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Home >> Signaling Pathways >> Microbiology & Virology >> HSV

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

    (9Z)-Hexadecen-1-ol, cis-9-Hexadecenol, Palmitoleyl Alcohol, (Z)-9-Hexadecen-1-ol, Z9-16:OH

     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

    16,16dimethyl PGA1

     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

    Uracil deoxyribose-d2

     An internal standard for the quantification of 2’-deoxyuridine 2′-Deoxyuridine-d2 Chemical Structure
  10. GC17430 2-Deoxy-D-glucose

    2-DG

     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-DG-d1; 2-Deoxy-D-arabino-hexose-d1; D-Arabino-2-deoxyhexose-d1

    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

    2’,3’-Dideoxythymidine, d2T, ddThd

     An antiviral nucleoside analog 3′-deoxy Thymidine Chemical Structure
  13. GC40641 5'-Ethynyl-2'-deoxycytidine

    EdC, 2'-deoxy-5-Ethynylcytidine

     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

    BRL 42359

     An inactive metabolite of famciclovir 6-Deoxypenciclovir Chemical Structure
  17. GC17186 Acyclovir

    ACV, BW 248U, NSC 645011

     Acyclovir is a potent oral antiviral drug. Acyclovir has anti-herpetic activity with IC50 values ​​of 0.85 μM and 0.86 μM for HSV-1 and HSV-2, respectively. Acyclovir induces cell cycle disruption and apoptosis. Acyclovir Chemical Structure
  18. GC46797 Acyclovir-d4

    ACV-d4

     An internal standard for the quantification of acyclovir Acyclovir-d4 Chemical Structure
  19. GC46805 Adefovir-d4

    PMEA-d4

     An internal standard for the quantification of adefovir Adefovir-d4 Chemical Structure
  20. GC19028 Amenamevir

    ASP2151

     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

    6-Bromoindirubin-3'-acetoxime, GSK3 Inhibitor X

    GSK-3α/β inhibitor

     BIO-acetoxime Chemical Structure
  24. GC17683 Brefeldin A

    Ascotoxin, BFA, Cyanein, Decumbin, Nectrolide, NSC 56310, NSC 89671, NSC 107456, NSC 244390, Synergisidin

     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. GC72705 BVDU 5′-Triphosphate ammonium BVDU 5′-Triphosphate ammonium is an antivirus agent with 5′-Triphosphate label, targeting viral DNA polymerase. BVDU 5′-Triphosphate ammonium Chemical Structure
  27. GC45413 Cridanimod (sodium salt)

    10-Carboxymethyl-9-Acridanone

       Cridanimod (sodium salt) Chemical Structure
  28. 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
  29. GC49863 Cytarabine 5′-monophosphate

    ara-CMP, 1-β-D-Arabinofuranosylcytosine 5'-monophosphate, Cytosine Arabinoside monophosphate, NSC 99445

     An active metabolite of cytarabine Cytarabine 5′-monophosphate Chemical Structure
  30. GC45800 Cytarabine-13C3

    Ara-C-13C3, 1-β-D-Arabinofuranosylcytosine-13C3

     A neuropeptide with diverse biological activities Cytarabine-13C3 Chemical Structure
  31. GC49153 Didemnin B

    NSC 325319, NSC 333841

     Didemnin B is a cyclic depsipeptide produced by marine tunicates that specifically binds the GTP-bound conformation of EEF1A, inhibiting its release from the ribosomal A site and preventing subsequent peptide elongation. Didemnin B Chemical Structure
  32. GC12881 Docosanol (Abreua)

    Behenyl Alcohol, n-Docosanol, Docosyl Alcohol, NSC 8407

     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
  33. GC30286 Docusate Sodium (Dioctyl sulfosuccinate sodium salt)

    Aerosol OT, AOT, Dioctyl sulfosuccinate, DOSS, KM 10-1610

     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
  34. GC47285 Elaidyl Alcohol

    NSC 72786, trans-9-Octadecenoyl Alcohol

     A monounsaturated fatty alcohol Elaidyl Alcohol Chemical Structure
  35. GC17947 Famciclovir

    BRL 42810

     Anti-herpesvirus oral prodrug of penciclovir Famciclovir Chemical Structure
  36. GC71512 Famciclovir-d4 Famciclovir-d4 is the deuterium labeled Famciclovir. Famciclovir-d4 Chemical Structure
  37. 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
  38. GC11943 Fialuridine

