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Home >> Signaling Pathways >> Microbiology & Virology

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.

Targets for  Microbiology & Virology

Products for  Microbiology & Virology

  1. Cat.No. Product Name Information
  2. GC38683 Benzyl isothiocyanate Benzyl isothiocyanate is a member of natural isothiocyanates with antimicrobial activity. Benzyl isothiocyanate Chemical Structure
  3. GC60639 Benzyldodecyldimethylammonium chloride dihydrate Benzyldodecyldimethylammonium chloride dihydrate is a quaternary ammonium compound (QAC) and can be used as a biocide to target antibiotic-resistant bacteria, such as methicillin-resistant?Staphylococcus aureus?(MRSA), multidrug-resistant (MDR)?P. Benzyldodecyldimethylammonium chloride dihydrate Chemical Structure
  4. GC35496 Bephenium Bephenium is an anthelmintic agent formerly used in the treatment of hookworm infections and ascariasis; B-type AChR activator. Bephenium Chemical Structure
  5. GC12697 Bephenium Hydroxynaphthoate Anthelmintic agent Bephenium Hydroxynaphthoate Chemical Structure
  6. GC68297 Bepirovirsen Bepirovirsen Chemical Structure
  7. GC14250 Bepotastine Besilate Non-sedating, selective antagonist of histamine 1 (H1) receptor Bepotastine Besilate Chemical Structure
  8. GN10221 Berberine

    Berberine (Natural Yellow 18) is an alkaloid isolated from the Chinese herbal medicine Huanglian, as an antibiotic. Berberine (Natural Yellow 18) induces reactive oxygen species (ROS) generation and inhibits DNA topoisomerase.

     Berberine Chemical Structure
  9. GC35497 Berberine chloride hydrate Berberine chloride hydrate (Natural Yellow 18 chloride hydrate) is an alkaloid that acts as an antibiotic. Berberine chloride hydrate induces reactive oxygen species (ROS) generation and inhibits DNA topoisomerase. Antineoplastic properties. Berberine chloride hydrate Chemical Structure
  10. GN10208 Berberine hydrochloride

    Berberine hydrochloride is an isoquinoline alkaloid derived from the Ranunculaceae medicinal plant Coptis chinensis. It has various pharmacological activities such as anti-tumor, anti-inflammatory, and hypoglycemic activities.

     Berberine hydrochloride Chemical Structure
  11. GN10523 Berberine Sulfate Berberine Sulfate Chemical Structure
  12. GC49387 Berberine-d6 (chloride) An internal standard for the quantification of berberine Berberine-d6 (chloride) Chemical Structure
  13. GN10539 Bergenin Bergenin Chemical Structure
  14. GC13475 Berninamycin A cyclic thiopeptide antibiotic Berninamycin A Chemical Structure
  15. GC63421 Bersacapavir Bersacapavir is a novel Hepatitis B Virus capsid assembly modulator. Bersacapavir Chemical Structure
  16. GC25135 Besifloxacin Besifloxacin is a fourth generation fluoroquinolone-type opthalmic antibiotic for the treatment of bacterial conjunctivitis. Besifloxacin Chemical Structure
  17. GC15920 Besifloxacin HCl Besifloxacin hydrochloride is a fourth-generation fluoroquinolone antibiotic. Besifloxacin HCl Chemical Structure
  18. GC38517 Besifovir Besifovir (LB80331), a parent drug converted by LB80380, further metabolizes to its active form, LB80317. Besifovir Chemical Structure
  19. GC33989 beta-L-D4A beta-L-D4A is a nucleoside HIV-1 reverse transcriptase inhibitor. beta-L-D4A Chemical Structure
  20. GC33078 beta-lactamase-IN-1 beta-lactamase-IN-1 is an inhibitor of β-Lactamase extracted from patent WO2016027249A1, page 77. beta-lactamase-IN-1 Chemical Structure
  21. GC10619 Betamipron Parenteral carbapenem antibiotic Betamipron Chemical Structure
  22. GC35507 Bethoxazin Bethoxazin(Bethoguard) is a new broad spectrum industrial microbicide with applications in material and coating preservation. Bethoxazin Chemical Structure
  23. GC48446 Betulin 3,28-diacetate A triterpene with antiviral and hepatoprotective activities Betulin 3,28-diacetate Chemical Structure
  24. GN10081 Betulinaldehyde Betulinaldehyde Chemical Structure
  25. GC10480 Betulinic acid A plant triterpenoid similar to bile acids Betulinic acid Chemical Structure
  26. GC48504 Betulinic Aldehyde oxime A derivative of betulin Betulinic Aldehyde oxime Chemical Structure
  27. GC35508 Bevirimat An inhibitor of HIV-1 virion maturation Bevirimat Chemical Structure
  28. GC32381 BF738735 BF738735 is a phosphatidylinositol 4-kinase III beta (PI4KIIIβ) inhibitor with an IC50 of 5.7 nM. BF738735 Chemical Structure
  29. GC46100 BHBM An acylhydrazone with antifungal activity BHBM Chemical Structure
  30. GC35510 BI 224436 BI 224436 is a novel HIV-1 noncatalytic site integrase inhibitor with EC50 values of less than 15 nM against different HIV-1 laboratory strains. BI 224436 Chemical Structure
  31. GC14204 Biapenem Highly broad spectrum antibiotic agent Biapenem Chemical Structure
  32. GC32060 Bictegravir (GS-9883) Bictegravir (GS-9883) (GS-9883) is a potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM. Bictegravir (GS-9883) Chemical Structure
  33. GC18304 Bicyclol Bicyclol is a hepatoprotective agent. Bicyclol Chemical Structure
  34. GC14866 Bicyclomycin Benzoate antibiotic Bicyclomycin Benzoate Chemical Structure
  35. GC39348 Bifendate Bifendate (DDB) is a synthetic intermediate of Schisandrin C with anti-HBV efficacy in research of chronic hepatitis B. Bifendate Chemical Structure
  36. GC17752 Bifonazole imidazole antifungal drug Bifonazole Chemical Structure
  37. GC45391 Bikaverin   Bikaverin Chemical Structure
  38. GC14233 BIO-acetoxime

