A new cytochalasin from endophytic Phomopsis sp. IFB-E060

Chinese Journal of Natural Medicines

Volumn 12, Issue 7, 2014, Pages 512-516

  Shen, Li ^a   Luo, Qian ^a,b   Shen, Zhi Ping ^a   Li, Ling Yu ^a   Zhang, Xiao Jun ^a   Wei, Zhong Qi ^a   Fu, Yi ^a   Song, Yong Chun ^c   Tan, Ren Xiang ^b,c  

^a CLINICAL MEDICAL COLLEGE OF YANGZHOU UNIVERSITY   (China)

^b NANKAI UNIVERSITY   (China)

^c NANJING UNIVERSITY   (China)

Author keywords

Cytochalasin; Endophyte; Phomopsis sp.; Sphaeropsidaceae; Vatica mangachapoi

Indexed keywords

18 METHOXYCYTOCHALASIN J; CEREVISTEROL; CYTOCHALASIN; CYTOCHALASIN H; ERGOSTEROL; FLUOROURACIL; NICOTINIC ACID; SEPHADEX; SILICA GEL; UNCLASSIFIED DRUG; CYTOCHALASIN J;

ARTICLE; CIRCULAR DICHROISM; COLUMN CHROMATOGRAPHY; CONTROLLED STUDY; CYTOTOXICITY; ENDOPHYTE; GEL FILTRATION; HUMAN; HUMAN CELL; IC 50; INFRARED SPECTROSCOPY; LIVER CANCER CELL LINE; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PHOMOPSIS; ULTRAVIOLET SPECTROSCOPY; ANGIOSPERM; ASCOMYCETES; BARK; CELL SURVIVAL; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; ISOLATION AND PURIFICATION; MICROBIOLOGY; TUMOR CELL LINE;

ANGIOSPERMS; ASCOMYCOTA; CELL LINE, TUMOR; CELL SURVIVAL; CYTOCHALASINS; ENDOPHYTES; HUMANS; MOLECULAR STRUCTURE; PLANT BARK;

EID: 84904417128     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.1016/S1875-5364(14)60080-7     Document Type: Article

References (15)

1. Fu J, Zhou Y, Li HF, et al. Antifungal metabolites from Phomopsis sp. By254, an endophytic fungus in Gossypium hirsutum [J]. Afr J Microbiol Res 2011, 5(10):1231-1236.
2. Adelin E, Servy C, Cortial S, et al. Isolation, structure elucidation and biological activity of metabolites from Sch-642305- producing endophytic fungus Phomopsis sp. CMU-LMA [J]. Phytochemistry 2011, 72(18):2406-2412.
3. Huang ZJ, Yang RY, Guo ZY, et al. A new naphtho-γ-pyrone from mangrove endophytic fungus ZSU-H26 [J]. Chem Nat Compd 2010, 46(1):15-18.
4. Rukachaisirikul V, Sommart U, Phongpaichit S, et al. Metabolites from the endophytic fungus Phomopsis sp. PSU-D15 [J]. Phytochemistry 2008, 69(3):783-787.
5. Izawa Y, Hirose T, Shimizu T, et al. Six new 10-phenyl- [11]cytochalasans, cytochalasins N-S from Phomopsis sp. [J]. Tetrahedron 1989, 45(8):2323-2335.
6. Liu YH, Xu LC, Wang JP, et al. Studies on the chemical constituents of Phylloporia ribis [J]. J Chin Med Mater 2005, 28(11):998-999.
7. Zhou ZY, Liu JK A chemical analysis of ascomycete Scutellinia ascoboloides [J]. J Yunnan National Univ (Nat Sci Ed) 2009, 18(1):1-4.
8. 13C NMR shift increments for 3-substituted pyridines [J]. Heterocycles 1981, 16(11):1893-1897.
9. Shen L, Jiao RH, Ye YH, et al. Absolute configuration of new cytotoxic and other bioactive trichothecene macrolides [J]. Chem Eur J 2006, 12(21):5596-5602.
10. Xu S Research and discovery of new cytochalasins [D] 2007, Nanjing University, Nanjing.
11. Beno MA, Cox RH, Wells JM, et al. Structure of a new cytochalasin, cytochalasin H or kodo-cytochalasin-I [J]. J Am Chem Soc 1977, 99:4123-4130.
12. Udagawa T, Yuan J, Panigrahy D, et al. Cytochalasin E, an epoxide containing Aspergillus-derived fungal metabolite, inhibits angiogenesis and tumor growth [J]. J Pharmacol Exp Ther 2000, 294(2):421-427.
13. Rochfort S, Ford J, Ovenden S, et al. A novel aspochalasin with HIV-1 integrase inhibitory activity from Aspergillus flavipes [J]. J Antibiot 2005, 58(4):279-283.
14. Taing O. Antibacterial cytochalasin-like substances and their manufacture with Zygosaccharomyces rouxii [P]. JP20012 18594, 2000.
15. Udagawa T, D'Amato RJ, Shah JH. Cytochalasin and isoindolinone derivatives as inhibitors of angiogenesis [P]. US Patent 5994388, 1999.