450408-59-0Relevant articles and documents
Synthetic studies on callipeltin A: Stereoselective synthesis of (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid
Zampella, Angela,Sorgente, Maria,D'Auria, Maria Valeria
, p. 681 - 685 (2002)
An efficient and highly stereocontrolled synthesis of protected (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid, the β-hydroxy acid unit that acylates the N-terminus of callipeltin A, has been devised starting from methyl (2S)-2-methyl-3-hydroxypropion
Total synthesis of odoamide, a novel cyclic depsipeptide, from an Okinawan marine cyanobacterium
Kaneda, Masato,Sueyoshi, Kosuke,Teruya, Toshiaki,Ohno, Hiroaki,Fujii, Nobutaka,Oishi, Shinya
, p. 9093 - 9104 (2016/10/07)
Odoamide is a novel cyclic depsipeptide with highly potent cytotoxic activity isolated from the Okinawan marine cyanobacterium Okeania sp. It contains a 26-membered macrocycle composed of a fatty acid moiety, a peptide segment and isoleucic acid. Four pos