt
ACS Central Science
|
August 5, 2017
New Tricks of the Trade for Crystal Structure Refinement
Jinjin Li, Yuriy A Abramov, Michael F Doherty
Fly
|
August 20, 2016
Trans-inactivation: Repression in a wrong place
Aleksei S Shatskikh, Yuriy A Abramov, Sergey A Lavrov
Chemical Science
|
June 24, 2026
Exploring celecoxib polymorph landscape using AIMNet2 machine learning interatomic potential
Peikun Zheng, Yuriy A Abramov, Changquan Calvin Sun, et al.
Molecular Pharmaceutics
|
January 14, 2020
Guiding Lead Optimization for Solubility Improvement with Physics-Based Modeling
Yuriy A Abramov, Guangxu Sun, Qiao Zeng, et al.
Page
of 3