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Cat. No. Product Name Information
PC-73148

Pritelivir mesylate

Antiviral

Pritelivir mesylate (AIC316) is an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro (HSV-1 and HSV-2, IC50=0.02 uM).
PC-73147

Pritelivir

Antiviral

Pritelivir (AIC316) is an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro (HSV-1 and HSV-2, IC50=0.02 uM).
PC-72691

MEDS433

DHODH inhibitor

MEDS433 is a potent DHODH inhibitor with IC50 of 1.2 nM (hDHODH), inhibits in vitro replication of HSV-1 and HSV-2 in the nanomolar range.
PC-72690

IM-250

HSV helicase primase inhibitor

IM-250 is a potent HSV-1 helicase primase inhibitor, inhibits HSV-1 replication with IC50 of 20 nM (clinical isolate of HSV-1).
PC-60382

Amenamevir

helicase-primase inhibitor

Amenamevir (ASP-2151) is a potent viral helicase-primase inhibitor that possesses antiviral activity against VZV, HSV1 and HSV2 with EC50 of 0.028-0.1 uM.
PC-45247

Valacyclovir

Viral DNA polymerase inhibitor

Valacyclovir is an antiviral agent that acts as a very potent inhibitor of viral DNA polymerase.
PC-45855

Fiacitabine

HSV inhibitor

Fiacitabine (NSC 382097, FIAC) is a synthesized pyrimidine analog that is a potent and selective anti-herpesvirus agent.
PC-45246

Penciclovir

HSV inhibitor

Penciclovir (VSA-671, BRL-39123) is a guanosine analogue antiviral agent used for the treatment of various herpesvirus (HSV) infections, inhibits viral DNA polymerase and exhibits low toxicity and good selectivity.
PC-45249

Famciclovir

HSV inhibitor

Famciclovir (BRL-42810) is a guanine analogue antiviral agent used for the treatment of various herpesvirus (HSV) infections.
PC-22614

L-BHDU

VZV inhibitor

L-BHDU is a potent and selective inhibitor of the varicella-zoster virus (VZV) with EC50 of 0.25 uM in human foreskin fibroblasts (HFFs).
PC-22223

HN0037

Viral helicase-primase inhibitor

HN0037 is a potent viral helicase-primase inhibitor, inhibits HSV-1 with IC50 of 7 nM.
PC-63468

FV-100

FV-100 (Valnivudine, CF-1743) is a potent, selective, bicyclic nucleoside analogue inhibitor of varicella zoster virus (VZV) with EC50 of subnanomolar range in vitro..

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