Antimicrobials
Antimicrobials are agents that destroy or inhibit the growth of microorganisms, including bacteria, viruses, fungi, and parasites. These compounds are essential in the prevention and treatment of infections, playing a crucial role in medicine, agriculture, and the food industry. At CymitQuimica, we offer an extensive range of high-quality, high-purity antimicrobials suitable for various scientific and industrial applications. Our catalog includes antibiotics, antifungals, antivirals, and disinfectants, all designed to meet the needs of research and development, as well as clinical and production applications. With our products, professionals can ensure the effectiveness and safety in infection control and public health protection.
Subcategories of "Antimicrobials"
- Antibiotics(4,137 products)
- Antifungals(904 products)
- Antiparasitics(700 products)
- Antivirals(767 products)
Found 2432 products of "Antimicrobials"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Gatifloxacin hydrochloride
CAS:Gatifloxacin hydrochloride is a fluoroquinolone antibiotic, which is synthesized chemically from quinolone compounds. It exhibits its mode of action by inhibiting bacterial DNA gyrase and topoisomerase IV, essential enzymes responsible for DNA replication and transcription processes in bacteria. This disruption of DNA processes leads to bacterial cell death, making it effective against a wide range of Gram-positive and Gram-negative bacteria.Formula:C19H23ClFN3O4Purity:Min. 95%Molecular weight:411.86 g/mol7-epi-Clindamycin 2-phosphate
CAS: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.Formula:C18H34ClN2O8PSPurity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:504.96 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:C23H29NO12Purity:Min. 95%Molecular weight:511.5 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•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:1,177.03 g/molLaidlomycin
CAS: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.
Formula:C37H62O12Purity:Min. 95%Molecular weight:698.88 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:C16H24BrN3O3Purity:Min. 95%Molecular weight:386.28 g/mol1-(6-Amino-3,5-difluoro-2-pyridinyl)-7-[3-[3-[[1-(6-amino-3,5-difluoro-2-pyridinyl)-3-carboxy-8-chloro-6-fluoro-1,4-dihydro-4-oxo-7- quinolinyl]amino]-2-hydroxypropoxy]-1-azetidinyl]-8-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
CAS:1-(6-Amino-3,5-difluoro-2-pyridinyl)-7-[3-[3-[[1-(6-amino-3,5-difluoro-2-pyridinyl)-3-carboxy-8-chloro-6-fluoro-1,4-dihydro-4-oxo-7-quinolinyl]amino]-2-hydroxypropoxy]-1-azetidinyl]-8-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid is a fluoroquinolone antibiotic, engineered through synthetic chemistry. It is derived from chemical sources involving complex organic synthesis, highlighting its intricate molecular architecture. Its mode of action is distinctive, as it inhibits bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication and transcription. This interference with bacterial DNA processes results in bactericidal effects, effectively eliminating susceptible bacterial strains.
Formula:C36H24Cl2F6N8O8Purity:Min. 95%Molecular weight:881.52 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:C56H98N16O13Molecular weight:1,203.5 g/molVidarabine monohydrate
CAS: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.Formula:C10H13N5O4·H2OPurity:(¹H-Nmr) Min. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:285.26 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:C53H67N9O10SPurity:Min. 95%Molecular weight:1,022.22 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:C70H113N25O13SPurity:Min. 95%Molecular weight:1,544.87 g/molLomefloxacin hydrochloride
CAS: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.Formula:C17H19F2N3O3•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:387.81 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:C15H14N4O6S2Purity:Min. 95%Molecular weight:410.43 g/molCeftizoxime
CAS: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.
Formula:C13H13N5O5S2Purity:Min. 95%Color and Shape:PowderMolecular weight:383.41 g/molNocardamine
CAS: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.
Formula:C27H48N6O9Purity:Min. 95%Molecular weight:600.71 g/molCefepime Related Compound E
CAS: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.
Formula:C13H20ClN3O3SPurity:Min. 95%Molecular weight:333.83 g/molParitaprevir
CAS: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.Purity:Min. 95%Dolutegravir sodium
CAS:Dolutegravir sodium is an HIV integrase strand transfer inhibitor with action on HIV integrase to block viral replication and is used for treating HIV/AIDS in combination with other antiretroviral medications.Formula:C20H19F2N3NaO5Purity:(Hplc) 98.0 To 102.0%Color and Shape:PowderMolecular weight:442.40 g/molFlucloxacillin
CAS: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.Formula:C19H17ClFN3O5SPurity:Min. 95%Molecular weight:453.87 g/molDMDNA31
CAS: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.Formula:C50H62N4O13Purity:Min. 95%Molecular weight:927 g/molSisomicin sulfate
CAS:Sisomicin sulfate is a sulfate salt form of sisomicin with similar action and applications as sisomicin.Formula:(C19H37N5O7)2•(H2SO4)5Purity:Min. 95%Color and Shape:PowderMolecular weight:1,385.45 g/molBCX4430 freebase
CAS:Adenosine analogue with antiviral activityFormula:C11H15N5O3Purity:Min. 95%Molecular weight:265.27 g/molDaclatasvir
CAS: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.
