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Patent Searching and Data


Title:
【発明の名称】マクロサイクリックラクトン、組成物、および使用方法
Document Type and Number:
Japanese Patent JP2001510838
Kind Code:
A
Abstract:
The present invention provides compound of the formula:wherein R1 and R2 are the same or different and are independently H, C1-C6 straight-chain or branched saturated or unsaturated alkyl, aryl, R6CH2-, R6CO-, or R6SO2-, wherein R6 is H, C1-C6 straight-chain or branched saturated or unsaturated alkyl, or aryl; R3 is H, C1->C6 straight-chain or branched-chain saturated alkyl, aryl, an oxime, or an oxime methyl ether; at least one aromatic ring position is optionally substituted with a substituent selected from the group consisting of halo, nitro, amino, hydroxyl, thio, acyl, C1-C6 alkyl, and cyano; and Z is a contiguous linker comprising a chain of 7-10 atoms (including heteroatoms) which atoms, together with the five atoms beginning with the carbon of the aromatic ring in meta-relationship with OR1 and ending with the carbon directly attached to the alkyl oxygen of the lactone, which carbons are covalently bonded to either end of linker Z, integrally form a 12-15 membered ring; or a pharmaceutically acceptable salt, an ester, or a prodrug thereof.The present invention further provides a pharmaceutical composition, and a method of preventing or treating cancer, using at least one compound of the present invention, optionally in conjunction with an additional compound other than a compound of the present invention.

Inventors:
Boyd, Michael Earl.
McKee, Tonya Si.
Cardelina The Second, John H.
Butler, John A.
Ericsson, Karen
Galinis, Deborah
Panel, lewis
Application Number:
JP2000504132A
Publication Date:
August 07, 2001
Filing Date:
July 23, 1998
Export Citation:
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Assignee:
US HEALTH (US)
International Classes:
A61K31/357; A61K31/365; A61P35/00; C07D313/00; C07D321/00; (IPC1-7): C07D313/00; A61K31/365; A61P35/00; C07D321/00
Attorney, Agent or Firm:
Takashima Hajime