Matthew Todd

Matthew Todd

University College London

H-index: 38

Europe-United Kingdom

About Matthew Todd

Matthew Todd, With an exceptional h-index of 38 and a recent h-index of 27 (since 2020), a distinguished researcher at University College London, specializes in the field of Organic Chemistry, Drug Discovery, Open Science.

His recent articles reflect a diverse array of research interests and contributions to the field:

Reaction hijacking inhibition of Plasmodium falciparum asparagine tRNA synthetase

Open Source Antibiotics: Simple Diarylimidazoles Are Potent against Methicillin-Resistant Staphylococcus aureus

Structure–Property Optimization of a Series of Imidazopyridines for Visceral Leishmaniasis

Illuminating the druggable genome through patent bioactivity data

Antifungal Activity of Natural Naphthoquinones and Anthraquinones against Madurella mycetomatis

Target 2035–an update on private sector contributions

Target 2035–update on the quest for a probe for every protein

Perphenazine–macrocycle conjugates rapidly sequester the Aβ42 monomer and prevent formation of toxic oligomers and amyloid

Matthew Todd Information

University

Position

___

Citations(all)

5559

Citations(since 2020)

2697

Cited By

3677

hIndex(all)

38

hIndex(since 2020)

27

i10Index(all)

78

i10Index(since 2020)

49

Email

University Profile Page

Google Scholar

Matthew Todd Skills & Research Interests

Organic Chemistry

Drug Discovery

Open Science

Top articles of Matthew Todd

Open Source Antibiotics: Simple Diarylimidazoles Are Potent against Methicillin-Resistant Staphylococcus aureus

ACS Infectious Diseases

2023/11/22

Structure–Property Optimization of a Series of Imidazopyridines for Visceral Leishmaniasis

ACS Infectious Diseases

2023/7/7

Illuminating the druggable genome through patent bioactivity data

PeerJ

2023/5/2

Antifungal Activity of Natural Naphthoquinones and Anthraquinones against Madurella mycetomatis

Chemistry & Biodiversity

2023/5

Matthew Todd
Matthew Todd

H-Index: 24

Perphenazine–macrocycle conjugates rapidly sequester the Aβ42 monomer and prevent formation of toxic oligomers and amyloid

ACS Chemical Neuroscience

2022/12/21

Metallaphotoredox-Catalyzed Decarboxylative sp3–sp3 Cou-pling with Iso (thio) chroman and Tetrahydroisoquinoline Cores

2022/6/16

Paul King
Paul King

H-Index: 16

Matthew Todd
Matthew Todd

H-Index: 24

CACHE (Critical Assessment of Computational Hit-finding Experiments): a public–private partnership benchmarking initiative to enable the development of computational methods …

2022/4

Screening the pandemic response box identified benzimidazole carbamates, Olorofim and ravuconazole as promising drug candidates for the treatment of eumycetoma

PLoS Neglected Tropical Diseases

2022/2/4

Matthew Todd
Matthew Todd

H-Index: 24

An open drug discovery competition: experimental validation of predictive models in a series of novel antimalarials

Journal of Medicinal Chemistry

2021/11/8

Molecular Docking with Open Access Software: Development of an Online Laboratory Handbook and Remote Workflow for Chemistry and Pharmacy Master’s Students to Undertake Computer …

Journal of Chemical Education

2021/8/18

Artificial Intelligence and Augmented Intelligence for Automated Investigations for Scientific Discovery

2021/3/15

Platinum binding preferences dominate the binding of novel polyamide amidine anthraquinone platinum (II) complexes to DNA

Dalton Transactions

2021

A critical overview of computational approaches employed for COVID-19 drug discovery

2021

There is no market for new antibiotics: this allows an open approach to research and development

Wellcome open research

2021

Copper (II) complexes of N-propargyl cyclam ligands reveal a range of coordination modes and colours, and unexpected reactivity

Dalton Transactions

2021

AI3SD Video: An Open Competition of People and Machines to Develop Predictive Models for Antimalarial Drug Discovery

2020/12/2

Matthew Todd
Matthew Todd

H-Index: 24

Perphenazine-macrocycle conjugates rapidly sequester the Aβ42 monomer and inhibit amyloid formation

2020/11/17

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