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Bacterial Related Products (8893)
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Antibodies (14)
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Related Compound Screening Libraries (1)
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LtaS-IN-2
0 ImagesCat. No.: HY-156416LtaS-IN-2 (compound 13) is a inhibitor of LTA synthesis, and shows antibacterial activity against S. aureus and S. epidermidis, with the MIC90 of 0.5 μg/mL and 1 μg/mL, respectively. LtaS-IN-2 is a derivative of LtaS-IN-1 (HY-135813). -
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Polymyxin S1
0 ImagesCat. No.: HY-N15119CAS No.: 63700-38-9Polymyxin S1 is found in Bacillus Polymyxa RS-6 and is resistant to Gram-positive bacteria. -
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Pacidamycin 5
0 ImagesCat. No.: HY-N14607CAS No.: 122855-43-0Pacidamycin 5 has inhibitory effect on Pseudomonas aeruginosa. Pacidamycin 5 also has effect on a few strains of bacteria such as Suppurative staphylococcus and Escherichia coli. -
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DprE1-IN-10
0 ImagesCat. No.: HY-158700CAS No.: 1254782-81-4DprE1-IN-10 (hit 2) is a Decaprenylphosphoryl-β-D-ribose-2′-epimerase (DprE1) inhibitor. DprE1-IN-10 can be used for tuberculosis research. -
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Cephamycin A
0 ImagesCat. No.: HY-N14005CAS No.: 34279-78-2Cephalomycin A shows weak activity against Gram-positive and negative bacteria. -
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4-Methylaeruginoic acid
0 ImagesCat. No.: HY-N14293CAS No.: 189820-27-74-Methylaeruginoic acid is an antibiotic and is cytotoxic to several human tumor cell lines. -
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Tioxacin
0 ImagesCat. No.: HY-167669CAS No.: 34976-39-1Tioxacin is an orally active bactericide agent. Tioxacin combined with aliphatic amines has activities against G(+) and G (-) bacteria, including Escherichia coli resistant to Nalidixic acid (HY-B0398) and Pseudomonas aeruginosa. -
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Neothramycin A
0 ImagesCat. No.: HY-129331CAS No.: 59593-16-7Neothramycin A is an antibiotic, which can be isolated from Streptomyces. Neothramycin A exhibits board spectrum antimicrobial activity, inhibits Staphylococcus aureus, Klebsiella pneumoniae, Escherichia coli W677, and Saccharomyces cerevisia with MIC of 25-50 μg/mL. Neothramycin A exhibits antitumor efficacy against leukemia in mouse models. -
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Fluoropolyoxin M
0 ImagesCat. No.: HY-N14392CAS No.: 50355-68-5Fluoropolyoxin M has the inhibitory activity of Escherichia coli and Streptococcus faecalis. -
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Topoisomerase inhibitor 6
0 ImagesCat. No.: HY-174227CAS No.: 2987726-03-2Topoisomerase inhibitor 6 (Compound REDX05931) is a dual irreversible inhibitor of DNA gyrase and topoisomerase IV (MIC=0.06 μg/mL against fluoroquinolone-resistant S. aureus). Topoisomerase inhibitor 6 blocks DNA strand break-reunion, inducing lethal DNA damage. Topoisomerase inhibitor 6 is promising for research of Gram-positive bacterial infections (e.g., S. aureus, S. pneumoniae). -
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Chartreusin sodium
0 ImagesCat. No.: HY-121136ACAS No.: 1393-72-2Chartreusin sodium is an antibiotic that is active against certain Gram-positive organisms and mycobacteria. Chartreusin is also active against the Micrococcus fiyogenes v. aureus phage. -
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Epelmycin C
0 ImagesCat. No.: HY-N14157CAS No.: 107807-23-8Epelmycin C has anti-Gram positive, negative bacteria and candida albicans activity, and has anti-leukemic L1210 activity, which is stronger than Aclacinomycin. -
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Helvecardin A
