Antimicrobici
Gli antimicrobici sono agenti che distruggono o inibiscono la crescita di microrganismi, inclusi batteri, virus, funghi e parassiti. Questi composti sono essenziali nella prevenzione e nel trattamento delle infezioni, svolgendo un ruolo cruciale nella medicina, nell'agricoltura e nell'industria alimentare. Presso CymitQuimica offriamo un'ampia gamma di antimicrobici di alta qualità e purezza, adatti a varie applicazioni scientifiche e industriali. Il nostro catalogo comprende antibiotici, antifungini, antivirali e disinfettanti, tutti progettati per soddisfare le esigenze della ricerca e dello sviluppo, nonché per applicazioni cliniche e di produzione. Con i nostri prodotti, i professionisti possono garantire l'efficacia e la sicurezza nel controllo delle infezioni e nella protezione della salute pubblica.
Sottocategorie di "Antimicrobici"
- Antibiotici(4.131 prodotti)
- Antimicotici(909 prodotti)
- Antiparassitari(702 prodotti)
- Antivirali(765 prodotti)
Trovati 2424 prodotti di "Antimicrobici"
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Spiromesifen-alcohol-4-hydroxymethyl
CAS:<p>Spiromesifen-alcohol-4-hydroxymethyl is a selective miticide, which is a derivative of spiromesifen. This compound is sourced from novel chemical synthesis approaches focusing on the manipulation of chemical structures to improve efficacy and selectivity. The mode of action of Spiromesifen-alcohol-4-hydroxymethyl centers on disrupting the lipid biosynthesis pathway within target mites and whiteflies. By inhibiting acetyl-CoA carboxylase, it leads to impaired energy storage and membrane biosynthesis, ultimately causing the mortality of these pests.</p>Formula:C17H20O4Purezza:Min. 95%Peso molecolare:288.34 g/molPyrimorph
CAS:Pyrimorph is a fungicide, which is a synthetic compound with specific activity against oomycete pathogens. It belongs to the chemical class of morpholines. Its mode of action involves the disruption of the biosynthetic pathways essential for the survival and proliferation of oomycetes, leading to their effective inhibition. Pyrimorph specifically targets the biosynthesis of cellulose in the cell walls of these pathogens, inhibiting their capacity to multiply and cause disease.Formula:C22H25ClN2O2Purezza:Min. 95%Peso molecolare:384.9 g/molWybutosine
CAS:<p>Modified nucleoside of phenylalanine tRNA</p>Formula:C21H28N6O9Purezza:Min. 95%Peso molecolare:508.48 g/molAtazanavir-d5
CAS:Atazanavir-d5 is an isotopically labeled variant of the antiretroviral drug Atazanavir, a non-peptidic HIV-1 protease inhibitor. It is synthesized using stable isotope labeling, specifically deuterium, which replaces five hydrogen atoms. The mechanism of action involves binding to the active site of the HIV-1 protease enzyme, a critical enzyme in the replication cycle of HIV, thereby preventing the cleavage of the viral gag-pol polyprotein precursors into the mature protein components of an infectious viral particle.Formula:C38H52N6O7Purezza:Min. 95%Peso molecolare:709.9 g/molA2ti-1
CAS:A2ti-1 is a specialized therapeutic agent, which is derived from recombinant DNA technology with the specific mode of action of targeting and modulating cytokine signaling pathways within the immune system. It is designed to interact with specific cytokine receptors, thereby inhibiting or modulating the downstream signaling cascades that are pivotal in the inflammatory response and immune regulation.Formula:C20H22N4O2SPurezza:Min. 95%Peso molecolare:382.5 g/molBleomycin A5 hydrochloride
CAS:Bleomycin A5 hydrochloride is an antineoplastic antibiotic, which is derived from the bacterium Streptomyces verticillus. Its mode of action involves binding to DNA and inducing strand breaks through the generation of free radicals, specifically targeting deoxyribose units. This leads to the inhibition of DNA synthesis and cell division, ultimately resulting in cell death.Formula:C57H89N19O21S2•HClPurezza:Min. 95%Colore e forma:PowderPeso molecolare:1,177.03 g/mol4-Demethyl daunomycinone
CAS:<p>4-Demethyl daunomycinone is an anthracycline derivative, which is a natural or semi-synthetic compound derived from the bacterium *Streptomyces*. It is primarily studied for its potential use in anticancer therapies, given its structural similarity to other well-known anthracyclines like daunorubicin and doxorubicin. These compounds are known to intercalate into DNA, thereby disrupting the function of DNA and RNA synthesis, leading to the inhibition of cell proliferation.</p>Formula:C20H16O8Purezza:Min. 95%Peso molecolare:384.34 g/molDaclatasvir
CAS:<p>Daclatasvir is a direct-acting antiviral agent, which is derived from synthetic chemical sources with a specific mode of action targeting the hepatitis C virus (HCV) replication process. It functions as an inhibitor of the HCV nonstructural protein 5A (NS5A), a vital component necessary for viral RNA replication and virion assembly. By binding to two distinct domains of NS5A, Daclatasvir disrupts its ability to function, thereby effectively halting the replication of the viral genome.</p>Formula:C40H50N8O6Purezza:Min. 95%Peso molecolare:738.88 g/molSulbactam pivoxyl
CAS:**Sulbactam pivoxyl** is a prodrug, which is a chemically modified form of sulbactam intended to improve its pharmacokinetic properties. Sulbactam itself is a beta-lactamase inhibitor of synthetic origin, specifically designed to combat antibiotic resistance by inhibiting the beta-lactamase enzymes produced by certain bacteria. These enzymes typically break down beta-lactam antibiotics, rendering them ineffective.Formula:C14H21NO7SPurezza:Min. 95%Peso molecolare:347.38 g/molOxibendazole-amine hydrochloride
CAS:<p>Oxibendazole-amine hydrochloride is a synthetic anthelmintic compound, which is a derivative of benzimidazole, known for its broad-spectrum efficacy against various helminths. It primarily acts by disrupting the polymerization of tubulin into microtubules, effectively impairing essential cellular structures and functions within parasitic worms, leading to their death.</p>Formula:C10H13N3O•HClPurezza:Min. 95%Colore e forma:PowderPeso molecolare:227.69 g/molOfloxacin Q acid