    FIAU,Fluoroiodoarauracil,5-Iodo-2’-Fluoroarauracil,NSC 678514

     nucleoside analog with antiviral activity Fialuridine Chemical Structure
  39. GC39811 FIT-039 FIT-039 is a selective, ATP-competitive and orally active CDK9 inhibitor with an IC50 of 5.8 μM for CKD9/cyclin T1. FIT-039 Chemical Structure
  40. 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
  41. GC67733 Gallic aldehyde Gallic aldehyde Chemical Structure
  42. GC11331 Ganciclovir

    BW 759, 2'Nor2'deoxyguanosine

     Antiviral drug for CMV infections Ganciclovir Chemical Structure
  43. GC60865 Ganciclovir sodium Ganciclovir (BW 759) sodium, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir sodium Chemical Structure
  44. GC49228 Ganoderol B

    Ganodermadiol, (+)-Ganoderol B

     A triterpenoid with diverse biological activities Ganoderol B Chemical Structure
  45. GN10156 Ginsenoside Rb1

    Gypenoside III, NSC 310103

     Ginsenoside Rb1 Chemical Structure
  46. GC38915 Glyceryl monocaprate Glyceryl monocaprate (Monolaurin) is a 1-monoglyceride of capric acid against gram-positive bacterial infections. Glyceryl monocaprate Chemical Structure
  47. GC74237 Guanosine-13C10,15N5

    DL-Guanosine-13C10,15N5; Vernine-13C10,15N5

     Guanosine-13C10,15N5 is the 13C and 15N labeled Guanosine. Guanosine-13C10,15N5 Chemical Structure
  48. GC74038 HN0037 HN0037 is a selective and orally active helicase-primase inhibitor. HN0037 Chemical Structure
  49. 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
  50. GC13247 Idoxuridine

    5-iodo-2′-deoxyuridine, NSC 39661, SKF 14287

     Antiviral agent Idoxuridine Chemical Structure
  51. GC16407 Imiquimod

    R-837, S-26308, TMX 101

    TLR-7 agonist,immunomodulator with antiviral and antitumor activity

     Imiquimod Chemical Structure
  52. GC47453 Imiquimod-d9

    R 837-d9

     A neuropeptide with diverse biological activities Imiquimod-d9 Chemical Structure
  53. GC69291 Isatin-β-thiosemicarbazone

    IBT

    Isatin-beta-thiosemicarbazone is an effective anti-poxvirus agent (including monkeypox virus, variola virus, cowpox virus, etc.). Isatin-beta-thiosemicarbazone is also an effective inhibitor of herpes simplex virus (HSV). Isatin-beta-thiosemicarbazone has antiviral activity against both HSV-1 and HSV-2.

     Isatin-β-thiosemicarbazone Chemical Structure
  54. GC40668 Isoborneol

    (±)-Isoborneol, DL-Isoborneol, Isobornyl Alcohol, NSC 26350

     Isoborneol is a monoterpene alcohol that has been found in a variety of plants, including C. Isoborneol Chemical Structure
  55. 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
  56. GC49382 L-Lysine-d3 (hydrochloride) An internal standard for the quantification of L-lysine L-Lysine-d3 (hydrochloride) Chemical Structure
  57. GC47584 L-Valacyclovir-d8 (hydrochloride) An internal standard for the quantification of valacyclovir L-Valacyclovir-d8 (hydrochloride) Chemical Structure
  58. GC19219 LDC4297 LDC4297 is a potent and selective CDK7 inhibitor with an IC50 of 0.13 nM. LDC4297 Chemical Structure
  59. GC90483 Magainin 1 (trifluoroacetate salt)

    An antimicrobial cationic peptide

     Magainin 1 (trifluoroacetate salt) Chemical Structure
  60. GC90544 Magainin 2 (trifluoroacetate salt)

    An antimicrobial cationic peptide

     Magainin 2 (trifluoroacetate salt) Chemical Structure
  61. GC46169 Mer-NF5003F

    F 1839M, NF 5003F, Stachybotrydial

     A sesquiterpene with diverse biological activities Mer-NF5003F Chemical Structure
  62. GC12557 ML324

    CID-44143209

     JMJD2 demethylase inhibitor, potent and cell-permeable ML324 Chemical Structure
  63. GC18769 MST-312

    Telomerase Inhibitor IX

     MST312 is a telomerase inhibitor (IC50 = 0.67 μM in a TRAP assay). MST-312 Chemical Structure
  64. GC47760 Nebularine

    Desaminoadenosine, NSC 65423, Purine riboside, Purinosine, Ribosylpurine

     A purine ribonucleoside with diverse biological activities Nebularine Chemical Structure
  65. GC17314 OG-L002 LSD1 inhibitor,potent and specific OG-L002 Chemical Structure
  66. GC48652 Olomoucine II A CDK inhibitor Olomoucine II Chemical Structure
  67. GC61771 Omaciclovir