    GSK-3α/β inhibitor

     BIO-acetoxime Chemical Structure
  39. 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
  40. GC12426 Birinapant (TL32711) An antagonist of cIAP1, cIAP2, and XIAP Birinapant (TL32711) Chemical Structure
  41. GC14716 Bisindolylmaleimide IV protein kinase C (PKC) inhibitor Bisindolylmaleimide IV Chemical Structure
  42. GC61825 Bismuth subcarbonate Bismuth subcarbonate (Bismuth carbonate oxide) is a typical Bi-based semiconductor that is widely applied as antibacterial, sensors, super capacitors, and photocatalysts. Bismuth subcarbonate Chemical Structure
  43. GC15357 Bismuth Subcitrate Potassium

    Antibiotic used to treat stomach ulcers

     Bismuth Subcitrate Potassium Chemical Structure
  44. GC15976 Bithionol potent inhibitor of soluble adenylyl cyclase (sAC) Bithionol Chemical Structure
  45. GC35526 Bithionol sulfoxide Bithionol sulfoxide is an anti-infection agent for parasites. Bithionol sulfoxide Chemical Structure
  46. GC32239 Bitoscanate (p-Phenylene diisothiocyanate) Bitoscanate (p-Phenylene diisothiocyanate) (p-Phenylene diisothiocyanate) is an organic chemical compound used in the treatment of hookworms. Bitoscanate (p-Phenylene diisothiocyanate) Chemical Structure
  47. GC35531 BKI-1369 BKI-1369 is a bumped kinase inhibitor (BKI). BKI-1369 Chemical Structure
  48. GC10909 Bleomycin A5 (hydrochloride) glycopeptide antibiotic that lead to nucleic acid cleavage Bleomycin A5 (hydrochloride) Chemical Structure
  49. GC60089 Bleomycin hydrochloride Bleomycin hydrochloride is a DNA synthesis inhibitor. Bleomycin hydrochloride is a DNA damaging agent. Bleomycin hydrochloride is an antitumor antibiotic. Bleomycin hydrochloride Chemical Structure
  50. GC15819 Bleomycin Sulfate

    Bleomycin is produced by Streptomyces verticillis.

