No abstract

This review describes recent progress in the design and development of inhibitors of human carbonic anhydrase IX (CA IX) based on space‐filling carborane and cobalt bis(dicarbollide) clusters. CA IX enzyme is known to play a crucial role in cancer cell proliferation and metastases. The new class of potent and selective CA IX inhibitors combines the structural motif of a bulky inorganic cluster with an alkylsulfamido or alkylsulfonamido anchor group for Zn2+ ion in the enzyme active site. Detailed structure‐activity relationship (SAR) studies of a large series containing 50 compounds uncovered structural features of the cluster‐containing inhibitors that are important for efficient and selective inhibition of CA IX activity. Preclinical evaluation of selected compounds revealed low toxicity, favorable pharmacokinetics and ability to reduce tumor growth. Cluster‐containing inhibitors of CA IX can thus be considered as promising candidates for drug development and/or for combination therapy in boron neutron capture therapy (BNCT).

Carbonic anhydrase IX (CAIX) is an enzyme expressed on the surface of cells in hypoxic tumors. It plays a role in regulation of tumor pH and promotes thus tumor cell survival and occurrence of metastases. Here, derivatives of the cobalt bis (dicarbollide)(1-) anion are reported that are based on substitution at the carbon sites of the polyhedra by two alkylsulfonamide groups differing in the length of the aliphatic connector (from C1 to C4, n = 1-4), which were prepared by cobalt insertion into the 7-sulfonamidoalkyl-7,8-dicarba-nidoundecaborate ions. Pure meso-and rac-diastereoisomeric forms were isolated. The series is complemented with monosubstituted species (n = 2). Synthesis by a direct method furnished similar derivatives (n = 2, 3), which are chlorinated at the B(8,8') boron sites. All compounds inhibited CAIX with subnanomolar inhibition constants and showed high selectivity for CAIX. The best inhibitory properties were observed for the compound with n = 3 and two substituents present in rac-arrangement with K i = 20 pM and a selectivity index of 668. X-ray crystallography was used to study interactions of these compounds with the active site of CAIX on the structural level.

The most significant result of this study is design and synthesis of boron-cluster-containing compounds that inhibit activity of the cancer-associated enzyme CA IX with picomolar inhibition constants. Moreover,X-ray crystallography,w as used to help understand their interactions at the active site of the enzyme on an atomic level.

Human carbonic anhydrase IX (CA IX), a protein specifically expressed on the surface of solid tumour cells, represents a validated target both for anticancer therapy and diagnostics. We recently identified sulfonamide dicarbaboranes as promising inhibitors of CA IX with favourable activities both in vitro and in vivo. To explain their selectivity and potency, we performed detailed X-ray structural analysis of their interactions within the active sites of CA IX and CA II. Series of compounds bearing various aliphatic linkers between the dicarbaborane cluster and sulfonamide group were examined. Preferential binding towards the hydrophobic part of the active site cavity was observed. Selectivity towards CA IX lies in the shape complementarity of the dicarbaborane cluster with a specific CA IX hydrophobic patch containing V131 residue. The bulky side chain of F131 residue in CA II alters the shape of the catalytic cavity, disrupting favourable interactions of the spherical dicarbaborane cluster.

Carbonic anhydrase IX (CA IX), at umor-associated metalloenzyme, represents avalidated target for cancertherapy and diagnostics. Herein, we report the inhibition properties of isomeric families of sulfonamidopropyl-dicarba-closododecaboranes group(s) prepared using an ew direct fivestep synthesis from the correspondingp arent cages. The protocol offers ar eliable solutionf or synthesis of singly and doubly substituted dicarba-closo-dodecaboranes with ad ifferent geometric positiono fc arbon atoms. The closo-compounds from the ortho-and meta-series were then degraded to corresponding 11-vertex dicarba-nido-undecaborate(1À) anions. All compounds show in vitro enzymatic activity against CA IX in the low nanomolar or subnanomolar range. This is accompanied by clear isomer dependence of the inhibition constant(K i)a nd selectivity towardsC AI X. Decreasing trends in K i ands electivity index (S I)v alues are observed with increasing separation of the cage carbon atoms. Interactions of compounds with the active sites of CA IX were explored with X-ray crystallography,a nd eight high-resolution crystal structures uncovered the structuralb asis of inhibition potencya nd selectivity.

We report the difunctional modification of anionic cobalta bis(dicarbollide)(1-) cluster with a B(8,8)-oxygen bridging unit that provides structural rigidity and an organic alkylazide substituent(s) on the carbon atoms of the...

A new method for previously inaccessible coupling of halogenated polyhedral ions with organic molecules is presented along with studies on the supramolecular complexation with cyclodextrin.