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(1 R,3 S)-3-(1 H -Benzo[ d ]imidazol-2-yl)-1,2,2-tri­methyl­cyclo­pentane-1-carb­oxy­lic acid as a new anti-diabetic active pharmaceutical ingredient
Kovalenko, S. M., Konovalova, I. S., Merzlikin, S. I., Chuev, V. P., Kravchenko, D. V.
The chiral title compound, C₁₆H₂₀N₂O₂, which can be used for producing active pharmaceutical
Validation of structural-based virtual screening protocols with the PDB Code 3G0B and prediction of the activity of Tinospora crispa compounds as inhibitors of dipeptidyl-peptidase-IV
Andri Prasetiyo, Shirly Kumala, Esti Mumpuni, Raymond R. Tjandrawinata
Brotowali (Tinospora crispa) has been traditionally used as an antidiabetic drug. DPP-IV inhibitor
Benzofurocaine: effects on experimental periodontitis, anti-diabetic activity and molecular mechanisms of action
Galenko-Yaroshevsky, P. A., Popkov, V. L., Bedrosova, K. A., Faustov, L. A., Sukoyan, G. V.
: To assess the influence of benzofuracaine on experimental periodontitis and to study its antidiabetic
Antidiabetic Biguanides as Anti-Aging Drugs
Anisimov V.N.
Evidence has emerged that metformin and other antidiabetic biguabides are promising candidates
Quick Identification of Piperidine Alkaloid from Roots of Grewia nervosa and Their Glucosidase Inhibitory Activity
Meena S.N., Majik M.S., Ghadi S.C., Tilve S.G.
-glucosidase inhibition activity with an IC50 value of 53.40 μm. Furthermore, N-methylmicrocosamine showed maximum α
Course and treatment of diabetes mellitus in the context of COVID-19
Shestakova M.V.
of the peculiarities of their immune response to a virus attack and due to their high susceptibility to viral activity
Synthesis, biological activity and molecular modeling of a new series of condensed 1,2,4-triazoles
Marmouzi I., Anouar E.H., Karthikeyan S., Harmaoui A., Faouzi M.E.A., Mague J.T., Essassi E.M., El Bakri Y., El Jemli M.
. The compounds showed interesting and promising antidiabetic activities compared to the reference drug Acarbose
Synthesis, α-Glucosidase Inhibitory Activity, and Molecular Docking Studies of Tri(benzo)-5-azacrownophanes with a γ-Piperidone Moiety
Nhung D.T., Tram N.N., Tam P.T.T., Alekseeva K.A., Khrustalev V.N., Hoang D.T., Duan L.T., Anh L.T.
and they were shown to be potential candidates in the search for new antidiabetic drugs. Among five tested
α-Glucosidase inhibition activity and in silico study of 2-(benzo[d][1,3]dioxol-5-yl)-4H-chromen-4-one, a synthetic derivative of flavone
Meena S.N., Kumar U., Naik M.M., Ghadi S.C., Tilve S.G.
by the one pot reaction method and assessed for α-glucosidase inhibitory activity. The BDC demonstrated dose
(1 R,3 S)-3-(1 H -Benzo[ d ]imidazol-2-yl)-1,2,2-tri­methyl­cyclo­pentane-1-carb­oxy­lic acid as a new anti-diabetic active pharmaceutical ingredient
Kovalenko, S. M., Konovalova, I. S., Merzlikin, S. I., Chuev, V. P., Kravchenko, D. V.
The chiral title compound, C 16 H 20 N 2 O 2, which can be used for producing active pharmaceutical

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