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Pavlova Alla Viktorovna
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, LPhR
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Personal publicalions (DB NIOCh)
2022
Reviews, articles
- A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927 - A. O. Finke, A. V. Pavlova, E. A. Morozova, T. G. Tolstikova, E. E. Shults
Synthesis of 1,2,3-Triazolyl-Substituted Derivatives of the Alkaloids Sinomenine and Tetrahydrothebaine on Ring A and Their Analgesic Activity
Chemistry of Natural Compounds, 2022, V. 58, N 5. Pp 895-902 doi:10.1007/s10600-022-03824-5, IF=0.83
2021
Reviews, articles
- Yu.V. Kharitonov, E.E. Shul'ts, T.V. Rybalova, A.V. Pavlova, T.G. Tolstikova
Synthetic Transformations of Higher Terpenoids. 40. Synthesis and Assessment of Analgesic Activity of N-Containing Derivatives of Lambertianic Acid Yu. V. Kharitonov, E. E. Shul’ts, T. V. Rybalova, A. V. Pavlova & T. G. Tolstikova
Chemistry of Natural Chemistry of Natural Compounds, 2021, V. 57, N 5, Pp 879-886 doi:10.1007/s10600-021-03502-y, IF=0.809
2020
Reviews, articles
- A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Effect of bispidine containing monoterpenoid moieties on physical performance in mice
2020 Cognitive Sciences, Genomics and Bioinformatics (CSGB), Novosibirsk, Russia, 2020, pp. 114-117 doi:10.1109/CSGB51356.2020.9214697 - V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88 - N.S. Li-Zhulanov, A.V. Pavlova, D.V. Korchagina, Yu.V. Gatilov, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
Synthesis of 1,3-Oxazine Derivatives Based on (-)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 936-941 doi:10.1007/s10593-020-02753-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I. Il'ina, E. Morozova, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of aliphatic ketones-derived chiral hexahydro-2H-chromenes
Medicinal Chemistry Research, 2020, V. 29, N 4, pp 738-747 doi:10.1007/s00044-020-02518-3, IF=1.783 - A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
2019
Reviews, articles
- O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
2017
Reviews, articles
- O.S. Patrusheva, A.V. Pavlova, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties
Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1066-1071 doi:10.1007/s10600-017-2202-1, IF=0.46 - K. Ponomarev, E. Morozova, A. Pavlova, E. Suslov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and Analgesic Activity of Amines Combining Diazaadamantane and Monoterpene Fragments
Medicinal Chemistry, 2017, V. 13 , N 8, Pp 773 - 779 doi:10.2174/1573406413666170525124316, IF=2.331 - I. Il'ina, A. Pavlova, D. Korchagina, O. Ardashov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of monoterpenoid-derived alkyl-substituted chiral hexahydro-2H-chromenes
Medicinal Chemistry Research, 2017, V. 26, N 7, pp 1415-1426 doi:10.1007/s00044-017-1847-4, IF=1.276 - A. Pavlova, O. Patrusheva, I. Il'ina, K. Volcho, T. Tolstikova, N. Salakhutdinov
The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8ahexahydro- 2H-chromene-4,8-diols in their Biological Activity
Letters in Drug Design & Discovery, 2017, V. 14, N 5, pp. 508-514 doi:10.2174/1570180813666161102142642, IF=1.169
2016
Reviews, articles
- A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472 - A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
2015
Reviews, articles
- K. Ponomarev, A. Pavlova, E. Suslov, O. Ardashov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of new compounds combining azaadamantane and monoterpene moieties
Medicinal Chemistry Research, 2015, V. 24, N 12, pp 4146-4156 doi:10.1007/s00044-015-1464-z, IF=1.401 - A. Pavlova, O. Mikhalchenko, A. Rogachev, I. Il'ina, D. Korchagina, Yu. Gatilov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
Medicinal Chemistry Research, 2015, V 24, N 11, pp 3821-3830 doi:10.1007/s00044-015-1426-5, IF=1.401
2014
Reviews, articles
- I. Il’ina, O. Mikhalchenko, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov, E. Pokushalov
Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
Medicinal Chemistry Research, 2014, V. 23, N 12, pp 5063-5073 doi:10.1007/s00044-014-1071-4, IF=1.402 - A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, S.Yu. Kurbakova, I.V. Sorokina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Potent Neuroprotective Activity of Monoterpene Derived 4-[(3aR,7aS)-1,3,3a,4,5,7a-Hexahydro-3,3,6-trimethylisobenzofuran-1-yl]-2-methoxyphenol in MPTP Mice Model
