2. Signaling Pathways
  3. Anti-infection
  4. HSV
  5. HSV-2 Isoform

HSV-2

 

HSV-2 Related Products (31):

Cat. No. Product Name Effect Purity
  • HY-15304
    Dynasore
    		Inhibitor 99.85%
    Dynasore is a cell-permeable dynamin inhibitor with an IC50 of 15 μM.
  • HY-13637
    Ganciclovir
    		Inhibitor 99.77%
    Ganciclovir (BW 759), a nucleoside analogue, is an orally active antiviral agent with activity against CMV.
  • HY-17422
    Acyclovir
    		Inhibitor 99.34%
    Acyclovir (Aciclovir) is a potent, orally active antiviral agent.
  • HY-129555
    Surfactin
    		Inhibitor
    Surfactin is a potent cyclic lipopeptide biosurfactants consists of four isomers (Surfactin A, B, C and D), which mediates flux of mono-and divalent cations, such as calcium, across lipid bilayer membranes.
  • HY-N1067
    Xanthohumol
    		Inhibitor 99.84%
    Xanthohumol is one of the principal flavonoids isolated from hops, the inhibitor of diacylglycerol acetyltransferase (DGAT), COX-1 and COX-2, and shows anti-cancer and anti-angiogenic activities.
  • HY-12653A
    LDC4297 hydrochloride
    		Inhibitor 98.25%
    LDC4297 hydrochloride is a selective inhibitor of CDK7 with an IC50 value of 0.13 nM.
  • HY-13637B
    Ganciclovir hydrate
    		Inhibitor
    Ganciclovir (BW 759) hydrate, a nucleoside analogue, is an orally active antiviral agent with activity against CMV.
  • HY-N10504
    Galactofucan
    		Inhibitor
    Galactofucan (Fucogalactan) is a sulfated polysaccharide.
  • HY-13637A
    Ganciclovir sodium
    		Inhibitor 99.85%
    Ganciclovir (BW 759) sodium, a nucleoside analogue, is an orally active antiviral agent with activity against CMV.
  • HY-A0061
    Trifluridine
    		Inhibitor 99.83%
    Trifluridine (Trifluorothymidine; 5-Trifluorothymidine; TFT) is an irreversible thymidylate synthase inhibitor, and thereby suppresses DNA synthesis.
  • HY-12653
    LDC4297
    		Inhibitor 98.25%
    LDC4297 is a selective inhibitor of CDK7 with an IC50 value of 0.13 nM.
  • HY-15303
    Pritelivir
    		Inhibitor 99.03%
    Pritelivir (AIC316), an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.
  • HY-A0181A
    Adenosine 5'-monophosphate monohydrate
    		Inhibitor 99.07%
    Adenosine 5'-monophosphate monohydrate is an adenosine A1 receptor agonist.
  • HY-B0277
    Vidarabine
    		Inhibitor ≥98.0%
    Vidarabine (Ara-A) an antiviral agent which is active against herpes simplex and varicella zoster viruses.
  • HY-17424
    Penciclovir
    		Inhibitor 99.90%
    Penciclovir (VSA 671) is a potent and selective anti-herpesvirus agent with EC50 values of 0.5, 0.8 µg/ml for HSV-1 (HFEM), HSV-2 (MS), respectively.
  • HY-14809
    Amenamevir
    		Inhibitor 99.91%
    Amenamevir is a helicase-primase inhibitor which has potent antiviral activity against HSVs with an EC50 of 14 ng/mL.
  • HY-N1430
    Oxyresveratrol
    		Inhibitor 98.87%
    Oxyresveratrol (trans-Oxyresveratrol) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 µM against DPPH free radicals).
  • HY-U00124B
    Tromantadine hydrochloride
    		Inhibitor ≥98.0%
    Tromantadine hydrochloride, an Amantadine derivative with antiherpetic activity, inhibits herpes simplex virus type 1 (HSV-1) and HSV-2 replication.
  • HY-N2584A
    Isoxanthohumol
    		Inhibitor 99.90%
    Isoxanthohumol is a prenylflavonoid from hops and beer.
  • HY-50735
    Fiacitabine
    		Inhibitor 98.83%
    Fiacitabine(NSC 382097; FIAC; FOAC) is a selective inhibitior of DNA replication of herpes simplex virus(HSV) with IC50 values of 2.5 nM and 12.6 nM for HSV1 and HSV2, respectively.