CAS:Ofloxacin Q acid is a quinolone analog, which is a synthetic derivative known for its significant antibacterial properties. This compound is sourced from the chemical synthesis of fluoroquinolone derivatives, designed to enhance reactivity and efficacy in pharmaceutical applications. Ofloxacin Q acid acts by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication, transcription, and repair, thereby leading to the cessation of bacterial growth and replication.Formula:C13H9F2NO4Purezza:Min. 95%Peso molecolare:281.21 g/molBCX4430 freebase
CAS:<p>Adenosine analogue with antiviral activity</p>Formula:C11H15N5O3Purezza:Min. 95%Peso molecolare:265.27 g/molCeftizoxime
CAS:<p>Ceftizoxime is a third-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating respiratory tract infections, urinary tract infections, and gonorrhea.</p>Formula:C13H13N5O5S2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:383.41 g/molAlamifovir
CAS:Alamifovir is an antiviral agent, which is synthetically derived. The mode of action of Alamifovir involves the inhibition of viral replication within host cells by targeting specific viral enzymes crucial for the replication process. This interference with the viral life cycle diminishes the ability of the virus to propagate and spread within the host organism.Formula:C19H20F6N5O5PSPurezza:Min. 95%Peso molecolare:575.42 g/mol3-Formyl rifamycin
CAS:<p>3-Formyl rifamycin is an intermediate in the synthesis of rifampicin that has been used to develop rifamycin derivatives with antibiotic activity. Rifampicin is aa anti-tuberculosis drug that inhibits bacterial DNA replication</p>Formula:C38H47NO13Purezza:Min. 95 Area-%Colore e forma:Red PowderPeso molecolare:725.78 g/molCefepime Related Compound E
CAS:<p>Cefepime Related Compound E is a chemical impurity, which is typically encountered as a byproduct in the synthesis or degradation of the antibiotic cefepime. This impurity is derived from synthetic processes used in the pharmaceutical industry and can originate from a variety of pathways during the manufacturing or storage of cefepime.</p>Formula:C13H20ClN3O3SPurezza:Min. 95%Peso molecolare:333.83 g/molHygromycin A
CAS:Hygromycin A is an antimicrobial compound isolated from the bacterium *Streptomyces hygroscopicus*. It functions by inhibiting protein synthesis within microbial cells. This compound disrupts the elongation phase of translation by binding to the ribosomal subunit, therefore impeding mRNA decoding during protein assembly.Formula:C23H29NO12Purezza:Min. 95%Peso molecolare:511.5 g/molDoripenem
CAS:<p>Doripenem is a carbapenem antibiotic with action on bacterial cell wall synthesis and is used for treating complicated bacterial infections like intra-abdominal infections and urinary tract infections.</p>Formula:C15H24N4O6S2Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:420.51 g/molNarasin sodium
CAS:Narasin sodium is an ionophore antibiotic, which is a type of compound that facilitates ion transport across biological membranes. It is derived from the fermentation of the bacterium *Streptomyces aureofaciens*. The mode of action involves the disruption of ion gradients in target organisms, specifically inhibiting the growth of certain pathogenic bacteria and protozoa by altering their cellular ionic balance.Formula:C43H71NaO11Purezza:Min. 95%Peso molecolare:787.02 g/molCefazolin
CAS:<p>Cefazolin is a broad-spectrum antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria. It is an effective cephalosporin antibiotic against both aerobic and anaerobic bacteria. Cefazolin is used in clinical isolates to inhibit the growth of methicillin-resistant staphylococcus, resistant microorganisms, and systemic inflammation. Some studies has shown good results to inhibit tumor necrosis factor-α (TNFα) production in cell culture.</p>Formula:C14H14N8O4S3Purezza:Min. 95%Peso molecolare:454.51 g/molQuinupristin
CAS:Quinupristin is a semi-synthetic antibiotic, which is derived from the natural compound pristinamycin IIA produced by the bacterium Streptomyces pristinaespiralis. It operates by binding to the 50S ribosomal subunit in bacterial cells, inhibiting protein synthesis and thus exerting a bacteriostatic effect. This mechanism effectively disrupts the growth and proliferation of susceptible bacteria.Formula:C53H67N9O10SPurezza:Min. 95%Peso molecolare:1,022.22 g/molSapecin
CAS:Sapecin is an antimicrobial peptide, which is derived from the hemolymph of the silk moth (Bombyx mori) with potent bactericidal action. The source of Sapecin is the immune system of the silk moth, where it acts as a natural defense mechanism against microbial infections. Its mode of action involves disrupting bacterial cell membranes, leading to cell lysis and death. The peptide achieves this by inserting itself into the lipid bilayer, creating pores that compromise the structural integrity of the membrane.Formula:C164H266N58O52S6Purezza:Min. 95%Peso molecolare:4,074.62 g/molNocardamine
CAS:<p>Nocardamine is a siderophore-based antioxidant, which is naturally derived from the soil-dwelling actinobacteria known as Streptomyces. Its primary mode of action involves the chelation of metal ions, effectively sequestering them and preventing metal-catalyzed oxidation reactions. By binding to iron and other transition metals, Nocardamine mitigates oxidative stress at a cellular level, which could otherwise contribute to cellular damage and dysfunction.</p>Formula:C27H48N6O9Purezza:Min. 95%Peso molecolare:600.71 g/molCecropin A
CAS:Cecropin A is an antimicrobial peptide, which is derived from the immune systems of insects, specifically moths. It displays potent antimicrobial properties through its ability to disrupt bacterial cell membranes, leading to cell lysis and death. This peptide primarily targets Gram-negative bacteria but is also effective against some Gram-positive strains. Cecropin A has garnered significant scientific interest due to its potential applications in developing new antimicrobial agents, particularly in the face of increasing antibiotic resistance. By integrating Cecropin A into therapeutic strategies, researchers aim to broaden the spectrum of antimicrobial options available for use in both clinical and agricultural settings, offering a promising avenue for future drug development.Formula:C184H313N53O46Purezza:Min. 95%Peso molecolare:4,003.78 g/molAzithromycin Dihydrate
