Synthesis and Receptor Binding Affinity of Conformationally Restricted Retinoic Acid Analogues. -Efforts to synthesize two conformationally restricted retinoids utilizing a cyclopropyl ring as bioisostere for the C9-C10 double bond are described. The attempted synthesis of the cisisomer leads mainl
ChemInform Abstract: Synthesis of a Series of Sulfinic Acid Analogues of GABA and Evaluation of Their GABAB Receptor Affinities.
β Scribed by Nicholas I. Carruthers; ET AL. ET AL.
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Synthesis of a Series of Sulfinic Acid Analogues of GABA and Evaluation of Their GABA B Receptor Affinities. -The replacement of the carboxyl group by a sulfinyl moiety in GABA analogues is investigated. The synthesis follows a similar procedure as shown for derivative (XII). Introduction of an additional carbon atom, cf. (IV), retains good GABA binding affinity, whereas the sulfinic moiety does not increase the desired activity. -(CARRUTHERS, NICHOLAS I.;
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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
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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
## 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