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Home >> Signaling Pathways >> Microbiology & Virology >> CMV

CMV

CMV (Cytomegalovirus) is a type of herpervirus and infects human.

Products for  CMV

  1. Cat.No. Product Name Information
  2. GC16841 Adefovir Dipivoxil

    GS 0840

     Adefovir Dipivoxil is an orally effective reverse transcriptase inhibitor. Adefovir Dipivoxil Chemical Structure
  3. GC33986 B220 B220 is an antiviral agent which can inhibit the growth of HSV-1, HSV-2 and human cytomegalovirus (CMV). B220 Chemical Structure
  4. GC14716 Bisindolylmaleimide IV

    Arcyriarubin A,BIM IV

     Bisindolylmaleimide IV is a potent cell-permeable inhibitor of protein kinase C (PKC) with IC50 values are 0.1- 0.55μM. Bisindolylmaleimide IV Chemical Structure
  5. GC50140 BRACO 19 trihydrochloride BRACO 19 trihydrochloride is a potent telomerase/telomere inhibitor with an IC50 value of 115±18nM, which prevents telomerase capping and catalysis. BRACO 19 trihydrochloride Chemical Structure
  6. GC68800 Braco-19

    Braco-19 is an effective telomerase/telomere inhibitor that prevents the catalytic activity of telomerase. As a quadruplex (GQ) binding ligand, Braco-19 stabilizes the formation of GQ quadruplexes at 3V telomeric DNA and can lead to rapid aging or selective cell death. Braco-19 is also an inhibitor of HAdV virus replication.

     Braco-19 Chemical Structure
  7. GC33923 Brivudine (Bromovinyldeoxyuridine)

    BVDU

     Brivudine (Bromovinyldeoxyuridine) is a thymidine analogue and an inhibitor of herpes simplex virus type 1 (HSV-1) and varicella-zoster virus (VZV) replication. Brivudine (Bromovinyldeoxyuridine) Chemical Structure
  8. GC35642 CEF20 CEF20 Chemical Structure
  9. GC12666 Cidofovir

    GS-0504, (S)-HPMPC, (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine

     Cidofovir dihydrate is an acyclic monophosphate nucleotide analog, a CMV inhibitor, possessing antiviral activity. Cidofovir Chemical Structure
  10. GC13936 Cidofovir dihydrate Cidofovir dihydrate is an acyclic monophosphate nucleotide analog, a CMV inhibitor, possessing antiviral activity. Cidofovir dihydrate Chemical Structure
  11. GC17689 CMX001

    Brincidofovir; HDP-CDV

     CMX001 is a lipophilic nucleotide analog formed by covalently linking 3-(hexdecyloxy)propan-1-ol to cidofovir (CDV) used for treatment of smallpox. CMX001 Chemical Structure
  12. GC35782 Cyclopropavir

    Filociclovir; ZSM-I-62; MBX-400

     Cyclopropavir (Filociclovir; ZSM-I-62; MBX-400) is a broad-spectrum anti-herpesvirus compound, has good antiviral activity against cytomegalovirus (CMV), herpes simplex virus (HHV)-6 and HHV-8 with EC50s of 0.7 μM to 8 μM. Cyclopropavir Chemical Structure
  13. GC78865 DNA polymerase-IN-6 formic DNA polymerase-IN-6 formic is an antiviral agent and a DNA polymerase inhibitor. DNA polymerase-IN-6 formic Chemical Structure
  14. GC11654 Enocitabine

    Behenoyl-ara-C, N4-Behenoyl-1-β-D-arabinofuranosylcytosine, behenoyl Cytarabine, NSC 239336

     nucleoside analog used as chemotherapy Enocitabine Chemical Structure
  15. GC74547 Fiztasovimab

    NPC-21; EV2038

     Fiztasovimab (NPC-21; EV2038) is a fully human IgG1λ mAb against human cytomegalovirus (hCMV). Fiztasovimab Chemical Structure
  16. GC67756 Fomivirsen

    ISIS-2922 free base

     Fomivirsen Chemical Structure
  17. GC64041 Fomivirsen sodium

    ISIS-2922

     Fomivirsen sodium is an antisense 21 mer phosphorothioate oligonucleotide. Fomivirsen sodium Chemical Structure
  18. GC60865 Ganciclovir sodium Ganciclovir sodium is a nucleoside antiviral drug. Ganciclovir sodium Chemical Structure
  19. GC12672 Letermovir

    AIC246

     Letermovir is an orally antiviral compound that inhibits the cytomegalovirus (CMV) DNA terminase, with an EC50 value of 4.0nM. Letermovir Chemical Structure
  20. GC10390 Maribavir

    1263W94; BW1263W94; GW257406X

    UL97 or pUL97 inhibitor

     Maribavir Chemical Structure
  21. GC78870 MLS8091 MLS8091 is a highly selective inhibitor of the human cytomegalovirus (HCMV) helicase-primase complex with antiviral activity. MLS8091 Chemical Structure
  22. GC70384 SB-734117 SB-734117 is a human cytomegalovirus (HCMV) replication inhibitor that prevents CREB and histone H3 post-translational modifications. SB-734117 Chemical Structure
  23. GC61284 Soyasaponin II Soyasaponin II is a saponin with antiviral activity. Soyasaponin II Chemical Structure
  24. GC78871 T-0902611 benzenesulfonate T-0902611 benzenesulfonate is a specific HCMV inhibitor. T-0902611 benzenesulfonate Chemical Structure
  25. GC32345 Tomeglovir (BAY 38-4766) Tomeglovir (BAY 38-4766) is a potent anti-CMV agent, inhibiting processing of viral DNA-concatemers, with IC50s of 0.34 μM and 0.039 μM for HCMV and MCMV. Tomeglovir (BAY 38-4766) Chemical Structure
  26. GC39158 Tricin Tricin is a natural flavonoid widely distributed in grasses and legumes, possessing various biological activities such as anti-inflammatory, antioxidant, and antitumor effects. Tricin Chemical Structure
  27. GC37882 Valganciclovir Valganciclovir, the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir Chemical Structure
  28. GC11924 Valganciclovir HCl

    Ro 1079070/194

     Valganciclovir (hydrochloride), the L-valyl ester of ganciclovir, is actually a prodrug for ganciclovir. Valganciclovir HCl Chemical Structure
  29. GA23665 VIP Antagonist VIP Antagonist is a novel, orally active vasoactive intestinal peptide (VIP) receptor antagonist. VIP Antagonist Chemical Structure

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