Evgeniya V. Nurieva - Concepedia

Author

Evgeniya V. Nurieva

Lomonosov Moscow State University

Also Known As

E. Nurieva, E. V. Nurieva, E.V. Nurieva, Evgeniya V. Nurieva, Nurieva, E.V., Nurieva, Evgeniya V., É. R. Nurieva

Publications

400

Citations

H-Index

Concepts

All Affiliations

Lomonosov Moscow State University Institute of Physiologically Active Compounds University of Rostock Chuvash State University Moscow State University

About

Evgeniya V. Nurieva is an author at Lomonosov Moscow State University specializing in drug discovery, medicine, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	76
2	Biochemistry	3	3	76
3	Natural Sciences	2	2	33
4	Biomolecular Engineering	2	2	50
5	Engineering	1	1	20

Evgeniya V. Nurieva

Publications

257

Citations

H-Index

Page 1

	Year	Citations
Taxol: Synthesis, Bioactive Conformations, and Structure-Activity Relationships in Its Analogs O. N. Zefirova, Evgeniya V. Nurieva, A. N. Ryzhov, Russian Journal of Organic Chemistry BiochemistryMedicineBioactive ConformationsPharmacologySynthetic Chemistry	2005	37
Reaction between 4-oxoalkane-1,1,2,2-tetracarbonitriles and morpholine: regioselective synthesis of 5-amino-2-(morpholin-4-yl)-3-(2-oxoalkyl)-3H-pyrrol-3,4-dicarbonitriles М. Yu. Belikov, A. V. Eremkin, Evgeniya V. Nurieva Tetrahedron Letters Organic ChemistryRegioselective SynthesisStereoselective SynthesisChemistrySynthetic Chemistry	2011	31
Synthesis and SAR requirements of adamantane–colchicine conjugates with both microtubule depolymerizing and tubulin clustering activities O. N. Zefirova, Evgeniya V. Nurieva, Dmitrii V. Shishov, Bioorganic & Medicinal Chemistry Tubulin Clustering ActivitiesAdamantane–colchicine ConjugatesBioconjugationChemistrySar Requirements	2011	30
Unusual Tubulin‐Clustering Ability of Specifically C7‐Modified Colchicine Analogues O. N. Zefirova, Heiko Lemcke, Margaréta Lantow, ChemBioChem α-Tubulin SubunitBiochemistryStable Tubulin ClustersPeptide SynthesisCytoskeleton	2013	26
Design, synthesis and bioactivity of simplified taxol analogues on the basis of bicyclo[3.3.1]nonane derivatives O. N. Zefirova, Evgeniya V. Nurieva, Heiko Lemcke, Mendeleev Communications	2008	22
Design, synthesis, and bioactivity of putative tubulin ligands with adamantane core O. N. Zefirova, Evgeniya V. Nurieva, Heiko Lemcke, Bioorganic & Medicinal Chemistry Letters Inorganic ChemistryBioorganic ChemistryEngineeringNatural SciencesAdamantane Core	2008	20
Design, synthesis and biotest of a bicyclo[3.3.1]nonane analogue of 2-amino-5,6-dihydro-4H-1,3-thiazine O. N. Zefirova, Evgeniya V. Nurieva, Vladimir Chupakhin, Mendeleev Communications	2010	18
Synthesis of 2-halo-6-hydroxy-5,5-dimethyl(ethyl)-5,6-dihydro-1H-pyridine-3,4,4-tricarbonitriles by the reaction of tetracyanoethylene with aldehydes A. V. Eremkin, Sergei N. Molkov, Yakov S. Kayukov, Mendeleev Communications	2006	14
Novel antimitotic agents related to tubuloclustin: synthesis and biological evaluation O. N. Zefirova, Evgeniya V. Nurieva, Birgit Wobith, Molecular Diversity Medicinal ChemistryBiochemistryAntiparasitic AgentMedicineNatural Sciences	2017	13
Synthesis and antihypotensive properties of 2-amino-2-thiazoline analogues with enhanced lipophilicity Evgeniya V. Nurieva, Alexander Alexeev, Alexey N. Proshin, Mendeleev Communications	2018	12

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