Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II ‘selective’ inhibitor celecoxib

2006 ◽  
Vol 16 (2) ◽  
pp. 437-442 ◽  
Author(s):  
Anna Di Fiore ◽  
Carlo Pedone ◽  
Katia D’Ambrosio ◽  
Andrea Scozzafava ◽  
Giuseppina De Simone ◽  
...  
2015 ◽  
Vol 51 (2) ◽  
pp. 302-305 ◽  
Author(s):  
Katia D'Ambrosio ◽  
Simone Carradori ◽  
Simona M. Monti ◽  
Martina Buonanno ◽  
Daniela Secci ◽  
...  

2-Benzylsulfinylbenzoic acid binds to human carbonic anhydrase II in a mode completely different from any other class of carbonic anhydrase inhibitors investigated so far.


2020 ◽  
Vol 56 (59) ◽  
pp. 8297-8300
Author(s):  
Murat Bozdag ◽  
Claudiu T. Supuran ◽  
Davide Esposito ◽  
Andrea Angeli ◽  
Fabrizio Carta ◽  
...  

2-Mercaptobenzoxazole represents an interesting lead compound alternative to the classical sulfonamides for the development of selective carbonic anhydrase inhibitors.


2015 ◽  
Vol 58 (3) ◽  
pp. 1494-1501 ◽  
Author(s):  
Rajendra P. Tanpure ◽  
Bin Ren ◽  
Thomas S. Peat ◽  
Laurent F. Bornaghi ◽  
Daniela Vullo ◽  
...  

2020 ◽  
Vol 56 (85) ◽  
pp. 13033-13036 ◽  
Author(s):  
Katia D'Ambrosio ◽  
Simone Carradori ◽  
Stefania Cesa ◽  
Andrea Angeli ◽  
Simona M. Monti ◽  
...  

Catechols adopt a peculiar binding mode to the CA active site which involves both the zinc bound water molecule and the “deep water”.


1983 ◽  
Vol 79 ◽  
pp. 151-152 ◽  
Author(s):  
E. Grell ◽  
B.S. Prabhananda ◽  
E. Rittger ◽  
H.H. Grünhagen

Molecules ◽  
2018 ◽  
Vol 23 (5) ◽  
pp. 1045 ◽  
Author(s):  
Srishti Singh ◽  
Carrie Lomelino ◽  
Mam Mboge ◽  
Susan Frost ◽  
Robert McKenna

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