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[DOI] [PMC free article] [PubMed] [Google Scholar] 29.Gomes R.D.S., Anay K., Galdino A.B.S., Oliveira J.P.F., Gama M.A.S., Medeiros C.A., Gavioli E.C., Porto A.L., Rangel A.H

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In this work, new cysteine-selective nucleoside-H 2 S-donor hybrid molecules were prepared by conjugating nucleoside biomolecules with a thiol-activatable dithioacetyl group

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Consequently, early strategies to enhance the efficacy of MM therapies focused on increasing the number of CD38 targets available for antibody binding