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bbSelect - An Open-Source Tool for Performing a 3D Pharmacophore-Driven Diverse Selection of R-Groups.
Rianjongdee, Francesco; Palmer, David; Pickett, Stephen D; Pogány, Peter; Tomkinson, Nicholas C O; Green, Darren V S.
Afiliación
  • Rianjongdee F; GSK Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, U.K.
  • Palmer D; Department for Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
  • Pickett SD; GSK Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, U.K.
  • Pogány P; GSK Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, U.K.
  • Tomkinson NCO; Department for Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
  • Green DVS; GSK Medicines Research Centre, Stevenage, Hertfordshire SG1 2NY, U.K.
J Chem Inf Model ; 64(12): 4687-4699, 2024 Jun 24.
Article en En | MEDLINE | ID: mdl-38822782
ABSTRACT
The design of compounds during hit-to-lead often seeks to explore a vector from a core scaffold to form additional interactions with the target protein. A rational approach to this is to probe the region of a protein accessed by a vector with a systematic placement of pharmacophore features in 3D, particularly when bound structures are not available. Herein, we present bbSelect, an open-source tool built to map the placements of pharmacophore features in 3D Euclidean space from a library of R-groups, employing partitioning to drive a diverse and systematic selection to a user-defined size. An evaluation of bbSelect against established methods exemplified the superiority of bbSelect in its ability to perform diverse selections, achieving high levels of pharmacophore feature placement coverage with selection sizes of a fraction of the total set and without the introduction of excess complexity. bbSelect also reports visualizations and rationale to enable users to understand and interrogate results. This provides a tool for the drug discovery community to guide their hit-to-lead activities.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Programas Informáticos / Descubrimiento de Drogas Idioma: En Revista: J Chem Inf Model Asunto de la revista: INFORMATICA MEDICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Programas Informáticos / Descubrimiento de Drogas Idioma: En Revista: J Chem Inf Model Asunto de la revista: INFORMATICA MEDICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido