Bacterial
Anything that destroys bacteria or suppresses their growth or their ability to reproduce. Heat, chemicals such as chlorine, and antibiotic drugs all have antibacterial properties. Many antibacterial products for cleaning and handwashing are sold today. Such products do not reduce the risk for symptoms of viral infectious diseases in otherwise healthy persons. This does not preclude the potential contribution of antibacterial products to reducing symptoms of bacterial diseases in the home.
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Bacterial Inhibitors
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Bacterial Agonists
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Bacterial Antagonists
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Bacterial Activators
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Bacterial Modulators
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Bacterial Chemicals
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Bacterial Inducers
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Bacterial Controls
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Bacterial Substrates
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Bacterial Ligand
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Bacterial Related Products (8852)
Related Products (8852)
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Antibodies (14)
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Related Compound Screening Libraries (1)
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Isohematinic acid
0 ImagesCat. No.: HY-N14234CAS No.: 86408-37-9Isohematinic acid has weak anti-anaerobic bacteria action.
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Ambazone monohydrate
0 ImagesAmbazone monohydrate is an orally active membrane active antitumor agent. Ambazone monohydrate also shows antibacterial and weak antiviral activities.
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Pyrisulfoxin A
0 ImagesCat. No.: HY-N14615CAS No.: 187337-07-1Pyrisulfoxin A is an antibiotic found in Streptomyces callfornicus BS-75.
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Anti-MRSA agent 28
0 ImagesCat. No.: HY-174323CAS No.: 2222727-47-9Anti-MRSA agent 28 is an antibacterial agent against multidrug resistant (MDR) gram-positive strains with MICs of 0.06-0.125 μg/mL. Anti-MRSA agent 28 can target DNA polymerase IIIC to reduce the amount of genomic DNA with the IC50 of 3.80 μg/mL. Anti-MRSA agent 28 has good antibacterial activity and reduces inflammation. Anti-MRSA agent 28 can be used against gram-positive strains and infectious conditions.
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Mycobacterium Tuberculosis-IN-7
0 ImagesCat. No.: HY-172397Mycobacterium Tuberculosis-IN-7 (Compound 4c) inhibits M. tuberculosis H37Ra with MIC of 5.34 μg/mL. Mycobacterium Tuberculosis-IN-7 exhibits slight cytotoxicity in cancer cell Vero, A549, and HepG2 (IC50s >50 μM).
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Chlorquinaldol (Standard)
0 ImagesChlorquinaldol (Standard) is the analytical standard of Chlorquinaldol. This product is intended for research and analytical applications. Chlorquinaldol (Chloquinan) is an antibacterial agent with the potential use in topical skin conditions and vaginal infections. Chlorquinaldol is a β-catenin/TCF4 inhibitor, showing anti-proliferation, anti-migration, and apoptosis-inducing activity in cancer cells.
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Demeclocycline (Standard)
0 ImagesCat. No.: HY-121268RCAS No.: 127-33-3Demeclocycline (Standard) is the analytical standard of Demeclocycline (HY-121268). This product is intended for research and analytical applications. Demeclocycline is an orally active tetracycline antibiotic. Demeclocycline impairs protein synthesis by binding to the 30S ribosomal subunit to inhibit binding of aminoacyl tRNA. Demeclocycline shows anti-bacterial activitise to a wide variety of bacterial infections.
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Conimine TFA
0 ImagesCat. No.: HY-N15435APurity: 99.78%Conimine TFA is a steroidal alkaloid, antibacterial agent and potentiator. Conimine TFA is isolated from the seeds of Holarrhena antidysenteriaca Wall.ex A.DC. Conimine TFA exhibits intrinsic antibacterial activity against methicillin-sensitive Staphylococcus aureus and methicillin-resistant Staphylococcus aureus. When combined with Penicillin, Conimine TFA shows synergistic antibacterial effects against methicillin-resistant Staphylococcus aureus; when combined with Vancomycin (HY-B0671), it exerts synergistic antibacterial effects against both methicillin-sensitive and methicillin-resistant Staphylococcus aureus.
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Neoaureothin
0 ImagesCat. No.: HY-N8504CAS No.: 59795-94-7Synonyms: NSC 260179; SpectinabilinNeoaureothin is a bacterial metabolite that has been found in Streptomyces. It is an androgen receptor (AR) antagonist that inhibits binding of dihydrotestosterone (DHT) to ARs (IC50=13 μM) and inhibits DHT-induced expression of prostate-specific antigen in LNCaP cells (IC50=1.75 nM). Neoaureothin is cytotoxic to A549, HCT116, and HepG2 cells (IC50s=34.3, 47, and 37.2 μg/mL, respectively). It also has nematocidal activity against the pine wood nematode B. xylophilus (LC50=0.84 μg/mL) and increases survival of P. densiflora trees inoculated with B. xylophilus.
