Bogdanov, A,
Tsivileva, O,
Voloshina, A,
Lyubina, A,
Amerhanova, S,
Burtceva, E,
Bukharov, S,
Samorodov, A,
Pavlov, V (2022) in the aromatic fragment have been synthesized. Their structure and composition were confirmed by
NMR-and IR-
spectroscopiesKHALIULLIN, F.A.,
KLEN, E.E.,
PAVLOV, V.N.,
SAMORODOV, A.V.,
SHEPILOVA, S.O.,
MAKAROVA, N.N.,
NURLANOVA, S.N.,
ABZALILOV, T.N. (2022) . The
structures of the synthesized compounds were established by IR, PMR, and 13C
NMR spectroscopy. In vitro
Khazhiev, S.Y.,
Khusainov, M.A.,
Khalikov, R.A.,
Kataev, V.A.,
Tyumkina, T.V.,
Mescheryakova, E.S.,
Khalilov, L.M.,
Kuznetsov, V.V. (2022) According to the
NMR 1Н, 13С and X-ray analysis data molecules of 5,5-bis(bromomethyl)-2
Borisova, Y.G.,
Dzhumaev, S.S.,
Khusnutdinova, N.S.,
Mryasova, L.M.,
Raskildina, G.Z.,
Zlotskii, S.S. (2022) with carbo- and heterocyclic fragments were obtained and characterized by mass spectrometry and
NMR. Studying
Bogdanov, AV,
Voloshina, AD,
Sapunova, AS,
Kulik, NV,
Bukharov, SV,
Dobrynin, AB,
Voronina, JK,
Terekhova, NV,
Samorodov, AV,
Pavlov, VN,
Mironov, VF (2022) and sodium heparin drugs. It has been shown by UV
spectroscopy and fluorescence microscopy that the mechanism
Parfenova, L.V.,
Galimshina, Z.R.,
Gil'fanova, G.U.,
Alibaeva, E.I.,
Danilko, K.V.,
Pashkova, T.M.,
Kartashova, O.L.,
Farrakhov, R.G.,
Mukaeva, V.R.,
Parfenov, E.V.,
Nagumothu, R.,
Valiev, R.Z. (2022) -ray photoelectron
spectroscopy (XPS). The contact angle measurements showed the increase in the hydrophilicity