LACTAM COMPOUNDS AND THEIR PHARMACEUTICAL USING Russian patent published in 2006 - IPC C07D487/04 C07D498/04 C07D513/04 A61K31/5517 A61K31/551 A61K31/55 A61P3/10 

Abstract RU 2287530 C2

FIELD: organic chemistry, medicine, pharmacy.

SUBSTANCE: invention relates to novel lactam compounds of the formula (I) or their pharmaceutically acceptable salts wherein A means phenyl, thienyl, pyridyl, pyrimidinyl, pyrazinyl; R2, R3 and R4 can be similar or different and mean independently of one another hydrogen atom (H), halogen atom, -OH, (C1-C6)-alkyl, (C1-C6)-alkoxy-group, -NH2, -NO2, -CF3, phenyl that can comprise substitute(s), benzyloxy-group that can comprise substitute(s), pnehylvinyl, and one among R2, R3 and R4 means -CF3-O- and others mean H; B means phenyl that can comprises substitute(s), monocyclic aliphatic (C3-C8)-ring, dihydropyrane ring; -X- and -Y- xan be similar or different and they mean independently -O-, -NH-, -NR5-, -S-; Z means -CH2-, -NH-; W means -NR1-, -CR8R9- wherein R1 means H; R8 and R9 are similar or different and mean H; wherein R5 represents a linear alkyl group that can comprise substitute(s), (C1-C8)-linear or branched alkoxycarbonyl group, acyl group chosen from formyl group, acyl group comprising (C1-C6)-alkyl, (C1-C6)-alkenyl or (C1-C6)-alkynyl group that can comprise substitute(s), carbamoyl group comprising (C1-C6)-alkyl group at nitrogen atom that can comprise substitutes, sulfonyl group comprising (C1-C6)-alkyl group at sulfur atom that can comprise substitute(s); each among a, b and c represents position of carbon atom under condition that: (i) substitute(s) is chosen from the group comprising halogen atom, -OH, (C1-C6)-alkyl, mercapto-group, (C1-C6)-alkoxy-group, -NO2, -COOH, -CF3, phenyl, -NH2, (C1-C8)-linear or branched alkoxycarbonyl group, (C1-C8)-linear or branched acyl group, (C1-C8)-linear or branched acyloxy-group; (ii) when B represents benzene ring, each among -X- and -Y- represents -NH-, -Z- represents -CH2- and -W- represents -NH- then R2, R3 and R4 can not mean phenyl group, 4-bromophenyl group, 4-hydroxyphenyl group, 4-methoxyphenyl group, 2-hydroxyphenyl group, 3,4-dimethoxyphenyl group or 3-methoxy-4-hydroxyphenyl group. Compounds of the formula (I) show the enhanced capacity for transport of sugar and can be used in pharmaceutical compositions for prophylaxis and/or treatment of diabetes mellitus and diabetic nephropathy.

EFFECT: valuable medicinal properties of compounds and pharmaceutical compositions.

