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Early bolt looseness state identification via generalized variational mode decomposition and similarity index

Journal of Mechanical Science and Technology, 2021, 35(3), , pp.861-873

2021

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Current screening, design, and delivery approaches to address low permeability of chemically synthesized modalities in drug discovery and early clinical development

Drug discovery today, 2023-09, Vol.28 (9), p.103685-103685, Article 103685

2023

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The solubilization of the poorly water soluble drug nifedipine by water soluble 4-sulphonic calix[ n]arenes

European journal of pharmaceutics and biopharmaceutics, 2004-11, Vol.58 (3), p.629-636

2004

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Pre-clinical Formulation Development of an in situ Meglumine Salt of AZD5991: A Novel Macrocyclic Mcl-1 Inhibitor

Pharmaceutical research, 2023-04, Vol.40 (4), p.977-988

2023

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Composite signal detection using multisynchrosqueezing wavelet transform

Digital signal processing, 2024-06, Vol.149, p.104482, Article 104482

2024

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Vibration-based looseness identification of bolted structures via quasi-analytic wavelet packet and optimized large margin distribution machine

Structural health monitoring, 2024-03, Vol.23 (2), p.856-875

2024

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Early evaluation of opportunities in oral delivery of PROTACs to overcome their molecular challenges

Drug discovery today, 2024-02, Vol.29 (2), p.103865-103865, Article 103865

2024

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Sparse representation of guided wave signals with differential norm penalty

Knowledge-based systems, 2024-01, Vol.284, p.111232, Article 111232

2024

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Unsupervised graph anomaly detection with discriminative embedding similarity for viscoelastic sandwich cylindrical structures

ISA transactions, 2024-04, Vol.147, p.36-54

2024

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An optimized variational mode decomposition for extracting weak feature of viscoelastic sandwich cylindrical structures

Measurement science & technology, 2018-03, Vol.29 (3), p.35006

2018

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Discovery solubility measurement and assessment of small molecules with drug development in mind

Drug discovery today, 2022-05, Vol.27 (5), p.1315-1325

2022

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Generalized variational mode decomposition for interlayer slipping detection of viscoelastic sandwich cylindrical structures

Measurement science & technology, 2018-09, Vol.29 (9), p.95001

2018

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A novel method to prepare highly encapsulated interferon-α-2b containing liposomes for intramuscular sustained release

European journal of pharmaceutics and biopharmaceutics, 2006-08, Vol.64 (1), p.9-15

2006

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Effect of para-sulfonato-calix[n]arenes on the solubility, chemical stability, and bioavailability of a water insoluble drug nifedipine

Current drug discovery technologies, 2008-06, Vol.5 (2), p.129

2008

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Application and Impact of Human Dose Projection from Discovery to Early Drug Development

AAPS PharmSciTech, 2020-01, Vol.21 (2), p.44, Article 44

2020

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The Evolving Druggability and Developability Space: Chemically Modified New Modalities and Emerging Small Molecules

The AAPS journal, 2020-01, Vol.22 (2), p.21, Article 21

2020

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Discovery of AZD9833, a Potent and Orally Bioavailable Selective Estrogen Receptor Degrader and Antagonist

Journal of medicinal chemistry, 2020-12, Vol.63 (23), p.14530-14559

2020

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Modulating target engagement of small molecules via drug delivery: approaches and applications in drug discovery and development

Drug discovery today, 2021-03, Vol.26 (3), p.713-723

2021

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Experimental design, development and evaluation of extended release subcutaneous thermo-responsive in situ gels for small molecules in drug discovery

Pharmaceutical development and technology, 2021-11, Vol.26 (10), p.1079-1089

2021

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Discovery of a Potent and Orally Bioavailable Zwitterionic Series of Selective Estrogen Receptor Degrader-Antagonists

Journal of medicinal chemistry, 2023-02, Vol.66 (4), p.2918-2945

2023

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Improving the aqueous solubility of triclosan by solubilization, complexation, and in situ salt formation

Journal of cosmetic science, 2003-11, Vol.54 (6), p.537-550

2003

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Abstract DDT01-02: AZD5991: A potent and selective macrocyclic inhibitor of Mcl-1 for treatment of hematologic cancers

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.DDT01-02-DDT01-02

2017

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Early bolt looseness state identification via generalized variational mode decomposition and similarity index

Current screening, design, and delivery approaches to address low permeability of chemically synthesized modalities in drug discovery and early clinical development

The solubilization of the poorly water soluble drug nifedipine by water soluble 4-sulphonic calix[ n]arenes

Pre-clinical Formulation Development of an in situ Meglumine Salt of AZD5991: A Novel Macrocyclic Mcl-1 Inhibitor

Composite signal detection using multisynchrosqueezing wavelet transform

Vibration-based looseness identification of bolted structures via quasi-analytic wavelet packet and optimized large margin distribution machine

Early evaluation of opportunities in oral delivery of PROTACs to overcome their molecular challenges

Sparse representation of guided wave signals with differential norm penalty

Unsupervised graph anomaly detection with discriminative embedding similarity for viscoelastic sandwich cylindrical structures

An optimized variational mode decomposition for extracting weak feature of viscoelastic sandwich cylindrical structures

Discovery solubility measurement and assessment of small molecules with drug development in mind

Generalized variational mode decomposition for interlayer slipping detection of viscoelastic sandwich cylindrical structures

Discovery of Mcl-1-specific inhibitor AZD5991 and preclinical activity in multiple myeloma and acute myeloid leukemia

A novel method to prepare highly encapsulated interferon-α-2b containing liposomes for intramuscular sustained release

Effect of para-sulfonato-calix[n]arenes on the solubility, chemical stability, and bioavailability of a water insoluble drug nifedipine

Application and Impact of Human Dose Projection from Discovery to Early Drug Development

The Evolving Druggability and Developability Space: Chemically Modified New Modalities and Emerging Small Molecules

Discovery of AZD9833, a Potent and Orally Bioavailable Selective Estrogen Receptor Degrader and Antagonist

Discovery of (2R)‑N‑[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]‑1H‑indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor

Modulating target engagement of small molecules via drug delivery: approaches and applications in drug discovery and development

Experimental design, development and evaluation of extended release subcutaneous thermo-responsive in situ gels for small molecules in drug discovery

Discovery of a Potent and Orally Bioavailable Zwitterionic Series of Selective Estrogen Receptor Degrader-Antagonists

Discovery of (2 R )- N -[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]-1 H -indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor

Improving the aqueous solubility of triclosan by solubilization, complexation, and in situ salt formation

Abstract DDT01-02: AZD5991: A potent and selective macrocyclic inhibitor of Mcl-1 for treatment of hematologic cancers

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