id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
eurjchem-1599	Radini, Ibrahim Ali; Hamed, Hany Mostafa; Kharir, Mohammed Abdo Yahya; Elwahab, Ashraf Hassan Fekry Abd	Heteroaromatization with 4-phenyldiazenyl-1-naphthol. Part II: Synthesis of some new benzochromens, benzochromenopyrimidines, benzochromenotriazolopyrimidines, benzochromenopyrimidotriazepine and antimicrobial activities	2017	8	.pdf	application/pdf	5892	350	74	Compounds 10a‐e, 12, and 13 were found to be the with inhibitory effects ranging 27.4±0.1 to 29.4±0.7 µg/mL more activities as compared to the standard antibiotics ampicillin and mycostatine, while compounds 9 and 11 with inhibitory effect of 13.7±0.2 to 19.2±0.4 µg/mL were exhibited moderate activities as compared to the standard antibiotics ampicillin and mycostatine and compounds 3 and 8 showed moderate activity against Pseudomonas aeruginosa with inhibitory effect ranging 16.6±0.1 and 18.2±0.1 µg/mL as compared to the standard antibiotics ampicillin, while compounds 3, 4, 5, 6 , 7 and 8 moderate to weak activity against Staphylococcus aureus, Bacillis subtilis and Pseudomonas aeruginosa with inhibitory effect ranging 13.2±0.3 and 18.1±0.1 µg/mL as compared to the standard antibiotics ampicillin. Compounds 4, 5, 6 and 7 inactive against Pseudomonas aeruginosa, while compounds 3, 4, 5, 6, 7 and 8 inactive against Escherichia coli, and Aspergillus fumigatus, respectively, compared to the standard antibiotics, ampicillin and mycostatine as reference drugs.	cache/eurjchem-1599.pdf	txt/eurjchem-1599.txt