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Cenicriviroc, an orally active CCR5 antagonist for the potential treatment of HIV infection

10.1248/bpb.b18-00967 58 KoskovacM.CuparaS.KipicM.BarjaktarevicA.MilovanovicO.KojicicK.et al (2017)

Subsequently, a 2-fold dilution series of unlabeled competitors ZZ1-SO 2 H or JQ1 (prepared in DMSO and then diluted with the binding buffer to reach the final DMSO concentration of 2% for all titration points) was combined with equal volumes of the mixture of 20 nM JQ1FITC and 60 nM BRD4 BD1 alone or premixed with 600 nM YPEL5WDR26 CTLH

doi: ^ Hansen A.E., Haggard M.E., Boelsche A.N., Adam D.J., Wiese H.F

311 XieY.ZamponiR.CharlatO.RamonesM.SwalleyS.JiangX.et al (2013)