Formula:C40H50N8O6Purity:Min. 95%Molecular weight:738.88 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:C21H28ClN3O7SPurity:Min. 95%Color and Shape:PowderMolecular weight:501.98 g/molCurvularin
CAS: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.Purity: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:C53H79F15N14O21Purity:Min. 95%Molecular weight:1,533.3 g/molMaribavir
CAS:Potent antiviral against HCMV and Epstein-Barr virus (EBV)
Formula:C15H19Cl2N3O4Purity:Min. 95%Molecular weight:376.24 g/mol4-Demethyl daunomycinone
CAS: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.Formula:C20H16O8Purity:Min. 95%Molecular weight:384.34 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:C13H9F2NO4Purity:Min. 95%Molecular weight:281.21 g/molDihydropenicillin 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•KPurity:Min. 95%Molecular weight:353.5 g/molMonensin
CAS: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.Formula:C36H62O11Purity:Min. 95%Molecular weight:670.87 g/molTaniborbactam hydrochloride
CAS: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.Formula:C19H30BCl2N3O5Purity:Min. 95%Molecular weight:462.2 g/molSTAADIUM™ PeptiZide L-Pyr
CAS: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.Formula:C17H17N3O3SPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:343.41 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:C25H31N3O9S2Purity:Min. 95%Molecular weight:581.7 g/molOteseconazole
CAS: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.
Formula:C23H16F7N5O2Purity:Min. 95%Molecular weight:527.4 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:C74H128N30O18S6Purity:Min. 95%Molecular weight:1,918.4 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:C184H313N53O46Purity:Min. 95%Molecular weight:4,003.78 g/mol14-Bromodaunorubicin HBr
CAS: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.Formula:C27H28BrNO10·BrHPurity:75%MinMolecular weight:687.33 g/molSulfadimethoxine sodium
CAS: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.Formula:C12H13N4NaO4SPurity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:332.31 g/molTenofovir alafenamide (free base)
CAS: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.Formula:C21H29N6O5PPurity:Min. 97 Area-%Color and Shape:PowderMolecular weight:476.47 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:C43H71NaO11Purity:Min. 95%Molecular weight:787.02 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·xH2OPurity:Min. 95%Color and Shape:PowderMolecular weight:307.3 g/molCefazolin
CAS: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.Formula:C14H14N8O4S3Purity:Min. 95%Molecular weight:454.51 g/molKasugamycin
CAS:Kasugamycin is an aminoglycoside antibiotic, which is derived from the actinomycete Streptomyces kasugaensis. Its mode of action involves the inhibition of protein synthesis by interfering with the function of the 30S ribosomal subunit, ultimately preventing the growth and proliferation of sensitive organisms. In agricultural contexts, Kasugamycin is primarily utilized to control bacterial and fungal diseases in a variety of crops, including rice and fruit trees. It is particularly effective against Xanthomonas oryzae, which causes bacterial leaf blight in rice, and other pathogenic organisms detrimental to plant health. The application of Kasugamycin has been an important tool for integrated pest management programs focusing on sustainable agricultural practices. As a compound with a specific mode of activity, it helps to reduce the environmental impact typically associated with broader-spectrum antibiotics, while offering target-specific disease control. Its careful application supports the minimization of resistance development, ensuring continued efficacy in protecting crop yields.Formula:C14H25N3O9Purity:Min. 95%Molecular weight:379.36 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:C164H266N58O52S6Purity:Min. 95%Molecular weight:4,074.62 g/molClindamycin 3-phosphate
CAS: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.Formula:C18H34ClN2O8PSPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:504.96 g/molSancycline hydrochloride
CAS: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.Formula:C21H23ClN2O7Purity:Min. 95%Molecular weight:450.87 g/molAzithromycin Dihydrate
CAS: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 synthesisFormula:C38H72N2O12·2H2OPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:785.02 g/molGentamicin C1 pentaacetate
CAS:Gentamicin C1 pentaacetate is an aminoglycoside antibiotic with action on bacterial protein synthesis inhibition and is used for research and analytical applications.Formula:C21H43N5O7•(C2H4O2)5Purity:Min. 90%Color and Shape:Off-White PowderMolecular weight:777.86 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:C35H52N8O20SPurity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:936.9 g/mol
