Pyrrolo[3,4-c]- and thieno- [3,4-c]isoquinolines — new heterocyclic hits for the drag design of oncolytic compounds
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Published:2020-07
Issue:7
Volume:
Page:62-71
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ISSN:1025-6415
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Container-title:Reports of the National Academy of Sciences of Ukraine
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language:
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Short-container-title:Dopov. Nac. akad. nauk Ukr.
Author:
Bogdan N.M., ,Bogza S.L.,Pendiukh V.V.,Stepanova D.S.,Sujkov S.Yu., , , , ,
Publisher
National Academy of Sciences of Ukraine (Co. LTD Ukrinformnauka)
Reference13 articles.
1. 1. Bogza, S. L., Kobrakov, K. I., Malienko, A. A., Perepichka, I. F., Sujkov, S. Yu., Bryce, M. R., Lyubchik, S. B., Batsanov, A. S. & Bogdan, N. M. (2005). A versatile synthesis of pyrasolo[3,4-c] isoquinoline derivatives by reaction of 4-aryl-5-amino-pyrazoles with aryl/heteroaryl aldehydes: the effect of heterocycle on the reaction pathways. Org. Biomol. Chem., 3, No. 5, pp. 932-940. https://doi.org/10.1039/B417002D 2. 2. Drug Data Report. (2007). Oncolytic drugs. № 29. 644 p. 3. 3. Pat. 7872014 US, IPC C07D471/02, A61K31/4745, A61K, A61K31/437, C07D471/04, A61P29/00. Anaplastic lymphoma kinase modulators and methods of use. Anand, N. K., Blazey, C. M., Bowles, O. J., Bussenius, J., Costanzo, S., Curtis, J. K., Dubenko, L., Kennedy, A. R., Khoury, R. G., Kim, A. I., Manalo, J. L., Peto, C. J., Rice, K. D. & Tsang, T. H., Publ. 18.01.2011. 4. 4. Kondratov, R. V., Komarov, P. G., Becker, Y., Ewenson, A. & Gudkov, A. V. (2001). Small molecules that dramatically alter multidrug resistance phenotype by modulating the substrate specificity of P-glycoprotein. Proc. Natl. Acad. Sci. USA., 98, Iss. 24, pp. 14078-14083. https://doi.org/10.1073/pnas.241314798 5. 5. Rochais, C., Lisowski, V., Dallemagne, P. & Rault, S. (2004). First synthesis of methyl 3-amino-4-(het)aryl- 1H-pyrrole-2-carboxylates as useful scaffolds in medicinal chemistry. Tetrahedron, 60, No. 10, pp. 2267-2270. https://doi.org/10.1016/j.tet.2004.01.019
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