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Microbiology & Virology

Microbiology & Virology

Microbiology & Virology

A virus is a small infectious agent that replicates inside living cells. Viruses cause many human diseases from small illnesses, like influenza, to more deadly diseases, like hepatitis B and HIV. Our body’s immune system defends against viral infection by generating specific antibodies to bind to and neutralize viral particles and by cell mediated immunity that destroys infected host cells.

Products for  Microbiology & Virology

  1. Cat.No. Product Name Information
  2. GC68473 Methyl carnosate Methyl carnosate  Chemical Structure
  3. GC68471 Nifurpirinol Nifurpirinol  Chemical Structure
  4. GC68465 SDH-IN-1 SDH-IN-1  Chemical Structure
  5. GC68457 Mab Aspartate Decarboxylase-IN-1 Mab Aspartate Decarboxylase-IN-1  Chemical Structure
  6. GC68449 CA inhibitor 1 CA inhibitor 1  Chemical Structure
  7. GC68428 Rimantadine-d4 hydrochloride Rimantadine-d4 hydrochloride  Chemical Structure
  8. GC68408 (R)-Praziquantel-d11 (R)-Praziquantel-d11  Chemical Structure
  9. GC68403 Dusquetide Dusquetide  Chemical Structure
  10. GC68402 Danofloxacin-d3 Danofloxacin-d3  Chemical Structure
  11. GC68401 Lehmannine Lehmannine  Chemical Structure
  12. GC68359 Pefloxacin-d5 Pefloxacin-d5  Chemical Structure
  13. GC68315 Salannin Salannin  Chemical Structure
  14. GC68300 Palivizumab Palivizumab  Chemical Structure
  15. GC68297 Bepirovirsen Bepirovirsen  Chemical Structure
  16. GC68286 Motavizumab Motavizumab  Chemical Structure
  17. GC68233 3-Aminobutanoic acid 3-Aminobutanoic acid  Chemical Structure
  18. GC68217 HCV-IN-30 HCV-IN-30  Chemical Structure
  19. GC68208 Salazopyridazine Salazopyridazine  Chemical Structure
  20. GC68144 Ticlatone Ticlatone  Chemical Structure
  21. GC68050 Pritelivir mesylate hydrate Pritelivir mesylate hydrate  Chemical Structure
  22. GC68026 SSAA09E3 SSAA09E3  Chemical Structure
  23. GC68023 HIV-1 inhibitor-48 HIV-1 inhibitor-48  Chemical Structure
  24. GC68005 Ceftobiprole medocaril sodium Ceftobiprole medocaril sodium  Chemical Structure
  25. GC67986 AMOZ-d5 AMOZ-d5  Chemical Structure
  26. GC67965 XR8-89 XR8-89  Chemical Structure
  27. GC67953 PNU-101603 PNU-101603  Chemical Structure
  28. GC67945 Sulfadimethoxine-d6 Sulfadimethoxine-d6  Chemical Structure
  29. GC67943 Triclosan-methyl-d3 Triclosan-methyl-d3  Chemical Structure
  30. GC67935 Sulfadoxine D3 Sulfadoxine D3  Chemical Structure
  31. GC67931 (+)-Medioresinol (+)-Medioresinol  Chemical Structure
  32. GC67913 Antiviral agent 5 Antiviral agent 5  Chemical Structure
  33. GC67842 Erythromycin thiocyanate Erythromycin thiocyanate  Chemical Structure
  34. GC67794 PA3552-IN-1 PA3552-IN-1  Chemical Structure
  35. GC67793 SARS-CoV-2-IN-13 SARS-CoV-2-IN-13  Chemical Structure
  36. GC67773 Levonadifloxacin Levonadifloxacin  Chemical Structure
  37. GC67756 Fomivirsen Fomivirsen  Chemical Structure
  38. GC67754 Molnupiravir-d7 Molnupiravir-d7  Chemical Structure
  39. GC67746 o-Vanillin o-Vanillin  Chemical Structure
  40. GC67733 Gallic aldehyde Gallic aldehyde  Chemical Structure
  41. GC67696 PRRSV/CD163-IN-1 PRRSV/CD163-IN-1  Chemical Structure
  42. GC67684 RSV-IN-7 RSV-IN-7  Chemical Structure
  43. GC52501 2',3'-Dideoxyadenosine 5'-triphosphate (lithium salt) An inhibitor of reverse transcriptases and DNA polymerases 2',3'-Dideoxyadenosine 5'-triphosphate (lithium salt)  Chemical Structure
  44. GC52492 Globotriaosylceramide (hydroxy) (porcine RBC) A sphingolipid Globotriaosylceramide (hydroxy) (porcine RBC)  Chemical Structure
  45. GC52491 Globotriaosylceramide (non-hydroxy) (porcine RBC) A sphingolipid Globotriaosylceramide (non-hydroxy) (porcine RBC)  Chemical Structure
  46. GC52468 Benanomicin B A microbial metabolite with antifungal, fungicidal, and antiviral activities Benanomicin B  Chemical Structure
  47. GC52427 Apelin-12 (human, mouse, rat, bovine) (acetate) An endogenous agonist of the APJ receptor Apelin-12 (human, mouse, rat, bovine) (acetate)  Chemical Structure
