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1.
Biomed Pharmacother ; 149: 112808, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35290889

RESUMEN

Krabbe disease is a rare, inherited neurodegenerative disease due to impaired lysosomal ß-galactosylceramidase (GALC) activity and formation of neurotoxic ß-galactosylsphingosine ('psychosine'). We investigated substrate reduction therapy with a novel brain-penetrant inhibitor of galactosylceramide biosynthesis, RA 5557, in twitcher mice that lack GALC activity and model Krabbe disease. This thienopyridine derivative selectively inhibits uridine diphosphate-galactose glycosyltransferase 8 (UGT8), the final step in the generation of galactosylceramides which are precursors of sulphatide and, in the pathological lysosome, the immediate source of psychosine. Administration of RA 5557, reduced pathologically elevated psychosine concentrations (72-86%) in the midbrain and cerebral cortex in twitcher mice: the inhibitor decreased galactosylceramides by about 70% in midbrain and cerebral cortex in mutant and wild type animals. Exposure to the inhibitor significantly decreased several characteristic inflammatory response markers without causing apparent toxicity to myelin-producing cells in wild type and mutant mice; transcript abundance of oligodendrocyte markers MBP (myelin basic protein) and murine UGT8 was unchanged. Administration of the inhibitor before conception and during several breeding cycles to mice did not impair fertility and gave rise to healthy offspring. Nevertheless, given the unchanged lifespan, it appears that GALC has critical functions in the nervous system beyond the hydrolysis of galactosylceramide and galactosylsphingosine. Our findings support further therapeutic exploration of orally active UGT8 inhibitors in Krabbe disease and related galactosphingolipid disorders. The potent thienopyridine derivative with effective target engagement here studied appears to have an acceptable safety profile in vivo; judicious dose optimization will be needed to ensure efficacious clinical translation.


Asunto(s)
Leucodistrofia de Células Globoides , Enfermedades Neurodegenerativas , Animales , Encéfalo/metabolismo , Modelos Animales de Enfermedad , Galactosilceramidas/metabolismo , Galactosilceramidas/farmacología , Leucodistrofia de Células Globoides/tratamiento farmacológico , Leucodistrofia de Células Globoides/metabolismo , Leucodistrofia de Células Globoides/patología , Ratones , Enfermedades Neurodegenerativas/patología , Psicosina/metabolismo , Tienopiridinas
2.
ACS Med Chem Lett ; 11(10): 2010-2016, 2020 Oct 08.
Artículo en Inglés | MEDLINE | ID: mdl-33062186

RESUMEN

Metachromatic leukodystrophy (MLD) is a rare, genetic lysosomal storage disorder caused by the deficiency of arylsulfatase A enzyme, which results in the accumulation of sulfatide in the lysosomes of the tissues of central and peripheral nervous systems, leading to progressive demyelination and neurodegeneration. Currently there is no cure for this disease, and the only approved therapy, hematopoietic stem cell transplant, has limitations. We proposed substrate reduction therapy (SRT) as a novel approach to treat this disease, by inhibiting ceramide galactosyltransferase enzyme (UGT8). This resulted in the identification of a thienopyridine scaffold as a starting point to initiate medicinal chemistry. Further optimization of hit compound 1 resulted in the identification of brain penetrable, orally bioavailable compound 19, which showed efficacy in the in vivo pharmacodynamic models, indicating the potential to treat MLD with UGT8 inhibitors.

3.
J Med Chem ; 55(6): 2641-8, 2012 Mar 22.
Artículo en Inglés | MEDLINE | ID: mdl-22339127

RESUMEN

We have studied the subtleties of fragment docking and binding using data generated in a Pim-1 kinase inhibitor program. Crystallographic and docking data analyses have been undertaken using inhibitor complexes derived from an in-house surface plasmon resonance (SPR) fragment screen, a virtual needle screen, and a de novo designed fragment inhibitor hybrid. These investigations highlight that fragments that do not fill their binding pocket can exhibit promiscuous hydrophobic interactions due to the lack of steric constraints imposed on them by the boundaries of said pocket. As a result, docking modes that disagree with an observed crystal structure but maintain key crystallographically observed hydrogen bonds still have potential value in ligand design and optimization. This observation runs counter to the lore in fragment-based drug design that all fragment elaboration must be based on the parent crystal structure alone.