CAS:<p>Azithromycin Dihydrate is a macrolide antibiotic and is used for the treatment of various bacterial infections. It binds to the 23S rRNA of the 50S ribosomal subunit, inhibiting protein synthesis</p>Formula:C38H72N2O12·2H2OPurezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:785.02 g/molCeftibuten
CAS:Ceftibuten is a third-generation cephalosporin antibiotic, which is a beta-lactam class of antimicrobial agents derived from Acremonium, a genus of fungi. This product is synthesized to resist degradation by beta-lactamase enzymes, which are commonly produced by resistant bacteria, thereby maintaining its efficacy against a wide range of bacterial pathogens.Formula:C15H14N4O6S2Purezza:Min. 95%Peso molecolare:410.43 g/molMaribavir
CAS:<p>Potent antiviral against HCMV and Epstein-Barr virus (EBV)</p>Formula:C15H19Cl2N3O4Purezza:Min. 95%Peso molecolare:376.24 g/molRef: 3D-AM178224
1gPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta250mgPrezzo su richiesta500mgPrezzo su richiestaDihydropenicillin F potassium
CAS:Dihydropenicillin F potassium is a novel antibiotic compound, which is semisynthetic in nature, derived from the penicillin family. It is sourced through the modification of natural penicillins, bringing about enhanced stability and efficacy against certain resistant bacterial strains. The mode of action involves the inhibition of bacterial cell wall synthesis, primarily targeting the penicillin-binding proteins (PBPs). This disruption consequently leads to cell lysis and the eventual bacterial death.Formula:C14H22N2O4S•KPurezza:Min. 95%Peso molecolare:353.5 g/molPolymyxin B1-I
CAS:Polymyxin B1-I is an antimicrobial peptide, which is sourced from the bacterium *Bacillus polymyxa*. It functions by interacting with and disrupting the bacterial cell membranes. The polypeptide inserts into the phospholipid bilayer, causing increased permeability and eventual cell lysis. This mechanism is particularly effective against Gram-negative bacteria due to the structural composition of their outer membranes.Formula:C56H98N16O13Peso molecolare:1,203.5 g/molVidarabine monohydrate
CAS:<p>Vidarabine monohydrate is an antiviral agent with action on viral DNA polymerase to inhibit replication and is used for treating herpes simplex virus infections and varicella-zoster virus infections.</p>Formula:C10H13N5O4·H2OPurezza:(¹H-Nmr) Min. 95 Area-%Colore e forma:White Off-White PowderPeso molecolare:285.26 g/molN-Acetal bromopride
CAS:N-Acetal bromopride is a chemical compound that serves as a derivative of bromopride, which is a selective dopamine D2 receptor antagonist. This derivative is synthesized from bromopride, typically through organic chemical processes, and modified to possess an acetal functional group. The presence of this functional group potentially alters its pharmacokinetic or pharmacodynamic properties, although these specific changes may still be under research.Formula:C16H24BrN3O3Purezza:Min. 95%Peso molecolare:386.28 g/molNatamycin
CAS:<p>Natamycin is a polyene macrolide antifungal agent with action on fungal cell membranes by binding to sterols and is used for treating fungal infections and as a food preservative.</p>Formula:C33H47NO13Purezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:665.73 g/molSisomicin sulfate
CAS:<p>Sisomicin sulfate is a sulfate salt form of sisomicin with similar action and applications as sisomicin.</p>Formula:C19H37N5O7·5H2SO4Purezza:Min. 95%Colore e forma:PowderPeso molecolare:1,385.45 g/molParitaprevir
CAS:<p>Paritaprevir is an antiviral medication, which is derived from chemical synthesis with its action targeting the hepatitis C virus (HCV). It operates primarily as a protease inhibitor, specifically targeting the NS3/4A protease, an essential enzyme for HCV replication. By inhibiting this protease, Paritaprevir effectively disrupts the viral life cycle, preventing the virus from maturing and proliferating within the host cells.</p>Purezza:Min. 95%Gentamicin C2 sulfate
CAS:<p>Gentamicin C2 sulfate is an aminoglycoside antibiotic with action on bacterial protein synthesis inhibition and is used for treating severe bacterial infections.</p>Formula:C20H41N5O7Purezza:(%) Min. 90%Colore e forma:PowderPeso molecolare:463.57 g/molTenofovir alafenamide (free base)
CAS:<p>Tenofovir alafenamide (free base) is a prodrug of tenofovir with action on viral reverse transcriptase to block replication and is used for treating HIV/AIDS and chronic hepatitis B with improved safety profile.</p>Formula:C21H29N6O5PPurezza:Min. 97 Area-%Colore e forma:PowderPeso molecolare:476.47 g/mol7-epi-Clindamycin 2-phosphate
CAS:<p>7-epi-Clindamycin 2-phosphate is a semisynthetic antibiotic derivative, which is sourced from chemical modifications of the natural antibiotic lincomycin. This compound operates by inhibiting bacterial protein synthesis. It achieves this by binding to the 50S subunit of the bacterial ribosome, thereby obstructing the translocation steps in protein elongation.</p>Formula:C18H34ClN2O8PSPurezza:Min. 95%Colore e forma:White to off-white solid.Peso molecolare:504.96 g/molCyclosporin V
CAS:<p>Cyclosporin V is an immunosuppressant medication with action on calcineurin inhibition and is used for preventing organ rejection in transplants and treating autoimmune diseases.</p>Formula:C63H113N11O12Purezza:Min. 95%Colore e forma:PowderPeso molecolare:1,216.64 g/molPefloxacin-d3
CAS:Prodotto controllatoPefloxacin-d3 is a deuterated fluoroquinolone antibiotic, which is a synthetic derivative of pefloxacin utilized primarily for research purposes. This compound is chemically modified to include deuterium atoms, a stable isotope of hydrogen, thus offering unique properties essential for precise quantitative analysis in pharmacokinetic studies.Formula:C17H17D3FN3O3Purezza:Min. 95%Peso molecolare:336.38 g/molCeftobiprole medocaril sodium
CAS:<p>Ceftobiprole medocaril sodium is a broad-spectrum cephalosporin antibiotic, which is a synthetically derived prodrug of ceftobiprole. Upon administration, ceftobiprole medocaril is rapidly converted into its active form, ceftobiprole, by the body's endogenous esterases. The mode of action involves binding to penicillin-binding proteins (PBPs) in the bacterial cell wall, leading to the inhibition of cell wall synthesis and ultimately the death of the bacteria. This action is effective against a wide range of gram-positive and gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and penicillin-resistant Streptococcus pneumoniae.</p>Formula:C26H26N8O11S2NaPurezza:Min. 95%Peso molecolare:713.65 g/molSterigmatocystin
CAS:<p>Sterigmatocystin is a mycotoxin, which is a secondary metabolite primarily produced by certain species of the fungi Aspergillus and Bipolaris. This compound exhibits its mode of action by interfering with DNA, RNA, and protein synthesis, ultimately disrupting cellular processes. As a precursor to the well-known aflatoxins, sterigmatocystin shares a similar structure and exhibits carcinogenic properties.</p>Purezza:Min. 95%Leptomycin B
CAS:<p>Leptomycin B is a bacterial secondary metabolite, which is derived from the bacterium Streptomyces sp. This compound is a potent nuclear export inhibitor with a mechanism of action that targets and inhibits the export receptor CRM1 (Chromosomal Maintenance 1), also known as Exportin 1. By binding irreversibly to CRM1, Leptomycin B prevents the nuclear export of proteins and RNA, disrupting the nuclear-cytoplasmic transport essential for cell function.</p>Formula:C33H48O6Purezza:Min. 95%Peso molecolare:540.73 g/molCurvularin
CAS:<p>Curvularin is a secondary metabolite, which is derived from the fungal genus *Curvularia*. This compound is produced through the natural biosynthetic pathways of filamentous fungi, specifically isolated from strains such as *Curvularia lunata*. Curvularin exerts its biological activity primarily through modulation of microtubule dynamics, making it a significant subject of study in cell biology. It disrupts the polymerization processes, impacting the assembly and stability of microtubules, which are critical components of the cytoskeleton involved in cell division, intracellular transport, and structural integrity.</p>Purezza:Min. 95%Polymyxin B nonapeptide TFA
CAS:Polymyxin B nonapeptide TFA is an antimicrobial peptide, which is derived from the bacterium *Bacillus polymyxa*. This peptide is a truncated form of polymyxin B, lacking the fatty acyl tail and N-terminal amino acid, resulting in a nonapeptide structure. Its mode of action involves binding to the lipid A portion of bacterial lipopolysaccharides, thereby disrupting the integrity of the bacterial cell membrane. This interaction increases membrane permeability and leads to cell lysis, particularly in Gram-negative bacteria.Formula:C53H79F15N14O21Purezza:Min. 95%Peso molecolare:1,533.3 g/molRetrocyclin-1 trifluoroacetate salt
CAS:Retrocyclin-1 trifluoroacetate salt is a synthetic antimicrobial peptide, which is derived from humanized sequences based on the theta-defensin family, originally found in certain primates. Retrocyclin-1 is particularly notable for its circular structure which contributes to its stability and biological activity. The peptide is produced through a process of solid-phase peptide synthesis, designed to mimic the native cyclic conformation of natural theta-defensins.Formula:C74H128N30O18S6Purezza:Min. 95%Peso molecolare:1,918.4 g/molBacampicillin Hydrochloride
CAS:Bacampicillin Hydrochloride is an aminopenicillin antibiotic and is used for the treatment of bacterial infections. It is a prodrug that is converted to ampicillin in the body, which then inhibits bacterial cell wall synthesis.Formula:C21H28ClN3O7SPurezza:Min. 95%Colore e forma:PowderPeso molecolare:501.98 g/molAripiprazole monohydrate
CAS:Prodotto controllato<p>Aripiprazole monohydrate is an atypical antipsychotic medication, which is synthesized through chemical processes involving aryl piperazine derivatives. It acts primarily as a partial agonist at dopamine D2 and serotonin 5-HT1A receptors and as an antagonist at 5-HT2A receptors, with additional activity at other neurotransmitter receptors. This unique mechanism of action sets it apart from typical antipsychotics that predominantly function as dopamine antagonists.</p>Formula:C23H29Cl2N3O3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:466.4 g/molClindamycin 3-phosphate
CAS:<p>Clindamycin 3-phosphate is an antibiotic prodrug, which is a derivative of clindamycin. It is semisynthetic with a synthetic origin, derived by chemically modifying the natural compound lincomycin obtained from the bacterium *Streptomyces lincolnensis*. The mode of action of Clindamycin 3-phosphate involves the inhibition of bacterial protein synthesis. It binds to the 50S subunit of the bacterial ribosome, thereby interfering with the translocation step in protein elongation, ultimately leading to the suppression of bacterial growth.</p>Formula:C18H34ClN2O8PSPurezza:Min. 95%Colore e forma:White To Off-White SolidPeso molecolare:504.96 g/molSTAADIUM™ PeptiZide L-Pyr
CAS:<p>STAADIUMTM PeptiZide L-Pyr is a targeted inhibitor for pyroglutamyl-aminopeptidase-producing bacteria. The antibacterial activity of STAADIUMTM PeptiZide L-Pyr is triggered by the enzyme pyroglutamyl aminopeptidase (a.k.a. pyrase or pyrrolidonyl peptidase) that is present, not only in bacteria, but also in archaea, plants and animals. STAADIUMTM PeptiZide can be used to suppress the growth of Citrobacter freundii on diagnostic agar plates for Salmonella. L-pyrrolidonyl peptidase activity has also been exploited to distinguish Enterococcus species and Streptococcus pyogenes from other Streptococaceae species. More details in the application notes document.</p>Formula:C17H17N3O3SPurezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:343.41 g/molOteseconazole
CAS:<p>Oteseconazole is an antifungal medication, which is a synthetic triazole-derived agent. It functions by inhibiting the activity of the fungal enzyme lanosterol 14α-demethylase. This inhibition disrupts the synthesis of ergosterol, a vital component of fungal cell membranes, thereby interfering with cell membrane integrity and function, ultimately leading to fungal cell death.</p>Formula:C23H16F7N5O2Purezza:Min. 95%Peso molecolare:527.4 g/molMicafungin FR-179642 impurity (acid)
CAS:Micafungin is an antifungal drug that inhibits the synthesis of ergosterol, a vital component of fungal cell membranes. It is a cyclic peptide with a lipophilic fatty acid chain that has been modified to allow penetration into cells. Micafungin is active against Candida and Aspergillus species and has shown activity against some strains of Cryptococcus neoformans. The MIC (minimum inhibitory concentration) for this drug ranges from 0.06 to 1 microgram/mL, depending on the bacterial strain being tested. Micafungin FR-179642 impurity (acid) is an impurity in micafungin that can be present as trace amounts in the final product and may contribute to hemolytic activity. This impurity is formed by hydrolysis during the synthesis process.Formula:C35H52N8O20SPurezza:Min. 95 Area-%Colore e forma:White PowderPeso molecolare:936.9 g/molTaniborbactam hydrochloride
CAS:<p>Taniborbactam hydrochloride is a β-lactamase inhibitor that is synthetically derived for use in combination with β-lactam antibiotics. Its mode of action involves the inhibition of β-lactamase enzymes, which are produced by certain bacteria to confer resistance to β-lactam antibiotics, including cephalosporins and carbapenems.</p>Formula:C19H30BCl2N3O5Purezza:Min. 95%Peso molecolare:462.2 g/molErythromycin C
CAS:<p>Erythromycin C is a macrolide antibiotic, which is a type of product derived from the bacterium *Saccharopolyspora erythraea*. It functions by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis through blocking translocation of peptidyl-tRNA. This mode of action effectively prevents bacterial growth and replication, making it a potent bacteriostatic agent.</p>Formula:C36H65NO13Purezza:Min. 95%Peso molecolare:719.9 g/molAmpicillin-sulbactam
CAS:Ampicillin-sulbactam is a combination antibiotic, which is a pharmaceutical product derived from the penicillin class of beta-lactam antibiotics. Its source involves semi-synthetic processes, combining ampicillin with sulbactam. The mode of action of this compound is through the inhibition of bacterial cell wall synthesis. Ampicillin specifically binds to penicillin-binding proteins, thereby disrupting the cross-linking process essential for maintaining cell wall structural integrity, leading to bacterial lysis. Sulbactam functions as a beta-lactamase inhibitor, enhancing the efficacy of ampicillin by preventing its degradation by beta-lactamase enzymes produced by certain resistant bacterial strains.Formula:C25H31N3O9S2Purezza:Min. 95%Peso molecolare:581.7 g/molLactoferricin B (4-14) (bovine) trifluoroacetate salt
CAS:Lactoferricin B (4-14) (bovine) trifluoroacetate salt is a peptide derivative, which is a fragment derived from bovine lactoferrin. It is obtained by enzymatic digestion of lactoferrin, a glycoprotein with a well-established role in the innate immune system. This specific peptide, Lactoferricin B (4-14), is known for its potent antimicrobial properties, attributed to its amphipathic structure that facilitates the disruption of microbial membranes. Additionally, it can modulate immune responses through interactions with immune cells, thereby influencing inflammatory processes.Formula:C70H113N25O13SPurezza:Min. 95%Peso molecolare:1,544.87 g/molMonensin
CAS:<p>Monensin is a polyether ionophore antibiotic, which is derived from the fermentation of the bacterium *Streptomyces cinnamonensis*. It operates by disrupting ion transport across biological membranes, primarily by facilitating the exchange of sodium and potassium ions. This ionophore action alters the osmotic balance in target cells, leading to their destabilization and death, particularly in Gram-positive bacteria and certain protozoa.</p>Formula:C36H62O11Purezza:Min. 95%Peso molecolare:670.87 g/molDoxorubicin Impurity 2
CAS:<p>Doxorubicin Impurity 2 is a chemical impurity of doxorubicin with no direct therapeutic action but used in research and quality control.</p>Formula:C19H12O6Purezza:Min. 95%Colore e forma:PowderPeso molecolare:336.29 g/molSpiramycin I
CAS:<p>Spiramycin I is a macrolide antibiotic with action on bacterial protein synthesis inhibition and is used for treating toxoplasmosis and bacterial infections.</p>Formula:C43H74N2O14Purezza:Min. 95 Area-%Colore e forma:White PowderPeso molecolare:843.05 g/molDMDNA31
CAS:<p>DMDNA31 is a synthetic nucleotide analog, which is a man-made compound designed to mimic the natural building blocks of DNA. It originates from advanced chemical synthesis processes, allowing precise control over its structure to mimic specific nucleotide sequences. DMDNA31 operates by integrating into DNA strands during replication, thereby enabling the study of genetic mutations and the mapping of genomic sequences.</p>Formula:C50H62N4O13Purezza:Min. 95%Peso molecolare:927 g/molLaidlomycin
CAS:<p>Laidlomycin is an ionophore compound with a mode of action that disrupts ion gradients in bacterial cells. It is used as a feed additive to improve feed efficiency in cattle.</p>Formula:C37H62O12Purezza:Min. 95%Peso molecolare:698.88 g/molGentamicin C1 pentaacetate
CAS:<p>Gentamicin C1 pentaacetate is an aminoglycoside antibiotic with action on bacterial protein synthesis inhibition and is used for research and analytical applications.</p>Formula:C21H43N5O7•(C2H4O2)5Purezza:Min. 90%Colore e forma:Off-White PowderPeso molecolare:777.86 g/molFlucloxacillin
CAS:<p>Flucloxacillin is a beta-lactam antibiotic, which is derived from the penicillin family. It is synthetically produced through chemical modification to enhance its stability against beta-lactamase enzymes. The mode of action of flucloxacillin involves inhibiting bacterial cell wall synthesis. It binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, which in turn inhibits the transpeptidation or cross-linking of peptidoglycan chains. This action leads to cell lysis and ultimately, bacterial death.</p>Formula:C19H17ClFN3O5SPurezza:Min. 95%Peso molecolare:453.87 g/molSulfadimethoxine sodium
