ENZYMES INHIBITION Russian patent published in 2017 - IPC C07D471/04 A61K31/4196 A61K31/437 A61P11/00 

Abstract RU 2638537 C2

FIELD: pharmacology.

SUBSTANCE: invention relates to the compound of the formula or its pharmaceutically acceptable salt. In the formula (I) R1 represents -CN; R2 is selected from (C1-C4)haloalkyl, (C1-C4)haloalkoxy; W represents the (i) 5-membered heteroaryl ring, where two or three ring-atoms represent the hetero-atom N, optionally substituted by one group, which is selected from the (C1-C4) alkyl, the group -NHR18, and from the group -COOR28; or (iii) phenyl group; R3 represents the group -CH2-R23; R5 represents the hydrogen; R6 represents the hydrogen; A1 represents the group -CR7=; A2 represents the group =CR8- or the group =N-; A3--A4 represents the group, which is selected from the group -CR4=N-, the group -CR4=CR9- and the group NR17-CO-; R4 represents the group, which is selected from the hydrogen, the (C1-C4) alkyl, -NR10R11, -NHCOR12, -NHCOO-R13, -NHCONR27-R14, the (C1-C4)alkoxy, -NH(CH2)n-SO2(C1-C4)alkyl, -(NH)q(CH2)n-(C6H4)-SO2(C1-C4)alkyl, -NHSO2(C1-C4) alkyl and -(NH)r(CH2)nCONR15R16; the other chemical groups value is indicated in the invention formula. The invention also relates to the pharmaceutical composition and to the method of the disease or state treatment, where HNE is implicated.

EFFECT: there are new compounds of the formula that offer the inhibitors' properties of the human neutrophil elastase.

14 cl, 97 ex

Similar patents RU2638537C2

Title Year Author Number
JAK-INHIBITING TRIAZOLOPYRIDINE COMPOUNDS AND METHODS 2009
  • Chzhu Bin-Jan'
  • Siu Majkl
  • Magnuson Stiven R.
  • Pastor Richard
  • Khajin Kheh
  • Isun Sjao
  • Tszifu Chzhehn
  • Sin Sjuj
  • Tszjun'Pin Chzhao
  • Kharli Kristofer A.
  • Ljan Tszjun'
  • Lju Vendi
  • Lissikatos Dzhozef P.
RU2560153C2
TRIAZOLOPYRIDINES AS PHOSPHODIESTERASE INHIBITORS FOR TREATING SKIN DISEASES 2009
  • Nil'Sen Simon Fel'Dbek
  • Vifian Tomas
  • Khorneman Anne Marija
  • Lau Jesper Fergemann
RU2544011C2
TRIAZOLOPYRIDINE JAK INHIBITOR COMPOUNDS AND METHODS 2009
  • Chzhu Bin-Jan'
  • Siu Majkl
  • Magnuson Stiven R.
  • Pastor Richard
  • Khajin Kheh
  • Isun Sjao
  • Tszifu Chzhehn
  • Sin Sjuj
  • Tszjun'Pin Chzhao
  • Lju Vendi
RU2561104C2
COMPOUNDS AND COMPOSITIONS AS ITPKb INHIBITORS 2007
  • Pan' Shifehn
  • Lju I
  • Si Jun'Fehn
  • Chehn Daj
  • Van' Juntsin'
  • Khan' Dun
  • Jan Jan
  • Gao Vehn'Tsi
  • Tszjan Tszitsin
  • Bursalaja Badri
  • Chamberlejn Filip
  • Karanevski Donald S.
  • Van Sja
RU2425826C2
MULTI-SUBSTITUTED AROMATIC COMPOUNDS AS THROMBIN INHIBITORS 2011
  • Short Kevin Majkl
  • Fam Son Minkh
  • Uillyams Devid Charlz
  • Datta Somalee
RU2639876C2
PESTICIDAL COMPOSITIONS 2009
  • Krauz Gari
  • Sparks Tomas
  • Makled Kasandra
  • Demeter Dehvid
  • Brajan Kristi
  • Braun Annett
  • Dehnt Uill'Jam
  • Kaduort Deniz
  • Nadzhent Dzhejm
  • Khanter Riki
  • Samaritoni Dzhek
RU2513723C2
BICYCLIC LACTAMS AND METHODS FOR USE THEREOF 2016
  • Patel Snakhel
  • Gamilton Gregori
  • Stivala Krejg
  • Chen Khuejfen
  • Chzhao Gujlin
RU2716136C2
PHENOXYMETHYL HETEROCYCLIC COMPOUNDS 2009
  • Shapiro Gideon
  • Ripka Ehmi
  • Chesuort Richard
RU2531274C2
TETRAHYDROTRIAZOLOPYRIMIDINE DERIVATIVES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE 2012
  • Blench Toby Jonathan
  • Edwards Christine
  • Heald Robert Andrew
  • Kulagowski Janusz Josef
  • Sutton Jonathan Mark
  • Capaldi Carmelida
RU2622643C2
SUBSTITUTED PYRAZOLES 2001
  • Brajtenbukher Dzh. Gaj
  • Kaj Kh'Jui
  • Ehdvards Dzhejms P.
  • Grajs Cheril A.
  • Gastin Darin Dzh.
  • Kkhatuja Kharipada
  • Meduna Stiven P.
  • Pajo Barbara A.
  • Tehjs Kevin L.
  • Vej Dzhianmej
RU2286343C2

RU 2 638 537 C2

Authors

Kapaldi Karmelida

Khild Robert Endryu

Rej Nikolas Charlz

Satton Dzhonatan Mark

Dates

2017-12-14Published

2013-07-10Filed