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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.

Targets for  Microbiology & Virology

Products for  Microbiology & Virology

  1. Cat.No. Product Name Information
  2. GC63814 Amantadine Amantadine (1-Adamantanamine) is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine  Chemical Structure
  3. GC10105 Amantadine HCl Amantadine (1-Adamantanamine) hydrochloride is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine HCl  Chemical Structure
  4. GC42777 Amastatin (hydrochloride) Amastatin is a slow, tight binding, competitive aminopeptidase (AP) inhibitor, first described as an inhibitor of human serum AP-A (glutamyl AP; IC50 = 0.54 μg/ml) but not of AP-B (arginine AP). Amastatin (hydrochloride)  Chemical Structure
  5. GC42780 Ambuic Acid Ambuic acid is a cyclohexanone originally isolated from Pestalotiopsis and Monochaetia species that has phytopathogenic antifungal, quorum sensing inhibitory, and antibacterial activities. Ambuic Acid  Chemical Structure
  6. GC10473 AMD 3465 CXCR4 antagonist,potent and selective AMD 3465  Chemical Structure
  7. GC16706 AMD 3465 hexahydrobromide potent, selective CXCR4 antagonist AMD 3465 hexahydrobromide  Chemical Structure
  8. GC12196 AMD-070 A CXCR4 antagonist AMD-070  Chemical Structure
  9. 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
  10. GN10484 Amentoflavone Amentoflavone  Chemical Structure
  11. GC33997 Amifloxacin (Win49375) Amifloxacin (Win49375) (Win49375) is a synthetic antibacterial agent of the quinolone class. Amifloxacin (Win49375)  Chemical Structure
  12. GC16285 Amikacin aminoglycoside antibiotic Amikacin  Chemical Structure
  13. GC38195 Amikacin (hydrate) Amikacin (hydrate)  Chemical Structure
  14. GC11093 Amikacin disulfate Semisynthetic aminoglycoside antibiotic Amikacin disulfate  Chemical Structure
  15. GC15685 Amikacin hydrate Aminoglycoside antibiotic Amikacin hydrate  Chemical Structure
  16. GC32149 Aminoacyl tRNA synthetase-IN-1 Aminoacyl tRNA synthetase-IN-1 is a bacterial aminoacyl tRNA synthetase (aaRS) inhibitor. Aminoacyl tRNA synthetase-IN-1  Chemical Structure
  17. GC18131 Aminothiazole Thyroid inhibitor Aminothiazole  Chemical Structure
  18. GC33983 Amitraz (BTS-27419) Amitraz (BTS-27419) is a non-systemic acaricide and insecticide, with alpha-adrenergic agonist activity, interaction with octopamine receptors of the central nervous system and inhibition of monoamine oxidases and prostaglandin synthesis. Amitraz (BTS-27419)  Chemical Structure
  19. GC60578 Ammonium lactate Ammonium lactate is the ammonium salt of lactic acid, with mild anti-bacterial properties. Ammonium lactate  Chemical Structure
  20. GC42790 Amodiaquine Amodiaquine is an aminoquinoline antimalarial compound. Amodiaquine  Chemical Structure
  21. GC60579 Amodiaquine dihydrochloride Amodiaquine dihydrochloride (Amodiaquin dihydrochloride), a 4-aminoquinoline class of antimalarial agent, is a potent and orally active histamine N-methyltransferase inhibitor with a Ki of 18.6 nM. Amodiaquine dihydrochloride  Chemical Structure
  22. GC10905 Amodiaquine dihydrochloride dihydrate histamine N-methyl transferase inhibitor Amodiaquine dihydrochloride dihydrate  Chemical Structure
  23. GC15052 Amorolfine HCl Amorolfine (Ro 14-4767/002) hydrochloride is a potent anti-fungal agent. Amorolfine HCl  Chemical Structure
  24. GC13989 Amoxicillin

