مدل سازی مولکولی و سنتز خاص ترکیبات آریل جایگزین شده دارای فعالیت ضدسرطانی بالقوه
Molecular modeling and synthesis of certain substituted aryl compounds which have a potential anticancer activity
نویسندگان |
این بخش تنها برای اعضا قابل مشاهده است ورودعضویت |
اطلاعات مجله |
Bulletin of Faculty of Pharmacy, Cairo University www.elsevier.com/locate/bfopcu |
سال انتشار |
2011 |
فرمت فایل |
PDF |
کد مقاله |
6245 |
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چکیده (انگلیسی):
Aim: The enzyme methionine synthase (MetS) is linked to the cancer pathogenesis disorders
such as myeloid leukemia, prostate and breast tumors. Inhibition of the biosynthesis of
methionine amino acid which provides the tumor nucleic acid with one carbon atom building units
occurred through the blocking of the natural substrate 5-methyltetrahydrofolate (MTHF) to bind
to its binding domain in MetS with the synthesized compounds in this article.
Design and methods: The target compounds were designed to interact with the binding site of
MTHF in much the same way as the substrate. The crystal structure of MTHF binding region from
human source has been deduced. A series of aromatic compounds was synthesized and docked separately
into the MTHF binding site of the enzyme. Thermodynamic algorithms were done and compared
to the results obtained from the biological cell line assay.
Results: The cytotoxicity assay (in vitro) of the most potent compounds 2-hydroxymethyl-5-nitro-
1H-benzimidazole and 1,3,5-trinitrobenzene showed IC50 of 50 ± 5 and 49 ± 5 lM, respectively,
with score of the lowest free energy of binding 1610.42 and 1737.10 kJ/mol, respectively.
Conclusion: The results of this study had led to the identification of two lead compounds with good
inhibitory activities that could overlay for the next generation of the inhibitors for methionine synthase.
Preparation of novel potential inhibitors for the methionine synthase that have the ability to
avoid the side effects of the other marketed anticancer drugs could be a good step forward towards
cancer treatment.
کلمات کلیدی مقاله (فارسی):
ساختار کریستالی؛ IC50؛ بازداری؛ متیونینسنتتاز ؛ متیل تتراهیدروفولات
کلمات کلیدی مقاله (انگلیسی):
Crystal structure; IC50; Inhibition; Methionine synthase; Methyltetrahydrofolate
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