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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. GC42816 Ansatrienin B

    Mycotrienin II, SDZ-115 962

     Ansatrienin B is an ansamycin antibiotic and antifungal agent first isolated from S. Ansatrienin B Chemical Structure
  3. GC72368 Ansuvimab Ansuvimab (Ansuvimab-zyk) is a recombinant human monoclonal IgG1 antibody that exhibits antiviral activity against Zaire ebolavirus. Ansuvimab Chemical Structure
  4. 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
  5. GC38312 Anthraquinone Anthraquinone is used as a precursor for dye formation. Anthraquinone Chemical Structure
  6. GC60051 Anti-MERS-2E6 mAb

    MERS-2E6; MERS Antibody-2E6

     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
  7. GC60052 Anti-MERS-3A1 mAb

    MERS-3A1; MERS Antibody-3A1

     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
  8. GC66241 Anti-MERS-D12 mAb

    MERS-D12; MERS Antibody-D12

     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
  9. 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
  10. GC60054 Anti-SARS-80R mAb

    SARS-80R; SARS Antibody-80R

     Anti-SARS-80R mAb (SARS-80R) is a human monoclonal IgG1 antibody produced in CHO cells. Anti-SARS-80R mAb Chemical Structure
  11. GC60055 Anti-SARS-CoV-2 Spike mAb (CR3022)

    SARS-CR3022; SARS-CoV-2 Antibody-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
  12. GC60056 Anti-Spike-RBD mAb

    SARS-CoV-2 (2019-nCoV) Spike RBD Antibody

     Anti-Spike-RBD mAb is a CHO cell derived human monoclonal IgG1 antibody. Anti-Spike-RBD mAb Chemical Structure
  13. GC60057 Anti-Spike-RBD Single Domain mAb

    SARS-CoV-2 (2019-nCoV) Single-Domain Antibodies; Humanized Single Domain Antibody

     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
  14. GC70589 anti-TB agent 1 anti-TB agent 1 is a potent and orally active anti-tuberculosis agent, with MICs of < 2 nM against the Mtb strains H37Rv, rRMP and rINH. anti-TB agent 1 Chemical Structure
  15. 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
  16. GC68664 Antibacterial agent 125

    Antibacterial agent 125 is an antibacterial agent. It has effective antibacterial activity against clinically relevant Gram-positive pathogens, with MIC50 values ranging from 0.25 - 8 μM. Antibacterial agent 125 can be used for research on antimicrobial resistance of active molecules.

     Antibacterial agent 125 Chemical Structure
  17. GC71202 Antibacterial agent 131 Antibacterial agent 131 is a quinoline derivative. Antibacterial agent 131 Chemical Structure
  18. GC62534 Antibacterial agent 18 Antibacterial agent 18 is a multi-arm AIE molecule extracted from patent CN110123801A, compound 23. Antibacterial agent 18 Chemical Structure
  19. GC68665 Antibacterial agent 19

    Antibacterial agent 19 is an effective antibacterial agent. Antibacterial agent 19 has antibacterial activity against K. pneumoniae, (M-R)S. aureus and (M-R,V-R)S. aureus, with MIC values of 0.022, 0.022 and 0.045 mg/mL respectively.