Letters in Drug Design & Discovery, 2014, V. 11 N 5 pp. 611-617. doi:10.2174/1570180811666131210000316, IF=0.961 - S. Kurbakova, I. Il'ina, A. Pavlova, D. Korchagina, O. Yarovaya, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of monoterpenoid-derived 2-aryl-4,4,7-trimethyl-4a,5,8,8a-tetrahydro-4H-benzo[d][1,3]dioxin-8-ols
Medicinal Chemistry Research, 2014, V. 23, N 4, pp 1709-1717. doi:10.1007/s00044-013-0772-4
2013
Reviews, articles
- O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
3-Methyl-6-(prop-1-en-2-yl) cyclohex-3-ene-1,2-diol: the Importance of Functional Groups for Antiparkinsonian Activity
Medicinal Chemistry, 2013, V. 9, N 5, P. 731-739. doi:10.2174/1573406411309050013, IF=1.373 - O. Mikhalchenko, I. Il’ina, A. Pavlova, E. Morozova, D. Korchagina, T. Tolstikova, E. Pokushalov, K. Volcho, N.Salakhutdinov
Synthesis and analgesic activity of new heterocyclic compounds derived from monoterpenoids
Medicinal Chemistry Research, 2013, V. 22, N 6, P. 3026-3034. doi:10.1007/s00044-012-0310-9, IF=1.611 - O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
Antiparkinsonian activity of some 9-N-, O-, S- and C-derivatives of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
Bioorganic & Medicinal Chemistry, 2013, V. 21, N 5, P. 1082-1087. doi:10.1016/j.bmc.2013.01.003, IF=2.903
2012
Reviews, articles
- А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, А.В. Павлова, М.В. Хвостов
Гель-хроматографическое и токсикологическое исследование механохимических превращений водорастворимых полисахаридов
Хим.-фарм. журн., 2012, Т. 46, № 10, 53-56. (Gel chromatographic and toxicological studies of the mechanochemical transformations of water-soluble polysaccharides/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, A. V. Pavlova, M. V. Khvostov// PHARM CHEM J+, 2012, V. 46, N 10, pp. 630-633. doi:10.1007/s11094-013-0859-8), IF=0.372 - T.G. Tolstikova, A.V. Pavlova, E.A. Morozova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov
The analgesic activity of 8- ( trifluoromethyl)-1,2,3,4,5-benzopentathiepine-6-amine and its hydrochloride
Lett. Drug Des. Discov., 2012, V. 9, N 5, 513-516. doi:10.2174/157018012800389296, IF=0.871
2011
Reviews, articles
- O.V. Ardashov, A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, E.V. Karpova, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in animal models of Parkinson's disease
J. Med. Chem., 2011, V. 54, N 11, 3866-74. doi:10.1021/jm2001579, IF=5.206
2010
Reviews, articles
- Т.Г. Толстикова, А.В. Павлова, Е.А. Морозова, О.В. Ардашов, И.В. Ильина, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
Высокоэффективное противопаркинсоническое средство нового структурного типа
Доклады Академии наук, 2010, Т. 435, N 5, C. 708–710. (A highly effective antiparkinsonian drug of a new structural type/ T. G. Tolstikova, A. V. Pavlova, Ye. A. Morozova, O. V. Ardashov, I. V. Il’ina, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 398-399. doi:10.1134/S0012496610060074) - А.В. Павлова, Т.Г. Толстикова, Е.А. Морозова, О.В. Ардашов, И.В. Ильина, К.П. Волчо, Н.Ф. Салахутдинов
Гидроксикетоны пара-ментанового ряда – перспективные анальгетики
Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 495-497. (Hydroxyketones of para-Menthane Series as Promising Analgetics/ A.V. Pavlova, T.G. Tolstikova, E.A. Morozova, O.V. Ardashov, I.V. Ilyina, K.P. Volcho, N.F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.423-455. (in russian))
2009
Reviews, articles
- Т.Г. Толстикова, А.В. Павлова, М.П. Долгих, И.В. Ильина, О.В. Ардашов, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
Новый высокоэффективный противосудорожный агент – (4S,5R,6R)-пара-мента-1,8-диен-5,6-диол
Доклады Академии наук (Биология), 2009, Т. 429, № 1, С. 139-141. ((4S,5R,6R)-para-mentha-1,8-dien-5,6-diol is a new highly effective anticonvulsant agent/ T.G. Tolstikova, A.V. Pavlova, M.P. Dolgikh, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Biological Sciences, 2009, V. 429, N 1, pp 494-496. doi:10.1134/S0012496609060039)
2008
Reviews, articles
- Т.Г. Толстикова, Е.А. Морозова, А.В. Павлова, А.В. Болкунов, М.П. Долгих, Е.А. Конева, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
Производные аминокислот пинанового ряда – новые противосудорожные агенты.
Доклады АН, 2008, Т. 422, № 4, 490-492. (Derivatives of Pinane Amino Acids as New Anticonvulsants/ T. G. Tolstikova, E. A. Morozova, A. V. Pavlova, A. V. Bolkunov, M. P. Dolgikh, E. A. Koneva, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Chemistry, 2008, V. 422, N 2, pp 248-250 doi:10.1134/S0012500808100029), IF=0.442
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