Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8250
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dc.contributor.authorBorisa, Ankit C.-
dc.contributor.authorBhatt, Hardik G.-
dc.date.accessioned2019-03-27T08:55:49Z-
dc.date.available2019-03-27T08:55:49Z-
dc.date.issued2017-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/8250-
dc.descriptionEuropean Journal of Medicinal Chemistry; 140 (2017) 1-19en_US
dc.description.abstractAurora kinase belongs to serine/threonine kinase family which controls cell division. Therapeutic inhibition of Aurora kinase showed great promise as probable anticancer regime because of its important role during cell division. Here, in this review, we have carried out exhaustive study of various synthetic molecules reported as Aurora kinase inhibitors and developed as lead molecule at various stages of clinical trials from its discovery in 1995 to till date. We reported details of small molecules, specifically inhibiting all 3 types of Aurora kinases, which includes extensive literature search in various database like various scientific journals, patents, scifinder and PubMed database, internet resources, books, etc. IC50 values of tumor growth inhibition, in-vitro and in-vivo activity along with clinical trial data. Here, we took efforts to describe essence of Aurora kinase and its inhibition which could be used to develop antimitotic drug for the treatment of cancer. In conclusion, we also discuss future perspectives for development of novel inhibitors and their scope in drug development process.en_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesIPFP0283;-
dc.subjectAurora kinaseen_US
dc.subjectAurora-Aen_US
dc.subjectAurora-Ben_US
dc.subjectAurora-Cen_US
dc.subjectINCENPen_US
dc.subjectSmall molecule inhibitorsen_US
dc.titleA comprehensive review on Aurora kinase: Small molecule inhibitors and clinical trial studiesen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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