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Synthesis of Novel Series of ۱-(۶-Hydroxy-۴-(۱H-indol-۳-yl)-۳,۶-dimethyl- ۴,۵,۶,۷-tetrahydro-۱H-indazol-۵-yl)ethan-۱-oneas Evaluations of their Antimicrobial Activity with Insilco Docking Study

عنوان مقاله: Synthesis of Novel Series of ۱-(۶-Hydroxy-۴-(۱H-indol-۳-yl)-۳,۶-dimethyl- ۴,۵,۶,۷-tetrahydro-۱H-indazol-۵-yl)ethan-۱-oneas Evaluations of their Antimicrobial Activity with Insilco Docking Study
شناسه ملی مقاله: JR_JMCH-5-2_011
منتشر شده در در سال 1401
مشخصات نویسندگان مقاله:

Milind Gaikwad - Department of Chemistry, Dr. D.Y. Patil Arts, Commerce & Science College; Pimpri, Pune-۴۱۱۰۱۸, India
Sunil Gaikwad - Department of Chemistry, Dr. D.Y. Patil Arts, Commerce & Science Women College; Pimpri, Pune-۴۱۱۰۱۸, India
Rahul Kamble - Department of Chemistry, Amruteshwar ACS, College, Vinzar, Pune (MH), India-۴۱۲۲۱۳

خلاصه مقاله:
This research study discusses the silico design, synthesis, and biological evaluation of novel effective phenyl, indole, ۳,۴-dimethyl substituted ۴,۵,۶,۷-tetrahydro-۱H-indazole derivatives. The novel multi- substituted indazole derivatives (۵A-۵J) was synthesized from the treatment of hydrazine hydrates in MeOH/H+ with multi substituted clohexanone derivatives (۴a-۴j). The final scaffold was characterized with the help of spectroscopic data such asIR, ۱H NMR, ۱۳C NMR, and mass spectra. The compound ۵A, ۵D, and ۵F shows excellent antibacterial activity and the compounds ۵B, ۵C, ۵H ۵I and ۵J exhibited moderate antibacterial activity against the S. aureus, Bacillus subtilis and E.Coli.  Finally, the molecular docking studies showes that the  compound ۵D and ۵F scaffolds display excellent bonding mode of interactions with the active site of DNA gyrase ۱KZN enzyme.

کلمات کلیدی:
Dihydro-multi substituted indazole, NH۲-NH۲-H۲O, Ph-NH۲-NH۲ Molecular docking, Antimicrobial activity

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1330657/