Mutagenic and prophage-inducing activities of 1-alkyl-3-nitro-1-nitrosoguanidines.

DOI: 10.1248/cpb.19.1809

Source and publish data:

Chemical and pharmaceutical bulletin p. 1914 - 1918 (1971)

Update date:2022-07-30

Topics:

Authors:

Iwahara Iwahara

Yanagimachi

Kamiya Kamiya

Nakadate

Suzuki Suzuki

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

Article abstract of DOI:10.1248/cpb.19.1809

Full text of DOI:10.1248/cpb.19.1809

NII-Electronic Library Service

Products guided by the article

Product name:1-Hexyl-3-nitro-1-nitrosoguanidine

Cas No:35089-70-4

R&D Labs maybe for 35089-70-4

xuri chemicals co., ltd

Contact:86-516-66656369

Address:The west road of Huaihai, Xuzhou, China
SYN Pharma Co., Ltd

Contact:86-21 60347964

Address:No.1304, West Meilong Road, Minhang District, Shanghai, China
Jintan City Mego Chemical Co., Ltd

Contact:+86-0519-82814387

Address:23# Dengguan Town, Jintan, Jiangsu Province, China
Hefei TNJ chemical industry co.,ltd

website:https://www.tnjchem.com

Contact:+86-551-65418695

Address:B911 Xincheng Business Center, Qianshan Road, Hefei Anhui China
Shandong Dayi Chemical Co., Ltd.

website:http://www.dayi.com.cn

Contact:+86- 535-7388728. 15306386031

Address:No 1 Danya west road, Laiyang City, Shandong province

Relevant to this article

Targeting ceramide metabolism with a potent and specific ceramide kinase inhibitor

Doi:10.1124/mol.108.048652
(2008)
Doi:10.1016/0040-4020(72)80064-4
(1972)
Synthesis and biological evaluation of novel Ani9 derivatives as potent and selective ANO1 inhibitors

Doi:10.1016/j.ejmech.2018.10.002
(2018)
Amide group coordination to the Hg²⁺ ion. Potentiometric, ¹H NMR and structural study on Hg²⁺-N-protected amino acid systems

Doi:10.1039/b100310k
(2001)
Oxidative and Redox-Neutral Approaches to Symmetrical Diamines and Diols by Single Electron Transfer/Hydrogen Atom Transfer Synergistic Catalysis

Doi:10.1002/ejoc.202001329
(2020)
Doi:10.1139/v71-674
(1971)

Article Doi