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Bacterial Related Products (8893)
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Antibodies (14)
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Plazomicin
0 ImagesCat. No.: HY-16955CAS No.: 1154757-24-0Synonyms: ACHN 490Plazomicin (ACHN 490) is a semi-synthetic aminoglycoside Antibiotic. Plazomicin acts as a substrate for Aminoglycoside acetyltransferase and Aminoglycoside phosphotransferase. Plazomicin is not modified by various common aminoglycoside-modifying enzymes. Plazomicin selectively inhibits MATE2-K. Plazomicin exhibits activity against multidrug-resistant bacteria, including carbapenem-resistant Enterobacterales. -
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Teicoplanin A2-2
0 ImagesCat. No.: HY-130337CAS No.: 91032-26-7Teicoplanin A2-2 is a glycopeptide antibiotic. Teicoplanin A2-2 exhibits antibacterial activity, particularly against coagulase-negative staphylococci (CNS). Teicoplanin A2-2 inhibits bacterial cell wall synthesis by competitively binding to the terminal D-Ala-D-Ala peptide bonds in the cell wall synthesis process, leading to bacterial death. Teicoplanin A2-2 can be used for research into bacterial resistance mechanisms and the development of new antibiotics. -
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Griseochelin
0 ImagesCat. No.: HY-N14612CAS No.: 91920-88-6Griseochelin has anti-Gram-negative bacterial activity, and has inhibitory effect on coccidioides. -
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Phleomycin E
0 ImagesCat. No.: HY-N14887CAS No.: 11031-13-3Phleomycin E is a heteropeptide antibiotic. Phleomycin E has anti-Gram-positive bacteria, negative bacteria and mycobacterium effects. Phleomycin E extends the survival time of mice transplanted with Ehrman's ascites cancer. Phleomycin E inhibits airy entity carcinoma in mice with an IC50 of 0.31 μg/mL. -
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Cyclo(Gly-His)
0 ImagesCat. No.: HY-P5033CAS No.: 15266-88-3Cyclo(Gly-His) is a liposome-encapsulated cyclic dipeptide with antimicrobial and anticancer activity. Cyclo(Gly-His) has cytotoxicity for HeLa and MCF-7 cell with IC50 values of 1.699 mM and 0.358 mM, respectively. Cyclo(Gly-His) can be used for the research of drug delivery systems. -
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10-Deoxymethymycin
0 ImagesCat. No.: HY-124111CAS No.: 36826-66-1Synonyms: Antibiotic YC 1710-Deoxymethymycin (Antibiotic YC 17) displays antibiotic activity against Gram positive bacteria. -
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Xanthobaccin A
0 ImagesCat. No.: HY-122955CAS No.: 227596-81-8Xanthobaccin A is a potent antibiotic that can be isolated from the culture fluid of Stenotrophomonas sp. strain SB-K88. Xanthobaccin A exhibits activity against fungi and G+ bacteria, induces zoospore immobilization and lysis, inhibits mycelial growth. Xanthobaccin A can be used for the research of beet damping-off disease, bacterial and fungal infection. -
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Josamycin (Standard)
0 ImagesCat. No.: HY-B1920RCAS No.: 16846-24-5Synonyms: EN-141 (Standard)Josamycin (Standard) is the analytical standard of Josamycin. This product is intended for research and analytical applications. Josamycin (EN-141) is an orally active macrolide antibiotic exhibiting antimicrobial activity against a wide spectrum of pathogens, such as bacteria. The dissociation constant Kd from ribosome for Josamycin is 5.5 nM. -
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Zarzissine
0 ImagesCat. No.: HY-N1051CAS No.: 160568-14-9Zarzissine is a cytotoxic guanidine alkaloid that can be isolated from the Mediterranean sponge Anchinoe paupertas. Zarzissine shows antimicrobial and anticancer activities. -
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Meptyldinocap (Standard)
0 ImagesMeptyldinocap (2,4-DNOPC) (Standard) is the analytical standard of Meptyldinocap. This product is intended for research and analytical applications. Meptyldinocap is a fungicide and cytotoxic agent that acts against powdery mildew. Meptyldinocap upregulates the phosphorylation levels of ERK1/2, JNK and p38. Meptyldinocap induces apoptosis and endoplasmic reticulum stress, disrupts calcium homeostasis, inhibits cell proliferation and migration, downregulates the expression of proliferation- and pregnancy-related genes, and triggers mitochondrial dysfunction. Meptyldinocap can be used in studies related to powdery mildew and implantation failure. -
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o-Cymen-5-ol
