Antimicrobianos

<p>Stability Hygroscopic<br>Applications α,α'-Dilaurin is a possible antimicrobial agent against gram-posistive organisms.<br>References Kabara, J., et al.; Antimicrob. Agents Chemother., 2, 23 (1972); Conley, A., et al.: Antimicrob. Agents Chemother., 4, 501 (1973)<br></p>

<p>Applications 1,14-Tetradecanediol is a bioactive component of Hybanthus enneaspermus with anti-microbial activity against microbes.<br>References Anand, T., et al.: Int. J. Pharm. Pharm. Sci., 4, 646 (2012)<br></p>

<p>Applications (+)-Ledene is an essential oil that is synthesized by viridiflorene synthase. It has been studied as an antioxidant, antimicrobial, antibiofilm and to treat various cancers.<br>References Negreiros, M.O., et al.: Pharm. Biol, 54, 3272-3279 (2016)<br></p>

<p>Stability Hygroscopic<br>Applications 1,3-Dibenzyl-1H-benzo[d]imidazol-3-ium Chloride is a useful reagent in the preparation of the antimicrobial benzimidazolium compounds via N-alkylation of benzimidazoles with benzyl chloride.<br>References Meng, J. P., et al.: Adv. Mat. Res., 554, 1686 (2012)<br></p>

<p>Stability Moisture Sensitive<br>Applications 3,6-Dichlorophthalic Anhydride is an intermediate in the synthesis of phthalic compounds, phthalazines, and quinones with antimicrobial activity.<br>References Hansongnern, K., et al. Appl. Magnetic. Resonance., 23, 333 (2003);<br></p>

<p>Stability Air Sensitive<br>Applications 4-(Phenylthio)-1,2-benzenediamine is used in the synthesis of bis(2-chloroethyl)aminophosphoryl-containing compounds which are potential anticancer agents. It is also used in the synthesis of 2-substituted-2,3-dihyrdro-5-thiophenoxy-1H-1,3,2-benzodiazaphosphole 2-oxides which exhibit antimicrobial activity.<br>References Rao, L. N., et al.: Phosphorus Sulfur, 177, 399 (2002); Rao, L. N., et al.: Phosphorus Sulfur, 158, 39 (2000)<br></p>

<p>Applications Silver Bromide is used in the spectroscopic study of silver halides in montmorillonite and their antibacterial activity, also used in the antimicrobial compositions for use in wound care products.<br>References Sohrabnezhad, S., et al.: J. Photochem. Photobiol., 163, 150 (2016); Adams, L. L., et al.: From U.S. Pat. Appl. Publ. (2016), US 20160220728 A1 20160804<br></p>

<p>Applications 4,7-Dichloro-2-phenyl-1H-isoindole-1,3(2H)-dione is an intermediate in the synthesis of phthalic compounds, phthalazines, and quinones with antimicrobial activity.<br>References Marriott, G. J., et al.: J. Chem. Soc., 134 (1939); Katayama, H., et al.: Tetrahedron., 63, 6642 (2007);<br></p>

<p>Applications K252a is a protein kinase inhibitor. It is an analogue of staurosporine (S685000). It shows potent antitumor activity but no antimicrobial activity in vitro, or in vivo toxicity in rodents.<br>References Kase, H., et al.: J. Antibiot., 39, 1059 (1986); Yasuzawa, T., et al.; J. Antibiot., 39, 1072 (1986)<br></p>

<p>Applications A 6-substituted 8-quinolinecarboxylic acid as antimicrobial and genotoxic agent.<br>References Weyer, R., et al.: Arzneim.-Forsch., 24, 269 (1974),<br></p>

<p>Stability Volatile<br>Applications 2,3-Dihydropyran is used in the synthesis of potent and selective myeloperoxidase inhibitors useful as antimicrobial oxidants. Also is used to synthesize novel and selective σ1 receptor ligands.<br>References Soubhye, J. et al.: J. Med. Chem., 56, 3943 (2013); Diaz, J. et al.: J. Med. Chem., 56, 3656 (2013);<br></p>

<p>Applications (Z)​-​Ethyl 2-​chloro-​2-​(2-​(4-​chlorophenyl)​hydrazono)​acetate is a reagent used in the preparation of pyrimidine and pyrimidinone-based compounds for their use as antimicrobials.<br>References Abbas, I et al.: J. Hetero. Chem., 54, 3447 (2017);<br></p>

