Synthesis of 2'-amino-2'-deoxyarbekacin and its analogs having potent activity against methicillin-resistant Staphylococcus aureus

DOI: 10.7164/antibiotics.47.821

Source and publish data:

Journal of Antibiotics p. 821 - 832 (1994)

Update date:2022-08-04

Topics: Synthesis Analog Potent activity

Authors:

Kondo Kondo

Ikeda Ikeda

Takeuchi

Usui Usui

Ishii Ishii

Kudo Kudo

Gomi Gomi

Shibahara

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

Article abstract of DOI:10.7164/antibiotics.47.821

Based on our studies on the enzymatic modifications of arbekacin by methicillin-resistant Staphylococcus aureus (MRSA), replacement of the 2'-hydroxyl group by an amino group in arbekacin was designed to synthesize derivatives that would be active against

Full text of DOI:10.7164/antibiotics.47.821

Products guided by the article

Product name:1,3''-bis(N-benzyloxycarbonyl)-3,2',6'-tris(N-tert-butoxycarbonyl)dibekacin

Cas No:161909-27-9

R&D Labs maybe for 161909-27-9

Nanjing Samwon International Limited

Contact:+86-25-84873444

Address:1108, BLDG B, New Century Plaza, No 1, South Taiping Rd.,
Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Guangzhou Probig Fine Chemical Co., Ltd.

Contact:020-86297874

Address:No.2, 1/F, No.20, Hetai Road,Hebian Village, Baiyun District,Guangzhou,China
LINAN HAIHUA CHEMICAL CO LTD

Contact:86-571-61063068

Address:LINAN
Tosta Enterprise Co., Ltd.

Contact:+86-134-5286-9121

Address:Add: Wing Tuck Commercial Centre, 177-183 Wing Lok Street, Hong Kong,

Relevant to this article

Copper-mediated hydroxylation of arenes and heteroarenes directed by a removable bidentate auxiliary

Doi:10.1021/ol5016064
(2014)
Cobalt-catalyzed chelation assisted C-H allylation of aromatic amides with unactivated olefins

Doi:10.1039/c6cc05330k
(2016)
Base-catalyzed domino cyclization of acetylenes with ketones to functionalized cyclopentenes

Doi:10.1021/ol501881e
(2014)
Oxidative skeletal rearrangement of 1,1′-binaphthalene-2,2′- diamines (BINAMs) via C-C bond cleavage and nitrogen migration: A versatile synthesis of U-shaped azaacenes

Doi:10.1039/c4cc04911j
(2014)
Doi:10.1021/jo01269a022
(1968)
Facile synthesis and NO-generating property of 4H-[1, 2, 5]oxadiazolo[3, 4-d]pyrimidine-5, 7-dione 1-oxides

Doi:10.1021/jo980732y
(1998)

Article Doi