Antibióticos
Os antibióticos são compostos projetados para destruir ou inibir o crescimento de vários microrganismos, desempenhando um papel crucial no tratamento de infecções e na prevenção da disseminação de doenças. Esta categoria oferece uma ampla variedade de ingredientes ativos especificamente para pesquisa no campo bioquímico. Esses compostos são ferramentas essenciais no estudo dos mecanismos bacterianos, padrões de resistência e no desenvolvimento de novos agentes terapêuticos. Os pesquisadores podem explorar uma grande variedade de antibióticos para entender seus efeitos, otimizar seu uso e desenvolver novos tratamentos para combater ameaças microbianas emergentes. A disponibilidade de um espectro tão amplo de antibióticos apoia a pesquisa avançada e a inovação em microbiologia e ciências farmacêuticas.
Subcategorias de "Antibióticos"
- Antibióticos macrolídeos(26 produtos)
- Antibióticos Esteróides(31 produtos)
- Antibióticos de tetraciclina(20 produtos)
- Antibióticos β-Lactâmicos(11 produtos)
Foram encontrados 4082 produtos de "Antibióticos"
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Lincophenicol
CAS:<p>Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor.</p>Fórmula:C18H27N3O5Pureza:98%Cor e Forma:SolidPeso molecular:365.42Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42Phenosulfazole
CAS:<p>Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].</p>Fórmula:C9H8N2O3S2Cor e Forma:SolidPeso molecular:256.3Vidarabine phosphate
CAS:<p>Vidarabine phosphate is an adenosine monophosphate analog.</p>Fórmula:C10H14N5O7PPureza:99.75%Cor e Forma:White Crystalline PowderPeso molecular:347.22Albitiazolium bromide
CAS:<p>Albitiazolium bromide is an antimalarial compound disrupting phosphatidylcholine biosynthesis in Plasmodium, transported via NPP and cation carriers.</p>Fórmula:C24H42BrN2O2S2Pureza:99.743%Cor e Forma:SolidPeso molecular:534.64Saquayamycin B
CAS:<p>Saquayamycin B, a glycoside, targets Gram-positive bacteria and both adriamycin-sensitive and -resistant P388 leukemia cells.</p>Fórmula:C43H48O16Cor e Forma:SolidPeso molecular:820.83Exeporfinium chloride
CAS:<p>Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.</p>Fórmula:C44H50Cl2N6O2Cor e Forma:SolidPeso molecular:765.81Abimtrelvir
CAS:<p>Abimtrelvir exhibited antiviral activity.</p>Fórmula:C24H17ClF3N7O2Cor e Forma:SolidPeso molecular:527.89Verticillin A
CAS:<p>Verticillin A, an apoptosis inducer, inhibits Leiomyosarcoma and Malignant peripheral nerve sheath tumor growth.</p>Fórmula:C30H28N6O6S4Pureza:98%Cor e Forma:SolidPeso molecular:696.84Pyrazofurin
CAS:<p>Pyrazofurin, a pyrimidine analogue, blocks cell growth and DNA synthesis by targeting UMP synthase & orotate-phosphoribosyltransferase (IC50: 0.06-0.37 μM).</p>Fórmula:C9H13N3O6Pureza:98%Cor e Forma:SolidPeso molecular:259.22Riodoxol
CAS:<p>Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.</p>Fórmula:C6H3I3O2Cor e Forma:SolidPeso molecular:487.8AFK-108
CAS:<p>AFK-108 is a fungicide agent.</p>Fórmula:C21H26Cl2N2OPureza:98%Cor e Forma:SolidPeso molecular:393.35FR900098 (sodium salt)
CAS:<p>FR900098, a fosmidomycin derivative, has potent antimalarial effects, targeting DOXP reductoisomerase and eradicating P. vinckei in mice at >10 mg/kg.</p>Fórmula:C5H12NNaO5PCor e Forma:SolidPeso molecular:220.117Chitin synthase inhibitor 2
CAS:<p>Chitin synthase inhibitor 2 (2b) has an IC50 of 0.09 mM, K i 0.12 mM, shows in vitro antimicrobial activity and boosts fluconazole/polyoxin B.</p>Fórmula:C20H19N3O3Cor e Forma:SolidPeso molecular:349.38Alalevonadifloxacin HCl
CAS:<p>Alalevonadifloxacin HCl is a novel l-alanine ester prodrug of levonadifloxacin.</p>Fórmula:C22H27ClFN3O5Pureza:98%Cor e Forma:SolidPeso molecular:467.92Pyrrofolic acid
