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HSV

HSV (herpes simplex virus) are ubiquitous and contagious that cause infection in human. HSV-1 infects the mouth and HSV-2 infects the genitals.

Products for  HSV

  1. Cat.No. Product Name Information
  2. GC49467 β-Aescin A triterpenoid saponin with diverse biological activities β-Aescin  Chemical Structure
  3. GC46356 (Z)-9-Hexadecenol An unsaturated long-chain fatty alcohol with diverse biological activities (Z)-9-Hexadecenol  Chemical Structure
  4. GC35010 (Z)-Capsaicin (Z)-Capsaicin is the cis isomer of capsaicin, acts as an orally active TRPV1 agonist, and is used in the research of neuropathic pain. (Z)-Capsaicin  Chemical Structure
  5. GC35048 11-Deoxymogroside IIE 11-Deoxymogroside IIE is a cucurbitane glycoside, isolated from Siraitia grosvenorii fruits. 11-Deoxymogroside IIE  Chemical Structure
  6. GC35050 11-Oxomogroside IIa 11-Oxomogroside IIa (11-oxomogroside II A1) is a cucurbitane glycoside extracted from the fruits of Siraitia grosVenorii. 11-Oxomogroside IIa  Chemical Structure
  7. GC18778 16,16-dimethyl Prostaglandin A1 16,16-dimethyl PGA1 is a metabolism resistant analog of PGA1. 16,16-dimethyl Prostaglandin A1  Chemical Structure
  8. GC41110 16-epi Latrunculin B 16-epi Latrunculin B, first isolated from the Red Sea sponge N. 16-epi Latrunculin B  Chemical Structure
  9. GC49514 2′-Deoxyuridine-d2 An internal standard for the quantification of 2’-deoxyuridine 2′-Deoxyuridine-d2  Chemical Structure
  10. GC17430 2-Deoxy-D-glucose

    2-Deoxy-D-glucose (2DG), is a glucose analogue, act as competitive glycolytic inhibitor.

    2-Deoxy-D-glucose  Chemical Structure
  11. GC68513 2-Deoxy-D-glucose-d

    2-Deoxy-D-glucose-d is the deuterated form of 2-Deoxy-D-glucose. 2-Deoxy-D-glucose is a glucose analogue and a glycolysis inhibitor that works by inhibiting hexokinase, an enzyme involved in glucose metabolism.

    2-Deoxy-D-glucose-d  Chemical Structure
  12. GC49122 3′-deoxy Thymidine An antiviral nucleoside analog 3′-deoxy Thymidine  Chemical Structure
  13. GC40641 5'-Ethynyl-2'-deoxycytidine 5'-Ethynyl-2'-deoxycytidine (EdC) is a nucleoside analog that inhibits replication of the herpes simplex virus-1 (HSV-1) KOS strain (ID50 = 0.2 μg/mL). 5'-Ethynyl-2'-deoxycytidine  Chemical Structure
  14. GC40527 5-(Hydroxymethyl)-2'-deoxyuridine 5-(Hydroxymethyl)-2'-deoxyuridine is a nucleoside analog with anticancer and antiviral activities. 5-(Hydroxymethyl)-2'-deoxyuridine  Chemical Structure
  15. GC66324 5-Nitrobarbituric acid 5-Nitrobarbituric acid is a herpes simplex virus type-1 (HSV-1) inhibitor (IC50=1.7 μM). 5-Nitrobarbituric acid  Chemical Structure
  16. GC49749 6-Deoxypenciclovir An inactive metabolite of famciclovir 6-Deoxypenciclovir  Chemical Structure
  17. GC17186 Acyclovir Antiviral agent Acyclovir  Chemical Structure
  18. GC46797 Acyclovir-d4 An internal standard for the quantification of acyclovir Acyclovir-d4  Chemical Structure
  19. GC46805 Adefovir-d4 An internal standard for the quantification of adefovir Adefovir-d4  Chemical Structure
  20. GC19028 Amenamevir Amenamevir is a helicase-primase inhibitor which has potent antiviral activity against HSVs with an EC50 of 14 ng/mL. Amenamevir  Chemical Structure
  21. GC33986 B220 B220 is an antiviral agent which can inhibit the growth of HSV-1, HSV-2 and human cytomegalovirus (CMV). B220  Chemical Structure
  22. GC11359 BAY 57-1293 BAY 57-1293 (AIC316), an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection. BAY 57-1293  Chemical Structure
  23. GC14233 BIO-acetoxime

    GSK-3α/β inhibitor

    BIO-acetoxime  Chemical Structure
  24. GC17683 Brefeldin A

    Brefeldin A (BFA) is a fungal macrocyclic lactone and a potent, reversible inhibitor of intracellular vesicle formation and protein trafficking between the endoplasmic reticulum (ER) and the Golgi apparatus.

