Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 13 de 13
Filter
Add more filters










Publication year range
1.
J Med Chem ; 61(1): 360-371, 2018 01 11.
Article in English | MEDLINE | ID: mdl-29240409

ABSTRACT

Aldehyde oxidase (AOX) is a molibdo-flavoenzyme that has raised great interest in recent years, since its contribution in xenobiotic metabolism has not always been identified before clinical trials, with consequent negative effects on the fate of new potential drugs. The fundamental role of AOX in metabolizing xenobiotics is also due to the attempt of medicinal chemists to stabilize candidates toward cytochrome P450 activity, which increases the risk for new compounds to be susceptible to AOX nucleophile attack. Therefore, novel strategies to predict the potential liability of new entities toward the AOX enzyme are urgently needed to increase effectiveness, reduce costs, and prioritize experimental studies. In the present work, we present the most up-to-date computational method to predict liability toward human AOX (hAOX), for applications in drug design and pharmacokinetic optimization. The method was developed using a large data set of homogeneous experimental data, which is also disclosed as Supporting Information .


Subject(s)
Aldehyde Oxidase/metabolism , Models, Molecular , Aldehyde Oxidase/chemistry , Cytochrome P-450 Enzyme System/metabolism , Drug Design , Humans , Molecular Docking Simulation , Molecular Dynamics Simulation , Protein Conformation , Substrate Specificity
2.
Proc Natl Acad Sci U S A ; 114(16): E3178-E3187, 2017 04 18.
Article in English | MEDLINE | ID: mdl-28373537

ABSTRACT

Aldehyde oxidase (AOX) is a metabolic enzyme catalyzing the oxidation of aldehyde and aza-aromatic compounds and the hydrolysis of amides, moieties frequently shared by the majority of drugs. Despite its key role in human metabolism, to date only fragmentary information about the chemical features responsible for AOX susceptibility are reported and only "very local" structure-metabolism relationships based on a small number of similar compounds have been developed. This study reports a more comprehensive coverage of the chemical space of structures with a high risk of AOX phase I metabolism in humans. More than 270 compounds were studied to identify the site of metabolism and the metabolite(s). Both electronic [supported by density functional theory (DFT) calculations] and exposure effects were considered when rationalizing the structure-metabolism relationship.


Subject(s)
Aldehyde Oxidase/chemistry , Aldehyde Oxidase/metabolism , Amides/chemistry , Aza Compounds/chemistry , Databases, Pharmaceutical , Hydrocarbons, Aromatic/chemistry , Biocatalysis , Humans , Oxidation-Reduction , Protein Conformation , Substrate Specificity
3.
J Med Chem ; 60(1): 517-523, 2017 01 12.
Article in English | MEDLINE | ID: mdl-27977195

ABSTRACT

The NorA efflux pump is a potential drug target for reversal of resistance to selected antibacterial agents, and recently we described indole-based inhibitor candidates. Herein we report a second class of inhibitors derived from them but with significant differences in shape and size. In particular, compounds 13 and 14 are very potent inhibitors in that they demonstrated the lowest IC50 values (2 µM) ever observed among all indole-based compounds we have evaluated.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial/drug effects , Indoles/pharmacology , Drug Design , Indoles/chemistry , Microbial Sensitivity Tests , Staphylococcus aureus/drug effects
4.
J Med Chem ; 60(1): 180-201, 2017 01 12.
Article in English | MEDLINE | ID: mdl-28004573

ABSTRACT

Phenotypic screens, which focus on measuring and quantifying discrete cellular changes rather than affinity for individual recombinant proteins, have recently attracted renewed interest as an efficient strategy for drug discovery. In this article, we describe the discovery of a new chemical probe, bisamide (CCT251236), identified using an unbiased phenotypic screen to detect inhibitors of the HSF1 stress pathway. The chemical probe is orally bioavailable and displays efficacy in a human ovarian carcinoma xenograft model. By developing cell-based SAR and using chemical proteomics, we identified pirin as a high affinity molecular target, which was confirmed by SPR and crystallography.


Subject(s)
Amides/chemistry , Carrier Proteins/chemistry , DNA-Binding Proteins/chemistry , Nuclear Proteins/chemistry , Quinolines/chemistry , Transcription Factors/chemistry , Administration, Oral , Amides/administration & dosage , Amides/pharmacology , Biological Availability , Carbon-13 Magnetic Resonance Spectroscopy , Dioxygenases , Drug Discovery , Heat Shock Transcription Factors , Ligands , Proton Magnetic Resonance Spectroscopy , Quinolines/administration & dosage , Quinolines/pharmacology , Spectrometry, Mass, Electrospray Ionization
5.
Eur J Med Chem ; 121: 658-670, 2016 Oct 04.
Article in English | MEDLINE | ID: mdl-27318985

ABSTRACT

Bosentan, the first-in-class drug used in treatment of pulmonary arterial hypertension, is principally metabolized by the cytochromes P450, and it is responsible for cytochromes induction and drug-drug interaction events with moderate to severe consequences. A strategy to reduce drug-drug interactions consists of increasing the metabolic stability of the perpetrator, and fluorinated analogues are often designed to block the major sites of metabolism. In this paper bosentan analogues were synthesized, and their metabolism and biological activity were evaluated. All synthesized compounds showed an improved metabolic stability towards CYP2C9, with one maintaining a moderate antagonist effect towards the ETA receptor.


