Design, in silico analysis, synthesis, and evaluation of novel benzofused nitrogen-containing heterocyclic N-substituted mercaptobenzimidazole derivatives as potential antimicrobial agent (Record no. 15644)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20211220145223.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 211220b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 14879
Author Patil, Tejaswini D.
245 ## - TITLE STATEMENT
Title Design, in silico analysis, synthesis, and evaluation of novel benzofused nitrogen-containing heterocyclic N-substituted mercaptobenzimidazole derivatives as potential antimicrobial agent
250 ## - EDITION STATEMENT
Volume, Issue number Vol.15 (3), Jul-Sept
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mandsaur
Name of publisher, distributor, etc. B.R. Nahata Smriti Sansthan
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 226-237p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: There is an urgent need for buy soma online overnight delivery the development of novel antimicrobial drugs due to the rapid<br/>development of antimicrobial drug resistance. Benzimidazole containing mercapto group at 2-position is attractive<br/>nucleus for modification with wider pharmacological activities. Objective: The aim of this study is to design<br/>benzofused nitrogen-containing heterocyclic derivatives of mercaptobenzimidazole using molecular docking,<br/>synthesis of active derivative and evaluation as potential antimicrobial agent. Materials and Methods: Using<br/>an effective procedure, N-substituted mercaptobenzimidazole derivatives were synthesized based on the<br/>literature review. The antimicrobial activity of all synthesized compounds was tested against four different<br/>organisms: Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans. Molecular<br/>docking of mercaptobenzimidazole derivatives against DNA gyrase subunit B Protein Data Bank (PDB): 5l3j and<br/>S. aureus tyrosyl-tRNA synthetase PDB: 1jij was performed using docking protocol. The compound binds to buy soma online usa the<br/>active site of DNA gyrase subunit B (1KZN) in a docking study, indicating that it may have antimicrobial activity.<br/>Conclusion: The compounds MB3 and MB5 have antimicrobial capacity, according to the findings of this report.<br/>MB4 has the high activity against C. albicans.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 14880
Co-Author Amrutkar, Sunil V.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Mandsaur B.R. Nahata Smriti Sansthan
Title International journal of green pharmacy
856 ## - ELECTRONIC LOCATION AND ACCESS
URL http://greenpharmacy.info/index.php/ijgp/article/view/3149
Link text Full Text
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 20/12/2021   2021-2022462 20/12/2021 20/12/2021 Articles Abstract Database
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