Studies on irreversible inhibition of serine proteases by α- sulfonyloxyketone derivatives

DOI: 10.1016/0960-894X(96)00178-3

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 1127 - 1132 (1996)

Update date:2022-08-05

Topics:

Authors:

Ohba Ohba

Wakayama

Ikeda Ikeda

Takei Takei

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0960-894X(96)00178-3

α-Sulfonyloxyketone derivatives were found to be active-site directed irreversible inhibitors of serine proteases.

Full text of DOI:10.1016/0960-894X(96)00178-3

Products guided by the article

Product name:4-Phenyl-3-trimethylsilanyloxy-butan-2-one

Cas No:119554-23-3

R&D Labs maybe for 119554-23-3

NIGNXIA XINDACHANG TECHNOLOGY CO.,LTD

website:https://xdcchemical.com/

Contact:86-311-85758226

Address:North Industry Area, Wuji
TAIZHOU XINGCHENG CHEMPHARM CO.,LTD.

Contact:0086-0576-88551200,88886292 ,88880039

Address:B Area. 10 Floor.Yaodadasha. 289#.Shifu Road.Taizhou.Zhejiang.China
C-LAB Chemievermittlung GmbH

Contact:+49-9398-993127

Address:Untertorstr. 27
Shanghai Mintchem Development ., Ltd

Contact:0086 21 5190 8570

Address:R602,4#,89Nong, Mudan Road Pudong Shanghai China
Fujian Huitian Biological Pharmacy Co., Ltd.

Contact:0086-598-8300831; 8339920

Address:No.46,Taijiang Road,Sanming City,Fujian,China

Relevant to this article

One-pot synthesis of symmetric and unsymmetric 1,1-bis-indolylmethanes via tandem iron-catalyzed C-H bond oxidation and C-O bond cleavage

Doi:10.1021/jo902093p
(2009)
SnCl₄/SiO₂: An efficient heterogeneous alternative for one-pot synthesis of β-acetamidoketones

Doi:10.1002/jccs.200900056
(2009)
Mechanistic studies on Ni(dppe)Cl₂-catalyzed chain-growth polymerizations: Evidence for rate-determining reductive elimination

Doi:10.1021/ja904197q
(2009)
Design and synthesis of substituted nicotinamides as inhibitors of soluble epoxide hydrolase

Doi:10.1016/j.bmcl.2009.08.074
(2009)
Synthesis of novel naphth[1,2-f][1,4]oxazepine-3,4-dione heterocycles

Doi:10.1002/jhet.166
(2009)
Potent biphenyl- and 3-phenyl pyridine-based inhibitors of acetyl-CoA carboxylase

Doi:10.1016/j.bmcl.2009.08.077
(2009)

Article Doi