Literature DB >> 32818604

Isolation, reactivity, pharmacological activities and total synthesis of hispanolone and structurally related diterpenes from Labiatae plants.

José L Marco1.   

Abstract

Hispanolone is a furolabdane diterpene isolated from Ballota hispanica, whose natural product chemistry has been summarized and updated here, including several aspects associated with the isolation, structure determination, hemisynthesis, total synthesis, and pharmacology, and related hispanolone diterpenoids that have attracted the interest of different laboratories from diverse perspective and expertise in the last forty-two years.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Ballota genus; Diterpenes; Hemisynthesis; Hispanolone; Isolation; Labiatae family; Natural products; Pharmacology; Reactivity; Total synthesis

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Substances:

Year:  2020        PMID: 32818604     DOI: 10.1016/j.bmcl.2020.127498

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Dehydroisohispanolone as a Promising NLRP3 Inhibitor Agent: Bioevaluation and Molecular Docking.

Authors:  Laura González-Cofrade; Irene Cuadrado; Ángel Amesty; Ana Estévez-Braun; Beatriz de Las Heras; Sonsoles Hortelano
Journal:  Pharmaceuticals (Basel)       Date:  2022-07-02
  1 in total

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