Activation of human α-carbonic anhydrase isoforms I, II, IV and VII with bis-histamine schiff bases and bis-spinaceamine substituted derivatives
A series of histamine bis-Schiff bases and bis-spinaceamine derivatives were synthesised and investigated as activators of four human (h) carbonic anhydrase (CA, EC 4.2.1.1) isoforms, the cytosolic hCA I, II and VII, and the membrane-associated hCA IV. All isoforms were effectively activated by the...
Main Authors: | Suleyman Akocak, Nabih Lolak, Silvia Bua, Alessio Nocentini, Claudiu T. Supuran |
---|---|
Format: | Article |
Language: | English |
Published: |
Taylor & Francis Group
2019-01-01
|
Series: | Journal of Enzyme Inhibition and Medicinal Chemistry |
Subjects: | |
Online Access: | http://dx.doi.org/10.1080/14756366.2019.1630616 |
Similar Items
-
Synthesis and biological evaluation of histamine Schiff bases as carbonic anhydrase I, II, IV, VII, and IX activators
by: Suleyman Akocak, et al.
Published: (2017-01-01) -
Discovery of novel 1,3-diaryltriazene sulfonamides as carbonic anhydrase I, II, VII, and IX inhibitors
by: Suleyman Akocak, et al.
Published: (2018-01-01) -
Activation of α-, β-, γ- δ-, ζ- and η- class of carbonic anhydrases with amines and amino acids: a review
by: Suleyman Akocak, et al.
Published: (2019-01-01) -
Antioxidant, acetylcholinesterase and butyrylcholinesterase inhibition profiles of histamine Schiff bases
by: Süleyman Akocak, et al.
Published: (2019-06-01) -
Activation of carbonic anhydrase isoforms involved in modulation of emotional memory and cognitive disorders with histamine agonists, antagonists and derivatives
by: Gustavo Provensi, et al.
Published: (2021-01-01)