Literature DB >> 590431

Completion of the natural groups of ergot alkaloids: syntheses and pharmacological profiles of beta-ergosine and beta-ergoptine.

P A Stadler, P Stütz, E Stürmer.   

Abstract

The syntheses and pharmacological potencies of beta-ergosine and beta-ergoptine, the missing links in the natural groups of ergot peptide alkaloids are described.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 590431     DOI: 10.1007/bf01933990

Source DB:  PubMed          Journal:  Experientia        ISSN: 0014-4754


  7 in total

1.  A SENSITIVE METHOD FOR ESTIMATION OF ERGOMETRINE, BASED UPON SEROTONIN ANTAGONISM ON ISOLATED RAT UTERUS.

Authors:  R B SUND
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1963

2.  Comparative study on the serotonin antagonism of amide derivatives of lysergic acid and of ergot alkaloids.

Authors:  A CERLETTI; W DOEPFNER
Journal:  J Pharmacol Exp Ther       Date:  1958-01       Impact factor: 4.030

3.  Chemical structure and sympathomimetic action of amines.

Authors:  G Barger; H H Dale
Journal:  J Physiol       Date:  1910-10-11       Impact factor: 5.182

4.  Beta-ergokryptine, a new alkaloid of the ergotoxine group.

Authors:  W Schlientz; R Brunner; A Rüegger; B Berde; E Stürmer; A Hofman
Journal:  Experientia       Date:  1967-12-15

5.  [Beta-ergokryptin, a new alkaloid of ergotoxin-group. 67. Report on ergot alkaloids].

Authors:  W Schlientz; R Brunner; A Rüegger; B Berde; E Stürmer; A Hofmann
Journal:  Pharm Acta Helv       Date:  1968-08

6.  [The synthesis of alkaloids of the ergotoxin group. 70. Section on ergot alkaloids].

Authors:  P A Stadler; S Guttmann; H Hauth; R L Huguenin; E Sandrin; G Wersin; H Willems; A Hofmann
Journal:  Helv Chim Acta       Date:  1969       Impact factor: 2.164

7.  [Synthesis of ergonine and ergoptine, two new analogs of the ergot alkaloids of the ergoxine group].

Authors:  P Stütz; P A Stadler; A Hofmann
Journal:  Helv Chim Acta       Date:  1970       Impact factor: 2.164

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.