<p>Stability Hygroscopic<br>Applications Berberrubine Chloride is a novel alkaloid with novel nitric-oxide donating activity. Antitumor and an antimicrobial agent.<br>References Chen, J. et al.: Eur. J. Med. Chem., 132, 173 (2017); Jeyakkumar, P. et al.: Bioorg. Med. Chem. Lett., 27, 1737 (2017);<br></p>

<p>Applications 2,3-Dichloro-6-nitroaniline is used as a reagent in the synthesis of 3-alkyl-, 3-halomethyl- and 3-carboxyethylquinoxaline-2-ones which have potential antimicrobial activity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Carta, A., et al.: Farmaco, 58, 1251 (2003)<br></p>

<p>Applications CSA (cationic steroid antibiotics) is a class of facial amphiphiles with same mechanism of antimicrobial action as that of CPAs (cationic peptide antibiotics).<br>References Sundriyal, S., et al.: J. Mol. Model, 14, 265 (2008).<br></p>

<p>Applications 1-Pyridin-2-yl-propan-2-one is an antimicrobial bioactive compound extracted from Lactarius vellereus fermenting liquor.<br>References Ji, H., et al.: Beijing Linye Daxue Xuebao, 30, 92 (2008); Song, R., et al.: From Faming Zhuanli Shenqing (2008), CN 101230368 A 20080730;<br></p>

AWZ1066S is a synthetic analog, which is a chemically engineered compound designed to mimic or influence biological molecules. This product is derived from sophisticated organic synthesis techniques that enable the precise modification of its molecular structure to enhance its specificity and efficacy. AWZ1066S operates through targeted binding to specific biomolecules or receptors, thereby modulating their function or facilitating their detection in complex biological systems.

Homoembelin is a chemical compound that is classified as a natural product alkaloid, which is derived from specific plant sources, notably the fruit of the plant Embelia ribes. It operates through a variety of biochemical interactions at the molecular level, including the inhibition of specific enzymes and modulation of signaling pathways. This mode of action has garnered interest due to its potential effects in various therapeutic contexts.

<p>Fenpicoxamid-phenol is a fungicide, which is a synthetic chemical compound primarily used in agriculture. It originates from advanced chemical synthesis methods that leverage specific molecular architectures to inhibit fungal growth effectively. The mode of action involves targeting and disrupting fungal respiration at the mitochondrial level, specifically inhibiting complex III of the electron transport chain. This selective interference curtails energy production in the fungal cells, thereby halting their growth and propagation.</p>

<p>Cefotiam is a broad-spectrum cephalosporin antibiotic, which is a beta-lactam compound derived from the mold Acremonium. It functions by inhibiting bacterial cell wall synthesis, particularly by targeting penicillin-binding proteins, which leads to cell lysis and death in susceptible bacteria. This mechanism of action makes it effective against various Gram-positive and Gram-negative bacteria.</p>

<p>6-[(1,1-Dimethylethyl)amino]-1,3,5-triazine-2,4(1H,3H)-dione, commonly known as Terbuthylazine, is a selective systemic herbicide, which is synthesized chemically and primarily sourced from the triazine group of compounds. It operates by inhibiting photosynthesis, specifically interfering with the electron transport in photosystem II. This disruption in the photosynthetic pathway effectively halts the growth of susceptible weed species.</p>

<p>Sulfamethylphenazole is a synthetic antibacterial compound, which is derived from sulfonamides. It functions by inhibiting bacterial dihydropteroate synthase, an enzyme crucial for the synthesis of folate in bacteria. This inhibition leads to the depletion of folate coenzymes, which are essential for DNA synthesis and cell replication in bacteria. As a result, Sulfamethylphenazole effectively halts bacterial growth by exploiting the reliance of bacteria on folate synthesis, a pathway absent in human cells, thereby offering selective toxicity.</p>

<p>Acetophos is an organophosphate insecticide, which is a synthetic chemical compound derived from phosphoric acid. It functions by inhibiting acetylcholinesterase, an essential enzyme in the nervous systems of insects. This inhibition leads to the accumulation of acetylcholine, causing continuous nerve impulses that result in the paralysis and eventual death of the pest.</p>

