Alexander Kornienko
Affiliations: | Chemistry | New Mexico Inistitue of Mining & Technology |
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Sign in to add trainee| Nikolai M. Evdokimov | grad student | 2008-2011 | New Mexico Inistitue of Mining & Technology |
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| Aksenov AV, Kirilov NK, Arutiunov NA, et al. (2022) Reductive Cleavage of 4'-Spiro[indole-3,5'-isoxazoles] En Route to 2-(1-Indol-3-yl)acetamides with Anticancer Activities. The Journal of Organic Chemistry |
| Mathieu V, Superchi S, Masi M, et al. (2022) In Vitro Effects of Fungal Phytotoxins on Cancer Cell Viability: First Insight into Structure Activity Relationship of a Potent Metabolite of Radicinin. Toxins. 14 |
| Goulart Stollmaier J, Thomson J, Endoma-Arias MA, et al. (2022) Conversion of Natural Narciclasine to Its C-1 and C-6 Derivatives and Their Antitumor Activity Evaluation: Some Unusual Chemistry of Narciclasine. Molecules (Basel, Switzerland). 27 |
| Habaz L, Bedard K, Smith M, et al. (2022) Design and Synthesis of C-1 Methoxycarbonyl Derivative of Narciclasine and Its Biological Activity. Molecules (Basel, Switzerland). 27 |
| Ticli V, Zhao Z, Du L, et al. (2021) Synthesis and biological evaluation of 10-benzyloxy-Narciclasine. Tetrahedron. 101 |
| Maslivetc V, Laguera B, Chandra S, et al. (2021) Polygodial and Ophiobolin A Analogues for Covalent Crosslinking of Anticancer Targets. International Journal of Molecular Sciences. 22 |
| Aksenov AV, Arutiunov NA, Kirilov NK, et al. (2021) [3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor. Organic & Biomolecular Chemistry |
| Aksenov NA, Aksenov AV, Kirilov NK, et al. (2020) Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity. Organic & Biomolecular Chemistry |
| Turner DN, Edwards L, Kornienko A, et al. (2020) Synergistic action of substituted indole derivatives and clinically used antibiotics against drug-resistant bacteria. Future Microbiology |
| Eyong KO, Ketsemen HL, Zhao Z, et al. (2020) Antiproliferative activity of naphthoquinones and indane carboxylic acids from lapachol against a panel of human cancer cell lines Medicinal Chemistry Research. 29: 1058-1066 |