0 ImagesCat. No.: HY-N14673CAS No.: 119979-33-8Helvecardin A is a glycopeptidtic antibiotic. Helvecardin A has strong activity of anti-aerobic and anaerobic Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus. -
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Sulfamethoxazole 1000 µg/mL in methanol
0 ImagesSulfamethoxazole (Ro 4-2130) 1000 μg/mL in methanol is a sulfonamide antibiotic with a widespread antibacterial activity. Sulfamethoxazole 1000 μg/mL in methanol inhibits bacterial folate metabolism by competing with 4-Aminobenzoic acid (HY-B1008) (PABA) to act on dihydropteroate synthetase and dihydropteroate reductase. Sulfamethoxazole 1000 μg/mL in methanol can be used for the study of urinary tract infections (UTIs), prostatitis, and bronchitis. -
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Aurantiogliocladin
0 ImagesCat. No.: HY-W399439CAS No.: 483-54-5Aurantiogliocladin is a weak antibiotic which was active against Staphylococcus epidermidis but not S. aureus. Aurantiogliocladin could inhibit biofilm formation. -
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1,4-Naphthoquinone (Standard)
0 Images1,4-Naphthoquinone is an inhibitor with broad-spectrum inhibitory activity targeting DNA polymerase, NF-κB and monoamine oxidase (MAO-A/B), with antibacterial and anti-biofilm efficacy. 1,4-Naphthoquinone is a competitive inhibitor of MAO-B (Ki=1.4 μM) and a non-competitive inhibitor of MAO-A (Ki=7.7 μM). 1,4-Naphthoquinone inhibits DNA polymerase pol α, β, γ, δ, ε, λ with IC50 ranging from 5.57-128 μM. 1,4-Naphthoquinone inhibits tumor cell proliferation, induces apoptosis and necrosis, and has anti-angiogenic and anti-inflammatory activities by inducing oxidative stress, depleting glutathione (GSH), inhibiting DNA polymerase-mediated DNA synthesis and blocking NF-κB nuclear translocation. 1,4-Naphthoquinone can be used in anti-bacterial , anti-tumor and anti-inflammatory studies, including inhibition of melanoma and colon cancer cell growth and endothelial cell function, as well as LPS-induced inflammation models. -
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Polymyxin B1-D-Leu-d7 TFA
0 ImagesCat. No.: HY-A0248AS1Polymyxin B1-D-Leu-d7 TFA is the deuterium labeled Polymyxin B1 (HY-A0248A). Polymyxin B1 is a potent antimicrobial lipopeptide first derived from Bacilus polymyxa. Polymyxin B1 is the major component in Polymyxin B (HY-A0248). Polymyxin B1 can induce lysis of bacterial cells through interaction with their membranes. Polymyxin B1 has the potential for multidrug-resistant Gram-negative bacterial infections treatment. -
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Naphthoquinomycin A
0 ImagesCat. No.: HY-N14829CAS No.: 101190-62-9Naphthoquinomycin A is an Ansa antibiotic with anti-Gram-positive bacteria and fungi activity, and can inhibit the synthesis of E. coli fatty acids. -
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Tropone (Standard)
0 ImagesCat. No.: HY-W035904RCAS No.: 539-80-0Synonyms: Cycloheptatrienone (Standard)Tropone (Standard) (Cycloheptatrienone (Standard)) is the analytical standard of Tropone (HY-W035904). This product is intended for research and analytical applications. Tropone (Cycloheptatrienone) is a non-benzenoid aromatic natural product that acts as a membrane reverse transporter and metal chelator. Tropone disrupts the proton motive force by affecting the transmembrane proton gradient and functions as a quorum sensing signal through LuxR-type transcriptional regulators. Tropone exhibits broad-spectrum antibiotic, anticancer, algicidal, and probiotic activities. As a virulence factor toxic to rice seedlings, Tropone promotes biofilm formation in Burkholderia plantarii and induces neurotoxicity involving mitochondrial and cytoskeletal damage, increased Ca2+ influx, and oxidative stress. Tropone is used in the study of bacterial infections. -
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