Cocrystals of a 1,2,4-thiadiazole-based potent neuroprotector with gallic acid: solubility, thermodynamic stability relationships and formation pathways-Reference-Cited by-同舟云学术

Cocrystals of a 1,2,4-thiadiazole-based potent neuroprotector with gallic acid: solubility, thermodynamic stability relationships and formation pathways

Published:2018 Issue:21 Volume:20 Page:14469-14481
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Surov Artem O.¹²³⁴^ORCID,Churakov Andrei V.⁵⁶⁴,Proshin Alexey N.⁷⁸⁴,Dai Xia-Lin⁹¹⁰¹¹¹²,Lu Tongbu¹³¹⁴¹⁵¹²,Perlovich German L.¹²³⁴^ORCID

Affiliation:

1. Institution of the Russian Academy of Sciences

2. G.A. Krestov Institute of Solution Chemistry RAS

3. 153045 Ivanovo

4. Russia

5. N.S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

6. Moscow

7. Institute of Physiologically Active Compounds of the Russian Academy of Sciences

8. Chernogolovka

9. School of Pharmaceutical Sciences

10. Sun Yat-Sen University

11. Guangzhou

12. China

13. Institute for New Energy Materials and Low Carbon Technologies

14. Tianjin University of Technology

15. Tianjin

Abstract

The thermodynamic stability relationships and the formation pathways of the cocrystals of 1,2,4-thiadiazole-based neuroprotector with gallic acid were investigated.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CP/C8CP02532K

Reference61 articles.

1. Pharmaceutical cocrystals: along the path to improved medicines

2. Pharmaceutical cocrystals: walking the talk

3. Co-crystallization and small molecule crystal form diversity: from pharmaceutical to materials applications