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Home >> Infectious Disease >> Viral Diseases

Viral Diseases

Products for  Viral Diseases

  1. Cat.No. Product Name Information
  2. GC49467 β-Aescin A triterpenoid saponin with diverse biological activities β-Aescin Chemical Structure
  3. GC40789 β-Cembrenediol

    β-CBD

     β-Cembrenediol (β-CBT) is a natural product from tobacco plants that is found in cigarette smoke condensate. β-Cembrenediol Chemical Structure
  4. GC41109 δ12-Prostaglandin J2

    Δ12PGJ2

     δ12-Prostaglandin J2 (δ12-PGJ2) is a cyclopentenone prostaglandin (PG) with anti-proliferative effect on various tumor cell growth. δ12-Prostaglandin J2, a naturally occurring dehydration product of prostaglandin D2, is able to induce apoptosis in HeLa cells via caspase activation. δ12-Prostaglandin J2 Chemical Structure
  5. GC52224 (±)-MMT5-14 A derivative of remdesivir with antiviral activity (±)-MMT5-14 Chemical Structure
  6. GC46304 (±)-Nebivolol-d4 (hydrochloride) A neuropeptide with diverse biological activities (±)-Nebivolol-d4 (hydrochloride) Chemical Structure
  7. GC49502 (-)-β-Sesquiphellandrene A sesquiterpene with antiviral and anticancer activities (-)-β-Sesquiphellandrene Chemical Structure
  8. GC45251 (-)-Neplanocin A S-Adenosylhomocysteine (SAH) hydrolase catalyzes the reversible hydrolysis of SAH to adenosine and homocysteine. (-)-Neplanocin A Chemical Structure
  9. GC65363 (1R)-Tenofovir amibufenamide

    (1R)-HS-10234

     (1R)-Tenofovir amibufenamide ((1R)-HS-10234) is the isomer of Tenofovir amibufenamide, is an orally active antiviral agent. (1R)-Tenofovir amibufenamide Chemical Structure
  10. GC64260 (2S,5S)-Censavudine

    (2S,5S)-OBP-601; (2S,5S)-BMS-986001

     (2S,5S)-Censavudine ((2S,5S)-OBP-601) is the (2S,5S)-enantiomer of Censavudine. (2S,5S)-Censavudine Chemical Structure
  11. GC41702 (E)-5-(2-Bromovinyl)uracil

    BVU

     (E)-5-(2-Bromovinyl)uracil (BVU) is a pyrimidine base and an inactive metabolite of the antiviral agents sorivudine and (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) that may be regenerated to BVDU in vivo. (E)-5-(2-Bromovinyl)uracil Chemical Structure
  12. GC49167 (R)-(+)-Trityl glycidyl ether

    (R)-Trityl Glycidol

     A synthetic precursor (R)-(+)-Trityl glycidyl ether Chemical Structure
  13. GC46352 (S)-DO271 An inactive control for DO264 (S)-DO271 Chemical Structure
  14. GC49294 1-(4-Chlorobenzhydryl)piperazine

    N-(p-Chlorobenzhydryl)-piperazine, Norchlorcyclizine, NSC 86164

     An inactive metabolite of meclizine and chlorcyclizine 1-(4-Chlorobenzhydryl)piperazine Chemical Structure
  15. GC46415 12-Bromododecanoic Acid

    12-Bromo-C12:0, 12-Bromododecanoate, 12-Bromolauric Acid, NSC 660375

     A halogenated form of lauric acid 12-Bromododecanoic Acid Chemical Structure
  16. GC72952 1E7-03 1E7-03, a low MW tetradroquinoline derivative targeting protein phosphatase-1, can inhibit HIV-1 transcription. 1E7-03 Chemical Structure
  17. GC49823 2′-C-β-Methylguanosine An active nucleoside metabolite of BMS-986094 2′-C-β-Methylguanosine Chemical Structure
  18. GC49514 2′-Deoxyuridine-d2

    Uracil deoxyribose-d2

     An internal standard for the quantification of 2’-deoxyuridine 2′-Deoxyuridine-d2 Chemical Structure
  19. GC41281 2'-C-Methyladenosine

    2-CMA

     2'-C-Methyladenosine is an inhibitor of hepatitis C virus (HCV) replication (IC50 = 0.3 μM in Huh-7 human hepatoma cells) that is not cytotoxic at concentrations up to 100 μM. 2'-C-Methyladenosine Chemical Structure
  20. GC46533 2-Amino-6-chloropurine

    6-Chloroguanine, NSC 29570

     A precursor in the synthesis of nucleoside analogs 2-Amino-6-chloropurine Chemical Structure
  21. GC42123 2-Aminopurine (hydrochloride)

    2-AP

     2-Aminopurine (hydrochloride) is a fluorescent analog of guanosine. 2-Aminopurine (hydrochloride) Chemical Structure
  22. 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
  23. GC40634 2-epi-Abamectin

    epi-Avermectin B1a

     2-epi-Abamectin is a degradation product of abamectin. 2-epi-Abamectin Chemical Structure
  24. GC42166 2-hydroxy Myristic Acid

    2-hydroxy Tetradecanoic Acid

     2-hydroxy Myristic acid is a hydroxy fatty acid that has been found in bovine, human, and horse milk, cow and buffalo cheeses, sea bass filet, seal oil, human vernix caseosa, and wool wax. 2-hydroxy Myristic Acid Chemical Structure
  25. GC46553 2-Nonylquinolin-4(1H)-one

    2-n-Nonyl-4-quinolone, 2-Nonyl-1H-quinolin-4-one, 2-Nonylquinolin-4(1H)-one, Pseudane IX

     A quinolone alkaloid with diverse biological activities 2-Nonylquinolin-4(1H)-one Chemical Structure
  26. GC52446 2-Nonylquinolin-4(1H)-one-d4

    2-n-Nonyl-4-quinolone-d4, 2-Nonyl-1H-quinolin-4-one-d4, 2-Nonylquinolin-4(1H)-one-d4, Pseudane IX-d4

     An internal standard for the quantification of 2-nonylquinolin-4(1H)-one 2-Nonylquinolin-4(1H)-one-d4 Chemical Structure
  27. GC41387 20-hydroxy Arachidic Acid

    ω-hydroxy Eicosanoic Acid

     20-hydroxy Arachidic acid is a hydroxylated fatty acid that has been found in the suberin component of silver birch (B. 20-hydroxy Arachidic Acid Chemical Structure
  28. GC48503 28-Deoxybetulin methyleneamine A derivative of betulin 28-Deoxybetulin methyleneamine Chemical Structure
  29. GC65085 3'-Azido-3'-deoxy-5-methylcytidine 3'-Azido-3'-deoxy-5-methylcytidine (CS-92) is a potent xenotropic murine leukemia-related retrovirus (XMRV) inhibitor with a CC50 of 43.5 μM in MCF-7 cells. 3'-Azido-3'-deoxy-5-methylcytidine Chemical Structure
  30. GC46608 4-(N-Boc-amino)piperidine

    4-(t-Butoxycarbonylamino)piperidine, 4-(tert-Butoxycarbonylamino)piperidine

     An organic building block 4-(N-Boc-amino)piperidine Chemical Structure
  31. GC46609 4-(Phenylcarbonyl)benzoic Acid

    4-Benzoylbenzoic Acid, 4-Carboxybenzophenone, NSC 37115, p-Benzoylbenzoic Acid, p-Carboxybenzophenone

     A photooxidant 4-(Phenylcarbonyl)benzoic Acid Chemical Structure
  32. GC42409 4-hydroxy Nebivolol (hydrochloride) 4-hydroxy Nebivolol is a major metabolite of nebivolol. 4-hydroxy Nebivolol (hydrochloride) Chemical Structure
  33. GC20095 5,7-Dihydroxy-4-methylcoumarin

    NSC 5302

    5,7-Dihydroxy-4-methylcoumarin is a coumarin derivative from Mexican tarragon. 5,7-Dihydroxy-4-methylcoumarin possesses antifungal and antibacterial activities.

     5,7-Dihydroxy-4-methylcoumarin Chemical Structure
  34. 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
  35. GC46721 6-Chloro-2-fluoropurine

    NSC 37363

     A heterocyclic building block 6-Chloro-2-fluoropurine Chemical Structure
  36. GC49749 6-Deoxypenciclovir

    BRL 42359

     An inactive metabolite of famciclovir 6-Deoxypenciclovir Chemical Structure
  37. GC46724 6-Hydroxypyridin-3-ylboronic Acid A heterocyclic building block 6-Hydroxypyridin-3-ylboronic Acid Chemical Structure
  38. GC63640 7-Hydroxyflavone

    NSC 94258, 7-hydroxy-2-Phenylchromone

     7-Hydroxyflavone is a flavonoid isolated from M. 7-Hydroxyflavone Chemical Structure
  39. GC52230 AA3-DLin

