Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yuri A. Piven"'
Autor:
Tatyana S. Khlebnicova, I. V. Sorokina, Yuri A. Piven, Tatyana G. Tolstikova, Dmitry S. Baev, Fedor A. Lakhvich, Tatiana S. Frolova
Publikováno v:
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry
Background: Prevention and treatment of chronic inflammatory diseases require effective and low-toxic medicines. Molecular hybridization is an effective strategy to enhance the biological activity of new compounds. Triterpenoid scaffolds are in the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3ff5bf821473ebc122f30fde30261ea
https://doi.org/10.2174/1871523018666190426152049
https://doi.org/10.2174/1871523018666190426152049
Autor:
Yuri A. Piven, Veronica G. Zinovich, Tatyana S. Khlebnicova, Margarita A. Yastrebova, Anton E. Matous, Danila V. Sorokin, Alexander M. Scherbakov, Yuri Yu. Shchegolev, Fedor A. Lakhvich
Publikováno v:
Organicbiomolecular chemistry. 19(47)
Effective method of synthesis of 8-aryl-4,5-dihydrothiazolo[4',5':3,4]benzo[1,2-c]isoxazol-2-amines was developed. The method includes α-keto bromination of 3-aryl-6,7-dihydrobenzo[c]isoxazol-4(5H)-ones followed by condensation of obtained bromo der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51bfe9b1b9907a315d926cb32d9eeea2
https://pubmed.ncbi.nlm.nih.gov/34846407
https://pubmed.ncbi.nlm.nih.gov/34846407
Autor:
Veronica G. Zinovich, Fedor A. Lakhvich, Tatyana S. Khlebnicova, Alexander V. Baranovsky, Victor V. Tatarskiy, Margarita A. Yastrebova, Alexander M. Scherbakov, Yuri A. Piven, Alvina I. Khamidullina, Julia A. Rusanova
Publikováno v:
Bioorganic & Medicinal Chemistry. 53:116521
Novel O-acylated (E)-3-aryl-6,7-dihydrobenzisoxazol-4(5H)-one oximes were designed as potential HSP90 inhibitors. A series of the compounds was synthesized by oximation of (E)-3-aryl-6,7-dihydrobenzisoxazol-4(5H)-ones followed by O-acylation with acy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e60c1489bff9fb42d1eb4565cbb684
https://doi.org/10.1016/j.bmc.2021.116521
https://doi.org/10.1016/j.bmc.2021.116521
Autor:
Fedor A. Lakhvich, Māris Turks, Irisa Rāviņa, Tatyana S. Khlebnicova, Viktors Kumpiņš, Inese Mieriņa, Svetlana V. Shishkina, Daina Zicāne, Alexander V. Baranovsky, Zenta Tetere, Inese Rijkure, Yuri A. Piven, Uldis Peipiņš
Publikováno v:
Steroids. 117:77-89
An efficient protocol for the synthesis of novel lupane triterpenoid-indazolone hybrids with oxime ester linkage has been developed from naturally accessible precursor betulin. For the first time a series of betulonic acid-indazolone hybrids have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ddac9b4b5529a8774b6daba90690c38
https://doi.org/10.1016/j.steroids.2016.08.002
https://doi.org/10.1016/j.steroids.2016.08.002
Autor:
I. V. Sorokina, Fedor A. Lakhvich, Yuri A. Piven, Tatyana S. Khlebnicova, Tatyana G. Tolstikova, Alexander V. Baranovsky
Publikováno v:
Steroids. 147
A series of novel fluorine-containing lupane triterpenoid acid derivatives with fluoroaromatic amide moieties at the C-28 position (1–8) or with 2-(fluoroacyl)cyclopentane-1,3-dione fragments at the C-3 position (9–18) of lupane skeleton was synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6deeec346251fc274f7cb51f55fa0bcd
https://pubmed.ncbi.nlm.nih.gov/30296549
https://pubmed.ncbi.nlm.nih.gov/30296549
Autor:
Fedor A. Lakhvich, Māris Turks, Kirils Gorovojs, Inta Strakova, Sergey Belyakov, Tatyana S. Khlebnicova, Yuri A. Piven
Publikováno v:
Tetrahedron. 68:6131-6140
A new route toward 4-acylamino- and 4-amino-substituted tetrahydroindazoles is disclosed. The title compounds are obtained in good to excellent yields in the Ritter reaction between 4-hydroxy-tetrahydroindazoles and various nitriles. The reactivity o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8062646623d4ed00b8def2ee5cd75db4
https://doi.org/10.1016/j.tet.2012.05.074
https://doi.org/10.1016/j.tet.2012.05.074
Autor:
Kirils Gorovojs, Sergey Belyakov, Fedor A. Lakhvich, Inta Strakova, Tatyana S. Khlebnicova, Yuri A. Piven, Māris Turks
Publikováno v:
ChemInform. 43
A new route to the title compounds proceeds via reaction of 4-hydroxytetrahydroindazoles with various nitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d660e7869d8dbd0b00c305f9b42979c5
https://doi.org/10.1002/chin.201250125
https://doi.org/10.1002/chin.201250125