<p>Napyradiomycin A is a secondary metabolite, classified as a type of antibiotic, which is derived from marine Streptomyces bacteria. This natural product is of considerable interest due to its unique biosynthetic origin, found specifically in marine ecosystems. Napyradiomycin A exhibits its mode of action primarily through the inhibition of bacterial RNA synthesis. This is achieved by interacting with bacterial enzymes, subsequently halting their reproductive and metabolic processes, which makes it a potent antibacterial agent.</p>

<p>SARS-CoV-IN-3 is a small-molecule inhibitor, which is derived through synthetic organic chemistry targeting SARS-CoV-2. It exhibits its mode of action by specifically inhibiting the viral RNA-dependent RNA polymerase (RdRp) enzyme. This enzyme is crucial for viral RNA synthesis, and by inhibiting its activity, SARS-CoV-IN-3 effectively suppresses viral replication within host cells.</p>

<p>Descarbamylnovobiocin is a synthetic derivative of the antibiotic novobiocin, which is originally sourced from Streptomyces species. As a derivative, it modifies certain structural elements of the parent compound to potentially enhance or alter its antimicrobial properties. Its mode of action is primarily through the inhibition of bacterial DNA gyrase and topoisomerase IV, essential enzymes for DNA replication and cell division. By impeding these enzymes, descarbamylnovobiocin disrupts the supercoiling of bacterial DNA, thereby inhibiting bacterial growth and proliferation.</p>

<p>DSHS00884 is a CRISPR-associated enzyme, which is a type of gene-editing tool derived from bacterial immune systems. This enzyme functions as a molecular scissor that targets specific DNA sequences and introduces breaks or modifications at defined loci. The mode of action involves recognizing specific guide RNA sequences that direct the enzyme to complementary DNA sites where it executes precise edits. This precision stems from its ability to form base-pair interactions with the targeted DNA, ensuring minimal off-target effects.</p>

<p>Omadacycline hydrochloride is a modern tetracycline-class antibiotic, which is a synthetic derivative sourced from tetracycline compounds. The mode of action involves binding to the bacterial 30S ribosomal subunit, thereby inhibiting protein synthesis, which ultimately interferes with bacterial growth. Omadacycline exhibits a broad spectrum of activity, showing efficacy against a range of Gram-positive and Gram-negative bacterial strains, including those resistant to other tetracyclines and antibiotics.</p>

<p>Dihydrostreptomycin sesquisulfate is an aminoglycoside antibiotic, which is derived from the bacterium Streptomyces griseus. Its mode of action involves binding to the 30S subunit of the bacterial ribosome, leading to the disruption of protein synthesis. This binding interferes with the initiation complex formation, causing misreading of mRNA and ultimately inhibiting bacterial growth.</p>

Afabicin is an antibiotic, which is a derivative of the natural product lipiarmycin. It acts by inhibiting the bacterial enzyme DNA-dependent RNA polymerase, crucial for bacterial growth and reproduction. This targeted action disrupts RNA synthesis, effectively halting the proliferation of susceptible bacterial strains.

<p>Please enquire for more information about MBX-4132 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

1-(4-Pentyloxy-3-trifluoromethylphenyl)-3-(pyridine-3-carbonyl)thiourea is a synthetic compound employed largely in biochemical research and potential medicinal applications. As a small molecule derivative, it is synthesized through meticulous organic chemistry protocols designed to yield compounds with specific biophysical properties. The compound acts primarily by modulating distinct biochemical pathways, interacting with molecular targets such as enzymes or receptors, thereby influencing biological processes at the cellular level.

<p>Tolnifanide is a fungicidal product, which is a synthetic compound derived from chemical synthesis. It operates by interfering with the normal cellular function of fungi, inhibiting their growth and reproduction. This mode of action involves disrupting key processes within the fungal cells, rendering them unable to thrive in their host environment.</p>

Cauloside A is a steroidal saponin, a type of glycoside compound, which is primarily isolated from the plant Caulophyllum robustum or related species. Saponins are known for their diverse biological activities and the ability to interact with cell membranes due to their amphipathic nature, allowing them to disrupt lipid bilayers.

