References
- Kawahara T, Nagai A, Takagi M, et al. JBIR-137 and JBIR-138, new secondary metabolites from Aspergillus sp. fA75. J Antibiot. 2012;65:535–538.
- Kawahara T, Itoh M, Izumikawa M, et al. New hydroxamate metabolite, MBJ-0003, from Micromonospora sp. 29867. J Antibiot. 2013;67(3):261–263.
- Kawahara T, Itoh M, Izumikawa M, et al. Cytotoxic sesquiterpenoids MBJ-0009 and MBJ-0010 from a saprobic fungus Nectria sp. f26111. J Antibiot. 2013;66(9):567–569.
- Kawahara T, Itoh M, Izumikawa M, et al. Three eremophilane derivatives, MBJ-0011, MBJ-0012 and MBJ-0013, from an endophytic fungus Apiognomonia sp. f24023. J Antibiot. 2013;66(5):299–302.
- Kawahara T, Itoh M, Izumikawa M, et al. New chaetoglobosin derivatives, MBJ-0038, MBJ-0039 and MBJ-0040, isolated from the fungus Chaetomium sp. f24230. J Antibiot. 2013;66(12):727–730.
- Kawahara T, Itoh M, Izumikawa M, et al. MBJ-0086 and MBJ-0087, new bicyclic depsipeptides, from Sphaerisporangium sp. 33226. J Antibiot. 2014;68:67–70.
- Kawahara T, Itoh M, Izumikawa M, et al. Novel aziridine-containing peptides MBJ-0034 and MBJ-0035 from Streptosporangium sp. 32552. J Antibiot. 2014;67(8):577–580.
- Furihata K, Seto H. Constant time HMBC (CT-HMBC), a new HMBC technique useful for improving separation of cross peaks. Tetrahedron Lett. 1998;39(40):7337–7340.
- Horiuchi M, Ohnishi K, Iwase N, et al. A novel isoindoline, porritoxin sulfonic acid, from Alternaria porri and the structure-phytotoxicity correlation of its related compounds. Biosci Biotechnol Biochem. 2003;67:1580–1583.
- Dale JA, Mosher HS. Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α-trifluoromethylphenylacetate (MTPA) esters. J Am Chem Soc. 1973;95:512–519.
- Ohtani I, Kusumi T, Kashman Y, et al. High-field FT NMR application of Mosher’s method. The absolute configurations of marine terpenoids. J Am Chem Soc. 1991;113:4092–4096.
- Marfey P. Determination of d-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene. Carlsberg Res Commun. 1984;49:591–596. .
- Kamalov LS, Aripova SF, Isaev MI. Low-molecular-mass metabolites of fungi I. Stachybotrin from Stachybotrys alternans. Chem Nat Compd. 1997;33:462–468.
- Kamalov LS, Aripova SF, Tashkhodzhaev BT, et al. Low-molecular-weight metabolites of fungi. II. Refinement of the structure of stachybotrin. Chem Nat Compd. 1998;34(5):605–608.
- Kamalov LS, Aripova SF, Isaev MI. Low-molecular-mass metabolites of fungi. III. Stachybotrolide from Stachybotrys alternans. Chem Nat Compd. 1998;34(5):616–619.
- Kamalov LS, Aripova SF, Isaev MI. Low-molecular-mass metabolites of fungi IV. The structures of stachybotrin A and stachybotral. Chem Nat Compd. 1999;35:82–85.
- Sakai K, Watanabe K, Masuda K, et al. Isolation, characterization and biological activities of novel triprenyl phenols as pancreatic cholesterol esterase inhibitors produced by Stachybotrys sp. F-1839. J Antibiot. 1995;48:447–456.
- Zhou D, Li L, Qi H, et al. A new stachybotrin congener from a soil fungus Stachybotrys parvispora strain HS-FG-843. J Antibiot. 2015;68:339–341.
- Li Y, Wu C, Liu D, et al. Chartarlactams A-P, phenylspirodrimanes from the sponge-associated fungus Stachybotrys chartarum with antihyperlipidemic activities. J Nat Prod. 2014;77:138–147.