Synthesis and Antiproliferative and Metabolic Evaluations of Novel Securinine Derivatives-Reference-Cited by-同舟云学术

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Synthesis and Antiproliferative and Metabolic Evaluations of Novel Securinine Derivatives

Published:2016-02-04 Issue:4 Volume:7 Page:403-407
ISSN:1948-5875
Container-title:ACS Medicinal Chemistry Letters
language:en
Short-container-title:ACS Med. Chem. Lett.

Author:

Perez Marc¹,Ayad Tahar¹,Maillos Philippe²,Poughon Valérie³,Fahy Jacques³,Ratovelomanana-Vidal Virginie¹

Affiliation:

1. PSL Research University, Chimie ParisTech - CNRS, Institut de Recherche de Chimie Paris, 75005 Paris, France

2. Institut de Recherche Pierre Fabre, 81600 Gaillac, France

3. Unité de Service et de Recherche CNRS-Pierre Fabre n°3388 ETaC CRDPF, 31035 Toulouse, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsmedchemlett.5b00441

Reference26 articles.

1. Securinega suffruticosa

2. Letter: Securinine

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1. A quinine-squaramide catalyzed enantioselective vinylogous Mannich reaction between benzothiazolimines and γ-butenolides for efficient preparation of chiral N-benzothiazole butyrolactones;Organic & Biomolecular Chemistry;2024

2. Bioactivities and mechanism of action of securinega alkaloids derivatives reported prior to 2022;Biomedicine & Pharmacotherapy;2023-02

3. Potential anticancer activities of securinine and its molecular targets;Phytomedicine;2022-11

4. Highly Diastereo‐ and Enantioselective Copper‐Catalyzed Dipropargylic Amination to Access Bispropargylic Diamines;Asian Journal of Organic Chemistry;2022-09-05

5. Asymmetric Synthesis of Propargylic α-Stereogenic Tertiary Amines by Reductive Alkynylation of Tertiary Amides Using Ir/Cu Tandem Catalysis;The Journal of Organic Chemistry;2022-04-18

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