    An ionizable cationic amino lipid

     AA3-DLin Chemical Structure
  40. GC46767 Abacavir-d4 An internal standard for the quantification of abacavir Abacavir-d4 Chemical Structure
  41. GC46775 Abiraterone Acetate-d4

    CB-7630-d4

     A neuropeptide with diverse biological activities Abiraterone Acetate-d4 Chemical Structure
  42. GC46797 Acyclovir-d4

    ACV-d4

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

    PMEA-d4

     An internal standard for the quantification of adefovir Adefovir-d4 Chemical Structure
  44. GC90949 Adenosine-5'-O-(3-thiotriphosphate) (sodium salt)

    A P2Y11 receptor agonist

     Adenosine-5'-O-(3-thiotriphosphate) (sodium salt) Chemical Structure
  45. GC19792 ALC-0315 ALC-0315 is a key component of the COVID‐19mRNA vaccine and a highly sought-after lipid for nucleic acid therapeutics research . ALC-0315 Chemical Structure
  46. GC63814 Amantadine Amantadine (1-Adamantanamine) is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine Chemical Structure
  47. GC70262 Amitivir Amitivir (LY 217896), a thiadiazole derivative, possesses broad antiviral activity against orthomyxo- and paramyxoviruses. Amitivir Chemical Structure
  48. GC73805 Antiviral agent 55 Antiviral agent 55 (Compound 95) is an inhibitor for human immunodeficiency virus 1 and 2 (HIV 1 and HIV 2), and exhibits antiviral activity. Antiviral agent 55 Chemical Structure
  49. GC68678 APOBEC3G-IN-1

    APOBEC3G-IN-1 (MN136.0185) is a potent HIV inhibitor that targets APOBEC3G.

     APOBEC3G-IN-1 Chemical Structure
  50. GC72208 Asp-Asp-Asp-Asp-Asp-Asp Asp-Asp-Asp-Asp-Asp-Asp is a polyaspartic acid. Asp-Asp-Asp-Asp-Asp-Asp Chemical Structure
  51. GC73486 Atevirdine Atevirdine is a potent non-nucleoside HIV-1 reverse transcriptase inhibitor. Atevirdine Chemical Structure
  52. GC46895 Aurintricarboxylic Acid (ammonium salt)

    ATA

     A protein synthesis inhibitor with diverse biological activities Aurintricarboxylic Acid (ammonium salt) Chemical Structure
  53. GC65963 AzddMeC

    CS-92

     AzddMeC (CS-92) is an antiviral nucleoside analogue and a potent potent, selective and orally active HIV-1 reverse transcriptase and HIV-1 replication inhibitor. In HIV-1-infected human PBM cells and HIV-1-infected human macrophages, the EC50 values of AzddMeC are 9 nM and 6 nM, respectively. AzddMeC Chemical Structure
  54. GC49057 Azelastine-13C-d3 (hydrochloride) An internal standard for the quantification of azelastine Azelastine-13C-d3 (hydrochloride) Chemical Structure
  55. GC46902 Azithromycin-13C-d3

    CP 62993-13C,d3

     A neuropeptide with diverse biological activities Azithromycin-13C-d3 Chemical Structure
  56. GC46903 Azithromycin-d3 An internal standard for the quantification of azithromycin Azithromycin-d3 Chemical Structure
  57. GC68719 AZT triphosphate tetraammonium

    3'-Azido-3'-deoxythymidine-5'-triphosphate tetraammonium

    AZT triphosphate (3'-Azido-3'-deoxythymidine-5'-triphosphate) tetraammonium is an active metabolite of Zidovudine (AZT). AZT triphosphate tetraammonium has antiretroviral activity and inhibits HIV replication. It can also inhibit HBV DNA polymerase. AZT triphosphate tetraammonium can activate the mitochondrial-mediated apoptosis pathway.

     AZT triphosphate tetraammonium Chemical Structure
  58. GC73412 BDM-2 BDM-2 is an IN-LEDGF allosteric inhibitor (INLAI) of HIV-1 integrase (IN refers to integrase) (IC50=47 nM) with potent anti-Retroviral (ARV) activity. BDM-2 Chemical Structure
  59. GC48458 Betulinic glycine amide A derivative of betulinic acid Betulinic glycine amide Chemical Structure
  60. GC52326 Biotin-PEG4-LL-37 (human) (trifluoroacetate salt) A biotinylated and pegylated form of LL-37 Biotin-PEG4-LL-37 (human) (trifluoroacetate salt) Chemical Structure
  61. GC68779 BMS-433771

    BMS-433771 is an effective oral respiratory syncytial virus (RSV) inhibitor. It is effective against both A and B groups of RSV, with an EC50 mean value of 20 nM. BMS-433771 can be used for research on respiratory diseases.

