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Bacterial Related Products (8736)
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Antibodies (14)
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Aureonuclemycin
0 ImagesCat. No.: HY-N12498CAS No.: 123970-01-4Aureonuclemycin can be isolated from Staphylococcus aureus to obtain its biosynthetic gene cluster. Aureonuclemycin exists in two forms: Type A and Type B. Aureonuclemycin A is a nucleoside antibiotic that is structurally similar to herbicides and contains adenine. Aureonuclemycin B contains 5′-deoxyadenosine and exhibits antibacterial activity. Aureonuclemycin can be used in the research of bacterial leaf blight in rice, citrus canker, and bacterial leaf spot in rice. . -
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Herbimycin B
0 ImagesCat. No.: HY-N15076CAS No.: 76207-83-5Herbimycin B is an ansamycin antibiotic that acts as a Src family kinase inhibitor. Herbimycin B has herbicidal effect on most monocotyledons and dicotyledons, inhibits the activity of tobacco Mosaic virus (TMV), HeLa cells and Ehrlich cells. -
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Apo6619
0 ImagesCat. No.: HY-165465CAS No.: 887774-94-9Apo6619 is an iron chelator with antibacterial activity that inhibits a variety of common bacteria associated with hospital-acquired infections. Apo6619 inhibits the growth of relevant bacterial strains in cation-adjusted Mueller-Hinton broth and RPMI 1640 tissue culture medium. Apo6619 can be used in antibacterial research on hospital-acquired infection-related bacteria based on the iron chelation mechanism. -
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Ciclopirox olamine (Standard)
0 ImagesSynonyms: Ciclopirox ethanolamine (Standard); HOE 296 (Standard)Ciclopirox (olamine) (Standard) is the analytical standard of Ciclopirox (olamine). This product is intended for research and analytical applications. Ciclopirox olamine (Ciclopirox ethanolamine) is a synthetic and orally active antifungal agent that can be used for superficial mycoses reseaech. Ciclopirox olamine has a very broad spectrum of activity and inhibits dermatophytes, yeasts, molds, and many Gram-positive and Gram-negative species pathogenic. Ciclopirox olamine also has anticancer and anti-inflammatory effect. -
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Mycinamicin V
0 ImagesCat. No.: HY-N14504CAS No.: 73684-72-7Monamycin V is an ester peptide antibiotic. Monamycin V has activity against Gram-positive bacteria. -
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Riboflavin-d8
0 ImagesCat. No.: HY-B0456S5Synonyms: Vitamin B2-d8 ; E101-d8Riboflavin-d8 (Vitamin B2-d8 ) is deuterium labeled Riboflavin. Riboflavin, an orally active and easily absorbed micronutrient, is a precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), which serve as coenzymes for numerous enzymatic reactions and perform key metabolic functions by mediating the transfer of electrons in biological oxidation-reduction reaction. -
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(S)-Dihydroaeruginoic acid
0 ImagesCat. No.: HY-129316CAS No.: 143209-04-5Synonyms: CGP 52547(S)-Dihydroaeruginoic acid is an antibiotic originally isolated from P. fluorescens. It has antimicrobial activity in a disc assay against R. solani, P. ultimum, B. cinera, S. rolfsii, C. gloeosporioide, F. oxysporum, and S. tritici fungi as well as B. subtilis, E. herbicola, and S. albus bacteria when used at a concentration of 200 μg/disc. -
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LpxH-IN-2
0 ImagesCat. No.: HY-161987CAS No.: 2923230-41-3LpxH-IN-2 (compound 014) is a potent LpxH inhibitor. LpxH-IN-2 shows antibacterial activity for E. coli. -
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LBM-415
0 ImagesCat. No.: HY-102008CAS No.: 478913-91-6Synonyms: NVP-PDF 713; VIC-104959LBM-415 (NVP-PDF 713) is a peptide deformylase (PDF) inhibitor that exhibits inhibitory activity against various antimicrobial-resistant gram-positive cocci, with a MIC90 range of 0.12-8 µg/ml. Additionally, inhibiting efflux pump activity can enhance bacterial sensitivity to LBM415, thereby improving its antibacterial efficacy. -
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Benzydamine
