IMIDAZOLE COMPOUNDS, METHOD FOR THEIR PREPARING, METHOD FOR INHIBITION OF ACTIVITY OF ADENOSINE DEAMINASE AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF Russian patent published in 2004 - IPC

Abstract RU 2243220 C2

FIELD: organic chemistry, biochemistry, medicine, pharmacy.

SUBSTANCE: invention relates to new imidazole compounds of the formula (I):

wherein R1 represents hydrogen atom, hydroxy-, protected hydroxy-group or aryl optionally substituted with suitable substitute(s) taken among the group consisting of halogen-(lower)-alkyl, halogen atom, hydroxy-, protected carboxy-group, carbamoyl, lower alkylenedioxy- lower alkoxy-group optionally substituted with aryl and lower alkyl optionally substituted with hydroxy- or protected carboxy-group; R2 represents hydrogen atom or lower alkyl; R3 represents hydroxy- or protected hydroxy-group; R4 represents cyano-group, (hydroxy)-iminoamino-(lower)-alkyl, carboxy-, protected carboxy-group, N-comprising heterocyclic group optionally substituted with amino-group or carbamoyl optionally substituted with suitable substitute(s) taken among the group consisting of amino-, hydroxy-group, lower alkyl, lower alkylsulfonyl and aminoimino-(lower)-alkyl optionally substituted with hydroxy-group; -A- represents -Q- or -O-Q- wherein Q means a single bond or lower alkylene, or its salt under condition that when R2 means lower alkyl then R1 represents hydroxy-, protected hydroxy-group or aryl optionally substituted with suitable substitute(s) given above, and also under condition that compound of the formula (I) doesn't represent 1-(hydroxyethyl)-4-(ethoxycarbonyl)-imidazole or 1-(2-hydroxyethyl)-imidazole 4-carboxylic acid anilide. Also, invention relates to a method for preparing these compounds, to a method for inhibition of activity of adenosine deaminase, and to a pharmaceutical composition eliciting inhibitory effect on activity of adenosine deaminase based on these compounds. Invention provides preparing new compounds and medicinal agents based on thereof used for prophylaxis and treatment of disease wherein adenosine shows the effectiveness.

EFFECT: improved inhibiting and preparing methods, valuable medicinal properties of compounds.

9 cl, 2 tbl, 32 ex

Similar patents RU2243220C2

Title Year Author Number
BENZOPYRANE DERIVATIVE AND MEDICINAL AGENT BASED ON THEREOF 2000
  • Tanikava Kejzo
  • Okhraj Kazukhiko
  • Janagikhara Kazufumi
  • Sigeta Jukikhiro
  • Tsukagosi Toru
  • Jamasita Toru
RU2234502C2
NEW β-LACTAMASE INHIBITOR AND A METHOD OF ITS PRODUCTION 2019
  • Abe, Takao
  • Furuuchi, Takeshi
  • Sakamaki, Yoshiaki
  • Inamura, Seiichi
  • Morinaka, Akihiro
RU2800050C2
NOVEL BETA-LACTAMASE INHIBITOR AND METHOD FOR PRODUCTION THEREOF 2013
  • Abe Takao
  • Furuuti Takesi
  • Sakamaki Josiaki
  • Inamura Seiiti
  • Morinaka Akikhiro
RU2693898C2
COMPOUNDS OF N,N-SUBSTITUTED CYCLIC AMINE 1999
  • Jamamoto Noboru
  • Komatsu Makoto
  • Suzuki Juiti
  • Kavano Koki
  • Kimura Teidzi
  • Ito Koiti
  • Nagato Satosi
  • Norimine Esikhiko
  • Niidome Tetsukhiro
  • Teramoto Tetsujuki
  • Iimura Eiti
  • Khatakejama Sindzi
RU2232156C2
AZOLE COMPOUNDS, METHOD OF THEIR SYNTHESIS, ANTIFUNGAL PHARMACEUTICAL COMPOSITION AND METHOD OF TREATMENT OF FUNGAL INFECTION 1998
  • Itokh Katsumi
  • Kitazaki Tomojuki
  • Okonogi Kendzi
RU2189982C2
DERIVATIVES OF DIAMINES 2002
  • 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 Suozo
  • Ono Makoto
RU2319699C2
DIAMINE DERIVATIVES 2002
  • 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
RU2314303C2
COMPOUNDS, PHARMACEUTICAL COMPOSITION, METHOD FOR PREVENTING NERVOUS CELL DEATH, METHOD FOR PROPHYLAXIS 2001
  • Jamamoto Noburu
  • Sudzuki Juiti
  • Kimura Manami
  • Nidome Tetsukhiro
  • Ijmura Joiti
  • Teramoto Tetsujuki
  • Kaneda Josikhisa
  • Kaneko Tosikhiko
  • Kurusu Nobujuki
  • Sinmio Daisuke
  • Josikava Jukie
  • Khatakejama Sindzi
RU2230060C2
DERIVATIVES OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND METHOD FOR TREATMENT OF DISORDERS WITH NEURONS INJURY 2000
  • Kanodzhia Ramesh M.
  • Dzhordan Al'Fonso D.
  • Rejtz Allen B.
  • Mehsilag Mark Dzh.
  • Zao Boui
RU2241709C2
DERIVATIVES OF IMIDAZOLE ELICITING INHIBITORY ACTIVITY WITH RESPECT TO FARNESYLTRANSFERASE, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS, PHARMACEUTICAL COMPOSITION 1998
  • Li Khiun Il
  • Kokh Dzong Sung
  • Li Dzin Kho
  • Dzung Von Khi
  • Shin Ju Seung
  • Chung Khiun Kho
  • Kim Dzong Khiun
  • Ro Seong Gu
  • Choj Tae Saeng
  • Dzeong Shin Vu
  • Kvak Tae Khvan
  • Akhn In Ae
  • Kim Khiun Sung
  • Li Sun Khva
  • Kim Kvi Khva
  • Joo Dzung Kvon
RU2179975C1

RU 2 243 220 C2

Authors

Terasaka Tadasi

Nakamura Katsuja

Seki Nobuo

Kuno Masako

Tsudzimoto Susumu

Sato Akikhiro

Nakanisi Isao

Kinosita Takaesi

Nisio Nobuja

Okumura Khirojuki

Tsudzi Kiesi

Dates

2004-12-27Published

1999-07-22Filed