Three alkaloids and one polyketide from Aspergillus cristatus harbored in Pinellia ternate tubers

[1]  R. Sarpong,et al.  A unified strategy to reverse-prenylated indole alkaloids: total syntheses of preparaherquamide, premalbrancheamide, and (+)-VM-55599† †Dedicated to the memory of Prof. Robert M. Williams (1953–2020). ‡ ‡Electronic supplementary information (ESI) available. See DOI: 10.1039/d0sc02296a , 2020, Chemical science.

[2]  G. Nichol,et al.  Total synthesis of brevianamide A , 2020, Nature Chemistry.

[3]  D. Sherman,et al.  Flavin‐Dependent Monooxygenases NotI and NotI′ Mediate Spiro‐Oxindole Formation in Biosynthesis of the Notoamides , 2019, Chembiochem : a European journal of chemical biology.

[4]  Dong-Lin Zhao,et al.  Angularly Prenylated Indole Alkaloids with Antimicrobial and Insecticidal Activities from an Endophytic Fungus Fusarium sambucinum TE-6L. , 2019, Journal of agricultural and food chemistry.

[5]  Xiaobing Wang,et al.  Asperones A–E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1–15 , 2018 .

[6]  Junjun Liu,et al.  Asperversiamides, Linearly Fused Prenylated Indole Alkaloids from the Marine-Derived Fungus Aspergillus versicolor. , 2018, The Journal of organic chemistry.

[7]  L. Kong,et al.  Aureochaeglobosins A-C, Three [4 + 2] Adducts of Chaetoglobosin and Aureonitol Derivatives from Chaetomium globosum. , 2018, Organic letters.

[8]  Junfeng Wang,et al.  Eurotiumins A–E, Five New Alkaloids from the Marine-Derived Fungus Eurotium sp. SCSIO F452 , 2018, Marine drugs.

[9]  Y. Jeon,et al.  Asperflavin, an Anti-Inflammatory Compound Produced by a Marine-Derived Fungus, Eurotium amstelodami , 2017, Molecules.

[10]  Xiaobing Wang,et al.  Citrifurans A-D, Four Dimeric Aromatic Polyketides with New Carbon Skeletons from the Fungus Aspergillus sp. , 2017, Organic letters.

[11]  Z. She,et al.  Depsidones from Talaromyces stipitatus SK-4, an endophytic fungus of the mangrove plant Acanthus ilicifolius , 2017 .

[12]  Chaozhong Li,et al.  Total Synthesis of Notoamides F, I, and R and Sclerotiamide. , 2016, Angewandte Chemie.

[13]  Robert M. Williams,et al.  Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids. , 2012, Journal of the American Chemical Society.

[14]  Robert M. Williams,et al.  Studies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic Conundrum. , 2011, Israel journal of chemistry.

[15]  Kenneth A. Miller,et al.  Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp. , 2010, Journal of the American Chemical Society.

[16]  H. Onuki,et al.  Notoamides F-K, prenylated indole alkaloids isolated from a marine-derived Aspergillus sp. , 2008, Journal of natural products.

[17]  Kenneth A. Miller,et al.  Calmodulin inhibitory activity of the malbrancheamides and various analogs. , 2008, Bioorganic & medicinal chemistry letters.

[18]  M. Figueroa,et al.  Malbrancheamide B, a novel compound from the fungus Malbranchea aurantiaca , 2008, Natural product research.

[19]  Kenneth A. Miller,et al.  Biomimetic total synthesis of malbrancheamide and malbrancheamide B. , 2008, The Journal of organic chemistry.

[20]  Robert M. Williams,et al.  Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, Aspergillus sp. , 2007 .

[21]  R. Mata,et al.  Malbrancheamide, a new calmodulin inhibitor from the fungus Malbranchea aurantiaca , 2006 .

[22]  Stella Huang,et al.  Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells. , 2002, Journal of the American Chemical Society.

[23]  Y. Sugie,et al.  A new antibiotic CJ-17,665 from Aspergillus ochraceus. , 2001, The Journal of antibiotics.

[24]  J. Gloer,et al.  Sclerotiamide: a new member of the paraherquamide class with potent antiinsectan activity from the sclerotia of Aspergillus sclerotiorum. , 1996, Journal of natural products.