    Moderate-spectrum, bacteriolytic, β-lactam antibiotic

    Amoxicillin  Chemical Structure
  25. GC16863 Amoxicillin Sodium moderate- spectrum, bacteriolytic, β-lactam antibiotic Amoxicillin Sodium  Chemical Structure
  26. GC14072 Amoxicillin trihydrate Broad spectrum antibiotic Amoxicillin trihydrate  Chemical Structure
  27. GC40232 Amoxicillin-d4 Amoxicillin-d4 is intended for use as an internal standard for the quantification of amoxicillin by GC- or LC-MS. Amoxicillin-d4  Chemical Structure
  28. GC67986 AMOZ-d5 AMOZ-d5  Chemical Structure
  29. GC15221 Amphomycin natural antibacterial lipopeptide Amphomycin  Chemical Structure
  30. GC14092 Amphotericin B Amphipathic polyene antibiotic Amphotericin B  Chemical Structure
  31. GC60047 Amphotericin B methyl ester Amphotericin B methyl ester is the methyl ester derivative of the polyene antibiotic Amphotericin B (A634250). Amphotericin B methyl ester  Chemical Structure
  32. GC33975 Ampicillin (D-(-)-α-Aminobenzylpenicillin) Ampicillin is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria. Ampicillin (D-(-)-α-Aminobenzylpenicillin)  Chemical Structure
  33. GC38372 Ampicillin (trihydrate)

    A broad-spectrum beta-lactam antibiotic

    Ampicillin (trihydrate)  Chemical Structure
  34. GC10036 Ampicillin sodium

    A broad-spectrum antibiotic

    Ampicillin sodium  Chemical Structure
  35. GC14152 Amprenavir (agenerase) A selective HIV protease inhibitor Amprenavir (agenerase)  Chemical Structure
  36. GC35328 Amprolium Amprolium is a coccidiostat used in poultry, is a thiamine analogue and blocks the thiamine transporter of Eimeria species by blocking thiamine uptake it prevents carbohydrate synthesis. Amprolium  Chemical Structure
  37. GC17445 Amprolium HCl Amprolium HCl is a coccidiostat used in poultry, is a thiamine analogue and blocks the thiamine transporter of Eimeria species by blocking thiamine uptake it prevents carbohydrate synthesis. Amprolium HCl  Chemical Structure
  38. GC62842 Amylmetacresol Amylmetacresol possesses antiviral (such HIV) effect. Amylmetacresol  Chemical Structure
  39. GC15026 AN-2690 A broad spectrum antifungal agent AN-2690  Chemical Structure
  40. GC63839 AN0128 AN0128 is a boron-containing antibacterial and anti-inflammatory agent. AN0128  Chemical Structure
  41. GC32324 AN2718 A broad-spectrum antifungal AN2718  Chemical Structure
  42. GC12345 AN3365 (hydrochloride) Epetraborole (GSK2251052) hydrochloride is a novel leucyl-tRNA synthetase (LeuRS) inhibitor (IC50=0.31 μM), thereby inhibiting protein synthesis. AN3365 (hydrochloride)  Chemical Structure
  43. GC60048 AN3661 AN3661, a potent antimalarial lead compound, targets a Plasmodium falciparum cleavage and polyadenylation specificity factor homologue subunit 3 (PfCPSF3). AN3661  Chemical Structure
  44. GC35336 AN7973 AN7973 is the 6-carboxamide benzoxaborole, blocks intracellular parasite development and inhibits Cryptosporidium growth. AN7973  Chemical Structure
  45. GN10045 Angelicin Angelicin  Chemical Structure
  46. GC14937 Anguizole Anguizole  Chemical Structure
  47. GC12754 Anidulafungin