CAS:<p>Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.</p>Fórmula:C23H21N7O7Pureza:98%Cor e Forma:SolidPeso molecular:507.46CRK12-IN-1
CAS:<p>CRK12-IN-1: strong inhibitor of CRK12, kills T.b. brucei & T. congolense (EC50s: 1.3 & 18 nM).</p>Fórmula:C20H26F2N4O3S2Pureza:99.72%Cor e Forma:SolidPeso molecular:472.57SQ109
CAS:<p>SQ109 (NSC-722041) is an effective inhibitor of the trypomastigote form of the parasite (IC50 = 50 nM). SQ109 is an antitubercular agent and targets MmpL3.</p>Fórmula:C22H38N2Pureza:99.70% - 99.91%Cor e Forma:SolidPeso molecular:330.55BRD-8000.3
CAS:<p>BRD-8000.3 is a narrow-spectrum antimycobacterial targeting EfpA, inhibiting lipid transport in drug-tolerant Mtb and useful in structural and functional.</p>Fórmula:C19H21BrN4OPureza:99.78% - 99.78%Cor e Forma:SolidPeso molecular:401.3MptpB-IN-1
CAS:<p>MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.</p>Fórmula:C17H11Cl2NO4Cor e Forma:SolidPeso molecular:364.18Acyclovir monophosphate
CAS:<p>Acyclovir monophosphate, a strong anti-HSV agent, inhibits viral DNA polymerase, blocking DNA synthesis and chain elongation.</p>Fórmula:C8H12N5O6PCor e Forma:SolidPeso molecular:305.18Amcinafal
CAS:<p>Amcinafal is an active diol,and used against virus replication and interferon production.</p>Fórmula:C26H35FO6Pureza:98%Cor e Forma:SolidPeso molecular:462.55LY 186826
CAS:<p>LY 186826 is an antibacterial agent with bicyclic pyrazolidinone properties.</p>Fórmula:C15H16N6O6SPureza:98%Cor e Forma:SolidPeso molecular:408.39Linogliride
CAS:<p>Linogliride: a guanidine derivative, inhibits insulin release, and enhances glucose tolerance by blocking ATP-sensitive K+ channels in pancreatic beta cells.</p>Fórmula:C16H22N4OPureza:98%Cor e Forma:SolidPeso molecular:286.37Lipoxamycin hemisulfate
CAS:<p>Lipoxamycin hemisulfate (Lipoxamycin) is an inhibitor of serine palmitoyltransferase (IC50 = 21 nM) with antifungal activity.</p>Fórmula:C38H74N4O14SPureza:99.14% - 99.93%Cor e Forma:SolidPeso molecular:843.08DDD01035881
CAS:<p>DDD01035881 is a anti-malarial drug that blocks parasite-to-mosquito transmission by targeting the Plasmodium vesicle membrane protein Pfs16.</p>Fórmula:C14H14BrNO4S2Pureza:99.78%Cor e Forma:SolidPeso molecular:404.3Pentachloropseudilin
CAS:<p>Pentachloropseudilin inhibits Myosin-1 and speeds up TGF-β receptor turnover, suppressing TGF-β activity.</p>Fórmula:C10H4Cl5NOPureza:98.14%Cor e Forma:SolidPeso molecular:331.41Ferric citrate
CAS:<p>Ferric citrate as a source of iron used in cell culture applications can provide iron with a less toxic form compared to free iron salts.</p>Fórmula:C6H8FeO7Cor e Forma:Limit Its Spread To The Environment It Is Used In Medicine In Making Blueprints And As A FeedPeso molecular:247.968Niclosamide monohydrate
CAS:<p>Niclosamide Monohydrate is used for the treatment of most tapeworm infections by inhibiting DNA replication.</p>Fórmula:C13H10Cl2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:345.14Epirubicin
CAS:<p>Epirubicin, a doxorubicin derivative, is an antineoplastic, inhibits topoisomerase, DNA/RNA synthesis, and Foxp3, reducing T cell activity.</p>Fórmula:C27H29NO11Cor e Forma:SolidPeso molecular:543.52SSJ-183
CAS:<p>SSJ-183 is a low-toxicity and orally available and anti-malarial drug with an IC50 = 7.6 nM against P. falciparum and no lethality at doses up to 2000 mg/kg po.</p>Fórmula:C25H22N4OPureza:99.71% - 99.83%Cor e Forma:SolidPeso molecular:394.47Pafuramidine maleate
CAS:<p>Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis.</p>Fórmula:C24H24N4O7Pureza:98%Cor e Forma:SolidPeso molecular:480.16Linogliride fumarate
CAS:<p>Linogliride fumarate, a guanidine derivative, stimulates insulin release by blocking ATP-sensitive K+ channels, enhancing glucose tolerance.</p>Fórmula:C20H26N4O5Pureza:98%Cor e Forma:SolidPeso molecular:402.451Tunicamine