     Bleomycin Sulfate Chemical Structure
  51. GC60648 BLT-1 BLT-1, a thiosemicarbazone copper chelator, is a selective scavenger receptor B, type 1 (SR-BI) inhibitor. BLT-1 Chemical Structure
  52. GC18217 BM212 BM212 is an antimycobacterial compound. BM212 Chemical Structure
  53. GC32204 BM635 BM635 is a MmpL3 inhibitor with outstanding anti-mycobacterial activity. BM635 Chemical Structure
  54. GC10263 BMS-378806 (BMS-806) BMS-378806 (BMS-806) is a potent HIV-1 attachment inhibitor that interferes with CD4-gp120 interactions. BMS-378806 (BMS-806) Chemical Structure
  55. GC10570 BMS-538203 HIV integrase inhibitor,highly efficient BMS-538203 Chemical Structure
  56. GC10794 BMS-626529 An HIV-1 attachment inhibitor BMS-626529 Chemical Structure
  57. GC13119 BMS-663068 BMS-663068 Chemical Structure
  58. GC11923 BMS-707035 BMS-707035 Chemical Structure
  59. GC32256 BMY-43748 BMY-43748 is a promising antibacterial agent, exhibiting great in vitro and in vivo antibacterial activity. BMY-43748 Chemical Structure
  60. GC32349 BO3482 BO3482 has Antimicrobial activity and can inhibit the growth of methicillin-resistant Staphylococci (MRS) with an MIC90 of 6.25 mg/mL. BO3482 Chemical Structure
  61. GC10959 Boceprevir An NS3/4A protease inhibitor Boceprevir Chemical Structure
  62. GC46936 Boceprevir-d9 An internal standard for the quantification of boceprevir Boceprevir-d9 Chemical Structure
  63. GC32299 Bombinin-Like Peptide BLP-1 Bombinin-Like Peptide BLP-1 is an antimicrobial peptide from Bombina species. Bombinin-Like Peptide BLP-1 Chemical Structure
  64. GC61885 Bonducellpin D Bonducellpin D is a furanoditerpenoid lactone isolated from Caesalpinia minax. Bonducellpin D Chemical Structure
  65. GC42967 Boromycin Boromycin is a boron-containing macrolide antibiotic that has been found in Streptomyces. Boromycin Chemical Structure
  66. GC11040 Borrelidin threonyl-tRNA synthetase (ThrRS) inhibitor Borrelidin Chemical Structure
  67. GC65355 BPH-715 BPH-715 is a bisphosphonate, inhibits Plasmodium liver-stage growth, with an IC50 of 10 μM for Plasmodium exoerythrocytic forms in HepG2 cells. BPH-715 Chemical Structure
  68. GC42969 bpV(phen) (potassium hydrate) bpV(phen) (potassium hydrate), a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. bpV(phen) (potassium hydrate) Chemical Structure
  69. GC32163 BQR-695 (NVP-BQR695) BQR-695 (NVP-BQR695) is a PI4KIIIβ inhibitor with IC50s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively. BQR-695 (NVP-BQR695) Chemical Structure
  70. GC50140 BRACO 19 trihydrochloride

    Telomerase inhibitor

     BRACO 19 trihydrochloride Chemical Structure
  71. GC38742 BRD-6929 An HDAC1 and HDAC2 inhibitor BRD-6929 Chemical Structure
  72. GC39238 BRD-K98645985 BRD-K98645985 is a BAF (mammalian SWI/SNF) transcriptional repression inhibitor with an EC50 of ~2.37 ?M. BRD-K98645985 Chemical Structure
  73. 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
  74. GC19082 Brequinar

    Brequinar is a potent inhibitor of dihydroorotate dehydrogenase, with potent activities against a broad spectrum of viruses.

