Literature DB >> 30730700

Structural Simplification of Natural Products.

Shengzheng Wang1,2, Guoqiang Dong1, Chunquan Sheng1.   

Abstract

Natural products (NPs) are important sources of clinical drugs due to their structural diversity and biological prevalidation. However, the structural complexity of NPs leads to synthetic difficulties, unfavorable pharmacokinetic profiles, and poor drug-likeness. Structural simplification by truncating unnecessary substructures is a powerful strategy for overcoming these limitations and improving the efficiency and success rate of NP-based drug development. Herein, we will provide a comprehensive review of the structural simplification of NPs with a focus on design strategies, case studies, and new technologies. In particular, a number of successful examples leading to marketed drugs or drug candidates will be discussed in detail to illustrate how structural simplification is applied in lead optimization of NPs.

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Year:  2019        PMID: 30730700     DOI: 10.1021/acs.chemrev.8b00504

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  26 in total

1.  Synthesis, conformational preferences, and biological activity of conformational analogues of the microtubule-stabilizing agents, (-)-zampanolide and (-)-dactylolide.

Authors:  Jeffrey L Henry; Matthew R Wilson; Michael P Mulligan; Taylor R Quinn; Dan L Sackett; Richard E Taylor
Journal:  Medchemcomm       Date:  2019-04-09       Impact factor: 3.597

2.  An amide mimic of desTHPdactylolide: Total synthesis and antiproliferative evaluation.

Authors:  Guanglin Chen; Maricarmen Gonzalez; Ziran Jiang; Qiang Zhang; Guangdi Wang; Qiao-Hong Chen
Journal:  Bioorg Med Chem Lett       Date:  2021-03-19       Impact factor: 2.823

3.  Design, synthesis and fungicidal evaluation of novel psoralen derivatives containing sulfonohydrazide or acylthiourea moiety.

Authors:  Jingyue Dong; Kun Li; Zeyu Hong; Lei Chen; Liangfu Tang; Lijun Han; Lai Chen; Zhijin Fan
Journal:  Mol Divers       Date:  2022-06-06       Impact factor: 3.364

4.  Identification of a 3-β-homoalanine conjugate of brusatol with reduced toxicity in mice.

Authors:  Nicky Hwang; Yonggang Pei; Jason Clement; Erle S Robertson; Yanming Du
Journal:  Bioorg Med Chem Lett       Date:  2020-09-21       Impact factor: 2.823

5.  Sugar-Pirating as an Enabling Platform for the Synthesis of 4,6-Dideoxyhexoses.

Authors:  Yinan Zhang; Jianjun Zhang; Larissa V Ponomareva; Zheng Cui; Steven G Van Lanen; Jon S Thorson
Journal:  J Am Chem Soc       Date:  2020-05-07       Impact factor: 15.419

Review 6.  Overcoming cancer therapeutic bottleneck by drug repurposing.

Authors:  Zhe Zhang; Li Zhou; Na Xie; Edouard C Nice; Tao Zhang; Yongping Cui; Canhua Huang
Journal:  Signal Transduct Target Ther       Date:  2020-07-02

7.  Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase.

Authors:  Abdullah Al Mamun; Jana Maříková; Daniela Hulcová; Jiří Janoušek; Marcela Šafratová; Lucie Nováková; Tomáš Kučera; Martina Hrabinová; Jiří Kuneš; Jan Korábečný; Lucie Cahlíková
Journal:  Biomolecules       Date:  2020-05-22

8.  Chagas Disease Treatment and Rational Drug Discovery: A Challenge That Remains.

Authors:  Ana Catarina Cristovão Silva; Maria Carolina Accioly Brelaz-de-Castro; Ana Cristina Lima Leite; Valéria Rêgo Alves Pereira; Marcelo Zaldini Hernandes
Journal:  Front Pharmacol       Date:  2019-08-02       Impact factor: 5.810

Review 9.  Structural simplification: an efficient strategy in lead optimization.

Authors:  Shengzheng Wang; Guoqiang Dong; Chunquan Sheng
Journal:  Acta Pharm Sin B       Date:  2019-06-06       Impact factor: 11.413

10.  Isolation of Quercetin from Rubus fruticosus, Their Concentration through NF/RO Membranes, and Recovery through Carbon Nanocomposite. A Pilot Plant Study.

Authors:  Muhammad Zahoor; Abdul Bari Shah; Sumaira Naz; Riaz Ullah; Ahmed Bari; Hafiz Majid Mahmood
Journal:  Biomed Res Int       Date:  2020-03-19       Impact factor: 3.411

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