     Antibacterial agent 19 Chemical Structure
  20. GC63959 Antibacterial agent 26 Antibacterial agent 26 is a potent antibacterial compound. Antibacterial agent 26 Chemical Structure
  21. GC63960 Antibacterial agent 27 Antibacterial agent 27 is a potent antibacterial compound against?Candida?species. Antibacterial agent 27 Chemical Structure
  22. GC32388 Antibacterial compound 1 Antibacterial compound 1 is a oxazolidinone extracted from patent WO1999037630A1 with antibacterial activities. Antibacterial compound 1 Chemical Structure
  23. GC32352 Antibacterial compound 2 Antibacterial compound 2 is a useful antibacterial agent extracted from patent US5652238, compound example 9. Antibacterial compound 2 Chemical Structure
  24. GC73563 Antibiofilm agent-1 Antibiofilm agent-1 is an antibacterial agent that inhibits growth of Gram-positive pathogens (WO2017011725A1; compound 17). Antibiofilm agent-1 Chemical Structure
  25. GC32220 Antibiotic-5d Antibiotic-5d is a synthesis and antimicrobial compound. Antibiotic-5d Chemical Structure
  26. GC32219 Antifungal agent 1 Antifungal agent 1 is a potent antifungal agent. Antifungal agent 1 Chemical Structure
  27. GC71238 Antifungal agent 48 Antifungal agent 48 (Example 308) is an antifungal agent. Antifungal agent 48 Chemical Structure
  28. GC71239 Antifungal agent 49 Antifungal agent 49 (Example 112) is an antifungal agent. Antifungal agent 49 Chemical Structure
  29. GC64396 Antimalarial agent 1 Antimalarial agent 1 is a potent antimalarial drug. Antimalarial agent 1 Chemical Structure
  30. GC70989 Antimalarial agent 13 Antimalarial agent 13 (Compound 1) is a potent antimalarial agent. Antimalarial agent 13 Chemical Structure
  31. GC71332 Antimalarial agent 33 Antimalarial agent 33 (compound 5g) has antiplasmodial activity against erythrocytic and hepatic stages of Plasmodium with an EC50 of 1.1 μM for K1 P. falciparum strain. Antimalarial agent 33 Chemical Structure
  32. GC73766 Antimalarial agent 38 Antimalarial agent 38 exhibits activity against antiplasmodial, which inhibits Plasmodium falciparum D6 strain, chloroquine-sensitive Thai strain and chloroquine-resistant FcB1 strain and K1 strain, with IC50s of 0.5, 13, 1 and 13 μM, respectively. Antimalarial agent 38 Chemical Structure
  33. GC73342 Antimicrobial agent-8 Antimicrobial agent-8 (Compound 15) is a potent antimicrobial agent, and shows potent antimicrobial activity with an MIC range of 2-8 μg/mL against Gram-negative and Gram-positive bacteria. Antimicrobial agent-8 Chemical Structure
  34. GC32296 Antimicrobial Compound 1 Antimicrobial Compound 1 is an alkylpyridinium compound, with antimicrobial activity. Antimicrobial Compound 1 Chemical Structure
  35. GC32169 Antimonyl potassium tartrate trihydrate (Potassium antimonyl tartrate trihydrate) Antimonyl potassium tartrate trihydrate (Potassium antimonyl tartrate trihydrate) Chemical Structure
  36. GC42819 Antimycin A3 Antimycin A3 is a component of the antimycin A antibiotic complex that is more polar than antimycin A1 and antimycin A2 but not antimycin A4. Antimycin A3 Chemical Structure
  37. 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
  38. 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
  39. GC70964 Antiviral agent 17 Antiviral agent 17 (Compound 4) is an anti-infection agent. Antiviral agent 17 Chemical Structure
  40. GC68675 Antiviral agent 24

    Antiviral agent 24 is an effective antiviral agent with EC50 values of 0.101, 19.9, and 91.2 µM against EV71, CVA21, and EV68 respectively. Antiviral agent 24 inhibits the activity of METTL3/METTL14 in a dose-dependent manner.

     Antiviral agent 24 Chemical Structure
  41. GC71087 Antiviral agent 38 Antiviral agent 38 (compound 2.1-1) is a potent antiviral agent. Antiviral agent 38 Chemical Structure
  42. GC67913 Antiviral agent 5 Antiviral agent 5 Chemical Structure
  43. 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
  44. GC52427 Apelin-12 (human, mouse, rat, bovine) (acetate)

    RPRLSHKGPMPF

     An endogenous agonist of the APJ receptor Apelin-12 (human, mouse, rat, bovine) (acetate) Chemical Structure
  45. GC91866 Apelin-36 (trifluoroacetate salt) The apelin gene encodes a preproprotein that is processed to generate a variety of bioactive peptides, including those having 36, 17, or 13 amino acids (apelin-36, apelin-17, and apelin-13, respectively). Apelin-36 (trifluoroacetate salt) Chemical Structure
  46. GC72291 Api137 TFA Api137 TFA is an antimicrobial peptide that interferes with bacterial growth by inhibiting translation. Api137 TFA Chemical Structure
  47. 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
  48. 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
  49. GC62610 Aplaviroc hydrochloride

    AK602 hydrochloride; GSK-873140 hydrochloride; GW-873140 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
  50. GC68678 APOBEC3G-IN-1

