ABSTRACT
FFA2, also called GPR43, is a G-protein coupled receptor for short chain fatty acids which is involved in the mediation of inflammatory responses. A class of azetidines was developed as potent FFA2 antagonists. Multiparametric optimization of early hits with moderate potency and suboptimal ADME properties led to the identification of several compounds with nanomolar potency on the receptor combined with excellent pharmacokinetic (PK) parameters. The most advanced compound, 4-[[(R)-1-(benzo[b]thiophene-3-carbonyl)-2-methyl-azetidine-2-carbonyl]-(3-chloro-benzyl)-amino]-butyric acid 99 (GLPG0974), is able to inhibit acetate-induced neutrophil migration strongly in vitro and demonstrated ability to inhibit a neutrophil-based pharmacodynamic (PD) marker, CD11b activation-specific epitope [AE], in a human whole blood assay. All together, these data supported the progression of 99 toward next phases, becoming the first FFA2 antagonist to reach the clinic.
Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/metabolism , Azetidines/metabolism , Butyrates/chemical synthesis , Receptors, Cell Surface/antagonists & inhibitors , Thiophenes/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Anti-Inflammatory Agents, Non-Steroidal/pharmacokinetics , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Azetidines/chemical synthesis , Azetidines/pharmacokinetics , Azetidines/pharmacology , Butyrates/pharmacokinetics , Butyrates/pharmacology , Humans , Immune System Diseases , Inhibitory Concentration 50 , Leukocyte Disorders , Mice , Microsomes, Liver/metabolism , Rats, Sprague-Dawley , Structure-Activity Relationship , Thiophenes/pharmacokinetics , Thiophenes/pharmacologyABSTRACT
Two rigid analogues of 5-ethylindolobenzazepinone 4, a potent cytotoxic agent and inhibitor of tubulin polymerization, were prepared. The first was the indane derivative 5, in which the ethyl group is attached to the benzo moiety. The second was the pyrrolidine analogue 6, in which the ethyl chain was bound to the lactam nitrogen. While both compounds were considerably less active inhibitors of KB cell growth as compared to 4, inhibition of tubulin polymerization was only moderately reduced. Tubulin docking studies indicated that the aR and aS atropoisomers of 5 and 6 occupy different binding pockets at the colchicine binding site. Conversely, both aS-5 and aS-6 occupy the same binding pocket as aSS-4 but do not benefit from the favorable hydrophobic interactions provided by the C5 alkyl group of 4, thus possibly explaining their lower activities.
Subject(s)
Indoles/chemistry , Catalysis , Imines/chemistry , Indole Alkaloids/chemistry , Isomerism , Oxidation-Reduction , Rhodium/chemistry , StereoisomerismABSTRACT
A direct ruthenium-catalyzed radical chloroalkylation of N-acyl oxazolidinones capitalizing on valence tautomerism of titanium enolates has been developed. The chloroalkylation method served as the centerpiece in the enantioselective total synthesis of trichloroleucine-derived marine natural product neodysidenin.
Subject(s)
Anions/chemical synthesis , Dipeptides/chemical synthesis , Thiazoles/chemical synthesis , Titanium/chemistry , Catalysis , Models, Molecular , Molecular Structure , StereoisomerismABSTRACT
This microreview provides a compilation of synthetic approaches and total syntheses of pinnatoxin A in a survey of the literature up to early 2010. Pinnatoxin A is the first discovered and representative member of a fascinating group of potent marine toxins that share a spiroimine subunit as a unifying structural element.
ABSTRACT
A series of 5-alkylindolobenzazepin-7-ones was synthesized by Suzuki coupling between 3-iodoindole-2-carboxylates and the appropriate alpha-alkylbenzylamino o-boronic acids followed by cyclization to the lactam. Derivatives having a linear alkyl chain at C5 were found to be highly cytotoxic to KB cells with IC50 values in the 30-80 nM range. These compounds also inhibited the polymerization of tubulin with IC50's of 1-2 microM. Compound 4f (( S)-5-ethyl) showed comparable antiproliferative activities (IC50's of 30-70 nM) in a variety of cancer cell lines, cell growth being arrested at the G2/M phase. Compound 4f induced apoptosis in a dose-dependent manner in three different cancer cell lines and was shown to affect cell morphology in a manner consistent with its inhibitory action on tubulin polymerization. Using the experimental model of glioma grafted on the chick chorio-allantoic membrane, local treatment with compound 4f markedly reduced tumor progression.
Subject(s)
Benzazepines/chemical synthesis , Indoles/chemical synthesis , Tubulin Modulators/chemical synthesis , Animals , Apoptosis/drug effects , Benzazepines/chemistry , Benzazepines/pharmacology , Biopolymers , Cell Cycle/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Chick Embryo , Drug Screening Assays, Antitumor , Humans , Indoles/chemistry , Indoles/pharmacology , Neoplasm Transplantation , Stereoisomerism , Structure-Activity Relationship , Transplantation, Heterologous , Tubulin/chemistry , Tubulin Modulators/chemistry , Tubulin Modulators/pharmacologyABSTRACT
An evaluation of two software tools dedicated to an automatic analysis of the CT scanner image spatial resolution is presented in this paper. The methods evaluated consist of calculating the Modulation Transfer Function (MTF) of the CT scanners; the first uses an image of an impulse source, while the second method proposed by Droege and Morin uses an image of cyclic bar patterns. Two Digital Test Objects (DTO) are created to this purpose. These DTOs are then blurred by doing a convolution with a two-dimensional Gaussian Point Spread Function (PSF(Ref)), which has a well known Full Width at Half Maximum (FWHM). The evaluation process consists then of comparing the Fourier transform of the PSF on the one hand, and the two mentioned methods on the other hand.
