Matches in SemOpenAlex for { <https://semopenalex.org/work/W4307842789> ?p ?o ?g. }
- W4307842789 abstract "Two series of 1,3,4-thiadiazole (40a-o) and 1,2,4-triazole-5-thione (41a-l) derivatives bearing a 2-pentyl-5-phenyl-1,2,4-triazole-3-one ring were synthesized and then studied for their urease inhibitory activities using thiourea as a standard drug. Among the two groups, the first group (40a-o) did not show good activity while the second group (41a-l) showed excellent activity. Compound 41j (1091.24 ± 14.02 µM) of the second series of compounds showed lower activity than thiourea, while the remaining 11 compounds (41a-i, k, and l) showed better activity than thiourea (183.92 ± 13.14 µM). Among the 11 compounds, 41b (15.96 ± 2.28 µM) having the 3-F group on the phenyl ring showed the highest inhibitory activity. Urease kinetic studies of 41b, which is the most active compound, determined it to have an un-competitive inhibition potential. Moreover, in silico analysis against urease from jack bean with 27 new heterocyclic compounds and the reference molecule was carried out to see the necessary interactions responsible for urease activity. The docking calculations of all compounds supported stronger binding to the receptor than the reference molecule, with high inhibition constants. In addition, compound 40m was characterized by single-crystal X-ray diffraction analysis. X-ray analysis reveals that the structures of the compound 40m crystallize in the monoclinic P21/c space group with the cell parameters: a = 10.2155(9) Å, b = 22.1709(18) Å, c = 21.4858(17) Å, β = 99.677(8)°, V = 4797.0(7) Å3 . X-ray diffraction analyses were also performed to gain insights into the role of weak intermolecular interactions and C-H…X (halogen) interactions in compound 40m that influence the crystal packing." @default.
- W4307842789 created "2022-11-06" @default.
- W4307842789 creator A5012770089 @default.
- W4307842789 creator A5017988475 @default.
- W4307842789 creator A5022751920 @default.
- W4307842789 creator A5042064295 @default.
- W4307842789 creator A5043199383 @default.
- W4307842789 creator A5061133955 @default.
- W4307842789 date "2022-10-31" @default.
- W4307842789 modified "2023-10-18" @default.
- W4307842789 title "1,3,4‐Thiadiazole and 1,2,4‐triazole‐5‐thione derivatives bearing 2‐pentyl‐5‐phenyl‐2,4‐dihydro‐3<i>H</i>‐1,2,4‐triazole‐3‐one ring: Synthesis, molecular docking, urease inhibition, and crystal structure" @default.
- W4307842789 cites W1527600411 @default.
- W4307842789 cites W1620160353 @default.
- W4307842789 cites W176484652 @default.
- W4307842789 cites W1913030039 @default.
- W4307842789 cites W1964970176 @default.
- W4307842789 cites W1966485019 @default.
- W4307842789 cites W1973558817 @default.
- W4307842789 cites W1975690500 @default.
- W4307842789 cites W1988846265 @default.
- W4307842789 cites W1990170643 @default.
- W4307842789 cites W1991347768 @default.
- W4307842789 cites W1993758577 @default.
- W4307842789 cites W1997439033 @default.
- W4307842789 cites W2006118174 @default.
- W4307842789 cites W2010091844 @default.
- W4307842789 cites W2023270354 @default.
- W4307842789 cites W2027753138 @default.
- W4307842789 cites W2033039564 @default.
- W4307842789 cites W2033127028 @default.
- W4307842789 cites W2036275281 @default.
- W4307842789 cites W2039773974 @default.
- W4307842789 cites W2040927552 @default.
- W4307842789 cites W2042758577 @default.
- W4307842789 cites W2046588215 @default.
- W4307842789 cites W2056426681 @default.
- W4307842789 cites W2059205366 @default.
- W4307842789 cites W2061271956 @default.
- W4307842789 cites W2070649140 @default.
- W4307842789 cites W2072442596 @default.
- W4307842789 cites W2076812690 @default.
- W4307842789 cites W2079816329 @default.
- W4307842789 cites W2084202792 @default.
- W4307842789 cites W2086617513 @default.
- W4307842789 cites W2090671413 @default.
- W4307842789 cites W2105668062 @default.
- W4307842789 cites W2108931847 @default.
- W4307842789 cites W2113110555 @default.
- W4307842789 cites W2117790879 @default.
- W4307842789 cites W2119007778 @default.
- W4307842789 cites W2125553099 @default.
- W4307842789 cites W2129319023 @default.
- W4307842789 cites W2130687287 @default.
- W4307842789 cites W2132454074 @default.
- W4307842789 cites W2143122357 @default.
- W4307842789 cites W2144896165 @default.
- W4307842789 cites W2173914872 @default.
- W4307842789 cites W2223244821 @default.
- W4307842789 cites W2320516419 @default.
- W4307842789 cites W2325407312 @default.
- W4307842789 cites W2333671104 @default.
- W4307842789 cites W2344703521 @default.
- W4307842789 cites W24899332 @default.
- W4307842789 cites W2506509580 @default.
- W4307842789 cites W2510927590 @default.
- W4307842789 cites W2606238720 @default.
- W4307842789 cites W2726508175 @default.
- W4307842789 cites W2750368943 @default.
- W4307842789 cites W2888026652 @default.
- W4307842789 cites W2896619532 @default.
- W4307842789 cites W2899437569 @default.
- W4307842789 cites W2901349652 @default.
- W4307842789 cites W2947606 @default.
- W4307842789 cites W2952579758 @default.
- W4307842789 cites W2952593686 @default.
- W4307842789 cites W2953742253 @default.
- W4307842789 cites W2965978788 @default.
- W4307842789 cites W2995486995 @default.
- W4307842789 cites W3016391295 @default.
- W4307842789 cites W3016762617 @default.
- W4307842789 cites W3044294667 @default.
- W4307842789 cites W3081357927 @default.
- W4307842789 cites W3081881156 @default.
- W4307842789 cites W3083350277 @default.
- W4307842789 cites W3086384262 @default.
- W4307842789 cites W3112334758 @default.
- W4307842789 cites W3119921885 @default.
- W4307842789 cites W3120285121 @default.
- W4307842789 cites W3158792255 @default.
- W4307842789 cites W3164296947 @default.
- W4307842789 cites W3170267201 @default.
- W4307842789 cites W3177474861 @default.
- W4307842789 cites W3183941090 @default.
- W4307842789 cites W3213319627 @default.
- W4307842789 cites W341207603 @default.
- W4307842789 cites W4200137642 @default.
- W4307842789 cites W4235312404 @default.
- W4307842789 cites W4251203264 @default.
- W4307842789 doi "https://doi.org/10.1002/ardp.202200355" @default.
- W4307842789 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36316247" @default.