Antibiotic

<p>Doxycycline hydrochloride (Hyclate) is a synthetic tetracycline derivative with similar antimicrobial activity.</p>

FSL-1 TFA activates TLR2/6, boosts HSV-2 defense, and triggers MMP-9 via TLR2, NF-κB/AP-1 in THP-1 cells.

<p>'6'-hydroxydihydrocinchonidine: quinine metabolite with antimicrobial, antitumor properties; inhibits Trypanosoma brucei, Streptococcus pneumoniae.</p>

<p>Adustin is an antifungal antibiotic characterized as a polypeptide that inhibits translation. It effectively suppresses translation in a cell-free rabbit reticulocyte lysate system, exhibiting an IC50 of 0.34 μM.</p>

<p>Ticarcillin disodium is a semi-synthetic, broad-spectrum penicillin, beta-lactamase resistant, inhibits cell wall synthesis, causing cell lysis.</p>

<p>(S)-5-chloro-N-(1-((4-chlorophenyl)amino)-1-oxo-3-phenylpropan-2-yl)-2-hydroxybenzamide has antifungal and tuberculostatic activities.</p>

<p>Acivicin (AT-125) is a chlorinated amino acid antibiotic produced by Streptomyces porcineus, a GGT inhibitor with anticancer and antiparasitic activity.</p>

<p>Borrelidin (Treponemycin) is an inhibitor of trehalose-6-phosphate synthase, a nitrogen-containing macrolide antibiotic isolated from Streptomyces rochei.</p>

<p>Stigmatellin is an antibiotic derived from the cell mass of the myxobacterium, effective against yeasts (yeasts), filamentous fungi (filamentous fungi), and several Gram-positive bacteria (Gram-positive bacteria). Additionally, it serves as a potent inhibitor of photosynthetic electron (photosynthetic electron) transfer. Stigmatellin utilizes various sugars, polysaccharides, and acids from the citric acid cycle as substrates, inhibiting RNA and protein synthesis. It has two different inhibitory sites: one located on the reducing side of photosystem II and the other at the cytochrome b6/f complex. Stigmatellin holds potential for use in antimicrobial and photosynthesis research.</p>

<p>Ac-Pro-Gly-Pro-OH can be used as a CXCR2 agonist with bactericidal and anti-inflammatory activity for the study of sepsis and lung inflammation.</p>

<p>Nanchangmycin, a polyether antibiotic similar to dianemycin, effectively combats diverse nematodes and insects, not mammals/plants.</p>

<p>10-Undecenoic acid (Undecylenic acid) is a natural or synthetic fungistatic fatty acid, with antifungal activity.</p>

<p>Nystatin A3 (Fungicidin) , which belongs to the polyene group of antimycotics, is frequently used as a topical agent in the treatment of oro-pharyngeal</p>

<p>Cefsulodin sodium (Sulcephalosporin) hydrate is a β lactam antibiotic.</p>

<p>6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine) is an antagonist of glutaminases (Ki : 6 μM).</p>

<p>Azlocillin sodium, an acylampicillin, is a broad-spectrum antibiotics</p>

<p>Bac8c is an antimicrobial peptide exhibiting potent activity against both Gram-negative and Gram-positive bacteria. The minimum inhibitory concentrations (MIC) of Bac8c for S. aureus, MRSA, S. epidermidis, E. coli, and P. aeruginosa are 2, 8, 4, 4, and 4 μg/mL, respectively.</p>

<p>C16G2 is a Specific Targeted Antimicrobial Peptide (STAMP) that selectively targets the cariogenic oral pathogen Streptococcus mutans. This compound operates by recognizing and disrupting the bacterial cell membrane, leading to small molecule leakage and the loss of membrane potential, which results in bacterial death. Unlike broad-spectrum antimicrobial peptides, C16G2 exhibits higher selectivity and efficacy against Streptococcus mutans.</p>

<p>Chitotriose, a low molecular weight chitosan oligosaccharide, is extractable from crab shell chitosan. It exhibits antibacterial properties against salmonella.</p>

<p>N-Demethylvancomycin is a glycopeptide antibiotic that can be extracted from Nocardia orientalis and exhibits activity against various strains of Staphylococcus aureus and Staphylococcus epidermidis. It is utilized in research related to infections.</p>