Search results for "Benzamide"
showing 10 items of 199 documents
The effects of enzalutamide and abiraterone on skeletal related events and bone radiological progression free survival in castration resistant prosta…
2017
Two new drugs, the CYP17 inhibitor abiraterone acetate and the androgen receptor (AR) antagonist enzalutamide, have recently shown to prolong OS prior chemotherapy or in docetaxel treated mCRPC patients, using steroidal therapy or placebo as control group. Updated analyses underlined the role of these new agents on two prostate-specific endpoints as radiographic progression-free survival (rPFS) and time to first skeletal-related event (tSRE). On the basis of these reports, we made an indirect comparison between abiraterone and enzalutamide. We obtained a clinically but not significant difference favouring enzalutamide over abiraterone in terms of rPFS (HR 0.48, 95% CI 0.22â1.02). No signi…
Hockey-Puck micelles from oligo(p-benzamide)-b-PEG rod-coil block copolymers.
2006
Analytical method for simultaneous determination of pesticide and veterinary drug residues in milk by CE-MS
2009
10 páginas, 2 figuras, 4 tablas.
Gold(ii) in redox-switchable gold(i) catalysis
2019
Chemical communications 55(32), 4615 - 4618 (2019). doi:10.1039/C9CC00283A
Protonation effects on the UV/Vis absorption spectra of imatinib: A theoretical and experimental study
2014
An experimental and theoretical investigation of protonation effects on the UV/Vis absorption spectra of imatinib showed systematic changes of absorption depending on the pH, and a new absorption band appeared below pH 2. These changes in the UV/Vis absorption spectra were interpreted using quantum chemical calculations. The geometry of various imatinib cations in the gas phase and in ethanol solution was optimized with the DFT/B3LYP method. The resultant geometries were compared to the experimentally determined crystal structures of imatinib salts. The semi-empirical ZINDO-CI method was employed to calculate the absorption lines and electronic transitions. Our study suggests that the forma…
N-(INDAZOLYL)BENZAMIDO DERIVATIVES AS CDK1 INHIBITORS: DESIGN, SYNTHESIS, BIOLOGICAL ACTIVITY, AND MOLECULAR DOCKING STUDIES
2009
A series of N-1H-indazole-1-carboxamides has been synthesized and their effects on both CDK1/cyclin B and the K-562 (human chronic myelogenus leukemia) cell line were evaluated. Using a computational model, we have observed that all the most active compounds 9e, f, i-n exhibited the same binding mode of purvanalol A in the ATP-binding cleft. Although they were able to moderately inhibit the leukemic cell line K-562 and to show inhibitory activity against the Cdc2-Cyclin B kinase in the low micromolar range, they turned out to be non-cytotoxic against HuDe (IZSL) primary cell cultures from human derm. These preliminary results are quite encouraging in view of the low toxicity demonstrated by…
CCDC 629530: Experimental Crystal Structure Determination
2007
Related Article: C.A.Jimenez, J.B.Belmar, F.S.Delgado, M.Julve, C.Ruiz-Perez|2007|CrystEngComm|9|746|doi:10.1039/b617605d
CCDC 1443023: Experimental Crystal Structure Determination
2016
Related Article: Pierre-Emmanuel Doulain, Christine Goze, Ewen Bodio, Philippe Richard, Richard A. Decréau|2016|Chem.Commun.|52|4474|doi:10.1039/C5CC10526A
CCDC 938974: Experimental Crystal Structure Determination
2014
Related Article: Lena Kaufmann, Nora L. Traulsen, Andreas Springer, Hendrik V. Schröder, Toni Mäkelä, Kari Rissanen, Christoph A. Schalley|2014|Org.Chem.Front.|1|521|doi:10.1039/C4QO00077C
CCDC 663805: Experimental Crystal Structure Determination
2007
Related Article: T.Lahtinen, K.Rissanen|2007|Acta Crystallogr.,Sect.E:Struct.Rep.Online|63|o4114|doi:10.1107/S1600536807044777