Matches in SemOpenAlex for { <https://semopenalex.org/work/W2953528566> ?p ?o ?g. }
- W2953528566 endingPage "355" @default.
- W2953528566 startingPage "347" @default.
- W2953528566 abstract "Background: Cancer can be considered as a disease in which normal cells start behaving badly, multiplying uncontrollably, ignoring signals to stop and accumulating to form a mass that is generally termed as a tumor. Apoptosis or programmed cell death is a physiological process that enables organisms to control their cell numbers in many developmental and physiological settings and to eliminate unwanted cells and it plays essential role in chemotherapy-induced tumor-cell killing. The correct balance between apoptosis and inhibition of apoptosis is important in animal development as well as in tissue homeostasis. The aim of this paper is to introduce the readers about the design strategy and synthesis of effective cytotoxic and apoptotic inducing agents based on benzo[d]imidazo[2,1-b]thiazole scaffold. Methods: Benzo[d]imidazo[2,1-b]thiazole-propenone conjugates were synthesized by the condensation of 7- methoxy-2-(aryl)benzo[d]imidazo[2,1-b]thiazol-3-yl)prop-2-yn-1-ones with aryl/hetero aryl amines in ethanol at room temperature. These in turn were obtained from 7-methoxy-2-(aryl)benzo[d]imidazo[2,1-b]thiazole-3- carbaldehydes on treatment with ethynylmagnesium bromide followed by oxidation. Results: 3-Arylaminopropenone linked 2-arylbenzo[d]imidazo[2,1-b]thiazole conjugates prepared in this investigation exhibited significant cytotoxic activity and arrested HeLa cancer cells in G1 phase. The treatment of the conjugate led to 40% of loss of mitochondrial membrane potential (DΨm) in HeLa cells and 4 fold increase in the levels of reactive oxygen species (ROS). In addition, it induces apoptosis in HeLa cells, this was examined by the wound healing assay, Actin filaments and Hoechst staining assay. Conclusion: The encouraging biological profile exhibited by these 3-arylaminopropenone 2-aryl linked benzo[d]imidazo[2,1-b]thiazole conjugates demonstrate that they have the potential to be developed as a lead by further structural modifications to obtain potential chemotherapeutic agents that are likely to target the HeLa cancer cells." @default.
- W2953528566 created "2019-07-12" @default.
- W2953528566 creator A5026940529 @default.
- W2953528566 creator A5028889608 @default.
- W2953528566 creator A5058560861 @default.
- W2953528566 creator A5062644316 @default.
- W2953528566 creator A5084168528 @default.
- W2953528566 creator A5090229898 @default.
- W2953528566 creator A5090906460 @default.
- W2953528566 date "2019-06-25" @default.
- W2953528566 modified "2023-09-26" @default.
- W2953528566 title "Synthesis of Benzo[d]imidazo[2,1-b]thiazole-Propenone Conjugates as Cytotoxic and Apoptotic Inducing Agents" @default.
- W2953528566 cites W1963951809 @default.
- W2953528566 cites W1966493552 @default.
- W2953528566 cites W1972779889 @default.
- W2953528566 cites W1975731421 @default.
- W2953528566 cites W1980480652 @default.
- W2953528566 cites W1988614680 @default.
- W2953528566 cites W1996271525 @default.
- W2953528566 cites W2000196730 @default.
- W2953528566 cites W2001126699 @default.
- W2953528566 cites W2005778575 @default.
- W2953528566 cites W2008117638 @default.
- W2953528566 cites W2009311211 @default.
- W2953528566 cites W2015082085 @default.
- W2953528566 cites W2015879631 @default.
- W2953528566 cites W2015908647 @default.
- W2953528566 cites W2028889221 @default.
- W2953528566 cites W2032028642 @default.
- W2953528566 cites W2034242236 @default.
- W2953528566 cites W2039048061 @default.
- W2953528566 cites W2041275386 @default.