     BMS-433771 Chemical Structure
  62. GC68780 BMS-433771 dihydrochloride hydrate

    BMS-433771 dihydrochloride hydrate is an effective inhibitor of respiratory syncytial virus (RSV) with oral activity. It is effective against both group A and B RSV, with an EC50 average of 20 nM. BMS-433771 dihydrochloride hydrate can be used for research on respiratory diseases.

     BMS-433771 dihydrochloride hydrate Chemical Structure
  63. GC46937 Boc-Glu-OBzl An amino acid-containing building block Boc-Glu-OBzl Chemical Structure
  64. GC46936 Boceprevir-d9 An internal standard for the quantification of boceprevir Boceprevir-d9 Chemical Structure
  65. 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
  66. GA21221 Bz-Nle-Lys-Arg-Arg-AMC

    Benzoyl-Nle-Lys-Arg-Arg-AMC, Benzoyl-Nle-Lys-Arg-Arg-7-amino-4-methylcoumarin, Bz-Nle-Lys-Arg-Arg-AMC

     Bz-Nle-Lys-Arg-Arg-AMC is a fluorogenic tetra-peptide substrate for yellow fever virus (YFV) non-structural 3 (NS3), dengue virus (DV) NS2B/3 serine proteases, and Zika virus (ZIKV) NS2B/NS3 serine proteases. Bz-Nle-Lys-Arg-Arg-AMC Chemical Structure
  67. GC91145 C12-113

    An ionizable cationic lipidoid

     C12-113 Chemical Structure
  68. GC90987 C12-SPM

    A polyamine branched-chain lipidoid

     C12-SPM Chemical Structure
  69. GC71273 C12-TLRa C12-TLRa is an adjuvant lipidoid. C12-TLRa Chemical Structure
  70. GC43071 C22 Sphingomyelin (d18:1/22:0)

    SM(d18:1/22:0), Sphingomyelin (d18:1/22:0), N-docosanoyl-D-erythro-Sphingosylphosphorylcholine

     C22 Sphingomyelin is a naturally occurring form of sphingomyelin. C22 Sphingomyelin (d18:1/22:0) Chemical Structure
  71. GC68449 CA inhibitor 1

    GS-6207 analog

     CA inhibitor 1 Chemical Structure
  72. GC66051 Cabotegravir sodium

    GSK-1265744 sodium; S/GSK1265744 sodium

     Cabotegravir (GSK-1265744) sodium is a orally active and long-acting HIV integrase inhibitor and organic anion transporter 1/3 (OAT1/OAT3) inhibitor with IC50 values of 2.5 nM, 0.41 μM and 0.81 μM for HIVADA, OAT3 and OAT1, respectively. Cabotegravir sodium is primarily metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A1, with low potential to interact with other antiretroviral drugs (ARVs). Cabotegravir sodium can be used to research AIDS. Cabotegravir sodium Chemical Structure
  73. GC47022 Camostat-d6 (hydrochloride) A neuropeptide with diverse biological activities Camostat-d6 (hydrochloride) Chemical Structure
  74. GC18322 CAY10567

    BML257

     Akt1, 2, and 3 are serine/threonine protein kinases in the phosphatidylinositol 3 (PI3)-kinase signalling pathway that play a critical role in the regulation of cell proliferation and survival. CAY10567 Chemical Structure
  75. GC43196 CAY10704 CAY10704 is a potent inhibitor of hepatitis C virus (HCV) infection (EC50 = 17 nM) that displays low cytotoxicity of virally-infected human hepatoma Huh7.5.1 cells (CC50 = 21.3 μM). CAY10704 Chemical Structure
  76. GC64261 Censavudine

    OBP-601; BMS-986001

     Censavudine (OBP-601; BMS-986001), a nucleoside analog, is a nucleoside reverse transcriptase inhibitor. Censavudine Chemical Structure
  77. GC45885 Chloroquine-d5 (phosphate)

    DL-Chloroquine-d5

     An internal standard for the quantification of chloroquine Chloroquine-d5 (phosphate) Chemical Structure
  78. GC71694 Chloroxylenol-d6 Chloroxylenol-d6 is the deuterium labeled Chloroxylenol. Chloroxylenol-d6 Chemical Structure
  79. GC66467 Claficapavir

    A1752

     Claficapavir (A1752) is a specific nucleocapsid protein (NC) inhibitor with an IC50 around 1 μM. Claficapavir strongly binds the HIV-1 NC (Kd=20 nM) thereby inhibiting the chaperone properties of NC and leading to good antiviral activity against the HIV-1. Claficapavir Chemical Structure
  80. GC70227 Clathrin-IN-1 Clathrin-IN-1 is a selective clathrin-mediated endocytosis (CME) inhibitor. Clathrin-IN-1 Chemical Structure
  81. GC68881 Clemastanin B

    Clemastanin B is a lignin that has strong anti-influenza activity by inhibiting virus proliferation, preventing and blocking virus attachment. Clemastanin B targets the internalization of viruses, uncoating or ribonucleoprotein (RNP) export from the cell nucleus. It also has antioxidant and anti-inflammatory activities.