<p>Aldicarb d3 is an isotopically labeled compound, categorized as a carbamate pesticide, which is derived from chemical synthesis using deuterium labeling. Its mode of action involves the inhibition of acetylcholinesterase, an enzyme essential for nerve function, leading to the disruption of neurological processes in pest organisms.</p>

(E)-Parthenolide is a sesquiterpene lactone, which is a naturally occurring organic compound often extracted from plants such as feverfew (Tanacetum parthenium). This compound exerts its effects primarily through the modulation of NF-kB signaling pathways, which play crucial roles in the regulation of immune responses, cell proliferation, and survival. By inhibiting NF-kB, (E)-Parthenolide can interfere with the expression of genes that promote cell growth and inflammation. This action makes it a compound of interest in cancer research, particularly as a potential therapeutic agent that targets cancer stem cells and reduces chemoresistance. Its applications extend to studying its efficacy in inhibiting tumor growth and inducing apoptosis in various cancer cell lines. Moreover, due to its natural source, (E)-Parthenolide is also being explored for its potential as an anti-inflammatory agent in the treatment of inflammatory conditions.

<p>Nocardicin G is a monocyclic β-lactam antibiotic, which is sourced from certain strains of the soil-dwelling actinobacterium *Nocardia*. This organism is known for its ability to synthesize various bioactive compounds. The mode of action of Nocardicin G involves inhibiting bacterial cell wall synthesis by targeting penicillin-binding proteins, resulting in the bactericidal effect against susceptible bacterial strains. This compound specifically disrupts the formation of the peptidoglycan layer, which is essential for bacterial integrity and survival.</p>

<p>Mafoprazine is an experimental psychotropic drug, which is an organic compound synthetically derived from the azapirone family. It functions primarily as a serotonin receptor agonist, specifically targeting the 5-HT1A receptors, while also exhibiting moderate affinity for dopamine and adrenergic receptors. This dual action on neurotransmitter systems is thought to contribute to its therapeutic effects.</p>

<p>Please enquire for more information about Noracronycine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(2,4,6-Trimethylphenylsulfonyl)-1,2,4-triazole is a sulfonyl-triazole reagent, which is widely utilized in the field of organic chemistry. This compound is synthetically derived, serving as an important tool in the construction of sulfonyl-protected intermediates and heterocyclic structures. Its mode of action involves acting as a versatile electrophile in conditions favoring nucleophilic attack, facilitating the formation of carbon-nitrogen and carbon-sulfur bonds.</p>

4-Epianhydrotetracycline hydrochloride is a chemically modified antibiotic derivative, originating from the structural transformation of tetracycline. It is derived through epimerization and dehydration processes, which alter the parent compound's structure.

<p>BAY-Y 3118 is a synthetic compound specifically designed as a radiolabeled dopamine D4 receptor antagonist. It is sourced from chemical synthesis processes that enable modification of molecular structures to target specific biological receptors. The mode of action of BAY-Y 3118 involves binding to the D4 subtype of dopamine receptors, which are G protein-coupled receptors located in the central nervous system. This binding is typically labeled with a radiolabel to facilitate tracking and visualization in biological assays.</p>

<p>Thiamphenicol is a semisynthetic derivative of chloramphenicol with action on bacterial protein synthesis inhibition and is used for treating bacterial infections, particularly in veterinary medicine.</p>

<p>Clindamycin 3,4-isopropylidene is a semi-synthetic antibiotic derivative of clindamycin, which is derived from the bacterial species Streptomyces lincolnensis. This compound is synthesized through chemical modification, specifically forming an isopropylidene group at positions 3 and 4 of the clindamycin molecule. The inclusion of the isopropylidene moiety alters its physicochemical properties, potentially enhancing its stability or spectrum of activity.</p>

<p>Cefmetazole lactone is an antibiotic, classified as a cephalosporin, which is a type of β-lactam antimicrobial compound. It is derived from the Cephalosporium fungus, known for its progenitor antimicrobial properties. As a second-generation cephalosporin, cefmetazole lactone operates by inhibiting bacterial cell wall synthesis, essentially interfering with the transpeptidation process of peptidoglycan, a critical component of the bacterial cell wall. This disruption leads to cell lysis and eventual bacterial death, mainly affecting Gram-positive and some Gram-negative bacteria.</p>