TY - JOUR
T1 - Structure determination, chemical synthesis, and evaluation of biological activity of super carbon chain natural products
AU - Oishi, Tohru
N1 - Funding Information:
I am grateful to professors Michio Murata (Osaka University), Nobuaki Matsumori (Kyushu Universiy), Keiichi Konoki (Tohoku University), and Masayuki Satake (The University of Tokyo) for collaboration. I thank all the co-workers for their significant contribution for this work. This work was supported by JSPS KAKENHI Grant Numbers JP16H04112, JP19H02720, JP16H01159 and JP18H04421 in Middle Molecular Strategy, and the Asahi Glass Foundation.
Publisher Copyright:
© 2020 The Chemical Society of Japan.
PY - 2020/11
Y1 - 2020/11
N2 - Marine microorganisms are known to produce natural products, so called super carbon chain compounds whose molecular weights (MWs) exceed one thousand, such as amphidinol 3 (AM3) and maitotoxin (MTX). AM3 (MW 1328) is a long linear compound containing polyol, bis-tetrahydopyran, and polyene moieties, and elicits potent antifungal activities. During the course of our studies on AM3, originally proposed absolute configuration was revised by the chemical synthesis of partial structures in combination with degradation of the natural product. Furthermore, the first total synthesis of AM3 has been achieved based on the convergent method via three components coupling. In addition, we have succeeded in design and synthesis of an artificial truncated analog of AM3 which elicits comparable antifungal activity with those of the natural product. On the other hand, MTX (MW 3422) is a ladder-shaped polyether comprised of thirty-two cyclic ethers, and it elicits potent Ca2+ influx activity. During the course of our structure-activity relationship studies of MTX, we have developed three methods for synthesizing ladder-shaped polyethers via two-ring construction through the coupling of two fragments. The synthetic partial structures corresponding to the hydrophobic parts of MTX inhibited the Ca2+ influx induced by MTX.
AB - Marine microorganisms are known to produce natural products, so called super carbon chain compounds whose molecular weights (MWs) exceed one thousand, such as amphidinol 3 (AM3) and maitotoxin (MTX). AM3 (MW 1328) is a long linear compound containing polyol, bis-tetrahydopyran, and polyene moieties, and elicits potent antifungal activities. During the course of our studies on AM3, originally proposed absolute configuration was revised by the chemical synthesis of partial structures in combination with degradation of the natural product. Furthermore, the first total synthesis of AM3 has been achieved based on the convergent method via three components coupling. In addition, we have succeeded in design and synthesis of an artificial truncated analog of AM3 which elicits comparable antifungal activity with those of the natural product. On the other hand, MTX (MW 3422) is a ladder-shaped polyether comprised of thirty-two cyclic ethers, and it elicits potent Ca2+ influx activity. During the course of our structure-activity relationship studies of MTX, we have developed three methods for synthesizing ladder-shaped polyethers via two-ring construction through the coupling of two fragments. The synthetic partial structures corresponding to the hydrophobic parts of MTX inhibited the Ca2+ influx induced by MTX.
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U2 - 10.1246/BCSJ.20200151
DO - 10.1246/BCSJ.20200151
M3 - Review article
AN - SCOPUS:85103900761
SN - 0009-2673
VL - 93
SP - 1350
EP - 1360
JO - Bulletin of the Chemical Society of Japan
JF - Bulletin of the Chemical Society of Japan
IS - 11
ER -