CAS:<p>Sulfadimethoxine sodium is a sulfonamide antibiotic with action on bacterial folate synthesis inhibition and is used for treating respiratory and urinary tract infections in veterinary medicine.</p>Formula:C12H13N4NaO4SPurezza:Min. 95%Colore e forma:White Off-White PowderPeso molecolare:332.31 g/molFaropenem sodium hydrate
CAS:Faropenem sodium hydrate is a hydrated form of faropenem sodium with similar action and applications as faropenem sodium hemipentahydrate.Formula:C12H14NNaO5S·xH2OPurezza:Min. 95%Colore e forma:PowderPeso molecolare:307.3 g/mol14-Bromodaunorubicin HBr
CAS:<p>14-Bromodaunorubicin HBr is a synthetic antitumor antibiotic derivative, which is a modified version of daunorubicin, an anthracycline antibiotic originally isolated from Streptomyces peucetius. With the inclusion of a bromine atom at the 14th position, this compound is designed to enhance the antitumor efficacy and alter pharmacokinetic properties compared to its parent molecule.</p>Formula:C27H28BrNO10·BrHPurezza:75%MinPeso molecolare:687.33 g/molSancycline hydrochloride
CAS:<p>Sancycline hydrochloride is a tetracycline antibiotic, which is derived from the natural fermentation process of Streptomyces bacteria. The mechanism of action involves the inhibition of protein synthesis by bindin directly to the 30S ribosomal subunit, thereby preventing the attachment of aminoacyl-tRNA to the A site of the ribosome. This action effectively halts the growth of bacteria by impeding protein production, making it bacteriostatic rather than bactericidal.</p>Formula:C21H23ClN2O7Purezza:Min. 95%Peso molecolare:450.87 g/molLomefloxacin hydrochloride
CAS:<p>Lumefantrine is an antimalarial compound with a mode of action that inhibits heme detoxification in Plasmodium parasites. It is used in combination with artemether for treating malaria.</p>Formula:C17H19F2N3O3•HClPurezza:Min. 95%Colore e forma:PowderPeso molecolare:387.81 g/molDicresulene Hydrate
CAS:Dicresulene Hydrate is an anti-inflammatory compound, which is derived from synthetic sources. It functions primarily by inhibiting specific enzymes involved in the inflammatory response. This inhibition reduces the production of pro-inflammatory mediators, thereby mitigating inflammation and associated symptoms.Formula:C15H16O8S2•(H2O)xPurezza:Min. 95%Colore e forma:PowderPeso molecolare:388.41 g/molCefmenoxime hydrochloride
CAS:Cefmenoxime hydrochloride is a third-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating gynecological and obstetric infections.Formula:C16H17N9O5S3HClPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:529.79 g/molNikkomycin Z from streptomyces tendae
CAS:<p>Nikkomycin Z is an antifungal agent, which is a secondary metabolite isolated from the bacterium Streptomyces tendae. This compound functions as a competitive inhibitor of chitin synthase, an essential enzyme responsible for the synthesis of chitin, a vital component of the fungal cell wall. By inhibiting this enzyme, Nikkomycin Z disrupts the structural integrity of the fungal cell wall, leading to impaired growth and cell lysis in susceptible fungi.</p>Formula:C20H25N5O10Purezza:Min. 95%Peso molecolare:495.4 g/molCeftriaxone sodium
CAS:<p>Ceftriaxone sodium is a third-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating severe bacterial infections like meningitis and pneumonia.</p>Formula:C18H18N8Na2O7S3Purezza:Min. 84 Area-%Colore e forma:White Yellow PowderPeso molecolare:600.56 g/molCarumonam
CAS:Carumonam is a synthetic monobactam antibiotic, which is derived from chemically modifying aztreonam to enhance its antimicrobial properties. Its source is entirely synthetic, allowing for precise structural modifications to target specific bacterial pathogens. The mode of action involves the inhibition of bacterial cell wall synthesis. Carumonam binds to penicillin-binding proteins (PBPs) on the surface of bacterial cell walls, disrupting the peptidoglycan cross-linking process necessary for cell wall strength and integrity. This action results in bacterial cell lysis and death, making it effective against a range of Gram-negative bacteria.Formula:C12H14N6O10S2Purezza:Min. 95%Peso molecolare:466.41 g/molN-Acetylamphotericin B
CAS:<p>N-Acetylamphotericin B is a derivative of the well-known antifungal agent Amphotericin B, which is derived from the bacterium *Streptomyces nodosus*. This compound is an acetylated version of Amphotericin B, designed to improve certain pharmacokinetic properties. It operates by binding to ergosterol, a key component of fungal cell membranes, leading to the formation of pores that disrupt membrane integrity, causing cell death. The acetylation is intended to reduce the compound's cytotoxicity and improve its solubility in aqueous solutions, potentially allowing for enhanced therapeutic applications.</p>Formula:C49H75NO18Purezza:(%) Min. 75%Colore e forma:Yellow To Brown SolidPeso molecolare:966.12 g/molOleandomycin
CAS:<p>Oleandomycin is a macrolide antibiotic, which is derived from the bacterium *Streptomyces antibioticus*. This antibiotic functions by binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis. The interruption of this essential process ultimately leads to the cessation of bacterial growth and replication.</p>Formula:C35H61NO12Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:687.86 g/molCasein
CAS:<p>Casein is a phosphoprotein, which is derived from milk. It originates primarily from cow's milk, where it constitutes about 80% of the total protein content. The mode of action for casein involves its ability to form a gel or clot in the stomach, which makes it highly efficient in nutrient delivery, especially the slow release of amino acids. This process is facilitated by its unique structural features, such as the presence of multiple phosphoryl groups that can bind calcium ions.</p>Purezza:Min. 95%Colore e forma:PowderEconazole
CAS:<p>Econazole is an imidazole antifungal agent with action on fungal cell membrane disruption and is used for treating fungal skin infections like athlete's foot and ringworm.</p>Formula:C18H15Cl3N2OPurezza:Min. 98 Area-%Colore e forma:White PowderPeso molecolare:381.68 g/molPuberulic acid
