Exploration of Indole Alkaloids from Marine Fungus Pseudallescheria boydii F44-1 Using an Amino Acid-Directed Strategy
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Title
Exploration of Indole Alkaloids from Marine Fungus Pseudallescheria boydii F44-1 Using an Amino Acid-Directed Strategy
Authors
Keywords
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Journal
Marine Drugs
Volume 17, Issue 2, Pages 77
Publisher
MDPI AG
Online
2019-01-25
DOI
10.3390/md17020077
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- Recent Progress in Biological Activities of Indole and Indole Alkaloids
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- Amino Acid-Directed Strategy for Inducing the Marine-Derived Fungus Scedosporium apiospermum F41–1 to Maximize Alkaloid Diversity
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- Two Additional New Compounds from the Marine-Derived Fungus Pseudallescheria ellipsoidea F42-3
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- Brønsted acid ionic liquid-catalyzed reductive Friedel–Crafts alkylation of indoles and cyclic ketones without using an external reductant
- (2015) Amir Taheri et al. GREEN CHEMISTRY
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- (2015) Jean-Baptiste Say Anouhe et al. Phytochemistry Letters
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- Synthesis of 1-indolyl substituted β-carboline natural products and discovery of antimalarial and cytotoxic activities
- (2014) Lydia P.P. Liew et al. TETRAHEDRON
- β-Carboline Derivatives and Diphenols from Soy Sauce Are in Vitro Quinone Reductase (QR) Inducers
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- (2010) Sheng-Xin Cai et al. HELVETICA CHIMICA ACTA
- Enhancement of Chemically-Induced HL-60 Cell Differentiation by 3,3′-Diindolylmethane Derivatives
- (2009) Tomomi Noguchi-Yachide et al. CHEMICAL & PHARMACEUTICAL BULLETIN
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