  48. GC52403 Ivermectin-d2 An internal standard for the quantification of ivermectin Ivermectin-d2  Chemical Structure
  49. GC52395 Indolicidin (trifluoroacetate salt) An antimicrobial peptide Indolicidin (trifluoroacetate salt)  Chemical Structure
  50. 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
  51. GC52315 GK241 An sPLA2 (Type IIA) inhibitor GK241  Chemical Structure
  52. GC52272 Jun9-72-2 A SARS-CoV-2 PLpro inhibitor Jun9-72-2  Chemical Structure
  53. GC52230 AA3-DLin An ionizable cationic amino lipid AA3-DLin  Chemical Structure
  54. GC52224 (±)-MMT5-14 A derivative of remdesivir with antiviral activity (±)-MMT5-14  Chemical Structure
  55. GC67632 ANS ammonium ANS ammonium is a potent antibacterial agent and a textile dye. ANS ammonium can be used as fluorescence probe. ANS ammonium blocks the binding of triiodothyronine to thyroxine binding globulin in radioimmunoassay of triiodothyronine. ANS ammonium  Chemical Structure
  56. GC67627 2'-Deoxy-5'-O-DMT-2'-fluorouridine 2'-Deoxy-5'-O-DMT-2'-fluorouridine, a nucleoside analogue, is a 5'-O-DMTr-5-FUDR derivative with potent anti-yellow fever (YFV) activity. 2'-Deoxy-5'-O-DMT-2'-fluorouridine  Chemical Structure
  57. GC67542 L-Azatyrosine L-Azatyrosine is an antitumor antibiotic isolated from Streptomyces chibaensis. L-Azatyrosine can restore normal phenotypic behavior to transformed cells bearing oncogenic Ras genes. L-Azatyrosine  Chemical Structure
  58. GC67328 2'-Deoxy-L-adenosine 2'-Deoxy-L-adenosine is an orally active synthon for modified oligodeoxyribonucleotides. 2'-Deoxy-L-adenosine is a potent, specific and selective inhibitor of the replication of hepatitis B virus (HBV) as well as the closely related duck and woodchuck hepatitis viruses (WHV). 2'-Deoxy-L-adenosine  Chemical Structure
  59. GC67195 Vidarabine phosphate Vidarabine phosphate (Ara-AMP), an antiviral agent, inhibits chronic HBV infection. Vidarabine phosphate also against herpes simplex and varicella zoster viruses. Vidarabine phosphate  Chemical Structure
  60. GC66890 2',3'-Dideoxy-5-iodocytidine 2',3'-Dideoxy-5-iodocytidine is used for gene sequencing can be used as an antibiotic. 2',3'-Dideoxy-5-iodocytidine is particular effective against Mycobacterium. 2',3'-Dideoxy-5-iodocytidine  Chemical Structure
  61. GC66467 Claficapavir 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
  62. GC66444 Eugenol-d3 Eugenol-d3 is the deuterium labeled Eugenol. Eugenol is an essential oil found in cloves with antibacterial, anthelmintic and antioxidant activity. Eugenol is shown to inhibit lipid peroxidation. Eugenol-d3  Chemical Structure
  63. GC66412 2-Hydroxy-1-methoxyanthraquinone 2-Hydroxy-1-methoxyanthraquinone could be isolated from the stem bark of Morinda lucida Benth. (Rubiaceae) and possesses antibacterial activity. 2-Hydroxy-1-methoxyanthraquinone  Chemical Structure
  64. GC66398 Thiabendazole-d4 Thiabendazole-d4 is the deuterium labeled EIDD-1931. EIDD-1931 (Beta-d-N4-hydroxycytidine; NHC) is a novel nucleoside analog and behaves as a potent anti-virus agent. EIDD-1931 effectively inhibits the replication activity of venezuelan equine encephaliti Thiabendazole-d4  Chemical Structure
  65. GC66395 CRS3123 dihydrochloride CRS3123 (REP-3123) dihydrochloride, a fully synthetic antibacterial agent, potently inhibits methionyl-tRNA synthetase (MetRS) of Clostridioides difficile, inhibiting Clostridioides difficile toxin production and spore formation. CRS3123 dihydrochloride is an oral agent for the research of Clostridioides difficile infection (CDI). CRS3123 dihydrochloride  Chemical Structure
  66. GC66376 Pirimiphos-methyl-d6 Pirimiphos-methyl-d6 is the deuterium labeled Pirimiphos-methyl. Pirimiphos-methyl is a rapid-acting organophosphorus insecticide and acaricide, causing inhibition of AChE in target organisms. Pirimiphos-methyl is often used for prevention and control of beetles, snout beetles, moths and Ephestia cautella during storage of agricultural grains. Pirimiphos-methyl-d6  Chemical Structure
