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Maribavir mbv

Manufactured by MedChemExpress
Sourced in United States, Luxembourg

Maribavir (MBV) is a small-molecule antiviral compound developed by MedChemExpress. It is a benzimidazole riboside that inhibits the human cytomegalovirus (HCMV) UL97 protein kinase, which is essential for viral DNA replication and capsid nuclear egress.

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2 protocols using maribavir mbv

1

Antiviral Drug Acquisition and Preparation

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Antiviral drugs were obtained from the following sources: abemaciclib (ABE) and maribavir (MBV; MedChemExpress, Monmouth Junction, NJ, USA); TF27 (Vichem Chemie Research Ltd., Budapest, Hungary) [30 (link),61 (link),62 (link)]; letermovir (LMV; Cayman Chemical Company, Ann Arbor, MI, USA); valganciclovir (VGCV; Ratiopharm, Ulm, Germany); LDC4297 (Lead Discovery Center GmbH, Dortmund, Germany). Stock aliquots were prepared in DMSO and stored at −20 °C.
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2

Synthesis and Characterization of CDK7 Inhibitors

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The synthesis and antiviral characterization of the parental, selective CDK7 inhibitor LDC4297 (Lead Discovery Center GmbH, Dortmund, Germany) have previously been described in detail [43 (link),44 (link),45 (link),47 (link),52 (link),53 (link),54 (link)]. The covalently binding derivatives QRS6, QRS7, and QRS were designed and synthesized by Qurient Co., Ltd. (C-dong, Pangyo-ro, Bundang-gu, Seongnam-si, Gyeonggi-do, Republic of Korea; Figure S1). The antiherpesviral drugs ganciclovir (GCV; Sigma-Aldrich, St. Louis, MO, USA), cidofovir (CDV; Pharmacia & Upjohn S.A., Luxembourg, Luxembourg), and maribavir (MBV; MedChemExpress, Monmouth Junction, NJ, USA) were purchased from the indicated sources and used as reference compounds. Stock aliquots were prepared in DMSO (Sigma-Aldrich, USA) at 10 mM and stored at −20 °C.
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