Progress in the Chemistry of Cytochalasans
125
152. Kawahara T, Itoh M, Izumikawa M, Sakata N, Tsuchida T, Shin-ya K (2013) New
chaetoglobosin derivatives, MBJ-0038, MBJ-0039 and MBJ-0040, isolated from the fungus
Chaetomium sp. f24230. J Antibiot 66:727
153. Yang MH, Gu ML, Han C, Guo XJ, Yin GP, Yu P, Kong LY (2018) Aureochaeglobosins
A–C, three [4 + 2] adducts of chaetoglobosin and aureonitol derivatives from Chaetomium
globosum. Org Lett 20:3345
154. Wang W, Zeng F, Bie Q, Dai C, Chen C, Tong Q, Liu J, Wang J, Zhou Y, Zhu H, Zhang Y
(2018) Cytochathiazines A–C: three merocytochalasans with a 2H-1,4-thiazine functionality
from coculture of Chaetomium globosum and Aspergillus flavipes. Org Lett 20:6817
155. Rukachaisirikul V, Khamthong N, Sukpondma Y, Pakawatchai C, Phongpaichit S, Sakayaroj
J, Kirtikara K (2009) An [11]cytochalasin derivative from the marine-derived fungus Xylaria
sp. PSU-F100. Chem Pharm Bull 57:1409
156. Keller-Schierlein W, Kupfer E (1979) Metabolites of microorganisms. 186. The aspochalasins
A, B, C, and D. Helv Chim Acta 62:1501
157. Neupert-Laves K, Dobler M (1982) Metabolic products of microorganisms. Part 215. X-ray
structural analysis of di-O-acetylaspochalasin C. Helv Chim Acta 65:1426
158. Tomikawa T, Shin-Ya K, Kinoshita T, Miyajima A, Seto H, Hayakawa Y (2001) Selective
cytotoxicity and stereochemistry of aspochalasin D. J Antibiot 54:379
159. Naruse N, Yamamoto H, Murata S, Sawada Y, Fukagawa Y, Oki T (1993) Aspochalasin E, a
new antibiotic isolated from a fungus. J Antibiot 46:679
160. Alvi KA, Nair B, Pu H, Ursino R, Gallo C, Mocek U (1997) Phomacins: three novel antitumor
cytochalasan constituents produced by a Phoma sp. J Org Chem 62:2148
161. Fang F, Ui H, Shiomi K, Masuma R, Yamaguchi Y, Zhang CG, Zhang XW, Tanaka Y, Omura
S (1997) Two new components of the aspochalasins produced by Aspergillus sp. J Antibiot
50:919
162. Kohno J, Nonaka N, Nishio M, Ohnuki T, Kawano K, Okuda T, Komatsubara S (1999) TMC169, a new antibiotic of the aspochalasin group produced by Aspergillus flavipes. J Antibiot
52:575
163. Tomikawa T, Shin-Ya K, Seto H, Okusa N, Kajiura T, Hayakawa Y (2002) Structure of
aspochalasin H, a new member of the aspochalasin family. J Antibiot 55:666
164. Zhou GX, Wijeratne EMK, Bigelow D, Pierson LSIII, VanEtten HD, Gunatilaka AAL (2004)
Aspochalasins I, J, and K: three new cytotoxic cytochalasans of Aspergillus flavipes from the
rhizosphere of Ericameria laricifolia of the Sonoran desert. J Nat Prod 67:328
165. Rochfort S, Ford J, Ovenden S, Wan SS, George S, Wildman H, Tait RM, Meurer-Grimes
B, Cox S, Coates J, Rhodes D (2005) A novel aspochalasin with HIV-1 integrase inhibitory
activity from Aspergillus flavipes. J Antibiot 58:279
166. Lin Z, Zhu T, Wei H, Zhang G, Wang H, Gu Q (2009) Spicochalasin A and new aspochalasins
from the marine-derived fungus Spicaria elegans. Eur J Org Chem 2009:3045
167. Lin ZJ, Zhu TJ, Chen L, Gu QQ (2010) Three new aspochalasin derivatives from the marinederived fungus Spicaria elegans. Chin Chem Lett 21:824
168. Liu J, Hu Z, Huang H, Zheng Z, Xu Q (2012) Aspochalasin U, a moderate TNF-α inhibitor
from Aspergillus sp. J Antibiot 65:49
169. Chen L, Liu YT, Song B, Zhang HW, Ding G, Liu XZ, Gu YC, Zou ZM (2014) Stereochemical
determination of new cytochalasans from the plant endophytic fungus Trichoderma gamsii.
