మా గ్రూప్ ప్రతి సంవత్సరం USA, యూరప్ & ఆసియా అంతటా 3000+ గ్లోబల్ కాన్ఫరెన్స్ ఈవెంట్లను నిర్వహిస్తుంది మరియు 1000 కంటే ఎక్కువ సైంటిఫిక్ సొసైటీల మద్దతుతో 700+ ఓపెన్ యాక్సెస్ జర్నల్లను ప్రచురిస్తుంది , ఇందులో 50000 మంది ప్రముఖ వ్యక్తులు, ప్రఖ్యాత శాస్త్రవేత్తలు ఎడిటోరియల్ బోర్డ్ సభ్యులుగా ఉన్నారు.
ఎక్కువ మంది పాఠకులు మరియు అనులేఖనాలను పొందే ఓపెన్ యాక్సెస్ జర్నల్స్
700 జర్నల్స్ మరియు 15,000,000 రీడర్లు ప్రతి జర్నల్ 25,000+ రీడర్లను పొందుతున్నారు
Nishu Singla
The balloning level of antimicrobial resistance in pathogenic bacteria, together with the lack of new potential drug scaffolds in the pipeline, make the problem of infectious diseases a major public health concern. Thus, in this context, a novel series of 1,3,4-oxadiazole-substituted thiophenes (4a-m) and 1,2,4-triazole (6a-m) substituted thiophene derivatives were synthesized in order to develop new compounds with improved efficacy, and to overcome the problem of drug resistance. Characterization of all the synthesized derivatives was done by various spectroscopic techniques such as 1H NMR, 13C NMR and mass spectroscopy, and evaluated for antimicrobial activity against various pathological strains such as gram positive and gram negative bacteria. The results obtained from antimicrobial evaluation of synthesized compounds revealed that all the compounds displayed moderate to significant antimicrobial activity. In particular, compound 6e and 4e exhibited significant inhibitory potential with MIC ranging from 2-7 µg/ml against S. aureus, B. subtilis, P. aeruginosa and E. coli. Additionally, compound 6e was found to be highly potent against methicillin resistant S. aureus (MRSA; MIC = 2 µg/ml). Molecular docking studies were also performed to confer the possible mode of action and association studies indicate the binding of potent active compound with DHFR enzyme. Further, the mechanism of action has also been explored by atomic force microscopy (AFM), which reveals the bacterial cell wall deformity and cell wall rupturing that may lead to bacteria cell death. Additionally, in silico ADME prediction study suggested the drug like properties of active compounds.