An efficient, catalyst-free, one-pot synthesis of 4H-chromene derivatives and investigating their biological activities and mode of interactions using molecular docking studies

An efficient, catalyst-free, one-pot synthesis of 4H-chromene derivatives and investigating their biological activities and mode of interactions using molecular docking studies


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نویسندگان: لیلا دین پرست , سالار همتی , علی اکبر علیزاده , حسین صمدی کفیل , سیاوش دستمالچی

کلمات کلیدی: ChromeneIonic liquidGreen chemistryCytotoxicityMolecular dockingEnzyme inhibition

نشریه: 55337 , 127426 , 1203 , 2020

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نویسنده ثبت کننده مقاله سیاوش دستمالچی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات بیوتکنولوژی(زیست فناوری)
کد مقاله 71028
عنوان فارسی مقاله An efficient, catalyst-free, one-pot synthesis of 4H-chromene derivatives and investigating their biological activities and mode of interactions using molecular docking studies
عنوان لاتین مقاله An efficient, catalyst-free, one-pot synthesis of 4H-chromene derivatives and investigating their biological activities and mode of interactions using molecular docking studies
ناشر 7
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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In the present study, the design and development of an efficient and green method for the synthesis of dialkyl 4-hydroxy-4H-chromene-2,3-dicarboxylate derivatives together with their biological evaluation are reported. A series of 4H-chromenes were synthesized in the presence of 1-hexyl-3-methylimidazolium bromide ([HMIM]Br) as an environmentally friendly media, without using any organic and toxic solvent and catalyst. The reaction was rapid and was conducted at room temperature with high-to-excellent yields. The antiproliferative potential of the synthesized compounds was evaluated against human lung (A549), breast (MCF-7), and colon (HT-29) cancerous cell lines by adopting MTT method. The tested chromenes showed cytotoxicity in the range of 8.8–82.3% against A549 cells at 200 μg/mL. Also, chromene derivatives were assessed for tyrosinase and α-glucosidase inhibitory activities. Based on IC50 values (2.99–4.39 mM), all chromenes exhibited significant α-glucosidase inhibition compared with acarbose (IC50 = 7.90 mM). Furthermore, the ability of the studied compounds to inhibit tyrosinase was evaluated and found to be moderate (IC50 = 3.50–12.20 mM). In silico studies were performed to explore the binding modes of the chromenes at the binding site of α-glucosidase and tyrosinase. Molecular docking results revealed the importance of hydrogen bonding, hydrophobic, π-π stacking, π-cation, and metal interactions between the target enzymes and the synthesized compounds. Collectively, the results obtained in the current work indicated that the studied chromenes may be regarded as lead compounds for designing new chemicals potentially effective in conditions such as skin disorders and diabetes mellitus.

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نویسنده نفر چندم مقاله
لیلا دین پرستاول
سالار همتیدوم
علی اکبر علیزادهسوم
حسین صمدی کفیلپنجم
سیاوش دستمالچیهفتم

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JMolStruct.pdf1398/11/141835672دانلود