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Bacterial

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN251858 Human β-defensin-1 452274-53-2

    Human β-defensin-1 (HβD-1) is a cysteine-rich cationicskin-antimicrobial peptide (SAP)produced by all epithelial surfaces, but also by circulatory cells and cells of the reproductive tract. Human β-defensin-1 has antimicrobial...

  • YN250617 SQ109 502487-67-4

    SQ109 is a potent inhibitor of thetrypomastigoteform of the parasite, with IC50for cell killing of 50±8nM. SQ109, targetsMmpL3, is an antitubercular agent.

  • YN250668 Deferasirox (Fe3+ chelate) 554435-83-5

    Deferasirox Fe3+ chelate is a rationally-designed oral iron chelator; its main use is to reduce chronic iron overload in patients who are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic ...

  • YN250686 AFN-1252 620175-39-5

    AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.

  • YN250640 CHIR-090 728865-23-4

    CHIR-090 is a potent, slow, tight-binding inhibitor of theLpxCdeacetylase. It binds toE. coliLpxCwith a Ki of 4.0nM.

  • YN251694 Tropodithietic acid 750590-18-2

    Tropodithietic acid is a sulfur-containing antibiotic produced by the marine bacteriumPhaeobacter inhibens. Tropodithietic acid exhibits a strong antibiotic activity against a broad spectrum of bacteria including alpha- and gammaproteo...

  • YN250765 Solithromycin 760981-83-7

    Solithromycin, belonging to the well-known class of macrolide antibiotics that also includes azithromycin, is a potent bacterial protein synthesis inhibitor.

  • YN250353 ML406 774589-47-8

    ML406 is a small molecule probe that showsanti-tubercularactivity viaM.tuberculosisBioA(DAPA synthase) enzyme inhibition with an IC50 of 30nM.M.tuberculosisBioA is an enzyme involved in biotin biosynthesis inM.tuberculosis.

  • YN250205 MCB-3681 790704-42-6

    MCB-3681 is the antibacterial Oxaquin's active substance, active against gram-positive bacterium.

  • YN251822 PBP10 794466-43-6

    PBP10 is a cell permeable and selective gelsolin-derived peptide inhibitor offormyl peptide receptor 2 (FPR2)over FPR1. PBP10 is a 10-AA peptide with rhodamine conjugated at its N terminus, exerts bactericidal activity agai...

  • YN251817 LF11 832729-13-2

    LF11 is a peptide withantibacterialactivity.

  • YN251816 Lauryl-LF 11 832729-14-3

    Lauryl-LF 11, N-terminally acylated analogue of LF11, is a peptide withantibacterialactivity.

  • YN250442 MAC-545496 838810-96-1

    MAC-545496 is a nanomolar glycopeptide-resistance-associated protein R(GraR) inhibitor with strong binding affinity to the full-length GraR protein (Kd ≤ 0.1 nM). MAC-545496 can reverse β-lactam resistance in methic...

  • YN250610 Bedaquiline 843663-66-1

    Bedaquiline(TMC207; R207910) is an anti-tuberculosis drug which selectively inhibit the mycobacterial energy metabolism i.e. ATP synthesis and found to be effective against all states of Mycobacterium tuberculosis.

  • YN250611 Bedaquiline fumarate 845533-86-0

    Bedaquiline fumarate, an oral diarylquinoline, is a bactericidal antimycobacterial drug. It is a proton-translocating ATP synthetase inhibitor.

  • YN250420 dmDNA31 845625-44-7

    dmDNA31 is a rifamycin-class antibiotic that inhibits bacterial DNA-dependent RNA polymerase with potent bactericidal activity against S.aureus.

  • YN250604 Tedizolid 856866-72-3

    Tedizolid phosphate is a novel oxazolidinone with activity against Gram-positive pathogens.

  • YN250605 Tedizolid phosphate 856867-55-5

    Tedizolid is an oxazolidinone-class antibiotic. Tedizolid phosphate is a phosphate ester prodrug of the active compound tedizolid.

  • YN250176 Salicyl-AMS 863238-55-5

    Salicyl-AMS is amycobactin biosynthesisinhibitor which can also inhibitM. tuberculosisgrowthin vitrounder iron-limited conditions.

  • YN250074 KKL-35 865285-29-6

    KKL-35 inhibits the trans-translation tagging reaction with an IC50 of 0.9 µM. It has broad-spectrum antibiotic activity.

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