CAS:Puberulic acid is a fungal metabolite that exhibits significant antimicrobial properties. It is derived from certain species of the Penicillium genus, a well-known source of various bioactive compounds. The mode of action of puberulic acid involves the disruption of microbial cell wall synthesis, leading to inhibited growth and eventual cell death of targeted microorganisms.Formula:C8H6O6Purezza:Min. 95%Peso molecolare:198.13 g/molLinearmycin A
CAS:Linearmycin A is an antibiotic compound, which is a secondary metabolite produced by the bacterium Streptomyces sp. Its mode of action involves disrupting bacterial protein synthesis, leading to the inhibition of bacterial growth. This compound exhibits strong efficacy against various Gram-positive and some Gram-negative bacteria, making it valuable in microbiological research.Formula:C64H101NO16Purezza:Min. 95%Peso molecolare:1,140.5 g/molFengycin
CAS:Fengycin is a cyclic lipopeptide from Bacillus subtilis acts as a biosurfactant and antifungal. As a fungicide, it has a mode of action that involves the formation of ion channels in the fungal lipid membrane, leading to membrane leakage This activity is negatively correlated to cholesterol levels, and may explain why mammalian cells, with higher cholesterol present, are not sensitive to fengycin.Formula:C72H110N12O20Purezza:Min. 90 Area-%Colore e forma:PowderPeso molecolare:1,463.71 g/molGramicidin S hydrochloride
CAS:Gramicidin S hydrochloride is a cyclic peptide antibiotic, which is a derivative of the naturally occurring antibiotic gramicidin S. It is sourced from Bacillus brevis, a type of soil bacterium. This peptide operates through a unique mode of action, whereby it disrupts bacterial cell membranes. By integrating into the lipid bilayer, it increases membrane permeability, leading to leakage of essential ions and molecules, and ultimately causing cell death.Formula:C60H92N12O10•(HCl)2Purezza:90%MinPeso molecolare:1,214.37 g/molDesoxymycin
CAS:Desoxymycin is an antibiotic product that belongs to the class of aminoglycosides, which is derived from natural sources such as certain species of Streptomyces bacteria. This compound exhibits its mode of action by specifically binding to the bacterial ribosomal RNA, interfering with protein synthesis. As a result, it inhibits the replication and growth of susceptible bacterial strains.Formula:C21H41N7O11Purezza:Min. 95%Peso molecolare:567.59 g/molAmoxicillin
CAS:<p>Amoxicillin is an aminopenicillin antibiotic and is used for the treatment of various bacterial infections. It works by inhibiting the synthesis of bacterial cell wall mucopeptides, leading to cell lysis and death</p>Formula:C16H19N3O5SPurezza:Min. 95%Colore e forma:PowderPeso molecolare:365.41 g/molSebuthylazine-2-hydroxy
CAS:<p>Sebuthylazine-2-hydroxy is a selective pre-emergent herbicide, which is a derivative of the sym-triazine compound family synthesized through chemical processes. It functions primarily as a soil-acting agent that inhibits photosynthesis by binding to the D1 protein in the photosystem II complex, thereby disrupting the electron transport chain. This biochemical action effectively curtails the growth of susceptible weed species by preventing their development, particularly annual grasses and broadleaf weeds.</p>Formula:C9H17N5OPurezza:Min. 95%Peso molecolare:211.26 g/mol(S)-HPMPA
CAS:(S)-HPMPA is a nucleotide analogue, which is a chemically synthesized compound designed to mimic nucleotides. It acts as both an antiviral and an antitumor agent, sourced primarily through synthetic chemistry involving the modification of naturally occurring nucleotide structures. The mode of action of (S)-HPMPA involves mimicking natural substrates of various viral polymerases and cellular enzymes, thereby inhibiting viral DNA synthesis and disrupting the replication cycle of DNA viruses. Additionally, it can interfere with certain cellular pathways contributing to its antitumor effects.Formula:C9H14N5O5PPurezza:Min. 95%Peso molecolare:303.21 g/molQuinofumelin
CAS:<p>Quinofumelin is a fungicide, which is synthetically derived with a novel mode of action targeting specific biochemical pathways in fungi. Its unique mechanism disrupts crucial cellular processes within pathogenic fungi, thereby halting their growth and spread. This fungicide has been meticulously developed through advanced chemical synthesis to ensure high efficacy and specificity against a broad spectrum of fungal pathogens affecting various crops.</p>Formula:C20H16F2N2Purezza:Min. 95%Peso molecolare:322.4 g/molAmicoumacin C
CAS:<p>Amicoumacin C is a biological product derived from certain strains of the Bacillus species, specifically fermented by Bacillus subtilis. It is recognized as a potent antibiotic compound, noted for its ability to inhibit bacterial protein synthesis, primarily by interacting with the 30S ribosomal subunit, thereby hindering the translation process.</p>Formula:C20H26N2O7Purezza:Min. 95%Peso molecolare:406.43 g/molHalauxifen
CAS:<p>Halauxifen is a synthetic herbicide, which is a product of chemical synthesis used in agricultural practices. Derived from advanced chemical research and development, its primary source is a laboratory setting where it is engineered to exhibit specific properties for plant management.</p>Formula:C13H9Cl2FN2O3Purezza:Min. 95%Peso molecolare:331.12 g/molBacitracin B1
CAS:<p>Bacitracin B1 is a polypeptide antibiotic and is used for the treatment of bacterial infections. Its mode of action is similar to bacitracin.</p>Formula:C65H101N17O16SPurezza:90%MinColore e forma:PowderPeso molecolare:1,408.67 g/mol4-Hydroxyvoriconazole
CAS:<p>Metabolite of voriconazole; sterol 14?-demethylase inhibitor</p>Purezza:Min. 95%2-Methyl-4-isothiazolin-3-one hydrochloride
CAS:<p>Methyl-4-isothiazolin-3-one HCl, also known as MIT hydrochloride is often used as a preservative in personal care products and other industrial applications. The product has shown to act as an antimicrobial and antifungal agent.</p>Formula:C4H6ClNOSPurezza:Min. 99 Area-%Peso molecolare:151.62 g/molRitonavir - Bio-X ™