    Brefeldin A  Chemical Structure
  25. GC32371 BRL44385 BRL44385 is a potent and selective inhibitor of the replication of herpes simplex virus types 1 and 2 (HSV-1 and HSV2), varicella zoster virus (VZV) and Epstein-Barr virus (EBV). BRL44385  Chemical Structure
  26. GC45413 Cridanimod (sodium salt)   Cridanimod (sodium salt)  Chemical Structure
  27. GC35782 Cyclopropavir 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
  28. GC49863 Cytarabine 5′-monophosphate An active metabolite of cytarabine Cytarabine 5′-monophosphate  Chemical Structure
  29. GC49153 Didemnin B

    Didemnin B is a cyclic depsipeptide produced by marine tunicates that specifically binds the GTP-bound conformation of EEF1A.

    Didemnin B  Chemical Structure
  30. GC12881 Docosanol (Abreua) Docosanol (Abreua) is a saturated fatty alcohol used traditionally as an emollient, emulsifier, and thickener in cosmetics, and nutritional supplement; inhibitor of lipid-enveloped viruses including herpes simplex. Docosanol (Abreua)  Chemical Structure
  31. GC30286 Docusate Sodium (Dioctyl sulfosuccinate sodium salt) Docusate Sodium (Dioctyl sulfosuccinate sodium salt) (Dioctyl sulfosuccinate sodium salt) is a laxative used to for the research of constipation, for constipation due to the use of opiates it maybe used with a stimulant laxative, can be taken by mouth or rectally. Docusate Sodium (Dioctyl sulfosuccinate sodium salt)  Chemical Structure
  32. GC47285 Elaidyl Alcohol A monounsaturated fatty alcohol Elaidyl Alcohol  Chemical Structure
  33. GC17947 Famciclovir Anti-herpesvirus oral prodrug of penciclovir Famciclovir  Chemical Structure
  34. GC36039 Fiacitabine 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. Fiacitabine  Chemical Structure
  35. GC11943 Fialuridine nucleoside analog with antiviral activity Fialuridine  Chemical Structure
  36. GC60860 FSL-1 TFA

    FSL-1 TFA, a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist, enhances resistance to experimental HSV-2 infection.

