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Title of Journal: Interdiscip Sci Comput Life Sci

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Abbravation: Interdisciplinary Sciences: Computational Life Sciences

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Springer Berlin Heidelberg

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10.1007/s00376-002-0039-3

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1867-1462

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Structural Interactions of Curcumin Biotransformed

Authors: Akhileshwar Kumar Srivastava Divya Singh Bijoy Krishna Roy
Publish Date: 2016/01/21
Volume: 9, Issue: 1, Pages: 116-129
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Abstract

Curcumin as a natural product has drawn considerable attention in recent years for its multiple pharmacological activities against various diseases but more studies are required to understand the curcumin pharmacological action considering its low bioavailability Though numerous reasons contribute to the low bioavailability of curcumin one of the important reasons is associated with biotransformation of curcumin through either conjugation or reduction depending on curcumin administration route The orally administered curcumin CUR is metabolised into curcumin glucuronidase CURGLR and curcumin sulphate by conjugation whereas dihydroxycurcumin tetrahydrocurcumin and hexahydrocurcumin HHC are formed by reduction after intraperitoneal administration of curcumin The main aim of the current study was to investigate the pharmacological properties of curcumin and its biotransformed molecules and its inhibitory potential against CagA cytotoxicassociated gene A oncoprotein of Helicobacter pylori All lead molecules followed the Lipinski’s five rules for biological activities except CURGLR whereas druglikeness scores were obtained for all molecules Subsequently molecular docking was employed to analyse the binding affinity of molecules with CagA The docking studies revealed that CURGLR has highest binding affinity with CagA whereas less interactive affinity was observed in HHC From the virtual screening and docking studies the current study suggests that the biotransformation of curcumin through conjugation has more potential for inhibition of oncogenic activities of CagA+ H pylori than reduction


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