Antibiótico

<p>BU-2313 A is a new antibiotic complex. It also active against anaerobes.</p>

Mycinamicin I is a macrolide antibiotic.

<p>Dactylarin: cytotoxic antibiotic from Dactylaria lutea, interacts with thiols, inhibits glycolytic enzymes.</p>

<p>Kijimicin is a polyether antibiotic and human immunodeficiency virus inhibitor in acutely and chronically infected cells.</p>

<p>Cefuzonam sodium: second-gen cephalosporin, effective against Staph aureus where third-gen fails.</p>

<p>Dehydrogriseofulvin is a natural product that can be used as a reference standard. The CAS number of Dehydrogriseofulvin is 3573-90-8.</p>

<p>AB023b is an antibiotic with antifungal properties.</p>

Altromycin C is a new pluramycin-like antibiotic.

<p>Lincosamine is a lincosamide antibiotic produced by Streptomyces lincolnensis.</p>

<p>AB023a is an antibiotic with antifungal properties.</p>

<p>Leucinostatin B is a peptide antibiotic from Paecilomyces lilacinus A-267.</p>

<p>Ruboxyl, a nitroxylated analog of daunorubicin, is an anthracycline antibiotic.</p>

<p>Dechlorogriseofulvin is a useful organic compound for research related to life sciences. The catalog number is T124937 and the CAS number is 3680-32-8.</p>

<p>PF-06647263 (anti-EFNA4-ADC) is a compound targeting EFNA4-ADC SDC, with anti-tumor activity.</p>

<p>Bismuth Subcitrate is an antibiotic used to treat stomach ulcers associated with Helicobacter pylori, a bacterial infection.</p>

Deltamycin A1 is a novel macrolide antibiotic.

<p>Sulbenicillin is an alpha-sulfobenzylpenicillin. It has been used in combination with dibekacin.</p>

<p>Nanaomycin A, a quinone antibiotic, reactivates cancer suppressor genes and inhibits DNMT3B (IC50=500nM).</p>

Landomycin A is a prominent angucycline hexasaccharide antibiotic from Streptomyces sp.

<p>TANDEM (quinoxaline) is a synthetic analog of antibiotics quinoxaline.</p>

<p>Prumycin is an agent of antifungal antibiotic.</p>

<p>Clindamycin sulfoxide, an active clindamycin metabolite formed by CYP3A4, inhibits P. prevotti, B. fragilis, C. sordelli with MICs 2, 2, 1 mg/L.</p>

<p>Propionylmaridomycin is a macrolide antibiotic.</p>

<p>Asterric Acid is a useful organic compound for research related to life sciences. The catalog number is T21860 and the CAS number is 577-64-0.</p>

<p>Fumitremorgin C (12α-Fumitremorgin C) is a mycotoxin and inhibits ABCG2/BRCP.</p>

<p>Biotinylated isoxazole is a biotin-conjugated derivative of isoxazole. It can induce the formation of aggregates associated with RNA granules.</p>

<p>Josamycin propionate is a macrolide antibiotic.</p>

<p>Amoxicillin, L- is an antibiotic. It is also useful for the treatment of a number of bacterial infections.</p>

<p>Oseltamivir acid methyl ester hydrochloride, a precursor to oseltamivir, is converted by CES1.</p>

<p>A-39183A, from Streptomyces NRRL 12049, targets penicillin-resistant S. aureus &amp; S. faecalis (MICs 32 μg/ml), plus other anaerobes (MICs 16-128 μg/ml).</p>

<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.

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

Farinomalein A, a maleimide derivative, is isolated from the entomopathogenic fungus Paecilomyces farinosus. It exhibits effective inhibitory activity against soybean pathogen Phytophtora sojae.

<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>