| Literature DB >> 28188066 |
Gary C Kemp1, Arnaud C Tiberghien2, Neki V Patel1, Francois D'Hooge1, Sanjay M Nilapwar1, Lauren R Adams1, Simon Corbett1, David G Williams1, John A Hartley1, Philip W Howard3.
Abstract
A novel pyrrolobenzodiazepine dimer payload, SG3227, was rationally designed based on the naturally occurring antitumour compound sibiromycin. SG3227 was synthesized from a dimeric core in an efficient fashion. An unexpected room temperature Diels-Alder reaction occurred during the final step of the synthesis and was circumvented by use of an iodoacetamide conjugation moiety in place of a maleimide. The payload was successfully conjugated to trastuzumab and the resulting ADC exhibited potent activity against a HER2-expressing human cancer cell line in vitro.Entities:
Keywords: Antibody-drug conjugate; DNA minor groove binding agent; Pyrrolobenzodiazepine dimer; SG3227; Sibiromycin
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Year: 2017 PMID: 28188066 DOI: 10.1016/j.bmcl.2017.01.074
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823