Journal ArticleDOI
122. The nature of the amino-group in aminoacridines. Part I. Evidence from electrometric studies
Adrien Albert,Reginald Goldacre +1 more
Reads0
Chats0
About:
This article is published in Journal of The Chemical Society (resumed).The article was published on 1943-01-01. It has received 18 citations till now. The article focuses on the topics: Aminoacridines.read more
Citations
More filters
Journal ArticleDOI
Interaction of aromatic compounds with alpha-chymotrypsin
Journal ArticleDOI
Some studies on cytisine and its methylated derivatives.
R. B. Barlow,L. J. McLEOD +1 more
TL;DR: In mice cytisine hydrochloride is less toxic intravenously than nicotine hydrogen tartrate, but more toxic by intraperitoneal or oral administration; if the drug is placed directly in the stomach there is no possibility of absorption through buccal mucous membranes.
Book ChapterDOI
Prototropic Tautomerism of Heteroaromatic Compounds: II. Six-Membered Rings
TL;DR: The most important cases of tautomerism in heterocyclic compounds containing six-membered rings involve the movement of a proton between a cyclic nitrogen atom and an atom adjacent to the ring as discussed by the authors.
Journal ArticleDOI
Combined mutagenicity of cobalt(II) salt and heteroaromatic compounds in Salmonella typhimurium
H. Iyehara Ogawa,Kazunori Sakata,Takashi Inouye,Shinichi Jyosui,Yoshiyuki Niyitani,Kohji Kakimoto,Masato Morishita,Satoshi Tsuruta,Yasuhiko Kato +8 more
TL;DR: Judging from visible and nuclear magnetic resonance spectral data, this increased mutagenicity may be attributable to the formation of moderate to weak complexes between these chemicals and the Co(II) cation.
Journal ArticleDOI
Effects of some isomers and analogues of nicotine on junctional transmission.
R. B. Barlow,J. T. Hamilton +1 more
TL;DR: A number of isomers and homologues of nicotine, (2-, 3- and 4-pyridylmethyl)- and [2-(2-(3-and-4-pyrs)ethyl)ethyl]- dialkylamines and trialkylammonium salts, have been prepared and the relationships between structure and dissociation constant, anticholinesterase activity, and activity in the pharmacological tests have been discussed.