volume 29 issue 14 pages 1765-1768

Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection

Publication typeJournal Article
Publication date2019-07-01
scimago Q2
wos Q2
SJR0.472
CiteScore5.1
Impact factor2.2
ISSN0960894X, 14643405
Organic Chemistry
Drug Discovery
Biochemistry
Molecular Biology
Pharmaceutical Science
Clinical Biochemistry
Molecular Medicine
Abstract
We report the first biological evaluation the 1,2,3-thiaselenazole class of compound and utilising a concise synthetic approach of sulfur extrusion, selenium insertion of the 1,2,3-dithiazoles. We created a small diverse library of compounds to contrast the two ring systems. This approach has highlighted new structure activity relationship insights and lead to the development of sub-micro molar anti-viral compounds with reduced toxicity. The 1,2,3-thiaselenazole represents a new class of potential compounds for the treatment of FIV and HIV.
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Asquith C. R. M. et al. Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection // Bioorganic and Medicinal Chemistry Letters. 2019. Vol. 29. No. 14. pp. 1765-1768.
GOST all authors (up to 50) Copy
Asquith C. R. M., Meili T., Rakitin O. A., Baranovsky I. V., Konstantinova L. S., Poso A., Hofmann-Lehmann R. Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection // Bioorganic and Medicinal Chemistry Letters. 2019. Vol. 29. No. 14. pp. 1765-1768.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1016/j.bmcl.2019.05.016
UR - https://linkinghub.elsevier.com/retrieve/pii/S0960894X19303026
TI - Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection
T2 - Bioorganic and Medicinal Chemistry Letters
AU - Asquith, Christopher R M
AU - Meili, Theres
AU - Rakitin, Oleg A.
AU - Baranovsky, Ilia V
AU - Konstantinova, Lidia S.
AU - Poso, Antti
AU - Hofmann-Lehmann, Regina
PY - 2019
DA - 2019/07/01
PB - Elsevier
SP - 1765-1768
IS - 14
VL - 29
PMID - 31101470
SN - 0960-894X
SN - 1464-3405
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Asquith,
author = {Christopher R M Asquith and Theres Meili and Oleg A. Rakitin and Ilia V Baranovsky and Lidia S. Konstantinova and Antti Poso and Regina Hofmann-Lehmann},
title = {Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection},
journal = {Bioorganic and Medicinal Chemistry Letters},
year = {2019},
volume = {29},
publisher = {Elsevier},
month = {jul},
url = {https://linkinghub.elsevier.com/retrieve/pii/S0960894X19303026},
number = {14},
pages = {1765--1768},
doi = {10.1016/j.bmcl.2019.05.016}
}
MLA
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MLA Copy
Asquith, Christopher R. M., et al. “Synthesis and comparison of substituted 1,2,3-dithiazole and 1,2,3-thiaselenazole as inhibitors of the feline immunodeficiency virus (FIV) nucleocapsid protein as a model for HIV infection.” Bioorganic and Medicinal Chemistry Letters, vol. 29, no. 14, Jul. 2019, pp. 1765-1768. https://linkinghub.elsevier.com/retrieve/pii/S0960894X19303026.