    FSL-1 TFA  Chemical Structure
  37. GC67733 Gallic aldehyde Gallic aldehyde  Chemical Structure
  38. GC11331 Ganciclovir Antiviral drug for CMV infections Ganciclovir  Chemical Structure
  39. GC60865 Ganciclovir sodium Ganciclovir (BW 759) sodium, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir sodium  Chemical Structure
  40. GC49228 Ganoderol B A triterpenoid with diverse biological activities Ganoderol B  Chemical Structure
  41. GN10156 Ginsenoside Rb1 Ginsenoside Rb1  Chemical Structure
  42. GC38915 Glyceryl monocaprate Glyceryl monocaprate (Monolaurin) is a 1-monoglyceride of capric acid against gram-positive bacterial infections. Glyceryl monocaprate  Chemical Structure
  43. GC36260 HSV-TK substrate HSV-TK substrate is a substrate for HSV-TK, and induces multi-log cytotoxicity in HSV-TK-expressing and bystander cells. HSV-TK substrate shows antitumor activity. HSV-TK substrate  Chemical Structure
  44. GC13247 Idoxuridine Antiviral agent Idoxuridine  Chemical Structure
  45. GC40668 Isoborneol Isoborneol is a monoterpene alcohol that has been found in a variety of plants, including C. Isoborneol  Chemical Structure
  46. GC60950 Isookanin Isookanin can be used for the research of various illnesses including cancers, skin rashes, snake and insects bites, diabetes mellitus, diarrhoea. Isookanin  Chemical Structure
  47. GC49382 L-Lysine-d3 (hydrochloride) An internal standard for the quantification of L-lysine L-Lysine-d3 (hydrochloride)  Chemical Structure
  48. GC47584 L-Valacyclovir-d8 (hydrochloride) An internal standard for the quantification of valacyclovir L-Valacyclovir-d8 (hydrochloride)  Chemical Structure
  49. GC19219 LDC4297 LDC4297 is a potent and selective CDK7 inhibitor with an IC50 of 0.13 nM. LDC4297  Chemical Structure
  50. GC46169 Mer-NF5003F A sesquiterpene with diverse biological activities Mer-NF5003F  Chemical Structure
  51. GC12557 ML324 JMJD2 demethylase inhibitor, potent and cell-permeable ML324  Chemical Structure
  52. GC18769 MST-312 MST312 is a telomerase inhibitor (IC50 = 0.67 μM in a TRAP assay). MST-312  Chemical Structure
  53. GC47760 Nebularine A purine ribonucleoside with diverse biological activities Nebularine  Chemical Structure
  54. GC17314 OG-L002 LSD1 inhibitor,potent and specific OG-L002  Chemical Structure
  55. GC48652 Olomoucine II A CDK inhibitor Olomoucine II  Chemical Structure
  56. GC61771 Omaciclovir Omaciclovir (H2G) is a potent and selective inhibitor of herpesvirus replication. Omaciclovir  Chemical Structure
  57. GC47828 Oosporein A mycotoxin with diverse biological activities Oosporein  Chemical Structure
  58. GC33464 Oxyresveratrol (trans-Oxyresveratrol) Oxyresveratrol (trans-Oxyresveratrol) (trans-Oxyresveratrol (trans-Oxyresveratrol)) is a potent naturally occurring antioxidant and free radical scavenger (IC50 of 28.9 μM against DPPH free radicals). Oxyresveratrol (trans-Oxyresveratrol)  Chemical Structure
  59. GC61164 Oxytetracycline hydrochloride Oxytetracycline hydrochloride is an antibiotic belonging to the tetracycline class. Oxytetracycline hydrochloride  Chemical Structure
  60. GC17848 Penciclovir HSV-1 DNA synthesis inhibitor Penciclovir  Chemical Structure
  61. GC49077 Podophyllotoxin-d6 An internal standard for the quantification of podophyllotoxin and picropodophyllotoxin Podophyllotoxin-d6  Chemical Structure
  62. GC62625 Pritelivir mesylate Pritelivir mesylate (BAY 57-1293 mesylate), an inhibitor of the viral helicase-primase complex, exhibits antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection. Pritelivir mesylate  Chemical Structure
  63. GC68050 Pritelivir mesylate hydrate Pritelivir mesylate hydrate  Chemical Structure
  64. GC46215 S-Acetyl-L-glutathione A derivative of glutathione S-Acetyl-L-glutathione  Chemical Structure
  65. GC49400 SN-011 A STING antagonist SN-011  Chemical Structure
  66. GC65198 Soyasapogenol C Soyasapogenol C is an oleanane-type triterpenoid. Soyasapogenol C  Chemical Structure
  67. GC61284 Soyasaponin II Soyasaponin II is a saponin with antiviral activity. Soyasaponin II  Chemical Structure
  68. GC46020 Stachybotrysin B A fungal metabolite with antiviral and anticancer activities Stachybotrysin B  Chemical Structure
  69. GC39448 Surfactin C1 A lipopeptide biosurfactant Surfactin C1  Chemical Structure
  70. GC13803 Triflurdine (Viroptic) Triflurdine (Viroptic) (Trifluorothymidine; 5-Trifluorothymidine; TFT) is an irreversible thymidylate synthase inhibitor, and thereby suppresses DNA synthesis. Triflurdine (Viroptic) is an antiviral drug for herpes simplex virus (HSV) infection. Trifluorothymidine also has anti-orthopoxvirus activity. Triflurdine (Viroptic)  Chemical Structure
  71. GC32214 Tromantadine Tromantadine hydrochloride, an Amantadine derivative with antiherpetic activity, inhibits herpes simplex virus type 1 (HSV-1) and HSV-2 replication. Tromantadine  Chemical Structure
  72. GC60373 Tromantadine hydrochloride Tromantadine hydrochloride, an Amantadine derivative with antiherpetic activity, inhibits herpes simplex virus type 1 (HSV-1) and HSV-2 replication. Tromantadine hydrochloride  Chemical Structure
  73. GC10955 Valaciclovir Valaciclovir  Chemical Structure
  74. GC30858 Valpromide Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. Valpromide  Chemical Structure
  75. GC13232 Verbascoside PKC/NF-κB inhibitor Verbascoside  Chemical Structure
  76. GC10082 Vidarabine antiviral drug for herpes viruses Vidarabine  Chemical Structure
  77. GC61785 Vidarabine monohydrate Vidarabine monohydrate is an adenine arabinoside. Vidarabine monohydrate  Chemical Structure
  78. GC46238 Yatein A lignan with diverse biological activities Yatein  Chemical Structure
  79. GA23863 Z-Leu-Val-Gly-diazomethylketone Z-Leu-Val-Gly-diazomethylketone is a cell-permeable and irreversible inhibitor of cysteine proteinase. Z-Leu-Val-Gly-diazomethylketone  Chemical Structure
  80. GC40902 Zerumbone Zerumbone is a natural monocyclic sesquiterpene first isolated from rhizomes of the wild ginger Z. Zerumbone  Chemical Structure

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