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1.
Chem Commun (Camb) ; 55(6): 802-805, 2019 Jan 15.
Article in English | MEDLINE | ID: mdl-30574643

ABSTRACT

Here we present 2shRNA, a shRNA-based nanobinder, which can simultaneously attack two therapeutic targets involved in drug resistance pathways and can additionally bind accessory molecules such as cell targeting peptides or fluorophores. We create 2shRNAs designed to specifically kill HER2+ breast cancer cells in the absence of a transfecting agent.


Subject(s)
Nanostructures/chemistry , RNA, Small Interfering/chemistry , Breast Neoplasms/drug therapy , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Cell Line, Tumor , Female , Humans , Microscopy, Confocal , Molecular Dynamics Simulation , Peptides/chemistry , Peptides/metabolism , RNA, Small Interfering/metabolism , RNA, Small Interfering/therapeutic use , Receptor, ErbB-2/antagonists & inhibitors , Receptor, ErbB-2/genetics , Receptor, ErbB-2/metabolism
2.
Chem Commun (Camb) ; 53(19): 2870-2873, 2017 Mar 02.
Article in English | MEDLINE | ID: mdl-28218319

ABSTRACT

Despite the broad applicability of the Huisgen cycloaddition reaction, the click functionalization of RNAs with peptides still remains a challenge. Here we describe a straightforward method for the click functionalization of siRNAs with peptides of different sizes and complexities. Among them, a promising peptide carrier for the selective siRNA delivery into HER2+ breast cancer cell lines has been reported.


Subject(s)
Breast Neoplasms/metabolism , Peptides/chemistry , Peptides/pharmacokinetics , RNA, Small Interfering/chemistry , RNA, Small Interfering/pharmacokinetics , Breast Neoplasms/genetics , Breast Neoplasms/pathology , Cell Line, Tumor , Click Chemistry , Drug Carriers/chemistry , Drug Carriers/pharmacokinetics , Female , Humans , Molecular Conformation , Receptor, ErbB-2/genetics
3.
J Org Chem ; 80(24): 11977-85, 2015 Dec 18.
Article in English | MEDLINE | ID: mdl-26556606

ABSTRACT

While B3LYP, M06-2X, and MP2 calculations predict the ΔG° values for exchange equilibria between enamines and ketones with similar acceptable accuracy, the M06-2X/6-311+G(d,p) and MP2/6-311+G(d,p) methods are required for enamine formation reactions (for example, for enamine 5a, arising from 3-methylbutanal and pyrrolidine). Stronger disagreement was observed when calculated energies of hemiaminals (N,O-acetals) and aminals (N,N-acetals) were compared with experimental equilibrium constants, which are reported here for the first time. Although it is known that the B3LYP method does not provide a good description of the London dispersion forces, while M06-2X and MP2 may overestimate them, it is shown here how large the gaps are and that at least single-point calculations at the CCSD(T)/6-31+G(d) level should be used for these reaction intermediates; CCSD(T)/6-31+G(d) and CCSD(T)/6-311+G(d,p) calculations afford ΔG° values in some cases quite close to MP2/6-311+G(d,p) while in others closer to M06-2X/6-311+G(d,p). The effect of solvents is similarly predicted by the SMD, CPCM, and IEFPCM approaches (with energy differences below 1 kcal/mol).

4.
J Org Chem ; 80(17): 8511-9, 2015 Sep 04.
Article in English | MEDLINE | ID: mdl-26079383

ABSTRACT

The total synthesis of (-)-amphidinolide K (1) based on asymmetric addition of allylsilane C1-C8 to enal C9-C22 is reported. The 1,9,18-tris-O-TBDPS ether was converted into the desired 9,18-dihydroxy acid. Its macrolactonization was accomplished by the Shiina method. Compound 1 together with some of its stereoisomers and analogues were subjected to evaluation of the possible disruption of the α,ß-tubulin-microtubule and/or G-actin-F-actin equilibria. Compound 1 behaves as a stabilizer of actin filaments (F-actin) in vitro.


Subject(s)
Actins/chemistry , Anti-Bacterial Agents/chemical synthesis , Macrolides/chemical synthesis , Tubulin/chemistry , Anti-Bacterial Agents/chemistry , Macrolides/chemistry , Molecular Structure , Stereoisomerism
5.
Aten. prim. (Barc., Ed. impr.) ; 46(9): 457-463, nov. 2014. ilus, tab
Article in Spanish | IBECS | ID: ibc-129689

ABSTRACT

OBJETIVO: Mejorar los conocimientos de la población sobre hábitos cardiosaludables mediante un programa de formación complementado por una Web y actividades comunitarias. DISEÑO: Ensayo clínico controlado donde la intervención es la participación en el Aula de Formación en Salud Cardiovascular (AFSC). Emplazamiento: Población de 80.000 habitantes. Participantes: Pacientes, ambos sexos, 55-70 años, con al menos un factor de riesgo cardiovascular (RCV). Intervención: El grupo intervención estaba formado por los pacientes que participaron en el AFSC. La intervención constaba de un curso presencial de 20 h en el que se ofrecía una Web de apoyo y se organizaban actividades complementarias. Las clases fueron impartidas por 3 enfermeras de atención primaria. Mediciones principales: La variable principal fue el conocimiento sobre el RCV. Variables secundarias: edad, sexo, factores de RCV, estilos de vida, visitas a los centros, consumo farmacéutico, adherencia terapéutica y satisfacción con el programa. RESULTADOS: Se evaluaron los datos de los pacientes de los 10 primeros cursos (n = 150). Se observa una mejora estadísticamente significativa en el conocimiento general sobre el RCV en el GI (de 87,3 al 100%) respecto al GC (84,5 al 92,7%), p < 0,001 y una mejora en la actividad física (GI: del 71,2 al 83,1% frente GC: del 72,6 al 78,2%), p = 0,05. El número de visitas totales en atención primaria (medicina y enfermería) disminuyó más en el GI que en el GC. La valoración del curso ha sido elevada. CONCLUSIONES: Se demuestra la efectividad de esta experiencia para mejorar conocimientos sobre salud cardiovascular y algunos hábitos de vida saludable


