Thieno[3,2-c]pyran-4-one based novel small molecules: Their synthesis, crystal structure analysis and in vitro evaluation as potential anticancer agents

dc.contributor.author Nakhi, Ali
dc.contributor.author Adepu, Raju
dc.contributor.author Rambabu, D.
dc.contributor.author Kishore, Ravada
dc.contributor.author Vanaja, G. R.
dc.contributor.author Kalle, Arunasree M.
dc.contributor.author Pal, Manojit
dc.date.accessioned 2022-03-27T01:02:11Z
dc.date.available 2022-03-27T01:02:11Z
dc.date.issued 2012-07-01
dc.description.abstract Novel thieno[3,2-c]pyran-4-one based small molecules were designed as potential anticancer agents. Expeditious synthesis of these compounds was carried out via a multi-step sequence consisting of few steps such as Gewald reaction, Sandmeyer type iodination, Sonogashira type coupling followed by iodocyclization and then Pd-mediated various C-C bond forming reactions. The overall strategy involved the construction of thiophene ring followed by the fused pyranone moiety and then functionalization at C-7 position of the resultant thieno[3,2-c]pyran-4-one framework. Some of the compounds synthesized showed selective growth inhibition of cancer cells in vitro among which two compounds for example, 5d and 6c showed IC 50 values in the range of 2.0-2.5 μM. The crystal structure analysis of an active compound along with hydrogen bonding patterns and molecular arrangement present within the molecule is described. © 2012 Elsevier Ltd. All rights reserved.
dc.identifier.citation Bioorganic and Medicinal Chemistry Letters. v.22(13)
dc.identifier.issn 0960894X
dc.identifier.uri 10.1016/j.bmcl.2012.04.109
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0960894X12005598
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/3938
dc.subject Alkynylation
dc.subject Heck
dc.subject Iodocyclization
dc.subject Sonogashira
dc.subject Suzuki
dc.subject Thienopyranone
dc.title Thieno[3,2-c]pyran-4-one based novel small molecules: Their synthesis, crystal structure analysis and in vitro evaluation as potential anticancer agents
dc.type Journal. Article
dspace.entity.type
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