Computed Properties of C8H8O2. In 2021 J IRAN CHEM SOC published article about ANTIMICROBIAL ACTIVITY; ANALGESIC ACTIVITY; HETEROCYCLES in [Elkanzi, Nadia A. A.; Alruwaili, May M.; Alruwaili, Enas D.; Almamtrfi, Rahaf W.; Alsharary, Hadeel Kh.] Jouf Univ, Coll Sci, Chem Dept, POB 2014, Sakaka, Saudi Arabia; [Elkanzi, Nadia A. A.] Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, Egypt; [Hrichi, Hajer] Carthage Univ, Ctr Urbain Nord, Natl Inst Appl Sci & Technol, BPN 676, Tunis 1080, Tunisia; [Bakr, Rania B.; Hendawy, O.] Jouf Univ, Coll Pharm, Dept Pharmacol, Sakaka 2014, Aljouf, Saudi Arabia; [Bakr, Rania B.] Beni Suef Univ, Fac Pharm, Dept Pharmaceut Organ Chem, Bani Suwayf 62514, Egypt; [Hendawy, O.] Beni Suef Univ, Fac Med, Dept Clin Pharmacol, Bani Suwayf, Egypt in 2021, Cited 34. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.
In the current study, a new series of pyrazole derivatives4a-d,5a-dand6a-dpossessing 1,5,10,10a-tetrahydrobenzo[g]quinoline-3-carbonitrile moiety were synthesized by treating chalcones (3a-d) with hydrazine monohydrate/acetic anhydride, hydrazine monohydrate/formic acid and 4-chlorophenylhydrazine in ethanol, respectively. These reactions proceeded smoothly with satisfactory yields, and the obtained compounds were characterized using FTIR,H-1-NMR,C-13-NMR and elemental analyses. All the synthesized compounds were subjected to antibacterial activity againstBacillus subtilis,Staphylococcus aureus,Escherichia coli, andPseudomonas aeruginosabacteria and molecular docking studies. The antibacterial studies showed that all compounds exhibited good to excellent antibacterial activity against the tested bacterial strains. The structure-activity relationship studies revealed that the compounds3b,4b,5band6bbearing a chlorine atom at the para position of the phenyl group attached to pyrazole moiety in displayed the highest antibacterial activity against all the tested bacteria exceeding the standard drug ampicillin. Moreover, the molecular docking results showed that the highest scores docking have been obtained from the most active antibacterial compounds3b,3d,4b,4d,4c,5band6bwith good energy binding score within the active site of topoisomerase II DNA gyrase enzymes (PDB ID: 2XCS), suggesting that they can act by the inhibition of DNA replication. These compounds are auspicious candidates as antibacterial agents that would deserve further investigations.
About 4-Methoxybenzaldehyde, If you have any questions, you can contact Elkanzi, NAA; Hrichi, H; Bakr, RB; Hendawy, O; Alruwaili, MM; Alruwaili, ED; Almamtrfi, RW; Alsharary, HK or concate me.. Computed Properties of C8H8O2
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles