Pegriseofamines A-E: Five cyclopiazonic acid related indole alkaloids from the fungus Penicillium griseofulvum.

[1]  Tao Yang,et al.  Cyclopiazonic Acid and Okaramine Analogues, Including Chlorinated Compounds, from Chrysosporium undulatum YT-1. , 2022, Journal of natural products.

[2]  Junjun Liu,et al.  Two pairs of undescribed enantiomers isolated from the fungus Penicillium griseofulvum. , 2022, Phytochemistry.

[3]  Zhen-Jie Li,et al.  Cyclopiazonic acid type indole alkaloids from Nicotiana tabacum-derived fungus Aspergillus versicolor and their anti-tobacco mosaic virus activities. , 2022, Phytochemistry.

[4]  Pingping Shen,et al.  A versatile tailoring tool for pentacyclic triterpenes of Penicillium griseofulvum CICC 40293 , 2021, Phytochemistry Letters.

[5]  Junjun Liu,et al.  Piperazine-2,5-dione derivatives and an α-pyrone polyketide from Penicillium griseofulvum and their immunosuppression activity. , 2021, Phytochemistry.

[6]  Shenmin Zhang,et al.  Asperorydines N-P, three new cyclopiazonic acid alkaloids from the marine-derived fungus Aspergillus flavus SCSIO F025. , 2021, Fitoterapia.

[7]  Weiming Zhu,et al.  New alkaloids from the diversity-enhanced extracts of an endophytic fungus Aspergillus flavus GZWMJZ-288. , 2021, Bioorganic chemistry.

[8]  Yanxing Jia,et al.  Seven-step total synthesis of α-cyclopiazonic acid , 2020 .

[9]  Guangming Liu,et al.  Penigrisacids A–D, Four New Sesquiterpenes from the Deep-Sea-Derived Penicillium griseofulvum , 2019, Marine drugs.

[10]  Fei Cao,et al.  A pair of enantiomeric 5-oxabicyclic[4.3.0]lactam derivatives and one new polyketide from the marine-derived fungus Penicillium griseofulvum , 2018, Natural product research.

[11]  Yonghui Zhang,et al.  Griseofamines A and B: Two Indole-Tetramic Acid Alkaloids with 6/5/6/5 and 6/5/7/5 Ring Systems from Penicillium griseofulvum. , 2018, Organic letters.

[12]  L. Debrauwer,et al.  From genomics to metabolomics, moving toward an integrated strategy for the discovery of fungal secondary metabolites. , 2018, Natural product reports.

[13]  Hongwei Liu,et al.  Asperorydines A-M: Prenylated Tryptophan-Derived Alkaloids with Neurotrophic Effects from Aspergillus oryzae. , 2018, The Journal of organic chemistry.

[14]  M. Ferrara,et al.  Enantioselective Synthesis of the Cyclopiazonic Acid Family Using Sulfur Ylides , 2018, Angewandte Chemie.

[15]  A. Carroll,et al.  Marine natural products. , 2018, Natural product reports.

[16]  Xuefu You,et al.  Griseofulvin Derivative and Indole Alkaloids from Penicillium griseofulvum CPCC 400528. , 2017, Journal of natural products.

[17]  Yanru Deng,et al.  Small-molecule inhibitors of the tuberculosis target, phenylalanyl-tRNA synthetase from Penicillium griseofulvum CPCC-400528 , 2016, Cogent Chemistry.

[18]  Yonghui Zhang,et al.  Penicamedine A, a Highly Oxygenated Hexacyclic Indole Alkaloid from Penicillium camemberti , 2015, Chemistry & biodiversity.

[19]  Xiao-nian Li,et al.  Aspergillines A-E, highly oxygenated hexacyclic indole-tetrahydrofuran-tetramic acid derivatives from Aspergillus versicolor. , 2014, Organic letters.

[20]  D. Knight,et al.  A total synthesis of (±)-α-cyclopiazonic acid using a cationic cascade as a key step , 2011 .

[21]  A. Stierle,et al.  Anticancer compounds derived from fungal endophytes: their importance and future challenges. , 2011, Natural product reports.

[22]  M. Schindler,et al.  Asymmetric total synthesis of the indole alkaloid cyclopiazonic acid and first structure–activity data , 2011 .

[23]  C. Walsh,et al.  Characterization of cyclo-acetoacetyl-L-tryptophan dimethylallyltransferase in cyclopiazonic acid biosynthesis: substrate promiscuity and site directed mutagenesis studies. , 2009, Biochemistry.

[24]  C. Walsh,et al.  Cyclopiazonic acid biosynthesis in Aspergillus sp.: characterization of a reductase-like R* domain in cyclopiazonate synthetase that forms and releases cyclo-acetoacetyl-L-tryptophan. , 2009, Biochemistry.

[25]  R. J. Cole,et al.  Cyclopiazonic acid inhibition of the Ca2+-transport ATPase in rat skeletal muscle sarcoplasmic reticulum vesicles. , 1988, Biochemical pharmacology.

[26]  C. Holzapfel The isolation and structure of cyclopiazonic acid, a toxic metabolite of Penicillium cyclopium Westling. , 1968, Tetrahedron.