CAS:<p>Ritonavir is a HIV protease inhibitor. It has an anti-retroviral activity as it inhibits the protease enzymes specific of both HIV-1 and HIV-2 and has been shown to be effective in controlling virus replication in humans and animals. Ritonavir works by preventing the HIV viral protease enzyme from cleaving the structural and replicative proteins produced by HIV genes such as gag and pol.</p>Formula:C37H48N6O5S2Purezza:Min. 98 Area-%Colore e forma:White PowderPeso molecolare:720.95 g/molGatifloxacin - Bio-X ™
CAS:<p>This product is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.</p>Formula:C19H22FN3O4Purezza:Min. 95%Colore e forma:PowderPeso molecolare:375.39 g/molMolnupiravir - Bio-X ™
CAS:Prodotto controllato<p>EIDD 2801 is an orally bioavailable prodrug of β-D-N4-hydroxycytidine and was shown to inhibit SARS-CoV-2 replication in human airway epithelial cells. EIDD 2801 was also tested in mice infected with SARS-CoV and MERS-CoV viruses. EIDD 2801 targets the RNA-dependent RNA polymerase (RdRp) and reduces virus titer and improved pulmonary function in experimental animals when used in prophylactic and therapeutic regime.</p>Formula:C13H19N3O7Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:329.31 g/molPotassium clavulanate
CAS:<p>Potassium clavulanate is a beta-lactamase inhibitor and an antibacterial agent. The presence of potassium clavulanate in culture media inhibits the activity of beta-lactamases, which are enzymes that confer resistance to penicillin and other beta-lactam antibiotics. It also has been shown to be active against bacterial infections such as tuberculosis, sepsis, and pneumonia, where it can inhibit the growth of bacteria by interfering with their ability to form cell walls. Potassium clavulanate is also used as an antimicrobial agent for blood culture technique and antimicrobial treatment.</p>Formula:C8H8NO5·KPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:237.25 g/molSTAADIUM™ GalactoZide II
CAS:<p>STAADIUMTM GalactoZide II is a targeted inhibitor for β-galactosidase producing bacteria. The antibacterial activity of STAADIUMTM GalactoZide II is triggered by the enzyme β-galactosidase which is produced by E.coli (EHEC), thermophilic lactic acid bacteria, and other coliform bacteria. STAADIUMTM GalactoZide II can help to selectively inhibit the growth of E. coli in complex bacterial cultures and canbe used in microbiome studies, food control, environmental safety, hygiene, and clinical diagnostics. STAADIUMTM GalactoZide II is not compatible with some experimental conditions, e.g. pH indicators such as neutral red, indigo stains, and possibly H2S staining. STAADIUMTM GalactoZide II can be added as an enzyme-specific selective supplement to agar plates and as an enrichment agent to broth culture.</p>Formula:C18H21NO7SPurezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:395.43 g/molAmphotericin A
CAS:<p>Amphotericin A is a polyene macrolide antibiotic, which is derived primarily from the soil bacterium *Streptomyces nodosus*. This compound functions by binding to ergosterol, an essential component of fungal cell membranes. This binding creates pores in the membrane, increasing its permeability and ultimately leading to cell death. Unlike its more widely used counterpart Amphotericin B, Amphotericin A is less frequently utilized but is critical in the study and understanding of antifungal activity.</p>Formula:C47H75NO17Purezza:Min. 95%Peso molecolare:926.09 g/molN-[5-[3-[(4-Hydroxyphenyl)sulfamoyl]-4-methoxyphenyl]-4-methyl-1,3-thiazol-2-yl]-2,2-dimethylpropanamide
CAS:<p>PI4KIII beta inhibitor</p>Formula:C22H25N3O5S2Purezza:Min. 98 Area-%Colore e forma:White PowderPeso molecolare:475.58 g/molAmicoumacin A
CAS:<p>Amicoumacin A is an antibiotic compound, which is derived from the bacterium Bacillus subtilis. This natural source is known for its production of a variety of biologically active compounds that contribute to its utility in numerous scientific contexts. The mode of action of Amicoumacin A involves the inhibition of bacterial protein synthesis by targeting the ribosomal subunit. Specifically, it interferes with the translation process, effectively disrupting the growth and proliferation of susceptible bacterial strains.<br><br>Amicoumacin A is primarily utilized in research settings to study bacterial resistance mechanisms, as well as to explore novel antibacterial therapies. Its application in scientific research extends to examining its potential synergistic effects with other antimicrobial agents, and it serves as a model compound for understanding ribosomal inhibition. The study of Amicoumacin A not only contributes to the broader field of antibiotic development but also offers insights into the molecular interactions that underlie bacterial protein synthesis and antibiotic resistance. This compound's unique properties make it an important subject of investigation for microbiologists and pharmacologists alike, emphasizing its relevance in the ongoing battle against antibiotic-resistant pathogens.</p>Formula:C20H29N3O7Purezza:Min. 95%Colore e forma:PowderPeso molecolare:423.46 g/molTicarcillin disodium salt - 80%
CAS:<p>Ticarcillin disodium salt is a beta-lactam antibiotic that has in vitro activity against Gram-positive and Gram-negative bacteria. Ticarcillin is active against penicillinase-producing strains of Staphylococcus aureus, Enterobacter aerogenes, Proteus mirabilis, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Serratia marcescens, Streptococcus pyogenes, Streptococcus faecalis, and Streptococcus pneumoniae. Furthermore, it inhibits transpeptidase activity of the cell wall of bacteria which prevents peptidoglycan synthesis. It is bactericidal for many bacteria at low concentrations.</p>Formula:C15H14N2Na2O6S2Purezza:Min. 90 Area-%Colore e forma:PowderPeso molecolare:428.4 g/molNigericin sodium - from Streptomyces hygroscopicus
CAS:<p>Membrane pore-forming agent; H+, K+, Pb2+ ionophore; polyether antibiotic</p>Formula:C40H67O11NaPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:746.94 g/mol
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