Subject(s)
Endothelin Receptor Antagonists/metabolism , Endothelin Receptor Antagonists/pharmacology , Sulfonamides/metabolism , Sulfonamides/pharmacology , Animals , Bosentan , CHO Cells , Cell Line, Tumor , Cell Survival/drug effects , Cricetinae , Cricetulus , Cytochrome P-450 CYP2C9/chemistry , Cytochrome P-450 CYP2C9/metabolism , Endothelin Receptor Antagonists/chemistry , Models, Molecular , Protein Conformation , Receptors, Endothelin/agonists , Receptors, Endothelin/metabolism , Sulfonamides/chemistry
6.
J Med Chem ; 59(3): 867-91, 2016 Feb 11.
Article in English | MEDLINE | ID: mdl-26757340

ABSTRACT

Antibiotic resistance represents a worldwide concern, especially regarding the outbreak of methicillin-resistant Staphylococcus aureus, a common cause for serious skin and soft tissues infections. A major contributor to Staphylococcus aureus antibiotic resistance is the NorA efflux pump, which is able to extrude selected antibacterial drugs and biocides from the membrane, lowering their effective concentrations. Thus, the inhibition of NorA represents a promising and challenging strategy that would allow recycling of substrate antimicrobial agents. Among NorA inhibitors, the indole scaffold proved particularly effective and suitable for further optimization. In this study, some unexplored modifications on the indole scaffold are proposed. In particular, for the first time, substitutions at the C5 and N1 positions have been designed to give 48 compounds, which were synthesized and tested against norA-overexpressing S. aureus. Among them, 4 compounds have NorA IC50 values lower than 5.0 µM proving to be good efflux pump inhibitor (EPI) candidates. In addition, preliminary data on their ADME (absorption, distribution, metabolism, and excretion) profile is reported.


Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bacterial Proteins/antagonists & inhibitors , Drug Resistance, Microbial/drug effects , Indoles/chemistry , Indoles/pharmacology , Methicillin-Resistant Staphylococcus aureus/drug effects , Multidrug Resistance-Associated Proteins/antagonists & inhibitors , Dose-Response Relationship, Drug , Molecular Structure , Structure-Activity Relationship
7.
Eur J Med Chem ; 102: 403-12, 2015 Sep 18.
Article in English | MEDLINE | ID: mdl-26301557

ABSTRACT

Bisphosphonates are the most important class of antiresorptive agents used against osteoclast-mediated bone loss, and, more recently, in oncology. These compounds have high affinity for calcium ions (Ca(2+)) and therefore target bone mineral, where they appear to be internalized selectively by bone-resorbing osteoclasts and inhibit osteoclast function. They are extensively used in healthcare, however they are affected by severe side effects; pharmacological properties of bisphosphonates depend on their molecular structure, which is frequently the cause of poor intestinal adsorption and low distribution. In this work we synthesized six novel bisphosphonate compounds having a variably substituted indole moiety to evaluate their extra- and intracellular calcium chelating ability in PE/CA-PJ15 cells. Preliminary in silico and in vitro ADME studies were also performed and the results suggested that the indole moiety plays an important role in cell permeability and metabolism properties.


Subject(s)
Chelating Agents/chemical synthesis , Chelating Agents/pharmacology , Diphosphonates/chemical synthesis , Diphosphonates/pharmacology , Indoles/chemistry , Apoptosis/drug effects , Calcium/metabolism , Cell Line, Tumor , Cell Survival/drug effects , Chelating Agents/chemistry , Diphosphonates/chemistry , Dose-Response Relationship, Drug , Humans , Molecular Structure , Structure-Activity Relationship
8.
Org Lett ; 17(11): 2740-3, 2015 Jun 05.
Article in English | MEDLINE | ID: mdl-25974178

ABSTRACT

Long-range bonding interactions were evaluated using variable-temperature NMR spectroscopy and suitable 2'-CH2X-substituted phenylpyridines (X = Me, NMe2, OMe, F). It was found that the arylpyridyl rotational barriers were lower when electronegative atoms were bound to the α carbon of the 2' moiety. This effect was ascribed to a stabilizing interaction in the transition state due to the lone pair of the heterocyclic nitrogen with the α carbon. Computational support for this hypothesis came from CCSD(T)/6-31+G(d) calculations. Steric effects of the X moiety were ruled out by comparison of the rotational barriers of analogous biphenyls.

