Antifection

Items 301-350 of 4946

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  1. Tolfenpyrad is a pesticide that was first approved in 2002 in Japan.
  2. Tulathromycin A is a macrolide antibiotic.
  3. protein kinase G (PknG) inhibitor

    AX20017 is a small-molecule protein kinase G (PknG) inhibitor with an IC50 of 0.39 μM.
  4. CMV inhibitor

    Letermovir is a novel inhibitor of CMV, which targets the viral terminase complex and remains active against virus resistant to DNA polymerase inhibitors.
  5. Carbendazim is a broad-spectrum benzimidazole fungicide which can be used to control a broad range of diseases on arable crops, fruits, vegetables, ornamentals and medicinal herbs.
  6. DprE1 inhibitor

    BTZ043 is an inhibitor of decaprenyl-phosphoribose-epimerase (DprE1), with MICs of of 2.3 nM and 9.2 nM for M. tuberculosis H37Rv and Mycobacterium smegmatis, respectively.
  7. peptide deformylase inhibitor

    Lanopepden (GSK 1322322) is a peptide deformylase inhibitor active against Staphylococcus aureus strains with MICs of 1 and 1 mg/L for ATCC 29213 and ATCC 25923 strain, respectively.
  8. Pyrindamycin B is an antibiotic, actives against gram-positive and gram-negative bacterias, and exhibits strong therapeutic effects against both drug-sensitive and resistant cells of P388 leukemia in mice.
  9. flaviviruse inhibitor

    NITD008 is a potent and selective flaviviruse inhibitor which can inhibit Dengue Virus Type 2 (DENV-2) with an EC50 of 0.64 μM.
  10. gyrase B inhibitor

    VXc-486 is a gyrase B inhibitor, with bactericidal activity.
  11. mycobactin biosynthesis inhibitor

    Salicyl-AMS is a mycobactin biosynthesis inhibitor which can also inhibit M. tuberculosis growth in vitro under iron-limited conditions.
  12. Amcinafal is an active diol, used against virus replication and interferon production.
  13. Levomecol (Chloramphenicol), made up of Chloramphenicol, Methyluracil, is a broad-spectrum antibiotic that is derived from the bacterium Streptomyces venezuelae.
  14. MCB-3681 is the antibacterial Oxaquin's active substance, active against gram-positive bacterium.
  15. Antibacterial compound 2 is a useful antibacterial agent extracted from patent US5652238, compound example 9.
  16. cyclophilin A inhibitor

    Cyclophilin inhibitor 1 is a potent and orally bioavailable cyclophilin A inhibitor, with a Kd of 5 nM, shows effective anti-HCV activity, with an EC50 of 98 nM for HCV 2a.
  17. LRS inhibitor

    Leu-AMS (compound 6), a leucine analogue, is a potent inhibitor of leucyl-tRNA synthetase (LRS) with an IC50 of 22.34 nM, which inhibits the catalytic activity of LRS but did not affect the leucine-induced mTORC1 activation.
  18. Cefotetan disodium is a semisynthetic cephamycin antibiotic that exerts its bactericidal effects by inhibition of cell-wall synthesis.
  19. DuP 105 is an orally active oxazolidinone, a new class of synthetic antimicrobial agent with activity against gram-positive bacteria.
  20. Moniliformin sodium salt is a potent, water-soluble mycotoxin isolate from Fusarium moniliforme.
  21. CRS400393 is a potent antimycobacterial agent, with MIC of 0.03, 2, and ?? 0.12 ?g/mL against M. abs., M. avium, M. intracellulare, and M. tuberculosis, respectively.
  22. DENV NS2B-NS3 protease inhibitor

    ZINC03129319 is a dengue virus (DENV) NS2B-NS3 protease inhibitor extracted from patent US20150141521A1, has inhibition constants (Ki1) of 92±15 μM and Ki3 of 20±4 μM.
  23. Xanthorrhizol, isolated from Curcuma xanthorrhiza Roxb, is a potential antibacterial agent.
  24. AHCY inhibitor

    Aristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor.
  25. Mycobacterium tuberculosis

    AU1235 is an adamantyl urea inhibitor of Mycobacterium tuberculosis.
  26. ribosome rescue inhibitor

    KKL-10 is a small-molecule ribosome rescue inhibitor with broad-spectrum antimicrobial activity against bacteria.
  27. PF 03709270 is an orally available ester prodrug form of sulopenem, with broad-spectrum antibacterial activity against most gram-positive and gram-negative bacteria.
  28. Nifursemizone is an antiprotozoal drug.
  29. MmpL3 inhibitor

    NITD-349 is an MmpL3 inhibitor that shows highly potent anti-mycobacterial activity with MIC50 of 23 nM against virulent Mycobacterium tuberculosis H37Rv.
  30. MmpL3 inhibitor

    BM635 is a MmpL3 inhibitor with outstanding anti-mycobacterial activity. BM635 has an MIC50 of 0.12 μM against M. tuberculosis H37Rv.
  31. WQ 2743 is a potent antimicrobial agent.
  32. Letrazuril is an anti-HIV agent.
  33. Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA) with the MIC90 value of 2 mcg/mL.
  34. Polymyxin B nonapeptide is a cyclic peptide obtained from Polymyxin B by proteolytic removal of its terminal amino acyl residue. Polymyxin B nonapeptide is less toxic, lacks bactericidal activity, and retains its ability to render gram-negative bacteria susceptible to several antibiotics by permeabilizing their outer membranes.
  35. cholesterol synthesis/Hedgehog inhibitor

    U18666A, a cell permeable drug, is a cholesterol synthesis and transport inhibitor.
  36. oxazolidinone antibiotic

    PNU288034 is a potent oxazolidinone antibiotic.
  37. antibacterial candidate for clinical trials

    Zabofloxacin (DW-224a Free base) is a novel fluoronaphthyridone quinolone with a 7-pyrrolidone substituent that is considered a potent antibacterial candidate for clinical trials.
  38. anti-tuberculosis agent

    TBAJ-587, a potent anti-tuberculosis agent, inhibits M.tb strain H37Rv growth with MIC90s of 0.006 and <0.02 ?g/mL in MABA and LORA assay, respectively.
  39. Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial drug, which is active against both Gram-negative and Gram-positive bacteria.
  40. Antifungal agent 1 is a potent antifungal agent.
  41. MF 5137 is a potent antibacterial agent.
  42. Nucleocidin is an antitrypanosomal antibiotic, inhibiting the transfer of labeled amino acid from S-RNA to protein.
  43. Dihydrofolate inhibitor

    Iclaprim is a new selective bacterial Dihydrofolate inhibitor, which can inhibit the growth of S. aureus (MRSA) with an MIC90 of 0.06 μg/mL.
  44. RMI 10874 is a tilorone analogue. Tilorone is a small-molecule, orally bioavailable antiviral agent. RMI 10874 completely abolishes lung colonization of an H-2 negative (GR9.B9) MCA-induced fibrosarcoma clone.
  45. DNA gyrase inhibitor

    Closthioamide is a potent inhibitor of bacterial DNA gyrase and highly active against Ec, MRSA, VRE and Mv), with MICs of 9.00 μM, 0.58 μM, 0.58 μM and 72.03 μM respectively.
  46. Xenalamine is a synthetic antiviral agent.
  47. antifungal drug

    Chlordantoin is an antifungal drug which can be used to treat vaginal candidiasis.
  48. Sulfasymazine is a sulfonamide drug and displays antibacterial properties.
  49. broad-spectrum arenavirus inhibitor

    ST-193 is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, Lassa and Machupo virus with IC50 values of 0.44, 0.62, 1.4 and 3.1 nM, respectively.
  50. HIV-1 reverse transcriptase inhibitor

    beta-L-D4A is a nucleoside HIV-1 reverse transcriptase inhibitor.

Items 301-350 of 4946

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