Introduction

Same author

Mass spectrometric characterization of a series of adenosylated peptides acting as bisubstrate analogs of protein kinases.

Journal of the American Society for Mass Spectrometry·2013

Same author

Specific inhibitors of Plasmodium falciparum thioredoxin reductase as potential antimalarial agents.

Bioorganic & medicinal chemistry letters·2006

Same author

A zinc ribbon protein in DNA replication: primer synthesis and macromolecular interactions by the bacteriophage T4 primase.

Biochemistry·2001

Same author

Intricacies in ATP-dependent clamp loading: variations across replication systems.

Structure (London, England : 1993)·2001

Same author

Unexpected formation of an epoxide-derived multisubstrate adduct inhibitor on the active site of GAR transformylase.

Biochemistry·2001

Same author

An unusually low pK(a) for Cys282 in the active site of human muscle creatine kinase.

Biochemistry·2001

Same journal

Tumor-targeted activatable molecular agent for synergistic chemo-photodynamic therapy.

Bioorganic chemistry·2026

Same journal

Computational design and experimental validation of peptide inhibitors targeting the p53-COP1 interaction to suppress p53 ubiquitination.

Bioorganic chemistry·2026

Same journal

Benzalkonium chloride disrupts human placental progesterone synthesis via locking NAD<sup>+</sup> pocket in 3β-Hydroxysteroid dehydrogenase 1 and rat homolog: docking evidence and 3D-QSAR, and experiment risk assessment.

Bioorganic chemistry·2026

Same journal

Terephthaloyl-based amide-linked derivatives and polymeric networks with selective cytotoxicity: In vitro evaluation, Molecular docking, Molecular dynamics, and DFT insights.

Bioorganic chemistry·2026

Same journal

Synthesis and biological evaluation of C6-modified Celastrol derivatives as anti-inflammatory agents targeting the NF-κB signaling pathway.

Bioorganic chemistry·2026

Same journal

Synthesis and biological evaluation of 6,9-disubstituted purine analogues inducing autophagy-mediated apoptosis and potentiating carboplatin response in high-grade serous ovarian cancer.

Bioorganic chemistry·2026

Related Experiment Videos

Introduction

Related Concept Videos

Mass spectrometric characterization of a series of adenosylated peptides acting as bisubstrate analogs of protein kinases.

Specific inhibitors of Plasmodium falciparum thioredoxin reductase as potential antimalarial agents.

A zinc ribbon protein in DNA replication: primer synthesis and macromolecular interactions by the bacteriophage T4 primase.

Intricacies in ATP-dependent clamp loading: variations across replication systems.

Unexpected formation of an epoxide-derived multisubstrate adduct inhibitor on the active site of GAR transformylase.

An unusually low pK(a) for Cys282 in the active site of human muscle creatine kinase.

Tumor-targeted activatable molecular agent for synergistic chemo-photodynamic therapy.

Computational design and experimental validation of peptide inhibitors targeting the p53-COP1 interaction to suppress p53 ubiquitination.

Benzalkonium chloride disrupts human placental progesterone synthesis via locking NAD<sup>+</sup> pocket in 3β-Hydroxysteroid dehydrogenase 1 and rat homolog: docking evidence and 3D-QSAR, and experiment risk assessment.

Terephthaloyl-based amide-linked derivatives and polymeric networks with selective cytotoxicity: In vitro evaluation, Molecular docking, Molecular dynamics, and DFT insights.

Synthesis and biological evaluation of C6-modified Celastrol derivatives as anti-inflammatory agents targeting the NF-κB signaling pathway.

Synthesis and biological evaluation of 6,9-disubstituted purine analogues inducing autophagy-mediated apoptosis and potentiating carboplatin response in high-grade serous ovarian cancer.

Related Experiment Videos

Introduction

Related Concept Videos

Related Articles

Mass spectrometric characterization of a series of adenosylated peptides acting as bisubstrate analogs of protein kinases.

Specific inhibitors of Plasmodium falciparum thioredoxin reductase as potential antimalarial agents.

A zinc ribbon protein in DNA replication: primer synthesis and macromolecular interactions by the bacteriophage T4 primase.

Intricacies in ATP-dependent clamp loading: variations across replication systems.

Unexpected formation of an epoxide-derived multisubstrate adduct inhibitor on the active site of GAR transformylase.

An unusually low pK(a) for Cys282 in the active site of human muscle creatine kinase.

Tumor-targeted activatable molecular agent for synergistic chemo-photodynamic therapy.

Computational design and experimental validation of peptide inhibitors targeting the p53-COP1 interaction to suppress p53 ubiquitination.

Benzalkonium chloride disrupts human placental progesterone synthesis via locking NAD<sup>+</sup> pocket in 3β-Hydroxysteroid dehydrogenase 1 and rat homolog: docking evidence and 3D-QSAR, and experiment risk assessment.

Terephthaloyl-based amide-linked derivatives and polymeric networks with selective cytotoxicity: In vitro evaluation, Molecular docking, Molecular dynamics, and DFT insights.

Synthesis and biological evaluation of C6-modified Celastrol derivatives as anti-inflammatory agents targeting the NF-κB signaling pathway.

Synthesis and biological evaluation of 6,9-disubstituted purine analogues inducing autophagy-mediated apoptosis and potentiating carboplatin response in high-grade serous ovarian cancer.