9.
J Phys Chem A ; 118(24): 4339-50, 2014 Jun 19.
Article in English | MEDLINE | ID: mdl-24840313

ABSTRACT

The role played by the C*-H based modes (C* being the chiral carbon atom) and the large amplitude motions in the vibrational absorption (VA) and vibrational circular dichroism (VCD) spectra is investigated. The example of an adduct of dimethyl fumarate and anthracene, i.e., dimethyl-(+)-(11R,12R)-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylate, and two deuterated isotopomers thereof specially synthesized for this goal, are considered. By comparing the experimental and DFT calculated spectra of the undeuterated and deuterated species, we demonstrate that the C*-H bending, rocking, and stretching modes in the VA and VCD spectra are clearly identified in well defined spectroscopic features. Further, significant information about the conformer distribution is gathered by analyzing the VA and VCD data of both the fingerprint and the C-H stretching regions, with particular attention paid to the band shape data. Effects related to the large amplitude motions of the two methoxy moieties have been simulated by performing linear transit (LT) calculations, which consists of varying systematically the relative positions of the two methoxy moieties and calculating VCD spectra for the partially optimized structures obtained in this way. The LT method allows one to improve the quality of calculated spectra, as compared to experimental results, especially in regard to relative intensities and bandwidths.


Subject(s)
Anthracenes/chemistry , Deuterium/chemistry , Fumarates/chemistry , Water/chemistry , Circular Dichroism , Dimethyl Fumarate , Motion , Quantum Theory , Stereoisomerism , Thermodynamics , Vibration
10.
J Med Chem ; 57(10): 4337-50, 2014 May 22.
Article in English | MEDLINE | ID: mdl-24785979

ABSTRACT

Influenza virus infections represent a serious concern to public health, being characterized by high morbidity and significant mortality. To date, compounds targeting the viral ion-channel M2 or the viral neuraminidase are the drugs available for treatment of influenza, but the emergence of drug-resistant viral mutants renders the search for novel targets and their possible inhibitors a major priority. Recently, we demonstrated that the viral RNA-dependent RNA polymerase (RdRP) complex can be an optimal target of protein-protein disruption by small molecules, with thiophene-3-carboxamide derivatives emerging as promising candidates for the development of new anti-influenza drugs with broad-spectrum activity. Here, we report a further dissection of the thiophene-3-carboxamide structure. By using a GRID molecular interaction field (MIF)-based scaffold-hopping approach, more potent and nontoxic polyamido derivatives were identified, highlighting a new space in the chemical variability of RdRP inhibitors. Finally, a possible pharmacophoric model highlighting the key features required for RdRP inhibition is proposed.


Subject(s)
Antiviral Agents/chemical synthesis , Orthomyxoviridae/drug effects , RNA-Dependent RNA Polymerase/antagonists & inhibitors , Thiophenes/chemical synthesis , Animals , Antiviral Agents/pharmacology , Dogs , Drug Design , HEK293 Cells , Humans , Madin Darby Canine Kidney Cells , Orthomyxoviridae/enzymology , Structure-Activity Relationship , Thiophenes/pharmacology
11.
Dalton Trans ; 43(4): 1636-50, 2014 Jan 28.
Article in English | MEDLINE | ID: mdl-24217639

ABSTRACT

Novel, optically pure 2-{4-methyl[2]paracyclo[2](5,8)quinolinophan-2-yl}-4-aryl/alkyloxazolines (QUIPHANOX) exhibiting both planar and central chirality have been prepared by reacting (Rp)- and (Sp)-2-cyano-4-methyl[2]paracyclo[2](5,8)quinolinophane with 2-aryl/alkyl-2-aminoethanols. The reaction of each of the above N,N-ligands with [Ru(η(6)-p-cymene)Cl2]2 in methanol, in the presence of either NH4PF6 or NaBPh4, gave the corresponding half-sandwich [(η(6)-p-cymene)Ru(QUIPHANOX)Cl](+)Y(-), (Y(-) = PF6(-), BPh4(-)) as stable complex salts exhibiting planar and carbon- and metal-centered chirality. The unknown absolute configuration (AC) at the metal was determined by (1)H NMR and by theoretical calculations of electronic circular dichroism (ECD) spectra and subsequently confirmed by crystallographic X-ray analysis. (Rp) and (Sp)-ligands afforded (RRu)- and (SRu)-configured complexes, respectively, independent of the AC at the chiral carbon of the oxazoline moiety.

12.
Org Biomol Chem ; 10(9): 1847-55, 2012 Mar 07.
Article in English | MEDLINE | ID: mdl-22268064

ABSTRACT

The free energies of activation for the aryl-aryl rotation of 17 biphenyl derivatives, bearing a heavy heteroatom (S, Se, Te, P, Si, Sn) as ortho substituent, have been measured by variable temperature NMR. These numbers, so called B values, represent a meaningful measure of the steric hindrance exerted by the selected substituents. DFT computations match quite satisfactorily the experimental barriers and the ground state geometries as well (determined, in two cases, by X-ray diffraction). The present values extend the available list of B values and thus provide an enlarged basis for the compilation of the space requirements of standard substituents, based solely on experimental determinations.

SELECTION OF CITATIONS
SEARCH DETAIL
...