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2-phenyl-4-(4-(4-phenylthiazol-2-yl)phenyl)thiazole is a complex organic compound characterized by its unique molecular structure. It features a thiazole ring at the core, which is fused with a phenyl group at the 2-position. Additionally, another phenyl group is attached at the 4-position, which itself is substituted with a 4-phenylthiazol-2-yl group. 2-phenyl-4-(4-(4-phenylthiazol-2-yl)phenyl)thiazole is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific chemical properties and reactivity. The intricate arrangement of its atoms and functional groups contributes to its distinct chemical behavior and possible uses in research and development.

7531-69-3

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7531-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7531-69-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7531-69:
(6*7)+(5*5)+(4*3)+(3*1)+(2*6)+(1*9)=103
103 % 10 = 3
So 7531-69-3 is a valid CAS Registry Number.

7531-69-3Downstream Products

7531-69-3Relevant academic research and scientific papers

New 2-phenylthiazoles as potential sortase a inhibitors: Synthesis, biological evaluation and molecular docking

Oniga, Smaranda Dafina,Araniciu, Catalin,Palage, Mariana Doina,Popa, Marcela,Chifiriuc, Mariana Carmen,Marc, Gabriel,Pirnau, Adrian,Stoica, Cristina Ioana,Lagoudis, Ioannis,Dragoumis, Theodoros,Oniga, Ovidiu

, (2017)

Sortase A inhibition is a well establish strategy for decreasing bacterial virulence by affecting numerous key processes that control biofilm formation, host cell entry, evasion and suppression of the immune response and acquisition of essential nutrients. A meta-analysis of structures known to act as Sortase A inhibitors provided the starting point for identifying a new potential scaffold. Based on this template a series of new potential Sortase A inhibitors, that contain the 2-phenylthiazole moiety, were synthesized. The physicochemical characterisation confirmed the identity of the proposed structures. Antibacterial activity evaluation showed that the new compounds have a reduced activity against bacterial cell viability. However, the compounds prevent biofilm formation at very low concentrations, especially in the case of E. faecalis. Molecular docking studies performed estimate that this is most likely due to the inhibition of Sortase A. The new compounds could be used as add-on therapies together with known antibacterial agents in order to combat multidrug-resistance enterococcal infections.

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