Russian Chemical Bulletin, volume 69, issue 11, pages 2215-2221
Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines
Publication type: Journal Article
Publication date: 2020-11-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
The protolytic properties and reactions with molecular iodine and blood serum proteins of 5,7-dimethyltetrahydro-1H-imidazo[4,5-e]-1,2,4-triazine-3,6(2H,4H)-dithione and (R)-1,3-dialkyl-4-[(2-hydroxybenzylidene)amino]-5-thioxohexahydroimidazo[4,5-d]imidazol-2(1H)-ones were studied. These compounds exhibit different chemical reactivities towards molecular iodine. The binding constants between these compounds and serum albumin attest to a considerable protein affinity of the compounds. The properties of the thiones make them promising as antithyroid agents.
Citations by journals
1
2
3
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
3 publications, 75%
|
New Journal of Chemistry
|
New Journal of Chemistry
1 publication, 25%
|
1
2
3
|
Citations by publishers
1
2
3
|
|
Springer Nature
|
Springer Nature
3 publications, 75%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 25%
|
1
2
3
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2021,2022],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[1,3],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["25","75"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Russian Chemical Bulletin","New Journal of Chemistry"],"ids":[10918,1404],"codes":[0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp"],"datasets":[{"label":"","data":[3,1],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":[75,25],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Springer Nature","Royal Society of Chemistry (RSC)"],"ids":[8,123],"codes":[0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp"],"datasets":[{"label":"","data":[3,1],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":[75,25],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Ivolgina V. A. et al. Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines // Russian Chemical Bulletin. 2020. Vol. 69. No. 11. pp. 2215-2221.
GOST all authors (up to 50)
Copy
Ivolgina V. A., POPOV L., Gazieva G. A., Kravchenko A. N. Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines // Russian Chemical Bulletin. 2020. Vol. 69. No. 11. pp. 2215-2221.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s11172-020-3024-z
UR - https://doi.org/10.1007%2Fs11172-020-3024-z
TI - Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines
T2 - Russian Chemical Bulletin
AU - Ivolgina, V A
AU - Gazieva, G A
AU - Kravchenko, A N
AU - POPOV, L.D.
PY - 2020
DA - 2020/11/01 00:00:00
PB - Springer Nature
SP - 2215-2221
IS - 11
VL - 69
SN - 1066-5285
SN - 1573-9171
ER -
Cite this
BibTex
Copy
@article{2020_Ivolgina,
author = {V A Ivolgina and G A Gazieva and A N Kravchenko and L.D. POPOV},
title = {Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines},
journal = {Russian Chemical Bulletin},
year = {2020},
volume = {69},
publisher = {Springer Nature},
month = {nov},
url = {https://doi.org/10.1007%2Fs11172-020-3024-z},
number = {11},
pages = {2215--2221},
doi = {10.1007/s11172-020-3024-z}
}
Cite this
MLA
Copy
Ivolgina, V. A., et al. “Protolytic and potential antithyroid properties of thioglycolurils and fused azolo-1,2,4-triazines.” Russian Chemical Bulletin, vol. 69, no. 11, Nov. 2020, pp. 2215-2221. https://doi.org/10.1007%2Fs11172-020-3024-z.
Profiles