Literature DB >> 30946980

Accelerated drug discovery by rapid candidate drug identification.

Fredrik Bergström1, Bo Lindmark2.   

Abstract

The eventual candidate drug (CD) is often already synthesized during early drug discovery but not nominated until much later. To facilitate the rapid identification of a potential CD, a thoroughly worked-out CD target profile (CDTP) with criteria acceptable for the disease target product profile (TPP) is required at the start of lead generation (LG). In addition to driving the compound property optimization, the preclinical project team has to understand the ultimate goal to be able to rapidly identify and progress a potential CD. A screening cascade with meaningful and well-balanced progression criteria based on the CDTP is required to rapidly filter out unwanted compounds and to progress a potential CD through the cascade to candidate selection.
Copyright © 2019 Elsevier Ltd. All rights reserved.

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Year:  2019        PMID: 30946980     DOI: 10.1016/j.drudis.2019.03.026

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  3 in total

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Authors:  Natesh Singh; Bruno O Villoutreix
Journal:  Comput Struct Biotechnol J       Date:  2021-04-26       Impact factor: 7.271

Review 2.  Anticancer Plants: A Review of the Active Phytochemicals, Applications in Animal Models, and Regulatory Aspects.

Authors:  Tariq Khan; Muhammad Ali; Ajmal Khan; Parveen Nisar; Sohail Ahmad Jan; Shakeeb Afridi; Zabta Khan Shinwari
Journal:  Biomolecules       Date:  2019-12-27

3.  Prediction of human pharmacokinetics for low-clearance compounds using pharmacokinetic data from chimeric mice with humanized livers.

Authors:  Kosuke Yoshida; Yuki Doi; Norihiko Iwazaki; Hidenori Yasuhara; Yuka Ikenaga; Hidetoshi Shimizu; Tomohisa Nakada; Tomoko Watanabe; Chise Tateno; Seigo Sanoh; Yaichiro Kotake
Journal:  Clin Transl Sci       Date:  2021-11-07       Impact factor: 4.689

  3 in total

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