    Antifungal drug

    Anidulafungin  Chemical Structure
  48. 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
  49. GC42816 Ansatrienin B Ansatrienin B is an ansamycin antibiotic and antifungal agent first isolated from S. Ansatrienin B  Chemical Structure
  50. 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
  51. GC38312 Anthraquinone Anthraquinone is used as a precursor for dye formation. Anthraquinone  Chemical Structure
  52. GC60051 Anti-MERS-2E6 mAb Anti-MERS-2E6 mAb (MERS-2E6; MERS Antibody-2E6), a human neutralizing antibody IgG1 (CHO expressed) that can compete for the binding of the virus Spike protein to the receptor (CD26), thereby inhibiting virus invasion into host cells. Anti-MERS-2E6 mAb  Chemical Structure
  53. GC60052 Anti-MERS-3A1 mAb Anti-MERS-3A1 mAb (MERS-3A1) is a human monoclonal IgG1 antibody with the high binding affinity produced in CHO cells. Anti-MERS-3A1 mAb  Chemical Structure
  54. 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
  55. GC35362 Anti-parasitic agent 3 Anti-parasitic agent 3 is an anti-parasitic agent which active against drug resistant parasites. Anti-parasitic agent 3  Chemical Structure
  56. GC60054 Anti-SARS-80R mAb Anti-SARS-80R mAb (SARS-80R) is a human monoclonal IgG1 antibody produced in CHO cells. Anti-SARS-80R mAb  Chemical Structure
  57. GC60055 Anti-SARS-CoV-2 Spike mAb (CR3022) Anti-SARS-CoV-2 Spike mAb (CR3022) is a a CHO cell derived human monoclonal IgG1 antibody. Anti-SARS-CoV-2 Spike mAb (CR3022)  Chemical Structure
  58. GC60056 Anti-Spike-RBD mAb Anti-Spike-RBD mAb is a CHO cell derived human monoclonal IgG1 antibody. Anti-Spike-RBD mAb  Chemical Structure
  59. GC60057 Anti-Spike-RBD Single Domain mAb Anti-Spike-RBD Single Domain mAb is a CHO cell derived Alpaca monoclonal VHH-huFc antibody, specifically binds to SARS-CoV-2 RBD with high affinity. Anti-Spike-RBD Single Domain mAb  Chemical Structure
  60. 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
  61. GC62534 Antibacterial agent 18 Antibacterial agent 18 is a multi-arm AIE molecule extracted from patent CN110123801A, compound 23. Antibacterial agent 18  Chemical Structure
  62. GC63959 Antibacterial agent 26 Antibacterial agent 26 is a potent antibacterial compound. Antibacterial agent 26  Chemical Structure
  63. GC63960 Antibacterial agent 27 Antibacterial agent 27 is a potent antibacterial compound against?Candida?species. Antibacterial agent 27  Chemical Structure
  64. GC32388 Antibacterial compound 1 Antibacterial compound 1 is a oxazolidinone extracted from patent WO1999037630A1 with antibacterial activities. Antibacterial compound 1  Chemical Structure
  65. GC32352 Antibacterial compound 2 Antibacterial compound 2 is a useful antibacterial agent extracted from patent US5652238, compound example 9. Antibacterial compound 2  Chemical Structure
  66. GC32220 Antibiotic-5d Antibiotic-5d is a synthesis and antimicrobial compound. Antibiotic-5d  Chemical Structure
  67. GC32219 Antifungal agent 1 Antifungal agent 1 is a potent antifungal agent. Antifungal agent 1  Chemical Structure
  68. GC64396 Antimalarial agent 1 Antimalarial agent 1 is a potent antimalarial drug. Antimalarial agent 1  Chemical Structure
  69. GC32296 Antimicrobial Compound 1 Antimicrobial Compound 1 is an alkylpyridinium compound, with antimicrobial activity. Antimicrobial Compound 1  Chemical Structure
  70. GC32169 Antimonyl potassium tartrate trihydrate (Potassium antimonyl tartrate trihydrate) Antimonyl potassium tartrate trihydrate (Potassium antimonyl tartrate trihydrate)  Chemical Structure
  71. GC39478 Antitrypanosomal agent 1 Antitrypanosomal agent 1 is a potent and selective trypanothione reductase (TR) inhibitor with an IC50 of 3.3 μM. Antitrypanosomal agent 1  Chemical Structure
  72. 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
  73. GC67913 Antiviral agent 5 Antiviral agent 5  Chemical Structure
  74. GC52427 Apelin-12 (human, mouse, rat, bovine) (acetate) An endogenous agonist of the APJ receptor Apelin-12 (human, mouse, rat, bovine) (acetate)  Chemical Structure
  75. GC32315 Apidaecin IB Apidaecin IB is a insect antimicrobial peptide, with minimum inhibitory concentration (MIC) values of 8 μM for E. Apidaecin IB  Chemical Structure
  76. GC32336 Aplaviroc (AK 602) Aplaviroc (AK 602) (AK 602), a SDP derivative, is a CCR5 antagonist, with IC50s of 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL and HIV-1MOKW. Aplaviroc (AK 602)  Chemical Structure
  77. GC62610 Aplaviroc hydrochloride Aplaviroc (AK 602) hydrochloride, a SDP derivative, is a CCR5 antagonist, with IC50s of 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL and HIV-1MOKW. Aplaviroc hydrochloride  Chemical Structure
  78. GC32288 Apramycin (Nebramycin II) Apramycin (Nebramycin II)  Chemical Structure
  79. GC48988 Apramycin (sulfate hydrate) An aminoglycoside antibiotic Apramycin (sulfate hydrate)  Chemical Structure
  80. GC12855 Apramycin Sulfate Aminoglycoside antibiotic Apramycin Sulfate  Chemical Structure
  81. GC15200 Aprepitant Substance P (SP) inhibitor Aprepitant  Chemical Structure
  82. GC49776 Apricitabine Apricitabine  Chemical Structure
  83. GC12900 Aprotinin