0 ImagesCat. No.: HY-149155CAS No.: 39660-61-2o-Cymen-5-ol is a broad-spectrum antimicrobial agent with direct antimicrobial activity. o-Cymen-5-ol showed effective minimum inhibitory concentrations (MICs) against a variety of bacteria and fungi, such as Streptococcus mutans and Candida albicans. The combination of o-Cymen-5-ol and zinc showed synergistic effects, enhancing the inhibitory effect against oral pathogens. o-Cymen-5-ol was able to inhibit the glycolysis process and co-enhanced this effect with zinc. o-Cymen-5-ol showed a stronger antibacterial effect in toothpaste than placebo. -
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Cephaibol D
0 ImagesCat. No.: HY-N5177CAS No.: 280774-64-3Cephaibol D is found in the strain of Acremonium tubaKii DSM 12774. Cephaibol D has weak antibacterial activity. -
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Thiethylperazine dimaleate (Standard)
0 ImagesThiethylperazine (dimaleate) (Standard) is the analytical standard of Thiethylperazine (dimaleate). This product is intended for research and analytical applications. Thiethylperazine dimaleate, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine dimaleate is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine dimaleate has anti-emetic, antipsychotic and antimicrobial effects. -
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ATP Synthesis-IN-2
0 ImagesCat. No.: HY-157046ATP Synthesis-IN-2 (Compound 5) is an antibacterial compound. ATP Synthesis-IN-2 is a potent ATP synthesis activity inhibitor with IC50 against Pseudomonas aeruginosa (PA) Value of 0.7 μg/mL. -
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N-Nitrosovancomycin
0 ImagesCat. No.: HY-182823CAS No.: 155386-25-7N-Nitrosovancomycin is an antibacterial agent and an N-terminal nitrosated derivative of vancomycin. N-Nitrosovancomycin exhibits antibacterial activity against Gram-positive bacteria in vitro, but shows no activity against Gram-negative E. coli. The modified N-terminal amino group of N-Nitrosovancomycin cannot be protonated, yet the compound still retains in vitro antibacterial activity. N-Nitrosovancomycin can be used in studies related to Gram-positive bacterial infections. -
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Antibacterial agent 357
0 ImagesCat. No.: HY-184313Antibacterial agent 357 is an Antibacterial agent. Antibacterial agent 357 disrupts bacterial cell membranes, induces ROS accumulation, and triggers metabolic disorders. Antibacterial agent 357 exhibits antibacterial activity against MRSA, Staphylococcus aureus, and Gram-negative bacteria. Antibacterial agent 357 can be used in research related to MRSA infections, S. aureus infections, and Gram-negative bacterial infections. -
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GDI-5755
0 ImagesCat. No.: HY-173617CAS No.: 849616-57-5Synonyms: SAM002706100GDI-5755 (SAM002706100), an antibacterial agent by inhibiting ClpP1P2, inhibits the growth of Mtb and M. bovis BCG, the model organism of mycobacteria. GDI-5755 can be used in the research for tuberculosis (TB). -
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Antitubercular agent-55
0 ImagesCat. No.: HY-180854Antitubercular agent-55 (Compound 2e) is an anti-tuberculous agent. Antitubercular agent-55 exhibits significant inhibitory activity against the standard strain of Mycobacterium tuberculosis H37Rv and also has moderate inhibitory activity against multidrug-resistant TB (MDR-TB). Antitubercular agent-55 has a strong affinity for the key enzyme InhA involved in the biosynthesis of mycotic acids. Antitubercular agent-55 can be used for research on tuberculosis infection caused by Mycobacterium tuberculosis. -
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10(R)-Hydroxystearic acid
0 ImagesCat. No.: HY-W983371CAS No.: 5856-32-6Synonyms: (R)-10-Hydroxyoctadecanoic acid; (R)-10-HSA10(R)-Hydroxystearic acid is a derivative of Oleic acid (HY-N1446). 10(R)-Hydroxystearic acid can be biocatalytically produced by Lactobacillus rhamnosus ATCC 53103. -
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D-Histidine (Standard)
0 ImagesD-Histidine (Standard) is the analytical standard of D-Histidine (HY-W012572). This product is intended for research and analytical applications. D-Histidine is an anti-biofilm agent that targets bacterial quorum sensing systems (such as RhlI/RhlR pathway) and has antibacterial activity. D-Histidine works by non-covalently binding to bacterial regulatory factors or copper ion complexes, selectively inhibiting bacterial biofilm formation and motility. D-Histidine downregulates quorum sensing-related gene expression, reduces the synthesis of virulence factors (such as alginate and proteases), and interferes with bacterial membrane stability, inhibiting biofilm formation, promoting the disintegration of mature biofilms, and enhancing antibiotic sensitivity. D-Histidine is also an efficient catalyst for the salt-induced peptide formation (SIPF) reaction, which promotes the condensation of amino acids to form dipeptides (such as dialanine and dilysine) by forming a complex with copper ions (Cu2+). -
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