Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine

Aksu, K; Nar, M; Tanc, M; Vullo, D; Gulcin, I; Goksu, S; Tumer, F; Supuran, CT

HERO ID

2280249

Reference Type

Journal Article

Year

2013

Language

English

PMID

23623256

HERO ID 2280249
In Press No
Year 2013
Title Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine
Authors Aksu, K; Nar, M; Tanc, M; Vullo, D; Gulcin, I; Goksu, S; Tumer, F; Supuran, CT
Journal Bioorganic & Medicinal Chemistry
Volume 21
Issue 11
Page Numbers 2925-2931
Abstract A series of novel sulfamides incorporating the dopamine scaffold were synthesized. Reaction of amines and tert-butyl-alcohol/benzyl alcohol in the presence of chlorosulfonyl isocyanate (CSI) afforded sulfamoyl carbamates, which were converted to the title compounds by treatment with trifluoroacetic acid or by palladium-catalyzed hydrogenolysis. Inhibition of six α-carbonic anhydrases (CAs, EC 4.2.1.1), that is, CA I, CA II, CA VA, CA IX, CA XII and CA XIV, and two β-CAs from Candida glabrata (CgCA) and Mycobacterium tuberculosis (Rv3588) with these sulfamides was investigated. All CA isozymes were inhibited in the low micromolar to nanomolar range by the dopamine sulfamide analogues. K(i)s were in the range of 0.061-1.822 μM for CA I, 1.47-2.94 nM for CA II, 2.25-3.34 μM for CA VA, 0.041-0.37 μM for CA IX, 0.021-1.52 μM for CA XII, 0.007-0.219 μM for CA XIV, 0.35-5.31 μM for CgCA and 0.465-4.29 μM for Rv3588. The synthesized sulfamides may lead to inhibitors targeting medicinally relevant CA isoforms with potential applications as antiepileptic, antiobesity antitumor agents or anti-infective.
Doi 10.1016/j.bmc.2013.03.077
Pmid 23623256
Wosid WOS:000319002600013
Is Certified Translation No
Dupe Override No
Comments Scopus URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84877801455&doi=10.1016%2fj.bmc.2013.03.077&partnerID=40&md5=ba92b4223a34df73181c07896d0ac5b6
Is Public Yes
Language Text English
Keyword Dopamine; Sulfamoyl carbamates; Sulfamide; Carbonic anhydrase; Enzyme inhibition