0 ImagesBenzydamine is an orally administered prostaglandin synthesis inhibitor that has anti-inflammatory, analgesic, antipyretic, and antibacterial properties. Benzydamine can inhibit TNF-α, stabilize cell membranes, and reduce oxidative stress within cells. -
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Kerriamycin A
0 ImagesCat. No.: HY-N14258CAS No.: 98474-20-5 -
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3-O-cis-p-Coumaroyl maslinic acid
0 ImagesCat. No.: HY-N7165CAS No.: 69297-40-13-O-cis-p-Coumaroyl maslinic acid (compound 16) is a natural compound isolated from the ethyl acetate extract of leaves of Miconia albicans.3-O-cis-p-Coumaroyl maslinic acid can inhibit PTP1B, with the IC50 of 0.46 μM, and shows antimicrobial activity on Gram-positive bacteria and yeasts. -
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Ethylhydrocupreine hydrochloride (Standard)
0 ImagesCat. No.: HY-136429ARCAS No.: 3413-58-9Synonyms: Optochin hydrochloride (Standard)Ethylhydrocupreine (hydrochloride) (Standard) is the analytical standard of Ethylhydrocupreine (hydrochloride). This product is intended for research and analytical applications. Ethylhydrocupreine hydrochloride (Optochin hydrochloride) is a quinine derivate with antimicrobial activity against S. pneumoniae. Ethylhydrocupreine hydrochloride also possesses antimalarial activity against Plasmodium falciparum, with an IC50 of 25.75 nM. Ethylhydrocupreine hydrochloride is a Gallus gallus taste 2 receptors (ggTas2r1, ggTas2r2 and ggTas2r7) agonist. -
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Erythromycin Ethylsuccinate (Standard)
0 ImagesSynonyms: Erythromycin ethyl succinate (Standard); EES (Standard)Erythromycin Ethylsuccinate (Standard) is the analytical standard of Erythromycin Ethylsuccinate. This product is intended for research and analytical applications. Erythromycin Ethylsuccinate is an antibiotic useful for the treatment of a number of bacterial infections, has an antimicrobial spectrum similar to or slightly wider than that of penicillin. Erythromycin Ethylsuccinate has antiviral activity against HIV-1. -
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Silodosin (Standard)
0 ImagesSynonyms: KAD 3213 (Standard); KMD 3213 (Standard)Silodosin (Standard) is the analytical standard of Silodosin. This product is intended for research and analytical applications. Silodosin (KAD 3213; KMD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH. -
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Napyradiomycin A2
0 ImagesCat. No.: HY-N14412CAS No.: 111216-62-7Napyradiomycin A2 is an antibiotic with anti-Gram-positive bacteria and mycobacterial activity. -
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Peptide 5g
0 ImagesCat. No.: HY-P5730CAS No.: 908065-91-8Peptide 5g is an antimicrobial peptide. Peptide 5g inhibits E. coli, S. aureus, and C. albicans with MIC values of 30, 10, 12.5 μg/mL respectively. -
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Etimicin
0 ImagesCat. No.: HY-182622CAS No.: 59711-96-5Etimicin is a fourth-generation semisynthetic aminoglycoside antibiotic. Etimicin exhibits broad spectrum of activity against gram-positive, gram-negative, and aminoglycoside-resistant bacterial strains, with lower ototoxicity and nephrotoxicity. Etimicin exerts rapid, concentration-dependent bactericidal activity against bacteria. Etimicin can be used for the research of bacterial infections. -
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Megovalicin H
0 ImagesCat. No.: HY-N14360CAS No.: 115932-37-1Megovalicin H has an effect against subtilis and E.coli, and it also has the effect against Pseudomonas aeruginosa. -
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Cinoxacin (Standard)
0 ImagesCat. No.: HY-B1085RCAS No.: 28657-80-9Synonyms: Compound 64716 (Standard)Cinoxacin (Standard) is the analytical standard of Cinoxacin. This product is intended for research and analytical applications. Cinoxacin (Compound 64716), a synthetic antimicrobial related to the quinolone class of orally active antibacterial agent. Cinoxacin has antibacterial activity against many gram-negative aerobic bacteria and inhibits bacterial DNA synthesis. Cinoxacin can be used for the research of urinary tract infections and bacterial prostatitis. -
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