    A serine protease inhibitor

    Aprotinin  Chemical Structure
  84. GC64848 APX2039 APX2039 is an orally active and potent inhibitor of the fungal Gwt1 enzyme. APX2039  Chemical Structure
  85. GC32313 AQ-13 dihydrochloride AQ-13 dihydrochloride is an aminoquinoline antimalarial drug that is effective against drug-resistant strains of Plasmodium falciparum. AQ-13 dihydrochloride  Chemical Structure
  86. GC13979 Arbidol HCl Arbidol HCl is a potent, orally active broad-spectrum antiviral with activity against a number of enveloped and non-enveloped viruses. Arbidol HCl  Chemical Structure
  87. GC35387 Aristeromycin Aristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor. Aristeromycin  Chemical Structure
  88. GC49103 Aromadendrene A sesquiterpene with diverse biological activities Aromadendrene  Chemical Structure
  89. GC35399 Artefenomel An antimalarial agent Artefenomel  Chemical Structure
  90. GC61598 Artelinic acid Artelinic acid, a derivative of Artemisinin, is an antimalarial drug for the treatment of multidrug resistant strains of Plasmodium falciparum. Artelinic acid  Chemical Structure
  91. GN10638 Artemether Artemether  Chemical Structure
  92. GC12784 Artemether (SM-224) An antiparasitic compound Artemether (SM-224)  Chemical Structure
  93. GC41610 Artemisinic Acid Artemisinic acid (Qing Hao acid), an amorphane sesquiterpene isolated from Artemisia annua L. Artemisinic Acid  Chemical Structure
  94. GN10647 Artemisinine Artemisinine  Chemical Structure
  95. GC34475 Artemisone Artemisone (Artemifone) is a potent and semi-synthetic antimalarial, inhibits P. Artemisone  Chemical Structure
  96. GC32205 Artemotil (β-Arteether) Artemotil (β-Arteether) (β-Arteether) has antimalarial activity for the treatment of chloroquine-resistant Plasmodium falciparum malaria with an IC50 of 1.61 nM. Artemotil (β-Arteether)  Chemical Structure
  97. GC32231 Arterolane (OZ 277) Arterolane (OZ 277) is an antimalarial agent, with IC50 of both 1.1 nM against P. Arterolane (OZ 277)  Chemical Structure
  98. GC10889 Artesunate Derivative of the natural product artemisinin Artesunate  Chemical Structure
  99. GC63501 ARX-1796 ARX-1796 (AV-006), an Avibactam prodrug, is an orally bioavailable β-lactamase inhibitor. ARX-1796  Chemical Structure
  100. GC13215 Ascomycin(FK 520) A potent macrolide immunosuppressant Ascomycin(FK 520)  Chemical Structure
  101. GC62290 Ascr#18 Ascr#18, an ascaroside, is a hormone of nematodes. Ascr#18  Chemical Structure

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