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

     APOBEC3G-IN-1 Chemical Structure
  51. GC32288 Apramycin (Nebramycin II) Apramycin (Nebramycin II), an aminoglycoside antibiotic for animals, is widely used to treat Salmonella, Escherichia coli, and other infections. Apramycin (Nebramycin II) Chemical Structure
  52. GC48988 Apramycin (sulfate hydrate)

    Nebramycin II

     An aminoglycoside antibiotic Apramycin (sulfate hydrate) Chemical Structure
  53. GC12855 Apramycin Sulfate Apramycin Sulfate, an aminoglycoside antibiotic for animals, is widely used to treat Salmonella, Escherichia coli, and other infections. Apramycin Sulfate Chemical Structure
  54. GC15200 Aprepitant

    Emend, L754,030, MK-869, ONO7436

     Substance P (SP) inhibitor Aprepitant Chemical Structure
  55. GC49776 Apricitabine

    AVX754, BCH 10618, (-)-BCH 10652, (-)-dOTC, SPD-754

     Apricitabine Chemical Structure
  56. GC12900 Aprotinin

    Bovine Pancreatic Trypsin Inhibitor, BPTI

     Aprotinin, a naturally occurring serine protease inhibitor, saves lives and decreases the risk of stroke and repeat surgery for massive bleeding. Aprotinin Chemical Structure
  57. GC64848 APX2039 APX2039 is an orally active and potent inhibitor of the fungal Gwt1 enzyme. APX2039 Chemical Structure
  58. 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
  59. GC73665 Arbemnifosbuvir

    AT-752 free base

     Arbemnifosbuvir is a nidovirus DdRp-associated nucleotidyltransferase (NiRAN) domain of non-structural protein 12 (nsp12)-interfering drugs. Arbemnifosbuvir Chemical Structure
  60. GC13979 Arbidol HCl

    Umifenovir hydrochloride

     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
  61. GC71253 ARC7 ARC7 can act as a probe for secondary metabolism in S. coelicolor. ARC7 Chemical Structure
  62. GC72189 Argadin Argadin is a cyclopentapeptide chitinase inhibitor. Argadin Chemical Structure
  63. GC35387 Aristeromycin Aristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor. Aristeromycin Chemical Structure
  64. GC49103 Aromadendrene

    (+)-Aromadendrene, 10(14)-Aromadendrene

     A sesquiterpene with diverse biological activities Aromadendrene Chemical Structure
  65. GC35399 Artefenomel

    OZ439

     An antimalarial agent Artefenomel Chemical Structure
  66. 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
  67. GC12784 Artemether (SM-224)

    (+)-Artemether, SM-224

     An antiparasitic compound Artemether (SM-224) Chemical Structure
  68. GC41610 Artemisinic Acid

    Artemisic Acid

     Artemisinic acid (Qing Hao acid), an amorphane sesquiterpene isolated from Artemisia annua L. Artemisinic Acid Chemical Structure
  69. GN10647 Artemisinine

    NSC 369397

     Artemisinine Chemical Structure
  70. GC34475 Artemisone Artemisone (Artemifone) is a potent and semi-synthetic antimalarial, inhibits P. Artemisone Chemical Structure
  71. GC32205 Artemotil (β-Arteether)

    Artemotil, Dihydroartemisinin ethyl ether, NSC 665971

     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
  72. GC32231 Arterolane (OZ 277)

    OZ277, RBx-11160

     Arterolane (OZ 277) is an antimalarial agent, with IC50 of both 1.1 nM against P. Arterolane (OZ 277) Chemical Structure
  73. GC10889 Artesunate

    Artesunic Acid, NSC 712571, WR 256283

     Artesunate is an antimalarial compound and an inhibitor of signal transducer and activator of transcription 3 (STAT-3) and membrane glutathione S-transferase (EXP1). Artesunate Chemical Structure
  74. GC63501 ARX-1796

    AV-006

     ARX-1796 (AV-006), an Avibactam prodrug, is an orally bioavailable β-lactamase inhibitor. ARX-1796 Chemical Structure
  75. GC72211 Arylomycin A2 Arylomycin A2, an antibiotic (Antibiotic), is a lipopeptide type I signal peptidase (SPase I) inhibitor. Arylomycin A2 Chemical Structure
  76. GC70506 Ascamycin Ascamycin is a 5'-O-sulfonamide ribonucleoside antibiotic produced by Streptomyces sp. Ascamycin Chemical Structure
  77. GC70457 Ascaridole Ascaridole is an anthelmintic and also has antimalarial activity. Ascaridole Chemical Structure
  78. GC13215 Ascomycin(FK 520)