Asunto(s)
Inhibidores Enzimáticos/química , Modelos Moleculares , Proteínas Proto-Oncogénicas c-pim-1/antagonistas & inhibidores , Proteínas Proto-Oncogénicas c-pim-1/química , Cristalografía por Rayos X , Diseño de Fármacos , Interacciones Hidrofóbicas e Hidrofílicas , Estructura Molecular , Unión Proteica , Estereoisomerismo , Relación Estructura-Actividad
4.
Bioorg Med Chem Lett ; 21(10): 3050-6, 2011 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-21507633

RESUMEN

Novel benzofuran-2-carboxylic acids, exemplified by 29, 38 and 39, have been discovered as potent Pim-1 inhibitors using fragment based screening followed by X-ray structure guided medicinal chemistry optimization. The compounds demonstrate potent inhibition against Pim-1 and Pim-2 in enzyme assays. Compound 29 has been tested in the Ambit 442 kinase panel and demonstrates good selectivity for the Pim kinase family. X-ray structures of the inhibitor/Pim-1 binding complex reveal important salt-bridge and hydrogen bond interactions mediated by the compound's carboxylic acid and amino groups.


Asunto(s)
Benzofuranos/química , Ácidos Carboxílicos/farmacología , Activación Enzimática/efectos de los fármacos , Inhibidores Enzimáticos/farmacología , Proteínas Proto-Oncogénicas c-pim-1/antagonistas & inhibidores , Animales , Ácidos Carboxílicos/síntesis química , Ácidos Carboxílicos/química , Cristalografía por Rayos X , Inhibidores Enzimáticos/síntesis química , Inhibidores Enzimáticos/química , Humanos , Concentración 50 Inhibidora , Microsomas Hepáticos/efectos de los fármacos , Microsomas Hepáticos/enzimología , Modelos Moleculares , Estructura Molecular , Ratas
7.
Bioorg Med Chem Lett ; 19(11): 2916-9, 2009 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-19419862

RESUMEN

Modification of the structure of trypanosomal AdoMetDC inhibitor 1 (MDL73811) resulted in the identification of a new inhibitor 7a, which features a methyl substituent at the 8-position. Compound 7a exhibits improved potencies against both the trypanosomal AdoMetDC enzyme and parasites, and better blood brain barrier penetration than 1.


Asunto(s)
Adenosina/análogos & derivados , Adenosina/síntesis química , Adenosilmetionina Descarboxilasa/antagonistas & inhibidores , Tripanocidas/síntesis química , Tripanosomiasis Africana/tratamiento farmacológico , Adenosina/química , Adenosina/farmacología , Adenosilmetionina Descarboxilasa/metabolismo , Animales , Barrera Hematoencefálica , Descubrimiento de Drogas , Humanos , Ratones , Tripanocidas/química , Tripanocidas/farmacocinética , Trypanosoma brucei brucei/enzimología
8.
Antimicrob Agents Chemother ; 53(8): 3269-72, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19451291

RESUMEN

Genzyme 644131, 8-methyl-5'-{[(Z)-4-aminobut-2-enyl](methylamino)}adenosine, is an analog of the enzyme activated S-adenosylmethionine decarboxylase (AdoMetDC) inhibitor and the trypanocidal agent MDL-7381, 5-{[(Z)-4-aminobut-2-enyl](methylamino)}adenosine. The analog differs from the parent in having an 8-methyl group on the purine ring that bestows favorable pharmacokinetic, biochemical, and trypanocidal activities. The compound was curative in acute Trypanosoma brucei brucei and drug-resistant Trypanosoma brucei rhodesiense model infections, with single-dose activity in the 1- to 5-mg/kg/day daily dose range for 4 days against T. brucei brucei and 25- to 50-mg/kg twice-daily dosing against T. brucei rhodesiense infections. The compound was not curative in the TREU 667 central nervous system model infection but cleared blood parasitemia and extended time to recrudescence in several groups. This study shows that AdoMetDC remains an attractive chemotherapeutic target in African trypanosomes and that chemical changes in AdoMetDC inhibitors can produce more favorable drug characteristics than the lead compound.


Asunto(s)
Adenosina/análogos & derivados , Adenosilmetionina Descarboxilasa/antagonistas & inhibidores , Tripanocidas/farmacología , Trypanosoma brucei brucei/efectos de los fármacos , Trypanosoma brucei rhodesiense/efectos de los fármacos , Adenosina/farmacología , Animales , Perros , Distribución Aleatoria , Ratas , Tripanocidas/síntesis química , Tripanocidas/química , Tripanocidas/uso terapéutico , Trypanosoma brucei brucei/patogenicidad , Trypanosoma brucei rhodesiense/patogenicidad , Tripanosomiasis Africana/tratamiento farmacológico , Tripanosomiasis Africana/microbiología
9.
Antimicrob Agents Chemother ; 53(5): 2052-8, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19289530