CAS:<p>Tunicamine is a reversible polyprenol-phosphate inhibitor.</p>Fórmula:C11H21NO9Pureza:98%Cor e Forma:SolidPeso molecular:311.29Antiviral agent 18
CAS:<p>Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.</p>Fórmula:C11H13ClN4O4Cor e Forma:SolidPeso molecular:300.7Rosaramicin
CAS:<p>Rosaramicin, a lipid-soluble basic macrolide, is an antibacterial substance similar to erythromycin but with a better activity against Gram-negative bacteria.</p>Fórmula:C31H51NO9Pureza:98%Cor e Forma:SolidPeso molecular:581.744-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS:<p>4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].</p>Fórmula:C16H16N2O5SCor e Forma:SolidPeso molecular:348.37Ormetoprim
CAS:<p>Ormetoprim (Ro 5-9754), an antibiotic approved for use in the United States, is used to prevent the spread of disease in freshwater aquaculture.</p>Fórmula:C14H18N4O2Pureza:99.92%Cor e Forma:SolidPeso molecular:274.32Ceftizoxime
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>Fórmula:C13H13N5O5S2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:383.41 g/molAntiviral agent 17
CAS:<p>Antiviral agent 17, EC50 0.015 μM in human assay, effective against murine norovirus, may aid infectious/malignant disease research.</p>Fórmula:C11H14N4O4Pureza:99.89%Cor e Forma:SolidPeso molecular:266.25Clofoctol
CAS:<p>Clofoctol is a bacteriostatic antibiotic with activity against Gram-positive bacteria, used in the treatment of upper and lower respiratory tract infections.</p>Fórmula:C21H26Cl2OPureza:98% - 99.87%Cor e Forma:SolidPeso molecular:365.34Hygromycin A
CAS:<p>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.</p>Fórmula:C23H29NO12Pureza:Min. 95%Peso molecular:511.5 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>Fórmula:C26H26N8O11S2NaPureza:Min. 95%Peso molecular:713.65 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>Fórmula:C43H74N2O14Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:843.05 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>Pureza:Min. 95%Sterigmatocystin
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>Pureza:Min. 95%Cefazolin
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>Fórmula:C14H14N8O4S3Pureza:Min. 95%Peso molecular:454.51 g/molCarnidazole
CAS:<p>Carnidazole (ME-108) shows antiprotozoal activity and can be used in studies about the treatment of Trichomonas infection.</p>Fórmula:C8H12N4O3SPureza:99.81%Cor e Forma:SolidPeso molecular:244.27Ceftriaxone 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>Fórmula:C18H18N8Na2O7S3Pureza:Min. 84 Area-%Cor e Forma:White Yellow PowderPeso molecular:600.56 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>Fórmula:C27H28BrNO10·BrHPureza:75%MinPeso molecular:687.33 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>Fórmula:C18H34ClN2O8PSPureza:Min. 95%Cor e Forma:White To Off-White SolidPeso molecular:504.96 g/molNortopixantrone HCl
CAS:<p>Nortopixantrone HCl (BBR 3438) is a novel 9-azacyclonopyrazole that shows antitumor activity in a human prostate cancer model.</p>Fórmula:C20H26Cl2N6O2Pureza:99.08% - 99.74%Cor e Forma:SolidPeso molecular:453.36Azidamfenicol
CAS:<p>Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 µM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.</p>Fórmula:C11H13N5O5Pureza:99.61%Cor e Forma:SolidPeso molecular:295.25Cyclosporin 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>Fórmula:C63H113N11O12Pureza:Min. 95%Cor e Forma:PowderPeso molecular:1,216.64 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>Fórmula:C12H13N4NaO4SPureza:Min. 95%Cor e Forma:White Off-White PowderPeso molecular:332.31 g/molQuinupristin
CAS:<p>Quinupristin, a macrolide-lincosamide-streptogramin antibiotic, inhibits protein synthesis in bacteria.</p>Fórmula:C53H67N9O10SPureza:98.05% - 98.16%Cor e Forma:SolidPeso molecular:1022.22Cefmenoxime hydrochloride
