Citrinin derivatives from the marine-derived fungus Penicillium citrinum.

Three new citrinin derivatives, penicitrinols C, D, and E (1-3), along with two known compounds, citrinin (4) and decarboxydihydrocitrinone (5), were isolated from Penicillium citrinum. Their structures were determined by spectroscopic methods and X-ray diffraction analysis. Compounds 1 and 3 demonstrated weak cytotoxicity against the HL-60 cell line.

[1]  T. Zhu,et al.  Novel carbon-bridged citrinin dimers from a volcano ash-derived fungus Penicillium citrinum and their cytotoxic and cell cycle arrest activities , 2010 .

[2]  Weiming Zhu,et al.  Pennicitrinone D, a new citrinin dimer from the halotolerant fungus Penicillium notatum B-52 , 2009, The Journal of Antibiotics.

[3]  Weiming Zhu,et al.  Citrinin dimers from the halotolerant fungus Penicillium citrinum B-57. , 2008, Journal of natural products.

[4]  Weiming Zhu,et al.  Penicillenols from Penicillium sp. GQ-7, an endophytic fungus associated with Aegiceras corniculatum. , 2008, Chemical & pharmaceutical bulletin.

[5]  S. Tsukamoto,et al.  (3R,4aR,5S,6R)-6-Hydroxy-5-methylramulosin: a new ramulosin derivative from a marine-derived sterile mycelium. , 2007, Chemical & pharmaceutical bulletin.

[6]  Liangxiong Xu,et al.  Three New Isochromans from the Mycelial Culture of a Cylindrocarpon Fungus , 2006 .

[7]  Galba Maria Campos Takaki,et al.  New citrinin derivatives isolated from Penicillium citrinum , 2006, Journal of Natural Medicines.

[8]  J. Kang,et al.  A new radical scavenging anthracene glycoside, asperflavin ribofuranoside, and polyketides from a marine isolate of the fungus microsporum. , 2006, Chemical & pharmaceutical bulletin.

[9]  E. Lacey,et al.  Citrinin revisited: from monomers to dimers and beyond. , 2006, Organic & biomolecular chemistry.

[10]  D. Oh,et al.  Cyanosporasides A and B, chloro- and cyano-cyclopenta[a]indene glycosides from the marine actinomycete "Salinispora pacifica". , 2006, Organic letters.

[11]  H. Kwon,et al.  Marinomycins A-D, antitumor-antibiotics of a new structure class from a marine actinomycete of the recently discovered genus "marinispora". , 2006, Journal of the American Chemical Society.

[12]  T. Mincer,et al.  Salinosporamide A: a highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora. , 2003, Angewandte Chemie.

[13]  G Goma,et al.  Characterization of monascidin A from Monascus as citrinin. , 1995, International journal of food microbiology.