RESUMEN

Trypanosomiasis remains a significant disease across the sub-Saharan African continent, with 50,000 to 70,000 individuals infected. The utility of current therapies is limited by issues of toxicity and the need to administer compounds intravenously. We have begun a program to pursue lead optimization around MDL 73811, an irreversible inhibitor of S-adenosylmethionine decarboxylase (AdoMetDC). This compound is potent but in previous studies cleared rapidly from the blood of rats (T. L. Byers, T. L. Bush, P. P. McCann, and A. J. Bitonti, Biochem. J. 274:527-533). One of the analogs synthesized (Genz-644131) was shown to be highly active against Trypanosoma brucei rhodesiense in vitro (50% inhibitory concentration, 400 pg/ml). Enzyme kinetic studies showed Genz-644131 to be approximately fivefold more potent than MDL 73811 against the T. brucei brucei AdoMetDC-prozyme complex. This compound was stable in vitro in rat and human liver microsomal and hepatocyte assays, was stable in rat whole-blood assays, did not significantly inhibit human cytochrome P450 enzymes, had no measurable efflux in CaCo-2 cells, and was only 41% bound by serum proteins. Pharmacokinetic studies of mice following intraperitoneal dosing showed that the half-life of Genz-644131 was threefold greater than that of MDL 73811 (7.4 h versus 2.5 h). Furthermore, brain penetration of Genz-644131 was 4.3-fold higher than that of MDL 73811. Finally, in vivo efficacy studies of T. b. brucei strain STIB 795-infected mice showed that Genz-644131 significantly extended survival (from 6.75 days for controls to >30 days for treated animals) and cured animals infected with T. b. brucei strain LAB 110 EATRO. Taken together, the data strengthen validation of AdoMetDC as an important parasite target, and these studies have shown that analogs of MDL 73811 can be synthesized with improved potency and brain penetration.


Asunto(s)
Adenosilmetionina Descarboxilasa/antagonistas & inhibidores , Desoxiadenosinas/química , Tripanocidas/química , Trypanosoma brucei brucei/efectos de los fármacos , Trypanosoma brucei rhodesiense/efectos de los fármacos , Tripanosomiasis Africana/tratamiento farmacológico , Animales , Encéfalo/metabolismo , Células CACO-2 , Desoxiadenosinas/síntesis química , Desoxiadenosinas/farmacocinética , Desoxiadenosinas/farmacología , Humanos , Cinética , Ratones , Pruebas de Sensibilidad Parasitaria , Ratas , Resultado del Tratamiento , Tripanocidas/síntesis química , Tripanocidas/farmacocinética , Tripanocidas/farmacología , Trypanosoma brucei brucei/patogenicidad , Trypanosoma brucei rhodesiense/patogenicidad , Tripanosomiasis Africana/mortalidad , Tripanosomiasis Africana/parasitología
10.
Bioorg Med Chem Lett ; 15(8): 2087-91, 2005 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-15808474

RESUMEN

A series of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid diamides that increase chloride transport in cells expressing mutant cystic fibrosis transmembrane conductance regulator (CFTR) protein has been identified from our compound library. Analoging efforts and the resulting structure-activity relationships uncovered are detailed. Compound potency was improved over 30-fold from the original lead, yielding several analogs with EC(50) values below 10nM in our cellular chloride transport assay.


Asunto(s)
Amidas/química , Cloruros/metabolismo , Regulador de Conductancia de Transmembrana de Fibrosis Quística/metabolismo , Tetrahidroisoquinolinas/química , Amidas/metabolismo , Animales , Línea Celular , Transporte Iónico , Ratones , Tetrahidroisoquinolinas/metabolismo
11.
Bioorg Med Chem Lett ; 13(24): 4463-6, 2003 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-14643347

RESUMEN

Ureas of 5-aminopyrazole and 2-aminothiazole emerged as lead compounds from a high-throughput screen assaying the growth of Staphylococcus aureus. Structure-activity relationships were developed for each compound series. Several compounds were also tested for activity against drug resistant strains of S. aureus in vivo.


Asunto(s)
Antibacterianos/síntesis química , Bacterias Grampositivas/efectos de los fármacos , Pirazoles/síntesis química , Pirazoles/farmacología , Tiazoles/síntesis química , Tiazoles/farmacología , Urea/análogos & derivados , Urea/síntesis química , Antibacterianos/química , Antibacterianos/farmacología , Resistencia a la Meticilina , Pruebas de Sensibilidad Microbiana , Conformación Molecular , Estructura Molecular , Pirazoles/química , Staphylococcus aureus/efectos de los fármacos , Relación Estructura-Actividad , Tiazoles/química , Urea/química , Urea/farmacología
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