  67. GC66366 Kansuinine B Kansuinine B inhibits IL-6-induced Stat3 activation. Kansuinine B possesses anti-viral activity and could be used in the study for COVID-19. Kansuinine B  Chemical Structure
  68. GC66340 β-Amyrone β-Amyrone (β-Amyron) is a triterpene compound which has anti-inflammatory activity through inhibiting the expression of COX-2. β-Amyrone has antifungal activity , as well as antiviral activity against Chikungunya virus. β-Amyrone also inhibits α-glucosidase and acetylcholinesterase (AChE) activity. β-Amyrone can be used in the research of disease like inflammation, infection, and obesity. β-Amyrone  Chemical Structure
  69. 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
  70. GC66241 Anti-MERS-D12 mAb Anti-MERS-D12 mAb (MERS-D12; MERS Antibody-D12) is a human monoclonal IgG1. Anti-MERS-D12 mAb binds directly to the DPP4 interacting region of the MERS-CoV Spike receptor binding domain (RBD) and effect neutralization by directly blocking receptor binding. Anti-MERS-D12 mAb  Chemical Structure
  71. GC66074 Methylprednisolone succinate sodium Methylprednisolone succinate (Methylprednisolone hydrogen succinate) sodium is a glucocorticoid of slightly longer half-life than that of Prednisolone. Methylprednisolone succinate sodium  Chemical Structure
  72. GC66070 TBT1 TBT1 is a first-generation inhibitor of the MsbA transporter. TBT1 is an LPS transport inhibitor and MsbA ATPase stimulator in strains from the Acinetobacter genus. TBT1 stimulated ATPase activity with an EC50 of 13 μM. TBT1  Chemical Structure
  73. GC66053 Clavulanic acid Clavulanic acid is a naturally occurring powerful bacterial β-lactamases inhibitor for research of infections caused by bacteria, including infections of the ears. Clavulanic acid is active against a wide spectrum of gram-positive and gram-negative bacterias. Clavulanic acid  Chemical Structure
  74. GC66051 Cabotegravir 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
  75. GC66045 ANT3310 sodium ANT3310 sodium is a broad-spectrum covalent Serine β-Lactamase inhibitor, with IC50 values ranging from 1 nM to 175 nM (a panel of Serine β-Lactamase). ANT3310 sodium potentiates activity of β-lactam antibiotics against Carbapenem-Resistant Enterobacterales (CRE) and Acinetobacter baumannii (CRAB). ANT3310 sodium can be used in the research of bacterial infection. ANT3310 sodium  Chemical Structure
  76. GC66027 Antituberculosis agent-5 Antituberculosis agent-5 (compound 52) is a nitrofuranylamide derivative, inhibits M. tuberculosis UDP-Gal mutase. Antituberculosis agent-5 inhibits Glf activity with an IC50 value of 99 μM/mL and resists tuberculosis (TB) with a MIC value of 1.6 μg/mL. Antituberculosis agent-5  Chemical Structure
  77. GC66018 Melarsomine dihydrochloride Melarsomine dihydrochloride is a trivalent arsenical compound used as an adulticide. Melarsomine dihydrochloride can be used for the reserach of canine heartworm disease and other helminth infections. Melarsomine dihydrochloride  Chemical Structure
  78. GC66003 Fluxapyroxad Fluxapyroxad is a synthetic broad-spectrum fungicide for the control of fungal diseases. It works by inhibiting succinate dehydrogenase in complex II of the mitochondrial respiratory chain, resulting in inhibition of spore germination, germ tubes and mycelia growth within the fungus target species. Fluxapyroxad  Chemical Structure
  79. GC65982 Antibacterial agent 117 Antibacterial agent 117, triazole derivative, is an antibacterial agent. Antibacterial agent 117 has against R. prowazekii MetAP1 (RpMetAP1) activity with an IC50 value of 15 μM. Antibacterial agent 117 also inhibits rickettsial growth and can be used for the research of infection. Antibacterial agent 117  Chemical Structure
  80. GC65981 SPHINX SPHINX is a selective SRPK1 inhibitor with an IC50 value of 0.58 μM. SPHINX effectively reduces Choroidal Neovascularization (CNV) in vivo. SPHINX can be used for the research of (age-related macular degenaration) AMD. SPHINX  Chemical Structure