CAS:<p>Cefmenoxime hydrochloride is a third-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating gynecological and obstetric infections.</p>Fórmula:C16H17N9O5S3HClPureza:Min. 95%Cor e Forma:White PowderPeso molecular:529.79 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>Fórmula:C36H65NO13Pureza:Min. 95%Peso molecular:719.9 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>Fórmula:C27H48N6O9Pureza:Min. 95%Peso molecular:600.71 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>Fórmula:C36H62O11Pureza:Min. 95%Peso molecular: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>Fórmula:C19H12O6Pureza:Min. 95%Cor e Forma:PowderPeso molecular:336.29 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>Fórmula:C37H62O12Pureza:Min. 95%Peso molecular:698.88 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>Fórmula:C18H34ClN2O8PSPureza:Min. 95%Cor e Forma:White to off-white solid.Peso molecular:504.96 g/molTrombodipine
CAS:<p>Trombodipine (PCA-4230) is a platelet aggregation inhibitor with antithrombotic activity and protection against Listeria monocytogenes.</p>Fórmula:C21H24N2O7SPureza:98.73% - 99.14%Cor e Forma:SolidPeso molecular:448.49Faropenem sodium hydrate
CAS:<p>Faropenem sodium hydrate is a hydrated form of faropenem sodium with similar action and applications as faropenem sodium hemipentahydrate.</p>Fórmula:C12H14NNaO5S·xH2OPureza:Min. 95%Cor e Forma:PowderPeso molecular:307.3 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>Fórmula:C19H17ClFN3O5SPureza:Min. 95%Peso molecular:453.87 g/molPefloxacin-d3
CAS:Produto Controlado<p>Pefloxacin-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.</p>Fórmula:C17H17D3FN3O3Pureza:Min. 95%Peso molecular:336.38 g/molGentamicin 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>Fórmula:C20H41N5O7Pureza:(%) Min. 90%Cor e Forma:PowderPeso molecular:463.57 g/molBleomycin A5 hydrochloride
CAS:<p>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.</p>Fórmula:C57H89N19O21S2•HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:1,177.03 g/molSisomicin sulfate
CAS:<p>Sisomicin sulfate is a sulfate salt form of sisomicin with similar action and applications as sisomicin.</p>Fórmula:C19H37N5O7·5H2SO4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:1,385.45 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>Fórmula:C21H43N5O7•(C2H4O2)5Pureza:Min. 90%Cor e Forma:Off-White PowderPeso molecular:777.86 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>Fórmula:C21H23ClN2O7Pureza:Min. 95%Peso molecular:450.87 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>Fórmula:C20H16O8Pureza:Min. 95%Peso molecular:384.34 g/molLeptomycin 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>Fórmula:C33H48O6Pureza:Min. 95%Peso molecular:540.73 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>Fórmula:C17H19F2N3O3•HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:387.81 g/molCeftibuten
CAS:<p>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.</p>Fórmula:C15H14N4O6S2Pureza:Min. 95%Peso molecular:410.43 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>Fórmula:C15H24N4O6S2Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:420.51 g/mol(-)-Neplanocin A
CAS:<p>S-Adenosylhomocysteine (SAH) hydrolase is responsible for the reversible hydrolysis of SAH into adenosine and homocysteine. Inhibition of this enzyme leads to the accumulation of SAH within cells, thereby increasing the SAH to S-adenosylmethionine (SAM) ratio and subsequently inhibiting SAM-dependent methyltransferases. (−)-Neplanocin A, a potent and irreversible inhibitor of SAH hydrolase (Ki= 8.39 nM), exhibits significant antitumor activity against mouse leukemia L1210 cells and holds broad-spectrum antiviral properties. Its efficacy notably surpasses that of the reversible inhibitor 3-deazaneplanocin, especially in combating vesicular stomatitis, evidencing a higher potency with ID50 values of 0.07 μg/ml for Neplanocin A versus 0.3 μg/ml for 3-deazaneplanocin.</p>Fórmula:C11H13N5O3Cor e Forma:SolidPeso molecular:263.3OM173-αA
