Otros inhibidores

<p>Wuweizidilactone H is a useful organic compound for research related to life sciences. The catalog number is T126503 and the CAS number is 1033288-82-2.</p>

<p>DDMU is a biochemical.</p>

<p>Eburnamonine is a useful organic compound for research related to life sciences and the catalog number is T131582.</p>

<p>Tetrachloroguaiacol, the predominant chlorinated phenol, is generated through the chlorine bleaching process of wood pulp.</p>

<p>2-hydroxy Tricosanoic Acid methyl ester can be used in related research in the field of life sciences.</p>

<p>Dinobuton is a biochemcial.</p>

<p>Biotinyl hexylamine aids in creating ANANAS and tumor-targeting drug conjugates.</p>

<p>Compound N016-0063 is a useful organic compound for research related to life sciences and the catalog number is T131335.</p>

<p>N-Boc-PEG-t-butyl ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules.</p>

<p>Cronaburmine is a useful organic compound for research related to life sciences and the catalog number is T124344.</p>

<p>ACG416B, a potent ChoK inhibitor, has an IC50 of 0.4 μM and strong anti-growth effects on HT-29 colon cancer cells.</p>

<p>Wedeloside is a biochemical.</p>

<p>4'-Hydroxy-5,7,3'-trimethoxyflavone is a useful organic compound for research related to life sciences and the catalog number is T126165.</p>

<p>Leucanthanolide is a sesquiterpene lactone from Montanoa leucantha.</p>

<p>4-Hydroxy-2-methoxyphenol 1-O-(6-O-syringoyl)glucoside is a useful organic compound for research related to life sciences and the catalog number is T123885.</p>

<p>Lysyltyrosine TFA is a dipeptide that may enhance brain function by boosting noradrenaline and tyrosine release.</p>

<p>Geranylgeranyl Pyrophosphate triammonium (GGPP triammonium) regulates endothelial cell proliferation and apoptosis during mouse embryo vasculogenesis.</p>

<p>Ecenofloxacin HCl, the salt form of Ecenofloxacin, is a novel fluoroquinolone antibiotic exhibiting potent antibacterial activity against Gram-positive bacteria, Gram-negative bacteria, and anaerobes.</p>

<p>Tefazoline is a cephalosporin antibiotic.</p>

<p>ADEP-14 (also known as Acyldepsipeptide-14) is an acyldepsipeptide antibiotic that functions by binding to the ClpP protein, thereby facilitating the degradation of newly synthesized proteins and the FtsZ protein within the cell. This process can potentially lead to cell death, making ADEP-14 a promising compound for development.</p>

<p>L-Homocysteine-d4 is the deuterium-labeled variant of L-Homocysteine.</p>

<p>Demethylflavasperone 10-O-β-D-glucopyranoside is a glycoside compound that can be found in the stems of Berchemia racemosa.</p>

<p>2,3,4,6,7,8-Hexachlorodibenzofuran (2,3,4,6,7,8-HxCDF) is a type of polychlorinated dibenzofuran (PCDF). It induces the expression of aryl hydrocarbon hydroxylase (AHH) and ethoxyresorufin-o-deethylase (EROD) genes in H-4-II-E rat hepatoma cells, with EC50 values of 0.687 and 0.575 nM, respectively.</p>

<p>Toralactone-9-O-β-D-glucopyranoside is a phenolic compound that can be extracted from Eriocaulon buergerianum.</p>

<p>4A3-SCC-PH is a degradable ionic lipid (LDIL) characterized by a unique cone-shaped structure responsive to GSH. This configuration enables exceptional endosomal escape and rapid mRNA release.</p>

<p>1,3-Dieicosapentaenoyl glycerol is a diacylglycerol compound featuring eicosapentaenoic acid (EPA) at both the sn-1 and sn-3 positions.</p>

<p>BB-83698 is a peptide deformylase inhibitor with potent antimicrobial against streptococci and Moraxella catarrhalis strains.</p>

<p>(2S)-(+)-2-Hydroxynaringenin-4'-O-β-D-glucopyranoside is a naturally occurring glycoside identified in the plant Baphicacanthus cusia.</p>

<p>Moxifloxacin-d4 hydrochloride (BAY 12-8039-d4) is the hydrochloride salt form of deuterium-labeled Moxifloxacin (Moxifloxacin). This compound acts as an orally effective antibacterial agent and is utilized in research concerning acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and infectious pneumonia.</p>

<p>Tigemonam is an orally administered monocyclic β-lactam antibiotic effective at inhibiting many bacterial strains at concentrations of 1 microgram/ml or lower. It targets Escherichia coli, Klebsiella spp., Enterobacter aerogenes, Citrobacter diversus, Proteus spp., Providencia spp., Aeromonas hydrophila, Salmonella spp., Shigella spp., Serratia marcescens, and Yersinia enterocolitica.</p>