  81. GC65968 JNJ4796 JNJ4796 is an oral active fusion inhibitor of influenza virus, neutralizing influenza A group 1 viruses by inhibiting hemagglutinin (HA)-mediated fusion. JNJ4796 mimics the functionality of the broadly neutralizing antibodies (bnAbs). JNJ4796  Chemical Structure
  82. GC65963 AzddMeC 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
  83. GC65943 SARS-CoV-2 3CLpro-IN-2 SARS-CoV-2 3CLpro-IN-2 (Compound 1) is a potent inhibitor of 3CL protease. SARS-CoV-2 3CLpro-IN-2 has the potential for the research of SARS-CoV-2 diseases. SARS-CoV-2 3CLpro-IN-2  Chemical Structure
  84. GC65913 Granilin Granilin, a sesquiterpene lactone, can be found in the flower buds of Carpesium triste. Granilin can be used as the bactericide and fungicide. Granilin  Chemical Structure
  85. GC65905 NBD-14189 NBD-14189 is a potent HIV-1 entry antagonist with an IC50 of 89 nM against the HIV-1HXB2 pseudovirus. NBD-14189 binds to HIV-1 gp120 and shows potent antiviral activity (EC50<200 nM). NBD-14189  Chemical Structure
  86. GC65903 NBD-14270 NBD-14270, a pyridine analogue, is a potent HIV-1 entry antagonist with an IC50 of 180 nM against 50 HIV-1 Env-pseudotyped viruses. NBD-14270 binds to HIV-1 gp120 and shows potent antiviral activity. NBD-14270 shows low cytotoxicity (CC50>100 μM). NBD-14270  Chemical Structure
  87. GC65875 Grepafloxacin hydrochloride Grepafloxacin (OPC-17116) hydrochloride is an oral actively fluoroquinolone antibiotic with potent activity against community-acquired respiratory pathogens including Streptococcus pneumonia. Grepafloxacin hydrochloride has high tissue penetration and a promising pharmacodynamic profile. Grepafloxacin hydrochloride  Chemical Structure
  88. GC65864 Policresulen Policresulen is a potent inhibitor of DENV2 NS2B/NS3 protease (IC50 of 0.48 μg/mL). Policresulen inhibits DENV2 replication in BHK-21 cells with IC50 of 4.99 μg/mL. Policresulen acts as a competitive inhibitor of the protease, and slightly affects the protease stability. Policresulen  Chemical Structure
  89. GC65613 Cefaclor Cefaclor is a well-absorbed orally active cephalosporin antibiotic. Cefaclor can specifically bind to specific for penicillin-binding protein 3 (PBP3). Cefaclor can be used for the research kinds of infections caused by bacteria, such as respiratory tract infections, bacterial bronchitis, pharyngitis and skin infections. Cefaclor  Chemical Structure
  90. GC65599 (±)-Leucine-d10 (±)-Leucine-d10  Chemical Structure
  91. GC65563 Spiramycin I Spiramycin I is a macrolide antibiotic and antiparasitic. Spiramycin I  Chemical Structure
  92. GC65557 Cladosporin Cladosporin is a fungal metabolite produced in good yield in the mycelium of Cladosporium cladosporioid. Cladosporin  Chemical Structure
  93. GC65545 Cyclo(L-Phe-L-Pro) Cyclo(L-Phe-L-Pro)  Chemical Structure
  94. GC65497 MCB-3681 MCB-3681 is the antibacterial Oxaquin's active substance, active against gram-positive bacterium. MCB-3681  Chemical Structure
  95. GC65495 Bruceine B Bruceine B inhibits protein synthesis and nucleic acid synthesis. Bruceine B  Chemical Structure
  96. GC65488 GP(33-41) TFA GP(33-41) TFA, a 9-aa-long peptide, is the optimal sequence of the GP1 epitope of lymphocytic choriomeningitis virus. GP(33-41) TFA  Chemical Structure
  97. GC65481 Dodecamethylpentasiloxane Dodecamethylpentasiloxane is a component of siloxanes and can be used as silicone oil. Dodecamethylpentasiloxane  Chemical Structure
  98. GC65468 LpxC-IN-10 LpxC-IN-10 (Compound A) is a high selectivity inhibitor of LpxC. LpxC-IN-10  Chemical Structure
  99. GC65454 UCT943 UCT943 is a next-generation Plasmodium falciparum PI4K inhibitor. UCT943  Chemical Structure
  100. GC65451 RR-11a analog RR-11a analog is a potent and irreversible inhibitor of Schistosoma mansoni legumain, with an IC50 of 31 nM. RR-11a analog  Chemical Structure
  101. GC65431 Tetradehydropodophyllotoxin Tetradehydropodophyllotoxin possesses antifungal activity. Tetradehydropodophyllotoxin  Chemical Structure

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