In vitro proliferative activity of 6-substituted uracil derivatives

Autor: Stanislav A. Grabovskiy, Natalia N. Kabal’nova, Nadezhda M. Andriayshina, Vladislav I. Egorov, Lenar R. Valiullin, Alexey A. Nabatov, Ivan S. Raginov, Yurii I. Murinov

Publikováno v: Journal of Pharmacy & Pharmacognosy Research, Vol 9, Iss 3, Pp 357-365 (2021)

Context: Previously, we investigated the relationship between the nature of the substituent at the 5-position of the uracil ring and the action of the corresponding uracil derivatives on immortalized lung cells. In the present study, we analyzed the

Externí odkaz: https://doaj.org/article/f657106ae9f44c748e4fed1df654e0fe

A case of pheochromocytoma in pregnancy diagnosed by 24-h ambulatory blood pressure monitoring

Autor: Farida Vadutovna Valeeva, Aidar R. Gosmanov, Ivan S. Raginov, Tatiana A. Kiseleva

Publikováno v: Journal of Clinical and Translational Endocrinology: Case Reports. 10:14-16

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::35e1ec14727054eacc0036fdb03ba6d5
https://doi.org/10.1016/j.jecr.2018.08.003

Morphological and functional evaluation of the effect of novel pyrimidine derivatives on regeneration of the sciatic nerve in rats

Autor: Lenar R. Valiullin, Konstantin V. Balakin, V.I. Egorov, Ivan S. Raginov, Daichi Watanabe, Yurii I. Murinov

Publikováno v: Neuroscience letters. 706

Two novel pyrimidine derivatives, RG2 and RG6, were studied using a rat’s model of peripheral nerve injury. Toe-spreading reflex and skin sensitivity to pinch in the foot were monitored to follow recovery of motor and sensory functions in the treat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::380a85adf5300597d9ec982502b862ff
https://pubmed.ncbi.nlm.nih.gov/31078677

Synthesis and In Vitro Anticancer Activity of 6-Ferrocenylpyrimidin-4(3H)-one Derivatives

Autor: † Natalie N. Kabal'nova, Lenar R. Valiullin, Stanislav A. Grabovskiy, Rinat S Muhammadiev, Ivan S. Raginov

Publikováno v: Current organic synthesis. 16(1)

Aim and Objective: Some ferrocenyl derivatives are active in vitro and in vivo against cancer. Generally, ferrocenyl derivatives for cancer research have three key components: a ferrocene moiety, a conjugated linker that lowers the oxidation potentia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb396eff16117cf8602e3aa5846c6fe3
https://pubmed.ncbi.nlm.nih.gov/31965930

The DC-SIGN-CD56 interaction inhibits the anti-dendritic cell cytotoxicity of CD56 expressing cells

Autor: Ivan S. Raginov, Alexey A. Nabatov

Publikováno v: Infectious Agents and Cancer
Infectious Agents and Cancer, 10:49. BioMed Central
Nabatov, A & Raginov, I S 2015, ' The DC-SIGN-CD56 interaction inhibits the anti-dendritic cell cytotoxicity of CD56 expressing cells ', Infectious Agents and Cancer, vol. 10, 49 . https://doi.org/10.1186/s13027-015-0043-8

Background This study aimed to clarify interactions of the pattern-recognition receptor DC-SIGN with cells from the HIV-infected peripheral blood lymphocyte cultures. Methods Cells from control and HIV-infected peripheral blood lymphocyte cultures we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47d7f3eaa3b9d8f763deaa9fbb952018
http://europepmc.org/articles/PMC4676137