19 cl, 21 tbl, 54 ex

Similar patents RU2287530C2

Title Year Author Number
PHOSPHOINDOLES AS HIV INHIBITORS 2005
  • Storer Richard
  • Dusson Siril
  • Aleksandr Fransua-Rene
  • Rolan Arlen
RU2393163C2
NITROGEN-CONTAINING AROMATIC DERIVATIVES, PHARMACEUTICAL COMPOSITION CONTAINING THEREOF, METHOD FOR TREATMENT AND USING 2003
  • Tsuruoka Akikhiko
  • Matsusima Tomokhiro
  • Matsukura Masajuki
  • Mijazaki Kazuki
  • Takakhasi Keiko
  • Kamata Dzjuniti
  • Fukuda Josio
RU2310651C2
ANTIVIRAL COMPOUND 2006
  • Betebenner Dehvid A.
  • Degoj Dehvid A.
  • Maring Klarens Dzh.
  • Krjuger Allan K.
  • Ivasaki Nobukhiko
  • Rokuehj Todd V.
  • Kuper Kert S.
  • Anderson Dehvid D.
  • Donner Pamela L.
  • Grin Brajan E.
  • Kempf Dejl Dzh.
  • Lju Dachun'
  • Makdehniel Kit F.
  • Mejdigan Dehrold L.
  • Motter Kristofer E.
  • Pratt Dzhon K.
  • Shehnli Dzhejson P.
  • T'Jufano Majkl D.
  • Vagner Rol'F
  • Chzhan Zhun
  • Molla Akkhteruzzaman
  • Mo Khunmehj
  • Pajlot-Matias Tami Dzh.
  • Masse Sheri Vl.
  • Kehrrik Robert Dzh.
  • Kheh Vepin
  • Lu Ljantszjun'
  • Grampovnik Dehvid Dzh.
RU2441010C2
HETEROARYLCARBOXYLIC ACID ESTER DERIVATIVES 2013
  • Kosiba Takakhiro
  • Tokumasu Munetaka
  • Itimaru Tajsuke
  • Osumi Kodzi
  • Nakagava Tadakie
  • Yamada Tatsukhiro
  • Matsumoto Kajo
  • Suzuki Tamotsu
RU2664544C2
NOVEL COMPOUND EXHIBITING ENTEROPEPTIDASE INHIBITING ACTIVITY 2019
  • Kim, Young Kwan
  • Kwon, Ohhwan
  • Park, Heedong
  • Park, Junggyu
  • Choi, Hwan Geun
  • Son, Jung Beom
  • Ko, Eunhwa
  • Kim, So Young
  • Lee, Seungyeon
  • Kang, Seock Yong
  • Ko, Yi Kyung
  • Park, Jin-Hee
RU2768755C1
5-SUBSTITUTED INDAZOLE AS KINASE INHIBITORS 2008
  • Akritopoulou-Zanze Irini
  • Uehjkfild Brajan D.
  • Mak Khel'Mut
  • Terner Shon K.
  • Gasiki Alan F.
  • Grasias Vidzhaja Dzh.
  • Sarris Kehti
  • Kalvin Duglas M.
  • Michmerkhuzen Melissa Dzh.
  • Shuaj Tsi
  • Patel Dzhioti R.
  • Bakker Margareta
  • Tojsh Nikol'
  • Dzhonson Ehrik F.
  • Kovar Piter Dzh.
  • D'Jurik Stiven V.
  • Long Ehndrju Dzh.
  • Vasudevan Anil
  • Khobson Adrian
  • St. Dzhon Mur Najdzhel
  • Van Lu
  • Dzhorzh Don
  • Li Bitsin'
  • Frank Kristin
RU2487873C2
MODULATORS OF ATP-BINDING CARTRIDGE TRANSPORTERS 2005
  • Adida Rua Sara S.
  • Khejzlvud Anna R.
  • Grotenkhejs Peter D.,J.
  • Van Gur Frederik F.
  • Singkh Ashvani K.
  • Chzhou Tszinlan'
  • Makkartni Dzhejson
RU2528046C2
DIAMINE DERIVATIVES 2003
  • Okhta Tosikharu
  • Komorija Satosi
  • Josino Tosikharu
  • Uoto Kouiti
  • Nakamoto Jumi
  • Naito Khirojuki
  • Motizuki Akijosi
  • Nagata Tsutomu
  • Kanno Khidejuki
  • Khaginoja Norijasu
  • Josikava Kendzi
  • Nagamoti Masatosi
  • Kobajasi Siozo
  • Ono Makoto
RU2333203C2
[1,8]NAPHTHYRIDINE DERIVATIVES, USEFUL AS INHIBITORS OF HCV VIRUS REPLICATION 2006
  • Rokuehj Todd V.
  • Betebenner Dehvid A.
  • Krjuger Allan K.
  • Ivasaki Nobukhiko
  • Kuper Kert S.
  • Anderson Dehvid D.
  • Kempf Dejl Dzh.
  • Mejdigan Dehrold L.
  • Motter Kristofer E.
  • Shehnli Dzhejson P.
  • T'Jufano Majkl D.
  • Vagner Rol'F
  • Chzhan Zhun
  • Molla Akkhteruzzaman
  • Mo Khunmehj
  • Pajlot-Matias Tami
  • Masse Sheri Vl.
  • Kehrrik Robert Dzh.
  • Kheh Vepin
  • Lu Ljantszjun'
RU2467007C2
ATP-BINDING CASETTE TRANSPORTER MODULATORS 2005
  • Adida Rua Sara S.
  • Khejzlvud Anna R.
  • Grotenkhejs Peter D. J.
  • Van Gur Frederik F.
  • Singkh Ashvani K.
  • Chzhou Tszinlan'
  • Makkartni Dzhejson
RU2382779C2

RU 2 287 530 C2

Authors

Jino Jukio

Ikenoue Takao

Kondo Nobuo

Matsueda Khirojuki

Khatanaka Tosikhiro

Khirama Riusuke

Masuzava Joko

Okhta Fumio

Jamazaki Akijo

Dates

2006-11-20Published

2001-11-29Filed