1233644-94-4Relevant academic research and scientific papers
Hamigeromycins C-G, 14-membered macrolides from the fungus Hamigera avellanea BCC 17816
Isaka, Masahiko,Chinthanom, Panida,Kongthong, Surisa,Supothina, Sumalee,Ittiworapong, Pataranun
, p. 955 - 961 (2010)
Five new 14-membered macrolides, hamigeromycins C-G, together with the previously described compounds, hamigeromycin A and 89-250904-F1 (radicicol analog A), were isolated from the fungus Hamigera avellanea BCC 17816. Hamigeromycins A, C, D, and E are stereoisomers differing from one another in the absolute configurations of the 4′,5′-diol moiety. Hamigeromycins F and G are unusual 5′-keto-analogs, and they are 6′-epimers to each other. The structures and the stereochemistry of the new compounds were deduced by analyses of the NMR spectroscopic and mass spectrometry data in combination with chemical means.
