【発明の名称】新規のロイコトリエン-B▲下4▼-誘導体、および製造法

Japanese Patent JP2921600

B2

PCT No. PCT/DE90/00397 Sec. 371 Date Mar. 25, 1991 Sec. 102(e) Date Mar. 25, 1991 PCT Filed May 25, 1990 PCT Pub. No. WO90/14329 PCT Pub. Date Nov. 29, 1990. (I) (a) (II) (III) (IV) Compounds of formula (I) in which the residues have the following meanings: a is (II) or (III); R1 is CH2OH, CH3, CF3, COOR5 with R5 or, A is a trans, trans-CH=CH-CH=CH-or tetramethylene group; B is an alkylene group with up to 10 C atoms; D is a direct bond, oxygen, sulphur, a -C 3BOND C-group or a -CH=CR7-group, or (IV); B and D together are a direct bond; R2 and R3 are the same or different and denote hydrogen or an organic acid residue with 1 to 15 C atoms, R1 and R2 together are a carbonyl group; R4 is a hydrogen atom or C1-10 alkyl, and if R5 denotes a hydrogen atom, their salts with physiologically acceptable bases and their cyclodextrin clathrates.

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WO/2018/191153	CANCER TREATMENT BY MALAT1 INHIBITION
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SUKUBARA UERUNAA
BUTSUFUMAN BERUNTO
HAINDORU YOZEFU
FUREERITSUHI UORUFUGANGU
EKERUTO ROORANTO

JP50789590A

July 19, 1999

May 25, 1990

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SHEERINGU AG

A61K31/16; A61K31/18; A61K31/19; A61K31/22; A61K31/365; A61K31/557; A61P29/00; A61P31/04; A61P37/08; A61P43/00; C07C33/14; A61K31/045; C07C59/46; C07C59/48; C07C69/16; C07C69/18; C07C69/73; C07C69/732; C07C235/08; C07C403/00; C07C405/00; C07D309/30; C07D333/02; C07F7/18; C07C; (IPC1-7): C07C33/14; C07C59/46; C07C69/16; C07C69/732; C07C235/08; C07D309/30

Toshio Yano (2 outside)

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