Bioorganic and Medicinal Chemistry Letters, volume 25, issue 2, pages 404-409
Design, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors
Ivanenkov Yan
1, 2
,
Vasilevski Sergei V
1
,
Beloglazkina Elena K.
1, 3
,
Kukushkin Maksim E
1
,
Machulkin Alexey E.
1, 4
,
Veselov Mark S.
5
,
Chufarova Nina V
2, 6
,
Chernyaginab Elizaveta S
5
,
Vanzcool Anton S
7
,
Zyk Nikolay V.
1
,
Skvortsov Dmitry
1
,
Khutornenko Anastasia A.
8
,
Rusanov Alexander L.
9
,
Tonevitsky Alexander
10, 11
,
Dontsova Olga A.
1, 8
,
Majouga Alexander G.
1, 12
1
7
ChemDiv, Inc., 6605 Nancy Ridge Drive, San Diego, CA 92121, USA.
|
10
SRC Bioclinicum, Ugreshskaya str 2/85, Moscow 115088, Russia
|
11
Publication type: Journal Article
Publication date: 2015-01-01
Quartile SCImago
Q2
Quartile WOS
Q2
Impact factor: 2.7
ISSN: 0960894X, 14643405
Organic Chemistry
Drug Discovery
Biochemistry
Molecular Biology
Pharmaceutical Science
Clinical Biochemistry
Molecular Medicine
Abstract
Regioselective synthesis, biological evaluation and 3D-molecular modeling for a series of novel diastereomeric 2-thioxo-5H-dispiro[imidazolidine-4,3-pyrrolidine-2,3-indole]-2,5(1H)-diones are described. The studied compounds have been tentatively identified as potent small molecule MDM2/p53 PPI inhibitors and can therefore be reasonably regarded as promising anticancer therapeutics.
Citations by journals
1
2
3
|
|
RSC Advances
|
RSC Advances
3 publications, 6.52%
|
Mendeleev Communications
|
Mendeleev Communications
3 publications, 6.52%
|
Molecules
|
Molecules
3 publications, 6.52%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
3 publications, 6.52%
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
3 publications, 6.52%
|
Russian Journal of Organic Chemistry
|
Russian Journal of Organic Chemistry
2 publications, 4.35%
|
International Journal of Molecular Sciences
|
International Journal of Molecular Sciences
2 publications, 4.35%
|
ChemistrySelect
|
ChemistrySelect
2 publications, 4.35%
|
European Journal of Medicinal Chemistry
|
European Journal of Medicinal Chemistry
2 publications, 4.35%
|
ChemMedChem
|
ChemMedChem
2 publications, 4.35%
|
Phosphorus, Sulfur and Silicon and the Related Elements
|
Phosphorus, Sulfur and Silicon and the Related Elements
1 publication, 2.17%
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 2.17%
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 2.17%
|
ACS Omega
|
ACS Omega
1 publication, 2.17%
|
Royal Society Open Science
|
Royal Society Open Science
1 publication, 2.17%
|
Anti-Cancer Agents in Medicinal Chemistry
|
Anti-Cancer Agents in Medicinal Chemistry
1 publication, 2.17%
|
Pharmaceuticals
|
Pharmaceuticals
1 publication, 2.17%
|
Biomolecules
|
Biomolecules
1 publication, 2.17%
|
Frontiers in Genetics
|
Frontiers in Genetics
1 publication, 2.17%
|
Tetrahedron
|
Tetrahedron
1 publication, 2.17%
|
Chinese Chemical Letters
|
Chinese Chemical Letters
1 publication, 2.17%
|
Medicinal Research Reviews
|
Medicinal Research Reviews
1 publication, 2.17%
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
1 publication, 2.17%
|
Journal of the American Chemical Society
|
Journal of the American Chemical Society
1 publication, 2.17%
|
Journal of Medicinal Chemistry
|
Journal of Medicinal Chemistry
1 publication, 2.17%
|
Chemical Communications
|
Chemical Communications
1 publication, 2.17%
|
Chemical Science
|
Chemical Science
1 publication, 2.17%
|
Synthesis
|
Synthesis
1 publication, 2.17%
|
Molecular Diversity
|
Molecular Diversity
1 publication, 2.17%
|
1
2
3
|
Citations by publishers
1
2
3
4
5
6
7
|
|
Elsevier
|
Elsevier
7 publications, 15.22%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
7 publications, 15.22%
|
Springer Nature
|
Springer Nature
7 publications, 15.22%
|
Wiley
|
Wiley
6 publications, 13.04%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
5 publications, 10.87%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
4 publications, 8.7%
|
Pleiades Publishing
|
Pleiades Publishing
2 publications, 4.35%
|
Taylor & Francis
|
Taylor & Francis
1 publication, 2.17%
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 2.17%
|
The Royal Society
|
The Royal Society
1 publication, 2.17%
|
Bentham Science
|
Bentham Science
1 publication, 2.17%
|
Frontiers Media S.A.
|
Frontiers Media S.A.
