The design and synthesis of novel adenosine agonists
β Scribed by P.J. Scammells; S.P. Baker; L. Bellardinelli; R.A. Olsson; R.A. Russell; S.A. Knevitt
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 244 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0960-894X
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β¦ Synopsis
The 2R and 2S-endo isomers of N6-(5,6-epoxynorbom-2-yl)adenosine have been synthesised and shown to be potent agonists for the AI adenosine receptor. The 2S-endo isomer was equipotent to N 6cyclopentyladenosine and 10-to 12-fold more potent than the 2R-endo isomer.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v