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Astringin

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For Research Use Only | Not For Clinical Use
CATAP29884499
CAS29884-49-9
Structure
MDL NumberMFCD03427331
Molecular Weight406.38
Assay≥95.0% (HPLC)
Size10MG
Storage Conditions2-8°C
1

Biosynthesis of the Major Tetrahydroxystilbenes in Spruce, Astringin and Isorhapontin, Proceeds via Resveratrol and Is Enhanced by Fungal Infection

Almuth Hammerbacher, Steven G Ralph, Joerg Bohlmann, Trevor M Fenning, Jonathan Gershenzon, Axel Schmidt

Plant Physiol. 2011 Oct;157(2):876-90.

PMID: 21865488

1

Highly Regioselective Hydroxylation of Polydatin, a Resveratrol Glucoside, for One-Step Synthesis of Astringin, a Piceatannol Glucoside, by P450 BM3

Thien-Kim Le, Hyun-Hee Jang, Ha Thi Huong Nguyen, Tiep Thi My Doan, Ga-Young Lee, Ki Deok Park, Taeho Ahn, Young Hee Joung, Hyung-Sik Kang, Chul-Ho Yun

Enzyme Microb Technol. 2017 Feb;97:34-42.

PMID: 28010771

1

High-performance Liquid Chromatography Coupled With Fluorescence Detection for the Determination of Trans-Astringin in Wine

S Carando, P L Teissedre, P Waffo-Téguo, J C Cabanis, G Deffieux, J M Mérillon

J Chromatogr A. 1999 Jul 23;849(2):617-20.

PMID: 10457456

1

Natural Stilbenoids Have Anti-Inflammatory Properties in Vivo and Down-Regulate the Production of Inflammatory Mediators NO, IL6, and MCP1 Possibly in a PI3K/Akt-Dependent Manner

Heikki Eräsalo, Mari Hämäläinen, Tiina Leppänen, Ilari Mäki-Opas, Mirka Laavola, Raisa Haavikko, Jari Yli-Kauhaluoma, Eeva Moilanen

J Nat Prod. 2018 May 25;81(5):1131-1142.

PMID: 29726680

1

Production of Bioactive 3'-Hydroxystilbene Compounds Using the Flavin-Dependent Monooxygenase Sam5

Kyung Taek Heo, Byeongsan Lee, Sangkeun Son, Jong Seog Ahn, Jae-Hyuk Jang, Young-Soo Hong

J Microbiol Biotechnol. 2018 Jul 28;28(7):1105-1111.

PMID: 30021423

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