Items 71 to 80 of 499 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Antibiotic TAN 420E | 91700-93-5 | sc-202058 | 500 µg | $250.00 | ||
Antibiotic TAN 420E demonstrates remarkable behavior as an acid halide, primarily through its ability to form stable intermediates during acylation processes. Its high electrophilicity promotes swift reactions with nucleophiles, particularly thiols and alcohols, resulting in a variety of functionalized products. The compound's unique steric configuration not only influences reaction kinetics but also enhances regioselectivity, making it a versatile participant in synthetic pathways. | ||||||
Cefdinir | 91832-40-5 | sc-217854 | 10 mg | $150.00 | ||
Cefdinir is distinguished by its unique structural configuration, which allows for effective hydrogen bonding and dipole-dipole interactions. This compound exhibits a notable tendency to undergo hydrolysis, leading to the formation of reactive intermediates that can participate in diverse chemical reactions. Its solubility in polar solvents enhances its reactivity, while its stereochemistry influences the selectivity of its interactions with other molecules, contributing to its dynamic behavior in various chemical environments. | ||||||
Lateropyrone | 93752-78-4 | sc-202206 | 5 mg | $147.00 | ||
Lateropyrone exhibits intriguing reactivity as an acid halide, primarily due to its electrophilic carbonyl group, which readily participates in nucleophilic acyl substitution reactions. Its unique cyclic structure contributes to a distinctive steric environment, influencing reaction rates and selectivity. The compound's ability to form stable intermediates enhances its reactivity, while its polar functional groups facilitate interactions with various nucleophiles, leading to diverse synthetic pathways. | ||||||
Cyproconazole | 94361-06-5 | sc-205641 sc-205641A | 5 g 10 g | $102.00 $145.00 | 2 | |
Cyproconazole is a triazole fungicide that operates through the inhibition of ergosterol biosynthesis, a critical component of fungal cell membranes. Its unique molecular structure allows for specific binding to the enzyme lanosterol demethylase, disrupting the conversion of lanosterol to ergosterol. This interaction alters membrane fluidity and integrity, leading to cell death. The compound's hydrophobic characteristics enhance its affinity for lipid-rich environments, influencing its distribution and efficacy in various substrates. | ||||||
Cefotiam Hexetil Hydrochloride | 95789-30-3 | sc-211042 sc-211042A | 10 mg 50 mg | $260.00 $970.00 | ||
Cefotiam Hexetil Hydrochloride exhibits unique reactivity as an acid halide, engaging in acylation reactions that facilitate the formation of amides and esters. Its electrophilic carbonyl group enhances nucleophilic attack, leading to rapid reaction kinetics. The compound's hydrophilic characteristics promote solubility in aqueous environments, while its structural configuration allows for specific interactions with nucleophiles, influencing reaction pathways and product formation. This behavior underscores its potential in diverse chemical applications. | ||||||
Streptothricin sulfate | 96736-11-7 | sc-203284 sc-203284A | 1 mg 5 mg | $38.00 $63.00 | 2 | |
Streptothricin sulfate is a complex glycoside that exhibits unique binding properties to ribosomal RNA, inhibiting protein synthesis in susceptible organisms. Its structure allows for specific interactions with the ribosomal A-site, leading to misreading of mRNA and subsequent production of faulty proteins. The compound demonstrates notable stability in various pH conditions, influencing its reactivity and efficacy in diverse environments. Its kinetic profile reveals a gradual accumulation of effects, contributing to its overall impact on cellular processes. | ||||||
Lemofloxacin | 98079-51-7 | sc-279272 | 100 mg | $250.00 | 1 | |
Lemofloxacin is a synthetic compound characterized by its unique ability to form chelate complexes with metal ions, enhancing its reactivity in various chemical environments. Its structure facilitates strong hydrogen bonding and dipole-dipole interactions, influencing solubility and stability in different solvents. The compound exhibits distinct kinetic behavior, with rapid reaction rates in alkaline conditions, allowing for versatile applications in complexation and catalysis. | ||||||
Lomefloxacin, Hydrochloride | 98079-52-8 | sc-218660 | 1 g | $55.00 | ||
Lomefloxacin, Hydrochloride is a synthetic fluoroquinolone distinguished by its unique ability to form chelate complexes with metal ions, enhancing its stability in various environments. Its structural features facilitate strong interactions with bacterial enzymes, particularly DNA gyrase, leading to the inhibition of DNA supercoiling. The compound's hydrophilic properties promote solubility in aqueous solutions, influencing its distribution and reactivity in biological systems. | ||||||
Bafilomycin D | 98813-13-9 | sc-202074 | 1 mg | $363.00 | 3 | |
Bafilomycin D is characterized by its selective inhibition of vacuolar ATPases, which plays a crucial role in modulating cellular ion gradients. Its unique molecular architecture facilitates strong interactions with the enzyme's catalytic site, effectively blocking proton translocation. This disruption leads to significant changes in cellular metabolism and energy production. Additionally, Bafilomycin D demonstrates remarkable solubility in organic solvents, enhancing its reactivity with lipid bilayers and membrane structures. | ||||||
Blasticidin A | 100513-53-9 | sc-202082 | 1 mg | $500.00 | 1 | |
Blasticidin A is notable for its selective inhibition of protein synthesis in eukaryotic cells, primarily through its interaction with the ribosomal machinery. It binds to the ribosomal A-site, preventing the incorporation of aminoacyl-tRNA, which disrupts peptide elongation. This compound exhibits a unique kinetic profile, characterized by a high affinity for ribosomes, leading to a pronounced effect on translation dynamics. Its structural features facilitate specific molecular interactions that enhance its potency as a translational inhibitor. | ||||||