     Clemastanin B Chemical Structure
  82. GC68883 Clesrovimab

    MK1654

    Clesrovimab (MK1654) is a fully human monoclonal antibody against respiratory syncytial virus fusion (RSV F) glycoprotein. Clesrovimab has the potential to study respiratory syncytial virus infections.

     Clesrovimab Chemical Structure
  83. GC18799 CPD77 CPD77is a racemate of X77. CPD77 Chemical Structure
  84. GC25306 CQ31

    CQ31, a small molecule, selectively activates caspase activation and recruitment domain-containing 8 (CARD8).

     CQ31 Chemical Structure
  85. GC47128 CU-32 A cGAS inhibitor CU-32 Chemical Structure
  86. GC64348 Cyanidin 3-sambubioside chloride Cyanidin 3-sambubioside chloride (Cyanidin-3-O-sambubioside chloride), a major anthocyanin, a natural colorant, and is a potent NO inhibitor. Cyanidin 3-sambubioside chloride Chemical Structure
  87. GC64068 Cyclotriazadisulfonamide Cyclotriazadisulfonamide (CADA) is a specific CD4-targeted HIV entry inhibitors. Cyclotriazadisulfonamide Chemical Structure
  88. GC68930 Cys-TAT(47-57) TFA

    Cys-[HIV-Tat (47-57)] TFA

    Cys-TAT(47-57) (Cys-[HIV-Tat (47-57)]) is a twelve-peptide rich in arginine that can penetrate cells and is a derivative of HIV-1 transactivator protein.

     Cys-TAT(47-57) TFA Chemical Structure
  89. GC45800 Cytarabine-13C3

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

     A neuropeptide with diverse biological activities Cytarabine-13C3 Chemical Structure
  90. GC43368 D,L-1′-Acetoxychavicol Acetate

    ACA, 1'-Acetoxychavicol Acetate, Galangal Acetate

     D,L-1′-Acetoxychavicol acetate is a natural compound first isolated from the rhizomes of ginger-like plants. D,L-1′-Acetoxychavicol Acetate Chemical Structure
  91. GC47266 D-Ornithine lactam

    (R)-3-Aminopiperidin-2-one

     A building block D-Ornithine lactam Chemical Structure
  92. GC45883 Daclatasvir-d6

    BMS-790052-d6; EBP 883-d6

     An internal standard for the quantification of daclatasvir Daclatasvir-d6 Chemical Structure
  93. GC64391 DDX3-IN-2 DDX3-IN-2 is an active DEADbox polypeptide 3 (DDX3) inhibitor with an IC50 value of 0.3 μM. DDX3-IN-2 Chemical Structure
  94. GC64270 Decanoyl-RVKR-CMK TFA

    DecRVKRcmk TFA

     Decanoyl-RVKR-CMK (DecRVKRcmk) TFA inhibits over-expressed gp160 processing and HIV-1 replication. Decanoyl-RVKR-CMK TFA Chemical Structure
  95. GC46130 Destruxin B2 A mycotoxin with antiviral, insecticidal, and phytotoxic activities Destruxin B2 Chemical Structure
  96. 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
  97. GC74090 Dimethyl fumarate-d2 Dimetl fumarate-d2 is the deuterium labeled Dimetl fumarate. Dimethyl fumarate-d2 Chemical Structure
  98. GC72450 Diridavumab Diridavumab is a monoclonal anti-HA stalk antibody. Diridavumab Chemical Structure
  99. GC45995 DO264 An ABHD12 inhibitor DO264 Chemical Structure
  100. GC70661 Dolutegravir-d3 Dolutegravir-d3 is the deuterium labeled Dolutegravir. Dolutegravir-d3 Chemical Structure
  101. GC70800 EFdA-TP tetrasodium EFdA-TP tetrasodium is a potent nucleoside reverse transcriptase (RT) inhibitor. EFdA-TP tetrasodium Chemical Structure

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