    H2G

     Omaciclovir (H2G) is a potent and selective inhibitor of herpesvirus replication. Omaciclovir Chemical Structure
  68. GC47828 Oosporein

    NSC 88466

     A mycotoxin with diverse biological activities Oosporein Chemical Structure
  69. GC33464 Oxyresveratrol (trans-Oxyresveratrol)

    trans2',3,4',5Tetramethoxystilbene

     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
  70. GC61164 Oxytetracycline hydrochloride Oxytetracycline hydrochloride is an antibiotic belonging to the tetracycline class. Oxytetracycline hydrochloride Chemical Structure
  71. GC91296 p-Carboxyphenyl Sulfate

    A sulfated phenolic acid

     p-Carboxyphenyl Sulfate Chemical Structure
  72. GC17848 Penciclovir

    BRL 39123

     HSV-1 DNA synthesis inhibitor Penciclovir Chemical Structure
  73. GC49077 Podophyllotoxin-d6

    PPT-d6

     An internal standard for the quantification of podophyllotoxin and picropodophyllotoxin Podophyllotoxin-d6 Chemical Structure
  74. 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
  75. GC68050 Pritelivir mesylate hydrate

    AIC316 mesylate hydrate; BAY 57-1293 mesylate hydrate

     Pritelivir mesylate hydrate Chemical Structure
  76. GC90883 Purine riboside-5'-O-triphosphate (sodium salt)

    An active metabolite of nebularine

     Purine riboside-5'-O-triphosphate (sodium salt) Chemical Structure
  77. GC46215 S-Acetyl-L-glutathione

    S-Acetylglutathione

     A derivative of glutathione S-Acetyl-L-glutathione Chemical Structure
  78. GC49400 SN-011

    GUN35901

     A STING antagonist SN-011 Chemical Structure
  79. GC65198 Soyasapogenol C Soyasapogenol C is an oleanane-type triterpenoid. Soyasapogenol C Chemical Structure
  80. GC61284 Soyasaponin II Soyasaponin II is a saponin with antiviral activity. Soyasaponin II Chemical Structure
  81. GC46020 Stachybotrysin B A fungal metabolite with antiviral and anticancer activities Stachybotrysin B Chemical Structure
  82. GC90785 STING Agonist 23

    A STING agonist

     STING Agonist 23 Chemical Structure
  83. GC39448 Surfactin C1 A lipopeptide biosurfactant Surfactin C1 Chemical Structure
  84. GC90702 Triciribine Phosphate

    An Akt activation inhibitor and active metabolite of triciribine

     Triciribine Phosphate Chemical Structure
  85. GC13803 Triflurdine (Viroptic)

    NSC 75520, NSC 529182, TFT, Trifluridine

     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
  86. 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
  87. 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
  88. GC10955 Valaciclovir Valaciclovir Chemical Structure
  89. GC11698 Valaciclovir HCl

    BW 256U, BW 256U87

     Valaciclovir HCl (Valaciclovir hydrochloride) is an orally active antiviral drug for herpes simplex, herpes zoster, and herpes B. Valaciclovir HCl Chemical Structure
  90. GC30858 Valpromide Valpromide is an amide derivative of valproic acid and inhibits human epoxide hydrolase. Valpromide Chemical Structure
  91. GC13232 Verbascoside

    Acteoside, NSC 603831

     PKC/NF-κB inhibitor Verbascoside Chemical Structure
  92. GC10082 Vidarabine

    Adenine Arabinoside, Ara-A, 9-β-D-Arabinofuranosyl adenine, Arabinosyladenine, NSC 247519, NSC 404241, Vira-A

     antiviral drug for herpes viruses Vidarabine Chemical Structure
  93. GC61785 Vidarabine monohydrate Vidarabine monohydrate is an adenine arabinoside. Vidarabine monohydrate Chemical Structure
  94. GC40740 WHI-P258 WHI-P258 is a quinazoline compound that modeling studies suggested would bind to the active site of JAK3 with an estimated Ki value of 72 μM. WHI-P258 Chemical Structure
  95. GC46238 Yatein

    Deoxypodorhizone, (-)-Yatein

     A lignan with diverse biological activities Yatein Chemical Structure
  96. 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
  97. GC40902 Zerumbone Zerumbone is a natural monocyclic sesquiterpene first isolated from rhizomes of the wild ginger Z. Zerumbone Chemical Structure

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