    Changchuanmycin, FK-520, FR900520, Immunomycin, L 683590

     A potent macrolide immunosuppressant Ascomycin(FK 520) Chemical Structure
  79. GC62290 Ascr#18 Ascr#18, an ascaroside, is a hormone of nematodes. Ascr#18 Chemical Structure
  80. GN10702 Asiatic acid

    Dammarolic Acid, NSC 166063

     Asiatic acid Chemical Structure
  81. 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
  82. GC15706 Aspirin (Acetylsalicylic acid)

    Acetylsalicylic Acid, NSC 27223, NSC 406186

     A non-selective, irreversible COX inhibitor Aspirin (Acetylsalicylic acid) Chemical Structure
  83. GC63886 Aspoxicillin Aspoxicillin is a broad-spectrum antimicrobial agent against 68 isolates of Actinobacillus pleuropneumoniae with an MIC90 value of <= 0.05 μg/ml. Aspoxicillin Chemical Structure
  84. GC14458 Asunaprevir (BMS-650032)

    BMS 650032

     An HCV NS3/4A protease inhibitor Asunaprevir (BMS-650032) Chemical Structure
  85. GC61821 AT-130 AT-130, a phenylpropenamide derivative, is a potent hepatitis B virus (HBV) replication non-nucleoside inhibitor. AT-130 Chemical Structure
  86. GC62320 AT-511

    AT-511

     AT-511 (AT-511) is a potent and orally active HCV viral replication inhibitor. AT-511 Chemical Structure
  87. GC62321 AT-527

    Bemnifosbuvir hemisulfate

    AT-527(Bemnifosbuvir hemisulfate), a hemisulfate salt of AT-511, a guanosine nucleotide proagent, is a potent and orally active HCV viral replication inhibitor.

     AT-527 Chemical Structure
  88. GC63412 AT-9010 tetrasodium

    AT-9010 tetrasodium, a triphosphate active metabolite of AT-527, is a potent inhibitor of NiRAN (a function essential for viral replication).

     AT-9010 tetrasodium Chemical Structure
  89. GC12945 Atazanavir

    BMS 232632, CGP 73547

     An inhibitor of HIV-1 protease Atazanavir Chemical Structure
  90. GC10240 Atazanavir sulfate (BMS-232632-05) An inhibitor of HIV-1 protease Atazanavir sulfate (BMS-232632-05) Chemical Structure
  91. GC46887 Atazanavir-d6 An internal standard for the quantification of atazanavir Atazanavir-d6 Chemical Structure
  92. GC73486 Atevirdine Atevirdine is a potent non-nucleoside HIV-1 reverse transcriptase inhibitor. Atevirdine Chemical Structure
  93. GC60604 Atherosperminine Atherosperminine（Atherospermine）is a nature occurring alkaloid, has antiplasmodial activities in vitro, with an IC50 of 5.80 μM. Atherosperminine Chemical Structure
  94. GC72370 Atoltivimab Atoltivimab (REGN3470), or maftivimab/odesivimab (Inmazeb) is the first Food and agent Administration (FDA)-approved monoclonal antibody to target Zaire ebolavirus (EBOVs) infection. Atoltivimab Chemical Structure
  95. GC17903 Atovaquone

    BW 566C, BW 556C-80

     unique naphthoquinone with broad-spectrum antiprotozoal activity Atovaquone Chemical Structure
  96. GC38889 Atovaquone D4 An internal standard for the quantification of atovaquone Atovaquone D4 Chemical Structure
  97. GC65088 Atovaquone-d5

    Atavaquone-d5

     Atovaquone-d5 Chemical Structure
  98. GC71142 ATP synthase inhibitor 2 ATP synthase inhibitor 2 is a Pseudomonas aeruginosa (PA) ATP synthase inhibitor (IC50=10 μg/mL). ATP synthase inhibitor 2 Chemical Structure
  99. GC35423 Atractylone Atractylone Chemical Structure
  100. GC65180 ATV006

    ATV006

     ATV006 is a potent, orally active antiviral agent and ester prodrugs of GS-441524. ATV006 Chemical Structure
  101. GC32095 AU1235 AU1235, an adamantyl urea, is a potent MmpL3 inhibitor. AU1235 Chemical Structure

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