Synthesis, Characterization and Complex Evaluation of Antibacterial Activity and Cytotoxicity of New Arylmethylidene Ketones and Pyrimidines with Camphane Skeletons-Reference-Cited by-同舟云学术

Synthesis, Characterization and Complex Evaluation of Antibacterial Activity and Cytotoxicity of New Arylmethylidene Ketones and Pyrimidines with Camphane Skeletons

Published:2022-05-03 Issue:17 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Slavchev Ivaylo M.¹,Mitrev Yavor¹,Shivachev Boris²,Valcheva Violeta³,Dogonadze Marine⁴,Solovieva Natalia⁴⁵,Vyazovaya Anna⁵,Mokrousov Igor⁵,Link Wolfgang⁶,Jiménez Lucía⁶,Cautain Bastien⁷,Mackenzie Thomas A.⁷,Portugal Isabel⁸,Lopes Francisca⁸,Capela Rita⁸,Perdigão João⁸,Dobrikov Georgi M.¹^ORCID

Affiliation:

1. Institute of Organic Chemistry with Centre of Phytochemistry Bulgarian Academy of Sciences bl. 9, Acad. G. Bonchev str. Sofia 1113 Bulgaria

2. Institute of Mineralogy and Crystallography Bulgarian Academy of Sciences, bl. 107, Acad. G. Bonchev str. Sofia 1113 Bulgaria

3. Stephan Angeloff Institute of Microbiology Bulgarian Academy of Sciences bl. 26, Acad. G. Bonchev str. Sofia 1113 Bulgaria

4. St. Petersburg Research Institute of Phthisiopulmonology St. Petersburg Russia

5. Laboratory of Molecular Epidemiology and Evolutionary Genetics St. Petersburg Pasteur Institute St. Petersburg Russia

6. Instituto de Investigaciones Biomédicas “Alberto Sols” (CSIC-UAM), Arturo Duperier 4 28029 Madrid Spain

7. Fundación MEDINA Centro de Excelencia en Investigación de Medicamentos Innovadores de Andalucía Parque Tecnológico de Ciencias de la Salud Avda. del Conocimiento 34 18016 Granada Spain

8. iMed.ULisboa – Instituto de Investigação do Medicamento Faculdade de Farmácia Universidade de Lisboa Lisboa Portugal

Funder

Bulgarian National Science Fund

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202201339

Reference62 articles.

1. New retinoid chemotypes: 9-cis-Retinoic acid analogs with hydrophobic rings derived from terpenes as selective RAR agonists

2. 1-(((7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo[2.2.1]heptan-1(S)-yl)methyl)sulfonyl)-4-(2-methylphenyl)piperazine (L-368,899): An Orally Bioavailable, Non-Peptide Oxytocin Antagonist with Potential Utility for Managing Preterm Labor

3. Orally active, nonpeptide oxytocin antagonists

4. Novel Tacrine Analogues for Potential Use against Alzheimer's Disease: Potent and Selective Acetylcholinesterase Inhibitors and 5-HT Uptake Inhibitors

5. Synthesis and biological activities of camphor-based non-peptide growth hormone secretagogues