Talk:Cefaclor
Latest comment: 5 years ago by Community Tech bot in topic A Commons file used on this page has been nominated for deletion
 | This article is rated Start-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | ||||||||||
| |||||||||||
 | Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Cefaclor.
|
reactions of cefachlor with amino acid derivatives such as phthalyl-, tosyl and 1,2,4-triazolyl amino acids using active ester, phosphorous oxy chloride and acid chloride methods to prepare some derivatives with higher antibacterial activities.
Structure image and Name edit
The structure lacks stereochemistry. The systematic name for this drug is
(6R,7R)-7-{[(2R)-2-amino-2-phenylacetyl]amino}-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid--ChemSpiderMan (talk) 01:26, 19 May 2008 (UTC)
- It also has methyl groups where there should be hydrogens :) I'll let the creator know and replace it with a correct version. Fvasconcellos (t·c) 18:49, 23 August 2008 (UTC)
A Commons file used on this page has been nominated for deletion edit
The following Wikimedia Commons file used on this page has been nominated for deletion:
Participate in the deletion discussion at the nomination page. —Community Tech bot (talk) 02:01, 3 November 2018 (UTC)
