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Results for "

176161-24-3

" in MedChemExpress (MCE) Product Catalog:

4

Inhibitors & Agonists

2

Isotope-Labeled Compounds

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-16305
    Maribavir
    10+ Cited Publications

    1263W94; BW1263W94; GW257406X

    		 EBV CMV Infection
    Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
    Maribavir
  • HY-16305S
    Maribavir-d6

    1263W94-d6; BW1263W94-d6; GW257406X-d6

    		 Isotope-Labeled Compounds Others
    Maribavir-d6 (1263W94-d6) is a deuterium labeled Maribavir (HY-16305). Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM .
    Maribavir-d6
  • HY-16305S1
    Maribavir-d6 TFA

    1263W94-d6 TFA; BW1263W94-d6 TFA; GW257406X-d6 TFA

    		 Bacterial Infection
    Maribavir-d6 TFA (1263W94-d6 TFA; BW1263W94-d6 TFA; GW257406X-d6 TFA) is a deuterium labeled Maribavir (HY-16305). Maribavir is an orally active antiviral agent for cytomegalovirus (CMV) through inhibition of protein kinase UL97 and the following CMV DNA replication .
    Maribavir-d6 TFA
  • HY-16305R
    Maribavir (Standard)

    		EBV CMV Infection
    Maribavir (Standard) is the analytical standard of Maribavir. This product is intended for research and analytical applications. Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
    Maribavir (Standard)

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