Structures of New Antibiotic Substances, Sakyomicin A, B, C, and D; X-Ray Crystal and Molecular Structure of Sakyomicin A

DOI: 10.1039/c39830000174

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 174 - 175 (1983)

Update date:2022-07-30

Topics:

Authors:

Irie, Hiroshi

Mizuno, Yukio

Kouno, Isao

Nagasawa, Toru

Tani, Yoshiki

et al. et al.

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

Article abstract of DOI:10.1039/c39830000174

The structure of a new antibiotic substance, sakyomicin A has been elucidated by X-ray crystallographic analysis and structures for its congeners, sakyomicin B, C, and D have been proposed from their spectroscopic properties.

Full text of DOI:10.1039/c39830000174

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:sakyomicin D

Cas No:86413-77-6

R&D Labs maybe for 86413-77-6

Weifang Yukai Chemical Co.,Ltd.

website:http://www.yukaichem.com/en.html

Contact:+86-536-8865336

Address:binhai economic development zone，262737 shangdong，china
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
Changzhou Litong Chemical Co., Ltd.

website:http://www.litonchem.com/

Contact:+86-519-86301238

Address:Laoba Rd, Hutang town Changzhou Jiangsu
Jiacheng-Chem Enterprises Limited(expird)

Contact:86-571-86711508

Address:19 Floor, CIBC Holley International Building, No. 198,Wuxing Road, Hangzhou, China,310020
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone

Relevant to this article

A synthetic approach to the stemona alkaloids

Doi:10.1021/jo0106391
(2001)
A Series of Ferulic Acid Amides Reveals Unexpected Peroxiredoxin 1 Inhibitory Activity with in vivo Antidiabetic and Hypolipidemic Effects

Doi:10.1002/cmdc.202000564
(2021)
DABCO-bis (sulfur dioxide), DABSO, as a convenient source of sulfur dioxide for organic synthesis: Utility in sulfonamide and sulfamide preparation

Doi:10.1021/ol201957n
(2011)
Daphnicyclidins A-H, novel hexa- or pentacyclic alkaloids from two species of Daphniphyllum

Doi:10.1021/ja016955e
(2001)
Studies directed towards the enantioselective synthesis of ethisolide and isoavenaciolide

Doi:10.1002/ejoc.200500884
(2006)
INTRODUCTION OF OXYGENATED FUNCTIONAL GROUPS INTO 3-CARENE AND 2-PINENE BY CULTURED CELLS

Doi:10.1016/0031-9422(94)85067-4
(1994)

Article Doi