1 publication, 2.17%
|
Thieme
|
Thieme
1 publication, 2.17%
|
1
2
3
4
5
6
7
|
- 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":[2015,2016,2017,2018,2019,2020,2021,2022,2023],"ids":[0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","",""],"datasets":[{"label":"Citations number","data":[3,7,1,6,3,9,8,6,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["6.52","15.22","2.17","13.04","6.52","19.57","17.39","13.04","6.52"],"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":["RSC Advances","Mendeleev Communications","Molecules","Chemistry of Heterocyclic Compounds","Russian Chemical Bulletin","Russian Journal of Organic Chemistry","International Journal of Molecular Sciences","ChemistrySelect","European Journal of Medicinal Chemistry","ChemMedChem","Phosphorus, Sulfur and Silicon and the Related Elements","Beilstein Journal of Organic Chemistry","Journal of Organic Chemistry","ACS Omega","Royal Society Open Science","Anti-Cancer Agents in Medicinal Chemistry","Pharmaceuticals","Biomolecules","Frontiers in Genetics","Tetrahedron","Chinese Chemical Letters","Medicinal Research Reviews","Advanced Synthesis and Catalysis","Journal of the American Chemical Society","Journal of Medicinal Chemistry","Chemical Communications","Chemical Science","Synthesis","Molecular Diversity"],"ids":[3100,5294,1770,16828,10918,5728,14627,8021,8171,1430,12904,21928,8697,18901,3859,9738,1203,13780,13242,3439,20341,18813,3906,4813,3673,9073,9646,10934,9362],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/BHBStD1OkQqtKFRRjS5njgNe7bXCAEgaDQVK7GTA_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp"],"datasets":[{"label":"","data":[3,3,3,3,3,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[6.52,6.52,6.52,6.52,6.52,4.35,4.35,4.35,4.35,4.35,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17,2.17],"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","Multidisciplinary Digital Publishing Institute (MDPI)","Springer Nature","Wiley","Royal Society of Chemistry (RSC)","American Chemical Society (ACS)","Pleiades Publishing","Taylor & Francis","Beilstein-Institut","The Royal Society","Bentham Science","Frontiers Media S.A.","Thieme"],"ids":[17,202,8,11,123,40,101,18,6139,259,39,208,135],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/BHBStD1OkQqtKFRRjS5njgNe7bXCAEgaDQVK7GTA_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[7,7,7,6,5,4,2,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[15.22,15.22,15.22,13.04,10.87,8.7,4.35,2.17,2.17,2.17,2.17,2.17,2.17],"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
Ivanenkov Y. et al. Design, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors // Bioorganic and Medicinal Chemistry Letters. 2015. Vol. 25. No. 2. pp. 404-409.
GOST all authors (up to 50)
Copy
Ivanenkov Y., Vasilevski S. V., Beloglazkina E. K., Kukushkin M. E., Machulkin A. E., Veselov M. S., Chufarova N. V., Chernyaginab E. S., Vanzcool A. S., Zyk N. V., Skvortsov D., Khutornenko A. A., Rusanov A. L., Tonevitsky A., Dontsova O. A., Majouga A. G. Design, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors // Bioorganic and Medicinal Chemistry Letters. 2015. Vol. 25. No. 2. pp. 404-409.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.bmcl.2014.09.070
UR - https://doi.org/10.1016%2Fj.bmcl.2014.09.070
TI - Design, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors
T2 - Bioorganic and Medicinal Chemistry Letters
AU - Ivanenkov, Yan
AU - Vasilevski, Sergei V
AU - Kukushkin, Maksim E
AU - Machulkin, Alexey E.
AU - Veselov, Mark S.
AU - Chufarova, Nina V
AU - Chernyaginab, Elizaveta S
AU - Vanzcool, Anton S
AU - Zyk, Nikolay V.
AU - Khutornenko, Anastasia A.
AU - Rusanov, Alexander L.
AU - Dontsova, Olga A.
AU - Beloglazkina, Elena K.
AU - Skvortsov, Dmitry
AU - Tonevitsky, Alexander
AU - Majouga, Alexander G.
PY - 2015
DA - 2015/01/01 00:00:00
PB - Elsevier
SP - 404-409
IS - 2
VL - 25
SN - 0960-894X
SN - 1464-3405
ER -
Cite this
BibTex
Copy
@article{2015_Ivanenkov,
author = {Yan Ivanenkov and Sergei V Vasilevski and Maksim E Kukushkin and Alexey E. Machulkin and Mark S. Veselov and Nina V Chufarova and Elizaveta S Chernyaginab and Anton S Vanzcool and Nikolay V. Zyk and Anastasia A. Khutornenko and Alexander L. Rusanov and Olga A. Dontsova and Elena K. Beloglazkina and Dmitry Skvortsov and Alexander Tonevitsky and Alexander G. Majouga},
title = {Design, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors},
journal = {Bioorganic and Medicinal Chemistry Letters},
year = {2015},
volume = {25},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016%2Fj.bmcl.2014.09.070},
number = {2},
pages = {404--409},
doi = {10.1016/j.bmcl.2014.09.070}
}
Cite this
MLA
Copy
Ivanenkov, Yan, et al. āDesign, synthesis and biological evaluation of novel potent MDM2/p53 small-molecule inhibitors.ā Bioorganic and Medicinal Chemistry Letters, vol. 25, no. 2, Jan. 2015, pp. 404-409. https://doi.org/10.1016%2Fj.bmcl.2014.09.070.