Analysis of hydroxylamine glycosidic linkages: Structural consequences of the NO bond in calicheamicin

DOI: 10.1021/ja00087a005

Source and publish data:

Journal of the American Chemical Society p. 3197 - 3206 (1994)

Update date:2022-08-05

Topics:

Authors:

Walker, Suzanne

Gange, David

Gupta, Varsha

Kahne, Daniel

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

Article abstract of DOI:10.1021/ja00087a005

The antitumor activity of calicheamicin is related to its ability to bind to and cleave double-stranded DNA. There is substantial evidence that the oligosaccharide-aryl tail of calicheamicin plays a critical role in the binding selectivity. The calicheami

Full text of DOI:10.1021/ja00087a005

Products guided by the article

Product name:C₂₅H₂₉NO₁₀

Cas No:157487-15-5

R&D Labs maybe for 157487-15-5

Xuzhou Tianrun Chemical Co.,Ltd

website:http://www.tianrunchem.cn

Contact:86-516-83832636

Address:fuxing road
New Forms

Contact:+31-24-3886056

Address:Binderskampweg 29 Unit 36
JiangXi Hong Run Chemical Co., Ltd

Contact:+86-0791-88521351

Address:XingHuo industrial zone in YongXiu county
Shangyu Sanhechemicals Co.,LTD.

Contact:86-0571-56696839

Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China
Zhejiang Chemicals Import & Export Corporation (ZHECHEM)

Contact:+86-571-87046953

Address:No. 37, Qingchun Road

Relevant to this article

Doi:10.1007/BF00468359
()
Facile organocatalytic domino oxidation of diols to lactones by in situ-generated TetMe-IBX

Doi:10.1016/j.tet.2014.01.034
(2014)
Facile Synthesis of (+)-Brefeldin A Utilizing Two Optically Active Synthons Prepared by Different Enzyme-catalysed Reactions

Doi:10.1039/c39940001085
(1994)
Synthesis and optical properties of new 5′-aryl-substituted 2,5-bis(3-decyl-2,2′-bithiophen-5-yl)-1,3,4-oxadiazoles

Doi:10.3762/bjoc.13.34
(2017)
Himbacine-derived thrombin receptor antagonists: C₇-Spirocyclic analogues of vorapaxar

Doi:10.1021/ml500008w
(2014)
Structural optimization of pyridine-type DAPY derivatives to exploit the tolerant regions of the NNRTI binding pocket

Doi:10.1016/j.ejmech.2016.05.054
(2016)

Article Doi