<script type="text/javascript">
<!--
document.write('<div id="oa_widget"></div>');
document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=undefined&type=result"></script>');
-->
</script>

COPY SCRIPT

For further information contact us at helpdesk@openaire.eu

The polarography of cephalosporin C derivatives

descriptionPublicationkeyboard_double_arrow_right Article 01 Dec 1968Publisher:Oxford University Press (OUP)Journal:Journal of Pharmacy and Pharmacology, volume 20, pages 45S-47S (issn: 0022-3573, eissn: 2042-7158,

Authors: C T Rhodes; I F Jones; J E Page;

doi: 10.1111/j.2042-7158.1968.tb09860.x

pmid: 4388171

The polarography of cephalosporin C derivatives

- Summary
- Subjects
- Related research
  (3)
- Metrics

Abstract

Abstract WE report some preliminary measurements on the polarographic reduction of cephalosporin C, cephalothin [7-(2-thienylacetamido)-cephalosporanic acid] and cephaloridine [7-(2-thienylacetamido)-3-(1-pyridylmethyl)-3-cephem-4-carboxylic acid betaine]. Green, Page & Staniforth (1965) have shown that cephalosporin C derivatives give well-defined infrared and nuclear magnetic resonance spectra that can be used for their qualitative identification. Martin & Shaw (1965) have reviewed the application of methods such as ultraviolet spectrophotometry, paper chromatography and paper electrophoresis for cephaloridine, while Chapman, Page & others (1968) have described infrared and X-ray powder measurements for this compound. The application of mass spectroscopy to the structural elucidation of cephalosporin derivatives has been reported by Richter & Biemann (1965).

Related Organizations

Portsmouth College
United Kingdom

Keywords

Cephalothin, Cephaloridine, Methods, Hydrogen-Ion Concentration, Cephalosporins, Polarography

3 Research products, page 1 of 1

ChemInform Abstract: 3‐ACYLOXYMETHYL‐7‐(2‐THIENYLACETAMIDO)‐3‐CEPHEM‐4‐CARBOXYLIC ACIDS. IMPROVED SYNTHESIS AND BIOLOGICAL PROPERTIES
1975IsAmongTopNSimilarDocuments
Reactions of Escherichia coli TEM beta-lactamase with cephalothin and with C10-dipeptidyl cephalosporin esters.
1986IsAmongTopNSimilarDocuments
Inactivation of alanine racemase by .beta.-chloro-L-alanine released enzymically from amino acid and peptide C10-esters of deacetylcephalothin
1987IsAmongTopNSimilarDocuments

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	16
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average