New synthesis and biological evaluation of uniflorine A derivatives: towards specific insect trehalase inhibitors-Reference-Cited by-同舟云学术

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New synthesis and biological evaluation of uniflorine A derivatives: towards specific insect trehalase inhibitors

Published:2015 Issue:3 Volume:13 Page:886-892
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

D'Adamio Giampiero¹²³⁴,Sgambato Antonella⁵⁶⁷⁴,Forcella Matilde⁵⁶⁷⁴,Caccia Silvia⁸⁹¹⁰⁴,Parmeggiani Camilla¹²³⁴¹¹,Casartelli Morena⁸⁹¹⁰⁴,Parenti Paolo¹²⁶⁷⁴,Bini Davide⁵⁶⁷⁴,Cipolla Laura⁵⁶⁷⁴,Fusi Paola⁵⁶⁷⁴,Cardona Francesca¹²³⁴

Affiliation:

1. Dipartimento di Chimica “Ugo Schiff”

2. University of Florence

3. 50019 Sesto Fiorentino

4. Italy

5. Department of Biotechnology and Biosciences

6. University of Milano-Bicocca

7. 20126 Milano

8. Department of Biosciences

9. University of Milano

10. 20133 Milano

11. CNR-INO

12. Dipartimento di Scienze dell'Ambiente e del Territorio e di Scienze della Terra

Abstract

(–)-Uniflorine A and 7-deoxy-uniflorine A are selective inhibitors of insect trehalases from C. riparius and S. littoralis.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C4OB02016B

Reference30 articles.

1. Australine and related alkaloids: easy structural confirmation by 13C NMR spectral data and biological activities

2. Casuarine: A very highly oxygenated pyrrolizidine alkaloid

3. Total Syntheses of Casuarine and Its 6-O-α-Glucoside: Complementary Inhibition towards Glycoside Hydrolases of the GH31 and GH37 Families

4. A membrane-bound trehalase from Chironomus riparius larvae: purification and sensitivity to inhibition

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