<p>YFJ-36 is an antibiotic that demonstrates superior and broad-spectrum antibacterial activity in vitro compared to cefiderocol, particularly against A. baumannii and K. pneumoniae. In a systemic infection model in mice, YFJ-36 exhibits strong in vivo efficacy. Additionally, the compound shows enhanced physicochemical stability in liquid media with a pH of 6-8 and is noteworthy for its potential to reduce allergy risk due to its quaternary ammonium bond.</p>

<p>1,2-Dipalmitoleoyl-3-11(Z)-octadecenoyl-rac-glycerol is a triacylglycerol that comprises cis-Vaccenic acid and Palmitoleic acid.</p>

<p>EDTA tetrasodium tetrahydrate is a metal chelator known for its ability to bind with divalent and trivalent metal cations, including calcium. It exhibits antihypercalcemic and anticoagulant properties. This compound reduces metal ion-catalyzed oxidative damage to proteins and maintains a reducing environment during protein purification processes, making it commonly used for protein purification and storage. Additionally, it helps in minimizing the formation of disulfide bonds.</p>

<p>Bis[2-(succinimidooxycarbonyloxy)ethyl] sulfone functions as a bifunctional amine-reactive crosslinker, facilitating the conjugation of β-endorphin with opioid receptors. It is utilized as the sulfone derivative of bis(2-hydroxyethyl) succinimide (BES) and plays a critical role in peptide and protein synthesis, as well as in studying enzyme reaction mechanisms.</p>

<p>Pyrenophorin ((-)-Pyrenophorin) is a fungal metabolite found in D. avenae with phytotoxic properties. It exhibits potent cytotoxicity against several cancer cell lines, with IC50 values ranging from 0.07 to 7.8 μM.</p>

<p>Trypanothione synthetase-IN-2: competitive inhibitor for Leishmania TryS, IC50 5.4 μM with spermidine.</p>

<p>28-Acetylbetulin, a lupane derivative of betulin, has anti-inflammatory, anticancer properties, and inhibits NO and PGE2.</p>

<p>3-Methyl-9H-carbazol-2-ol is a useful organic compound for research related to life sciences and the catalog number is T125227.</p>

<p>6-Deoxy-D-glucose is a useful organic compound for research related to life sciences and the catalog number is T124253.</p>

<p>Heleurine is a useful organic compound for research related to life sciences and the catalog number is T124789.</p>

<p>XE 820 is a biochemical.</p>

<p>AI 3-27211 is an insecticide.</p>

<p>Deoxyadenosine diphosphate sodium is a diphosphate nucleoside featuring deoxyadenosine as its nucleoside component. It plays a role in the synthesis and repair of DNA. Deoxyadenosine diphosphate sodium acts as an inhibitor of polynucleotide phosphorylase, thereby interfering with the polymerization of ADP and CDP.</p>

<p>Sporidesmolide II is a cyclic depsipeptide that was initially isolated from P. chartarum.</p>

<p>Relacidine B is an innovative non-ribosomal lipopeptide antibiotic that demonstrates promising activity against Gram-negative pathogens.</p>

<p>Synucleozid-2.0 is an innovative compound under investigation for neurodegenerative disease research, potentially acting by modulating neurotransmitters and cellular signaling pathways.</p>

<p>(S)-C12-200, the (S)-isomer of C12-200, is an ionizable cationic lipid and an auxiliary lipid. It is utilized in the formulation of lipid nanoparticles for mRNA delivery.</p>

<p>1-Stearoyl-2-linoleoyl-3-oleoyl-rac-glycerol is a triglyceride composed of Stearic acid at the sn-1 position, Linoleic acid at the sn-2 position, and Oleic acid at the sn-3 position.</p>

<p>Eniclobrate (Sgd 33374) is a diphenylmethane derivative known for its lipid-lowering effects.</p>

<p>Gramicidin S 2HCl, is an antibiotic. At concentrations of 40-80 μg/mL, GS can reduce planktonic cell numbers within 20-40 minutes. For established biofilms, it effectively kills cells at concentrations of 100-200 μg/mL without regrowth. This anti-biofilm effect results from peptide transmembrane transport and complexation with intracellular nucleotides (including the alarmone ppGpp). GS demonstrates wide-ranging activity against biofilm-forming, drug-resistant infections caused by E. faecalis, proving its efficacy in endodontic treatment. The successful treatment of persistent infections in two volunteer cases further confirms GS's potent therapeutic performance. These studies indicate that GS can be applied in certifying compounds used in endodontics.</p>