Russian Chemical Bulletin, volume 59, issue 12, pages 2268-2275
Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity
Konyushkin L D
1
,
Godovikova T I
1
,
Vorontsova S K
1
,
Tsyganov D V
2
,
Karmanova I B
1
,
Raihstat M M
1
,
Firgang S I
1
,
Pokrovskii” M A
2
,
Pokrovskii A G
2
,
Semenova M. N.
3
,
Semenov V. V.
1
Publication type: Journal Article
Publication date: 2010-12-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
Polyalkoxy-5-(4-hydroxyphenyl)-3-phenyl-1,2,4-oxadiazoles were prepared from allylpolyalkoxybenzenes, the main metabolites of parsley and dill seeds. Due to the spatial arrangement of the aryl substituents provided by 1,2,4-oxadiozole fragment, these compounds can be considered as structural analogs of natural antimitotic combretastatins. The antimitotic activity of the synthesized compounds was evaluated in vivo using sea urchin embryo test.
Citations by journals
|
1
2
|
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
2 publications, 28.57%
|
|
Fitoterapia
|
Fitoterapia
2 publications, 28.57%
|
|
Russian Journal of General Chemistry
|
Russian Journal of General Chemistry
1 publication, 14.29%
|
|
Mendeleev Communications
|
Mendeleev Communications
1 publication, 14.29%
|
|
Chemical Reviews
|
Chemical Reviews
1 publication, 14.29%
|
|
1
2
|
Citations by publishers
|
1
2
3
|
|
|
Elsevier
|
Elsevier
3 publications, 42.86%
|
|
Springer Nature
|
Springer Nature
2 publications, 28.57%
|
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 14.29%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 14.29%
|
|
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":[2015,2016,2017,2018,2019,2020,2021],"ids":[0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0],"imageUrls":["","","","","","",""],"datasets":[{"label":"Citations number","data":[2,1,1,2,0,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["28.57","14.29","14.29","28.57",0,0,"14.29"],"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","Fitoterapia","Russian Journal of General Chemistry","Mendeleev Communications","Chemical Reviews"],"ids":[10918,13573,13581,5294,13718],"codes":[0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[2,2,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[28.57,28.57,14.29,14.29,14.29],"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":["Elsevier","Springer Nature","Pleiades Publishing","American Chemical Society (ACS)"],"ids":[17,8,101,40],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[3,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[42.86,28.57,14.29,14.29],"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
Konyushkin L. D. et al. Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity // Russian Chemical Bulletin. 2010. Vol. 59. No. 12. pp. 2268-2275.
GOST all authors (up to 50)
Copy
Konyushkin L. D., Godovikova T. I., Vorontsova S. K., Tsyganov D. V., Karmanova I. B., Raihstat M. M., Firgang S. I., Pokrovskii” M. A., Pokrovskii A. G., Semenova M. N., Semenov V. V. Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity // Russian Chemical Bulletin. 2010. Vol. 59. No. 12. pp. 2268-2275.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s11172-010-0387-6
UR - https://doi.org/10.1007%2Fs11172-010-0387-6
TI - Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity
T2 - Russian Chemical Bulletin
AU - Konyushkin, L D
AU - Godovikova, T I
AU - Vorontsova, S K
AU - Tsyganov, D V
AU - Karmanova, I B
AU - Raihstat, M M
AU - Firgang, S I
AU - Pokrovskii”, M A
AU - Pokrovskii, A G
AU - Semenova, M. N.
AU - Semenov, V. V.
PY - 2010
DA - 2010/12/01 00:00:00
PB - Springer Nature
SP - 2268-2275
IS - 12
VL - 59
SN - 1066-5285
SN - 1573-9171
ER -
Cite this
BibTex
Copy
@article{2010_Konyushkin,
author = {L D Konyushkin and T I Godovikova and S K Vorontsova and D V Tsyganov and I B Karmanova and M M Raihstat and S I Firgang and M A Pokrovskii” and A G Pokrovskii and M. N. Semenova and V. V. Semenov},
title = {Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity},
journal = {Russian Chemical Bulletin},
year = {2010},
volume = {59},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007%2Fs11172-010-0387-6},
number = {12},
pages = {2268--2275},
doi = {10.1007/s11172-010-0387-6}
}
Cite this
MLA
Copy
Konyushkin, L. D., et al. “Polyalkoxybenzenes from plant raw materials 4. Parsley and dill seed extracts in the synthesis of polyalkoxy-3,5-diaryl-1,2,4-oxadiazoles with antiproliferative activity.” Russian Chemical Bulletin, vol. 59, no. 12, Dec. 2010, pp. 2268-2275. https://doi.org/10.1007%2Fs11172-010-0387-6.
Profiles