Temperini Claudia, Cecchi Alessandro, Boyle Nicholas A, Scozzafava Andrea, Cabeza Jaime Escribano, Wentworth Paul, Blackburn G Michael, Supuran Claudiu T
Università degli Studi di Firenze, Polo Scientifico, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy.
Bioorg Med Chem Lett. 2008 Feb 1;18(3):999-1005. doi: 10.1016/j.bmcl.2007.12.022. Epub 2007 Dec 15.
2-N,N-Dimethylamino-1,3,4-thiadiazole-5-methanesulfonamide was tested for its interaction with the 12 catalytically active mammalian carbonic anhydrase (CA, EC 4.2.1.1) isozymes, CA I-XIV. The compound is a potent inhibitor of CA IV, VII, IX, XII, and XIII (K(I)s of 0.61-39 nM), a medium potency inhibitor of CA II and VA (K(I)s of 121-438 nM), and a weak inhibitor against the other isoforms (CA III, VB, VI, and XIV), making it a very interesting candidate for situations in which a strong/selective inhibition of certain isozymes is needed. The crystal structure of the hCA II adduct of this sulfonamide revealed interesting interactions between the inhibitor and the enzyme which are quite different from those observed in the adducts of CA II with the structurally related aliphatic derivatives zonisamide, 2-amino-1,3,4-thiadiazolyl-5-difluoromethanesulfonamide, and 2-dimethylamino-5-[sulfonamido-(aminomethyl)]-1,3,4-thiadiazole reported earlier.
对2-N,N-二甲基氨基-1,3,4-噻二唑-5-甲磺酰胺与12种具有催化活性的哺乳动物碳酸酐酶(CA,EC 4.2.1.1)同工酶CA I - XIV的相互作用进行了测试。该化合物是CA IV、VII、IX、XII和XIII的强效抑制剂(抑制常数K(I)为0.61 - 39 nM),是CA II和VA的中效抑制剂(抑制常数K(I)为121 - 438 nM),对其他同工酶(CA III、VB、VI和XIV)是弱抑制剂,这使其成为在需要对某些同工酶进行强/选择性抑制的情况下非常有吸引力的候选物。这种磺酰胺的hCA II加合物的晶体结构揭示了抑制剂与酶之间有趣的相互作用,这些相互作用与之前报道的CA II与结构相关的脂肪族衍生物唑尼沙胺、2-氨基-1,3,4-噻二唑基-5-二氟甲磺酰胺以及2-二甲基氨基-5-[磺酰胺基-(氨基甲基)]-1,3,4-噻二唑的加合物中观察到的相互作用有很大不同。