Pinoresinol–lariciresinol reductases, key to the lignan synthesis in plants-Reference-Cited by-同舟云学术

Pinoresinol–lariciresinol reductases, key to the lignan synthesis in plants

Published:2019-03-20 Issue:6 Volume:249 Page:1695-1714
ISSN:0032-0935
Container-title:Planta
language:en
Short-container-title:Planta

Author:

Markulin Lucija,Corbin Cyrielle,Renouard Sullivan,Drouet Samantha,Gutierrez Laurent,Mateljak Ivan,Auguin Daniel,Hano Christophe,Fuss Elisabeth,Lainé Eric^ORCID

Funder

Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation

Publisher

Springer Science and Business Media LLC

Subject

Plant Science,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00425-019-03137-y.pdf

Reference131 articles.

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2. Al-Jumaily EF, AL-Azawi AH (2015) antioxidant and hepatoprotective activity of purelignan from flaxseed (Linum usitatissimum l.) on acetaminophen induced toxicity in male rabbit. Int J Res Stud Biosci 3:8–16

3. Allen KL, Tschantz DR, Awad KS et al (2007) A plant lignan, 3′-O-methyl-nordihydroguaiaretic acid, suppresses papillomavirus E6 protein function, stabilizes p53 protein, and induces apoptosis in cervical tumor cells. Mol Carcinog 46:564–575. https://doi.org/10.1002/mc.20305

4. Basini G, Baioni L, Bussolati S et al (2012) Antiangiogenic properties of an unusual benzo[k, l]xanthene lignan derived from CAPE (caffeic acid phenethyl ester). Invest New Drugs 30:186–190. https://doi.org/10.1007/s10637-010-9550-z

5. Baumgartner L, Sosa S, Atanasov AG et al (2011) Lignan derivatives from Krameria lappacea roots inhibit acute inflammation in vivo and pro-inflammatory mediators in vitro. J Nat Prod Prod 74:1779–1786. https://doi.org/10.1021/np200343t

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