98892-19-4Relevant academic research and scientific papers
Synthetic spiroketal pyranes as potent anti-cancer agents
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Example 2, (2010/11/29)
Novel tubulin binding compounds (SPIKETS) having potent tubulin depolymerization activity and inhibitory activity against tubulin polymerization. The compounds are effective agents for inhibiting cellular proliferation, for example, in cancer cells. The compounds are adapted to interact favorably with a novel SP binding pocket on tubulin, which pocket is useful for screening of anti-tubulin, anti-proliferation, and anti-cancer drugs.
Novel chiral glycerol analogues building blocks. Application to the synthesis of bioactive glycoglycerolipid analogues
Ferraboschi,Colombo,Compostella,Reza-Elahi
, p. 1379 - 1382 (2007/10/03)
Monoacylglycosylglycerols show anti-tumor promoting effects: in order to study the role of the ester function we have prepared by simple methods (R)-1-O-benzyl-1,2-decandiol, (R)-3-O-benzyl-1-O-hexyl-sn-glycerol, and (R)-1-O-benzyl-5-oxo-1,2-decandiol; these optically active compounds are building blocks for the synthesis of monohexanoylglycosylglycerol isosters.
Structure-based design of a novel synthetic spiroketal pyran as a pharmacophore for the marine natural product Spongistatin 1
Uckun, Fatih M.,Mao, Chen,Vassilev, Alexei O.,Huang, He,Jan, Shyi-Tai
, p. 541 - 545 (2007/10/03)
SPIKET-P, a novel synthetic spiroketal pyran, was rationally designed as a pharmacophore for the tubulin depolymerizing marine natural product Spongistatin 1. SPIKET-P was prepared from the commercially available benzyl (R)-(-)-glycidyl ether using a versatile 11-step synthetic scheme in a stereocontrolled fashion. At nanomolar concentrations, SPIKET-P caused tubulin depolymerization in cell-free turbidity assays and exhibited potent cytotoxic activity against cancer cells as evidenced by destruction of microtubule organization, and prevention of mitotic spindle formation in human breast cancer cells. (C) 2000 Elsevier Science Ltd. All rights reserved.
Stereocontrolled synthesis of a novel pharmacophore of the tubulin- depolymerizing marine natural product spongistatin
Huang, He,Mao, Chen,Jan, Shyi-Tai,Uckun, Fatih M.
, p. 1699 - 1702 (2007/10/03)
We report here the synthesis and X-ray structure of a novel spiroketal pyran, SPIKET-P1, as a pharmocophore for the tubulin-depolymerizing marine natural product spongistatin 1. Following its retro-synthetic analysis, SPIKET-P1 was prepared using a versatile 11-step synthetic scheme in a stereocontrolled fashion. (C) 2000 Elsevier Science Ltd.
SYNTHESIS OF CLAVULONES (CLAVIRIDENONES)
Hashimoto, Shinsuke,Arai, Yoshinobu,Hamanaka, Nobuyuki
, p. 2679 - 2682 (2007/10/02)
New marine eicosanoid clavulones (claviridenones) were synthesized from the Corey lactone and D-glutamic acid.