OBJECTIVE: To improve the knowledge of the population about heart-healthy habits through a training program supplemented by a web site and community activities. DESIGN: A controlled clinical trial with intervention done through participation in the Cardiovascular Health Training Classroom (CHTC) Location: A town of 80,000 inhabitants. Participants: Patients: both sexes, aged 55 to 70 years, with at least one cardiovascular risk factor (CVRF). Intervention: The intervention group (IG) consisted of patients who participated in the CHTC. Intervention was carried out through a 20-hour presential group course in which a support web site was offered and complementary activities were organized. Classes were taught by three Primary Care nurses. Main measurements: The primary endpoint was knowledge of CVRF. The secondary variables were age, sex, CVRF, lifestyle, visits to health centers, pharmaceutical use adherence, and satisfaction with the program. RESULTS: Data from patients in the first 10 courses (n = 150) were evaluated. A statistically significant improvement was observed in overall knowledge of CVRF in the IG (87.3% to 100%) compared with control group (GC) (84.5% to 92.7%), p<.001, as well as an improvement in physical activity is (IG: 71.2% to 83.1% versus CG: 72.6% to 78.2%), p=.05. The total number of Primary Care visits (medical and nursing) decreased in the IG more than in the CG. The satisfaction rate of the course was very high. CONCLUSIONS: This experience is effective in improving cardiovascular health knowledge and promoting some healthy habits


Subject(s)
Humans , Consumer Health Information/organization & administration , Cardiovascular Diseases/epidemiology , Patient Compliance , Primary Health Care/statistics & numerical data , Health Education/trends , Patient Education as Topic/organization & administration , Evaluation of Results of Preventive Actions
6.
Org Lett ; 16(11): 2900-3, 2014 Jun 06.
Article in English | MEDLINE | ID: mdl-24824532

ABSTRACT

Enamines from 3-methylbutanal and several Pro- and Phe-derived secondary amines were prepared in DMSO-d6, CD3CN, and CDCl3. For the first time, the relative thermodynamic stabilities of these and other enamines were compared, and rapid exchanges of 1-alkenyl groups were demonstrated. Competition experiments showed that the most favored enamines (without significant steric inhibition of resonance) react more rapidly with electrophiles.

7.
Aten Primaria ; 46(9): 457-63, 2014 Nov.
Article in Spanish | MEDLINE | ID: mdl-24768658

ABSTRACT

OBJECTIVE: To improve the knowledge of the population about heart-healthy habits through a training program supplemented by a web site and community activities. DESIGN: A controlled clinical trial with intervention done through participation in the Cardiovascular Health Training Classroom (CHTC) LOCATION: A town of 80,000 inhabitants. PATIENTS: both sexes, aged 55 to 70 years, with at least one cardiovascular risk factor (CVRF). INTERVENTION: The intervention group (IG) consisted of patients who participated in the CHTC. Intervention was carried out through a 20-hour presential group course in which a support web site was offered and complementary activities were organized. Classes were taught by three Primary Care nurses. MAIN MEASUREMENTS: The primary endpoint was knowledge of CVRF. The secondary variables were age, sex, CVRF, lifestyle, visits to health centers, pharmaceutical use adherence, and satisfaction with the program. RESULTS: Data from patients in the first 10 courses (n=150) were evaluated. A statistically significant improvement was observed in overall knowledge of CVRF in the IG (87.3% to 100%) compared with control group (GC) (84.5% to 92.7%), p<.001, as well as an improvement in physical activity is (IG: 71.2% to 83.1% versus CG: 72.6% to 78.2%), p=.05. The total number of Primary Care visits (medical and nursing) decreased in the IG more than in the CG. The satisfaction rate of the course was very high. CONCLUSIONS: This experience is effective in improving cardiovascular health knowledge and promoting some healthy habits.


Subject(s)
Cardiovascular Diseases/prevention & control , Health Education , Aged , Female , Humans , Male , Middle Aged , Pilot Projects
8.
Org Lett ; 14(2): 536-9, 2012 Jan 20.
Article in English | MEDLINE | ID: mdl-22224938

ABSTRACT

Equilibria between carbonyl compounds and their enamines (from O-TBDPS-derived prolinol) have been examined by NMR spectroscopy in DMSO-d(6). By comparing the exchange reactions between pairs (enamine A + carbonyl B → carbonyl A + enamine B), a quite general scale of the tendency of carbonyl groups to form enamines has been established. Aldehydes quickly give enamines that are relatively more stable than those of ketones, but there are exceptions to this expected rule; for example, 1,3-dihydroxyacetone acetals or 3,5-dioxacyclohexanones (2-phenyl-1,3-dioxan-5-one and 2,2-dimethyl-1,3-dioxan-5-one) show a greater tendency to afford enamines than many α-substituted aldehydes.

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