     Brequinar Chemical Structure
  75. GC50377 Brequinar sodium Potent and selective DHODH inhibitor Brequinar sodium Chemical Structure
  76. GC30156 Brevianamide F (Cyclo(L-Pro-L-Trp)) Brevianamide F (Cyclo(L-Pro-L-Trp)) (Cyclo(L-Pro-L-Trp)) is a mycotoxin isolated from Colletotrichum gloeosporioides, with antibacterial activity. Brevianamide F (Cyclo(L-Pro-L-Trp)) Chemical Structure
  77. GC32238 Brilacidin (PMX 30063) Brilacidin (PMX 30063) (PMX 30063) is an anti-infective antimicrobial with MIC90s of 1 and 8 μg/mL for Gram-positive bacteria Streptococcus pneumonia and Streptococcus viridans, and MIC90 of 8 and 4 μg/mL for Gram-negative bacteria Haemophilus influenza and Pseudomonas aeruginosa. Brilacidin (PMX 30063) Chemical Structure
  78. GC39353 Brilliant Black BN A sulfonated azo dye with antiviral activity Brilliant Black BN Chemical Structure
  79. GC61529 BRITE-338733 BRITE-338733 is a RecA ATPase inhibitor, with an IC50 of 4.7 ?M. BRITE-338733 Chemical Structure
  80. GC33923 Brivudine (Bromovinyldeoxyuridine) Brivudine (Bromovinyldeoxyuridine) is a thymidine analogue with antiviral activity, indicated for the early treatment of acute herpes zoster. Brivudine (Bromovinyldeoxyuridine) Chemical Structure
  81. 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
  82. GC63622 Brodimoprim Brodimoprim (Ro 10-5970), a trimethoprim analogue, is an orally active dihydrofolate reductase inhibitor. Brodimoprim Chemical Structure
  83. GC30921 Bronopol (BNPD) Bronopol (BNPD) is an antimicrobial, with low mammalian toxicity (at in-use levels) and high activity against bacteria (especially the troublesome Gram-negative species). Bronopol (BNPD) Chemical Structure
  84. GC32155 Broxaldine (Brobenzoxaldine) Broxaldine (Brobenzoxaldine) (Brobenzoxaldine) is an antiprotozoal agent. Broxaldine (Brobenzoxaldine) Chemical Structure
  85. GC10347 Broxyquinoline Antiprotozoal agent Broxyquinoline Chemical Structure
  86. GC17948 Bruceine A antibabesial activity Bruceine A Chemical Structure
  87. GC65495 Bruceine B Bruceine B inhibits protein synthesis and nucleic acid synthesis. Bruceine B Chemical Structure
  88. GC60667 BSH-IN-1 An inhibitor of bile salt hydrolases BSH-IN-1 Chemical Structure
  89. GC40680 BTZ043 BTZ043 is an antibiotic with antimycobacterial activity. BTZ043 Chemical Structure
  90. GC18127 BTZ043 Racemate DprE1 inhibitor BTZ043 Racemate Chemical Structure
  91. GC35569 Buparvaquone An electron transport chain inhibitor Buparvaquone Chemical Structure
  92. GC25181 Butenafine Butenafine is a synthetic benzylamine antifungal agent. Butenafine Chemical Structure
  93. GC13207 Butenafine HCl Butenafine HCl (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase. Butenafine HCl Chemical Structure
  94. GC49136 Butenafine-13C-d3 (hydrochloride) An internal standard for the quantification of butenafine Butenafine-13C-d3 (hydrochloride) Chemical Structure
  95. GC25182 Butoconazole Butoconazole is an imidazole antifungal used in gynecology. Butoconazole Chemical Structure
  96. GC12984 Butoconazole nitrate Antifungal agent Butoconazole nitrate Chemical Structure
  97. GC32255 Butylparaben (Butyl parahydroxybenzoate) Butylparaben (Butyl parahydroxybenzoate) is an organic compound, has proven to be a highly successful antimicrobial preservative in cosmetics, also used in medication suspensions, and as a flavoring additive in food. Butylparaben (Butyl parahydroxybenzoate) Chemical Structure
  98. GC39739 Bz-RS-iSer(3-Ph)-OMe Bz-RS-iSer(3-Ph)-OMe (compound 2), a Taxol derivative, inhibits HSV replication cycle at low cytotoxicity, blocks mitotic divisions of Vero cells, influences M-MSV induced tumor size and affects immune response by inhibiting PHA-induced T lymphocyte proliferation. Bz-RS-iSer(3-Ph)-OMe Chemical Structure
  99. GC13643 c-di-AMP

    C-di-AMP is a STING agonist, which binds to the transmembrane protein STING, thereby activating the TBK3-IRF3 signaling pathway, subsequently triggering the production of type I IFN and TNF.

     c-di-AMP Chemical Structure
  100. GC62198 c-di-AMP sodium

    C-di-AMP is a STING agonist, which binds to the transmembrane protein STING, thereby activating the TBK3-IRF3 signaling pathway, subsequently triggering the production of type I IFN and TNF.

     c-di-AMP sodium Chemical Structure
  101. GC43020 C12E8 C12E8 (C12E8) is an non-ionic detergent that can be used for membrane protein extraction. C12E8 Chemical Structure

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