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A-867191 hydrochloride
0 ImagesCat. No.: HY-19951ACAS No.: 162763-53-3A-867191 hydrochloride is a 2-pyridone DNA gyrase inhibitor. A-867191 hydrochloride has antibacterial activity. A-867191 hydrochloride can be used for research on infections.
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Fluconazole hydrate
0 ImagesCat. No.: HY-B0101ACAS No.: 155347-36-7Synonyms: UK 49858 hydrateFluconazole (UK-49858) hydrate is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole hydrate inhibits C. albicans and Candida kefyr with IC99s range from 0.20 μg/mL to 0.39 μg/mL.
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Cissetin
0 ImagesCat. No.: HY-N15059CAS No.: 691407-97-3Cissetin shows activity against Gram-positive bacteria, including drug-resistant strains.
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BDM31827
0 ImagesCat. No.: HY-120138CAS No.: 1388658-04-5BDM31827 is an EthR inhibitor. BDM31827 can be used for multidrug-resistant-tuberculosis research.
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Monamycin D2
0 ImagesCat. No.: HY-N14077CAS No.: 31556-79-3Monamycin D2 is an ester peptide antibiotic. Monamycin D2 has activity against Gram-positive bacteria.
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Balofloxacin (Standard)
0 ImagesCat. No.: HY-B0159RCAS No.: 127294-70-6Synonyms: Q-35 (Standard)Balofloxacin (Standard) is the analytical standard of Balofloxacin. This product is intended for research and analytical applications. Balofloxacin (Q-35) is an orally active fluoroquinolone antibiotic with broad-spectrum antibacterial activity against gram-negative, gram-positive, and anaerobic bacteria. Balofloxacin can be used for the research of respiratory, intestinal, and urinary tract infections.
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Kikumycin A
0 ImagesCat. No.: HY-124431CAS No.: 37913-77-2Kikumycin A is an antibiotic, which can be generated from Streptomyces. Kikumycin A exhibits antibacterial activity against Gram-positive and Gram-negative bacteria. Kikumycin A exhibits antitrichomonal activity, with MIC of 25 μg/mL for Trichomonas foetus.
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Rubiadin (Standard)
0 ImagesRubiadin (Standard) is the analytical standard of Rubiadin (HY-N0444). This product is intended for research and analytical applications. Rubiadin is an orally active free radical scavenger that inhibits the activation of the NF-κB pathway. Rubiadin inhibits osteoclast formation, bone resorption, lipid peroxidation, HBV DNA replication and cancer cell proliferation; reduces pro-inflammatory cytokine levels; induces cancer cell apoptosis; and possesses antifungal, antimalarial, antibacterial and anticonvulsant activities. Rubiadin can be used in the research of osteoporosis, acute inflammation, chronic inflammation, carbon tetrachloride-induced liver injury, Alzheimer's disease, breast cancer, iron overload disorders, hepatitis B virus infection, colon cancer, liver cancer, T-lymphocytic leukemia, cervical cancer, diabetic nephropathy, epileptic seizures, fungal infections, malaria and bacterial infections.
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Antibiotic adjuvant 4
0 ImagesCat. No.: HY-181935CAS No.: 2493985-50-3Antibiotic adjuvant 4 (Compound 13) is an Antibiotic adjuvant and efflux pump inhibitor. Antibiotic adjuvant 4 exhibits potent efflux pump inhibitory activity. Antibiotic adjuvant 4 significantly downregulates virulence-related genes of Staphylococcus aureus when used alone or in combination with antibiotics. Antibiotic adjuvant 4 enhances the efficacy of Ciprofloxacin (HY-B0356) against multiagent-resistant Staphylococcus aureus strains.
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Valifenalate (Standard)
0 ImagesSynonyms: IR5885 (Standard); Valiphenal (Standard)Valifenalate (Standard) is the analytical standard of Valifenalate. This product is intended for research and analytical applications. Valifenalate (IR5885; Valiphenal) is an insecticide agent and fungicide, which is approved for application on high-value crops such as grapes, tomatoes and other vegetables. Valifenalate interferes with cell-wall synthesisValifenalate is effective against various types of mildew. Valifenalate can be used against crown rot of rose cuased by Phytophthora citrophthora. Valifenalate induces non-adverse thyroid changes via adaptive induction of uridine 5’-diphosphoglucuronosyltransferase (UGT) in the liver of dogs and rats.