Fitoterapia 96:115
170. Liu Y, Zhao S, Ding W, Wang P, Yang X, Xu J (2014) Methylthio-aspochalasins from a
marine-derived fungus Aspergillus sp. Mar Drugs 12:5124
171. Wei G, Tan D, Chen C, Tong Q, Li XN, Huang J, Liu J, Xue Y, Wang J, Luo Z, Zhu H,
Zhang Y (2017) Flavichalasines A–M, cytochalasan alkaloids from Aspergillus flavipes. Sci
Rep 7:42434
172. Xu D, Luo M, Liu F, Wang D, Pang X, Zhao T, Xu L, Wu X, Xia M, Yang X (2017) Cytochalasan and tyrosine-derived alkaloids from the marine sediment-derived fungus Westerdykella
dispersa and their bioactivities. Sci Rep 7:11956
125
152. Kawahara T, Itoh M, Izumikawa M, Sakata N, Tsuchida T, Shin-ya K (2013) New
chaetoglobosin derivatives, MBJ-0038, MBJ-0039 and MBJ-0040, isolated from the fungus
Chaetomium sp. f24230. J Antibiot 66:727
153. Yang MH, Gu ML, Han C, Guo XJ, Yin GP, Yu P, Kong LY (2018) Aureochaeglobosins
A–C, three [4 + 2] adducts of chaetoglobosin and aureonitol derivatives from Chaetomium
globosum. Org Lett 20:3345
154. Wang W, Zeng F, Bie Q, Dai C, Chen C, Tong Q, Liu J, Wang J, Zhou Y, Zhu H, Zhang Y
(2018) Cytochathiazines A–C: three merocytochalasans with a 2H-1,4-thiazine functionality
from coculture of Chaetomium globosum and Aspergillus flavipes. Org Lett 20:6817
155. Rukachaisirikul V, Khamthong N, Sukpondma Y, Pakawatchai C, Phongpaichit S, Sakayaroj
J, Kirtikara K (2009) An [11]cytochalasin derivative from the marine-derived fungus Xylaria
sp. PSU-F100. Chem Pharm Bull 57:1409
156. Keller-Schierlein W, Kupfer E (1979) Metabolites of microorganisms. 186. The aspochalasins
A, B, C, and D. Helv Chim Acta 62:1501
157. Neupert-Laves K, Dobler M (1982) Metabolic products of microorganisms. Part 215. X-ray
structural analysis of di-O-acetylaspochalasin C. Helv Chim Acta 65:1426
158. Tomikawa T, Shin-Ya K, Kinoshita T, Miyajima A, Seto H, Hayakawa Y (2001) Selective
cytotoxicity and stereochemistry of aspochalasin D. J Antibiot 54:379
159. Naruse N, Yamamoto H, Murata S, Sawada Y, Fukagawa Y, Oki T (1993) Aspochalasin E, a
new antibiotic isolated from a fungus. J Antibiot 46:679
160. Alvi KA, Nair B, Pu H, Ursino R, Gallo C, Mocek U (1997) Phomacins: three novel antitumor
cytochalasan constituents produced by a Phoma sp. J Org Chem 62:2148
161. Fang F, Ui H, Shiomi K, Masuma R, Yamaguchi Y, Zhang CG, Zhang XW, Tanaka Y, Omura
S (1997) Two new components of the aspochalasins produced by Aspergillus sp. J Antibiot
50:919
162. Kohno J, Nonaka N, Nishio M, Ohnuki T, Kawano K, Okuda T, Komatsubara S (1999) TMC169, a new antibiotic of the aspochalasin group produced by Aspergillus flavipes. J Antibiot
52:575
163. Tomikawa T, Shin-Ya K, Seto H, Okusa N, Kajiura T, Hayakawa Y (2002) Structure of
aspochalasin H, a new member of the aspochalasin family. J Antibiot 55:666
164. Zhou GX, Wijeratne EMK, Bigelow D, Pierson LSIII, VanEtten HD, Gunatilaka AAL (2004)
Aspochalasins I, J, and K: three new cytotoxic cytochalasans of Aspergillus flavipes from the
rhizosphere of Ericameria laricifolia of the Sonoran desert. J Nat Prod 67:328
165. Rochfort S, Ford J, Ovenden S, Wan SS, George S, Wildman H, Tait RM, Meurer-Grimes
B, Cox S, Coates J, Rhodes D (2005) A novel aspochalasin with HIV-1 integrase inhibitory
activity from Aspergillus flavipes. J Antibiot 58:279
166. Lin Z, Zhu T, Wei H, Zhang G, Wang H, Gu Q (2009) Spicochalasin A and new aspochalasins
from the marine-derived fungus Spicaria elegans. Eur J Org Chem 2009:3045
167. Lin ZJ, Zhu TJ, Chen L, Gu QQ (2010) Three new aspochalasin derivatives from the marinederived fungus Spicaria elegans. Chin Chem Lett 21:824
168. Liu J, Hu Z, Huang H, Zheng Z, Xu Q (2012) Aspochalasin U, a moderate TNF-α inhibitor
from Aspergillus sp. J Antibiot 65:49
169. Chen L, Liu YT, Song B, Zhang HW, Ding G, Liu XZ, Gu YC, Zou ZM (2014) Stereochemical
determination of new cytochalasans from the plant endophytic fungus Trichoderma gamsii.
Fitoterapia 96:115
170. Liu Y, Zhao S, Ding W, Wang P, Yang X, Xu J (2014) Methylthio-aspochalasins from a
marine-derived fungus Aspergillus sp. Mar Drugs 12:5124
171. Wei G, Tan D, Chen C, Tong Q, Li XN, Huang J, Liu J, Xue Y, Wang J, Luo Z, Zhu H,
Zhang Y (2017) Flavichalasines A–M, cytochalasan alkaloids from Aspergillus flavipes. Sci
Rep 7:42434
172. Xu D, Luo M, Liu F, Wang D, Pang X, Zhao T, Xu L, Wu X, Xia M, Yang X (2017) Cytochalasan and tyrosine-derived alkaloids from the marine sediment-derived fungus Westerdykella
dispersa and their bioactivities. Sci Rep 7:11956