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Title:
ベンゾイルグリシン誘導体およびその作製および使用の方法
Document Type and Number:
Japanese Patent JP7012289
Kind Code:
B2
Abstract:
Disclosed are compounds of formulae:and pharmaceutically acceptable salts thereof, wherein the variables, R1, R2, R3, R4, R5, R6, R7, R11, R12, R13, R14, R15, R16, R17, n, and m are defined herein. These compounds are useful for treating Gram-negative bacteria infections. Also disclosed are methods of making these compounds.

Inventors:
Robert A. Nicholas
Liang Xiaofei
Pei butterfly
Eric Jay Toon
Ramesh Gopalaswamy
Frank Navas, The Third
Application Number:
JP2018556890A
Publication Date:
February 14, 2022
Filing Date:
April 25, 2017
Export Citation:
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Assignee:
Duke University
THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
International Classes:
C07C259/06; A61K31/198; A61K31/396; C07C229/22; C07C311/06; C07D309/06
Domestic Patent References:
JP51076220A
JP2012502946A
JP2010280684A
JP62255460A
JP2010530372A
Foreign References:
WO2015024011A1
US20150225388
WO2014165075A1
WO2015024010A1
WO2012031298A1
WO2013170030A1
Other References:
LIANG, X. et al.,A scalable synthesis of the difluoromethyl-allo-threonyl hydroxamate-based LpxC inhibitor lpc-058,The journal of Organic Chemistry,2016年,Vol.81,pp.4393-4398
SOLOSHONOK, V. et al.,Transition metal/base-catalyzed aldol reactions of isocyanoacetic acid derivatives with prochiral ketones, a straightforward approach to stereochemically defined β,β-disubstituted-β-hydroxy-α-amino acids. Scope and limitations,J. Org. Chem.,1997年,Vol.62,pp.3470-3479
SOLOSHONOK, V. A. et al.,Transition metal-catalyzed diastereoselective aldol reactions of prochiral ketones with methyl isocyanoacetate,Tetrahedron Letters,1996年,Vol.37, No.43,pp.7845-7848
LEE, C. J. et al.,Drug design from the cryptic inhibitor envelope,NATURE COMMUNICATIONS,2016年,pp.1-7,Supplementary Data,doi:10.1038/ncomms10638
Registry(STN)[online],2015年12月03日,CAS登録番号 1822350-04-8
Attorney, Agent or Firm:
Aoki Atsushi
Shinji Mihashi
Youichi Watanabe
Nakajima Masaru
Ryotaro Takei
Michiko Uehara