Anu V. Chandran

Didcot, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 11 publications

Crystallographic Fragment Screening of the Dengue Virus Polymerase Reveals Multiple Binding Sites for the Development of Non-nucleoside Antiflavivirals.

Crystallographic Fragment Screening of the Dengue Virus Polymerase Reveals Multiple Binding Sites for the Development of Non-nucleoside Antiflavivirals.

Journal: Journal of medicinal chemistry
Published: September 02, 2025

Crystallographic fragment screening of the dengue virus polymerase reveals multiple binding sites for the development of non-nucleoside antiflavivirals.

Crystallographic fragment screening of the dengue virus polymerase reveals multiple binding sites for the development of non-nucleoside antiflavivirals.

Journal: bioRxiv : the preprint server for biology
Published: April 16, 2025

Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

Journal: Research square
Published: February 24, 2025

Combined crystallographic fragment screening and deep mutational scanning enable discovery of Zika virus NS2B-NS3 protease inhibitors.

Combined crystallographic fragment screening and deep mutational scanning enable discovery of Zika virus NS2B-NS3 protease inhibitors.

Journal: Nature communications
Published: January 21, 2025

Identifying novel chemical matter against the Chikungunya virus nsP3 macrodomain through crystallographic fragment screening.

Identifying novel chemical matter against the Chikungunya virus nsP3 macrodomain through crystallographic fragment screening.

Journal: bioRxiv : the preprint server for biology
Published: September 04, 2024

Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

Journal: bioRxiv : the preprint server for biology
Published: May 15, 2024

High-throughput crystallographic fragment screening of Zika virus NS3 Helicase.

High-throughput crystallographic fragment screening of Zika virus NS3 Helicase.

Journal: bioRxiv : the preprint server for biology
Published: May 15, 2024

Crystallographic Fragment Screen of Coxsackievirus A16 2A Protease identifies new opportunities for the development of broad-spectrum anti-enterovirals.

Crystallographic Fragment Screen of Coxsackievirus A16 2A Protease identifies new opportunities for the development of broad-spectrum anti-enterovirals.

Journal: bioRxiv : the preprint server for biology
Published: May 15, 2024

Yop1 stability and membrane curvature generation propensity are controlled by its oligomerisation interface.

Yop1 stability and membrane curvature generation propensity are controlled by its oligomerisation interface.

Journal: The Biochemical journal
Published: April 16, 2024

A quinolin-8-ol sub-millimolar inhibitor of UGGT, the ER glycoprotein folding quality control checkpoint.

A quinolin-8-ol sub-millimolar inhibitor of UGGT, the ER glycoprotein folding quality control checkpoint.

Journal: iScience
Published: November 28, 2022

Clamping, bending, and twisting inter-domain motions in the misfold-recognizing portion of UDP-glucose: Glycoprotein glucosyltransferase.

Clamping, bending, and twisting inter-domain motions in the misfold-recognizing portion of UDP-glucose: Glycoprotein glucosyltransferase.

Journal: Structure (London, England : 1993)
Published: March 05, 2020
Showing 1-11 of 11

Last Updated: 09/26/2026