6637-30-5

Usage

Chemical Structure

A complex structure consisting of a pyrazole, benzoxazine, and ethanone moiety.

Substituents

Contains a chloro-substituted phenyl group.

Biological Activity

Potent inhibitor of a variety of biological processes.

Pharmaceutical Applications

Potential candidate for pharmaceutical applications due to its biological activity.

Research Interest

Of interest to researchers in the fields of medicinal chemistry and drug development.

Further Study

Its chemical properties and potential biological activities make it a subject of interest for further study and investigation.

Upstream product

• 51908-29-3 4-isothiocyanatobenzene sulfonamide 
• 150-13-0 4-amino-benzoic acid 
• 2131-62-6 4-isothiocyanatobenzoic acid 
• 63-74-1 sulfanilamide 

Relevant academic research and scientific papers

Carbonic anhydrase inhibitors: Water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects

A series of sulfonamides has been obtained by reaction of 4-isothiocyanatobenzenesulfonamide with amines, amino acids, and oligopeptides. The new thiourea derivatives showed strong affinities toward isozymes I, II, and IV of carbonic anhydrase (CA, EC 4.2.1.1). In vitro inhibitory power was good (in the low-nanomolar range) for the derivatives of β-phenylserine and α-proportionalto-phenylglycine, for those incorporating hydroxy and mercapto amino acids (Ser, Thr, Cys, Met), hydrophobic amino acids (Val, Leu, Ile), aromatic amino acids (Phe, His, Trp, Tyr, DOPA), and dicarboxylic amino acids as well as di/tri/tetrapeptides among others. Such CA inhibitors displayed very good water solubility (in the range of 2-3%) mainly as sodium (carboxylate) salts, with pH values of the obtained solutions being 6.5-7.0. Some of these preparations (such as the derivatives of Ser, β-Ph-Ser, Leu, Asn, etc.) strongly lowered intraocular pressure (IOP) when applied topically, directly into the normotensive/glaucomatous rabbit eye, as 2% water solutions. It is interesting to note that not all the powerful CA inhibitors designed in the present study showed topical IOP-lowering effects (such as, for instance, the Cys and Lys derivatives, devoid of such properties) whereas the Pro, Arg, and oligopeptidyl thiourea derivatives showed reduced efficacy when administered topically. This may be due to the very hydrophilic nature of some of these compounds, whereas inhibitors with balanced hydro- and liposolubility also showed optimal in vivo effects. The interesting pharmacological properties of this new type of CA inhibitors, correlated with the neutral pH of their solutions used in ophthalmologic applications, make them attractive candidates for developing novel antiglaucoma drugs devoid of major ocular side effects.