- W2953528566 cites W2044377404 @default.
- W2953528566 cites W2057810394 @default.
- W2953528566 cites W2059988098 @default.
- W2953528566 cites W2084461102 @default.
- W2953528566 cites W2084889020 @default.
- W2953528566 cites W2087072319 @default.
- W2953528566 cites W2099365146 @default.
- W2953528566 cites W2105809801 @default.
- W2953528566 cites W2107714285 @default.
- W2953528566 cites W2125873364 @default.
- W2953528566 cites W2167637849 @default.
- W2953528566 cites W2522573946 @default.
- W2953528566 cites W3004118171 @default.
- W2953528566 doi "https://doi.org/10.2174/1871520619666181127112621" @default.
- W2953528566 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30479221" @default.
- W2953528566 hasPublicationYear "2019" @default.
- W2953528566 type Work @default.
- W2953528566 sameAs 2953528566 @default.
- W2953528566 citedByCount "7" @default.
- W2953528566 countsByYear W29535285662020 @default.
- W2953528566 countsByYear W29535285662021 @default.
- W2953528566 countsByYear W29535285662022 @default.
- W2953528566 countsByYear W29535285662023 @default.
- W2953528566 crossrefType "journal-article" @default.
- W2953528566 hasAuthorship W2953528566A5026940529 @default.
- W2953528566 hasAuthorship W2953528566A5028889608 @default.
- W2953528566 hasAuthorship W2953528566A5058560861 @default.
- W2953528566 hasAuthorship W2953528566A5062644316 @default.
- W2953528566 hasAuthorship W2953528566A5084168528 @default.
- W2953528566 hasAuthorship W2953528566A5090229898 @default.
- W2953528566 hasAuthorship W2953528566A5090906460 @default.
- W2953528566 hasConcept C121608353 @default.
- W2953528566 hasConcept C134306372 @default.
- W2953528566 hasConcept C1491633281 @default.
- W2953528566 hasConcept C154317977 @default.
- W2953528566 hasConcept C185592680 @default.
- W2953528566 hasConcept C190283241 @default.
- W2953528566 hasConcept C197336794 @default.
- W2953528566 hasConcept C202751555 @default.
- W2953528566 hasConcept C2777366897 @default.
- W2953528566 hasConcept C2778464347 @default.
- W2953528566 hasConcept C33923547 @default.
- W2953528566 hasConcept C54355233 @default.
- W2953528566 hasConcept C55493867 @default.
- W2953528566 hasConcept C71240020 @default.
- W2953528566 hasConcept C86803240 @default.
- W2953528566 hasConcept C96232424 @default.
- W2953528566 hasConceptScore W2953528566C121608353 @default.
- W2953528566 hasConceptScore W2953528566C134306372 @default.
- W2953528566 hasConceptScore W2953528566C1491633281 @default.
- W2953528566 hasConceptScore W2953528566C154317977 @default.
- W2953528566 hasConceptScore W2953528566C185592680 @default.
- W2953528566 hasConceptScore W2953528566C190283241 @default.
- W2953528566 hasConceptScore W2953528566C197336794 @default.
- W2953528566 hasConceptScore W2953528566C202751555 @default.
- W2953528566 hasConceptScore W2953528566C2777366897 @default.
- W2953528566 hasConceptScore W2953528566C2778464347 @default.
- W2953528566 hasConceptScore W2953528566C33923547 @default.
- W2953528566 hasConceptScore W2953528566C54355233 @default.
- W2953528566 hasConceptScore W2953528566C55493867 @default.
- W2953528566 hasConceptScore W2953528566C71240020 @default.
- W2953528566 hasConceptScore W2953528566C86803240 @default.
- W2953528566 hasConceptScore W2953528566C96232424 @default.
- W2953528566 hasIssue "3" @default.
- W2953528566 hasLocation W29535285661 @default.
- W2953528566 hasLocation W29535285662 @default.