CAS:<p>OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M.</p>Fórmula:C17H16O6Cor e Forma:SolidPeso molecular:316.31Gusperimus trihydrochloride
CAS:<p>Gusperimus trihydrochloride is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity.</p>Fórmula:C17H40Cl3N7O3Pureza:98%Cor e Forma:SolidPeso molecular:496.9Annamycin
CAS:<p>Annamycin, a semi-synthetic doxorubicin derivative, binds DNA, blocks topoisomerase II, and evades MDR, inhibiting DNA/RNA/protein synthesis.</p>Fórmula:C26H25IO11Cor e Forma:SolidPeso molecular:640.37Nilofabicin
CAS:<p>Nilofabicin (CG-400549) is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated</p>Fórmula:C19H20N2O2SPureza:98.66%Cor e Forma:SolidPeso molecular:340.44Myxopyronin A
CAS:<p>Myxopyronin A is an inhibitor of bacterial RNA polymerase.</p>Fórmula:C23H31NO6Pureza:98%Cor e Forma:SolidPeso molecular:417.5N-Acetylpurinomycin
CAS:<p>N-Acetylpurinomycin is a selective agonist of CB2 receptor.</p>Fórmula:C24H31N7O6Cor e Forma:SolidPeso molecular:513.55AS-2077715
CAS:<p>AS-2077715, an antifungal agent, exhibits inhibitory activity against Trichophyton species and is derived from the fermentation broth of Capnodium sp. 339855. It is utilized in the study of fungal infections [1].</p>Fórmula:C25H41NO7Cor e Forma:SolidPeso molecular:467.6Alatrofloxacin
CAS:<p>Alatrofloxacin is a prodrug of trovafloxacin.</p>Fórmula:C26H25F3N6O5Cor e Forma:SolidPeso molecular:558.51Rosoxacin
CAS:<p>Rosoxacin (Acrosoxacin) shows antibacterial activities against a broad spectrum of Gram-negative bacteria including Neisseria gonorrhoeae (MIC90 = 0.03mg/ml).</p>Fórmula:C17H14N2O3Pureza:99.1%Cor e Forma:SolidPeso molecular:294.34'-Acetyl-chrysomycin B
CAS:<p>4'-Acetyl-chrysomycin B, a 4'-acetylated analog of chrysomycin B, exhibits anti-Gram-positive bacterial and antimicrobial activities [1].</p>Fórmula:C29H30O10Cor e Forma:SolidPeso molecular:538.54Trovafloxacin mesylate
CAS:<p>Trovafloxacin: broad-spectrum fluoroquinolone, blocks DNA gyrase/topoisomerase IV and PANX1 channel (IC50=4μM).</p>Fórmula:C21H19F3N4O6SPureza:99.18%Cor e Forma:SolidPeso molecular:512.46Aranciamycin
CAS:<p>Aranciamycin (Compound 1), an anthracycline antibiotic, exhibits collagenase inhibitory activity (IC50 3.7*10^-7 M) and can inhibit DNA synthesis in tumor cells</p>Fórmula:C27H28O12Cor e Forma:SolidPeso molecular:544.5Pristinamycin IA
CAS:<p>Pristinamycin IA (Mikamycin B) is a substrate for the P-glycoprotein and a cyclo-peptidic macrolactone antibiotic.</p>Fórmula:C45H54N8O10Pureza:97.44%Cor e Forma:SolidPeso molecular:866.96Berkeleylactone E
CAS:<p>Berkeleylactone E, a macrolide antibiotic [1], exhibits antimicrobial properties.</p>Fórmula:C20H32O7Cor e Forma:SolidPeso molecular:384.469Calicheamicin
CAS:<p>Calicheamicin (Calicheamicin γ1) is an antitumor antibiotic and is a DNA synthesis inhibitor. It also is a cytotoxic agent that causes double-strand DNA breaks.</p>Fórmula:C55H74IN3O21S4Pureza:98.22% - 98.78%Cor e Forma:SolidPeso molecular:1368.35Oseltamivir acid methyl ester
CAS:<p>Oseltamivir acid methyl ester, a CES1-convertible neuraminidase inhibitor, serves as an antiviral prodrug.</p>Fórmula:C15H26N2O4Pureza:98.78%Cor e Forma:SolidPeso molecular:298.38Cladosporin
CAS:<p>Cladosporin, from Cladosporium cladosporioid fungus, halts dermatophyte growth on agar at 75 μg/mL.</p>Fórmula:C16H20O5Cor e Forma:SolidPeso molecular:292.33CcpA-IN-1
CAS:<p>CcpA-IN-1 is a Staphylococcus aureus antibiotic exhibiting significant bactericidal activity (MICs=460 nM) [1].</p>Fórmula:C77H82F12N8OP3RuPureza:98%Cor e Forma:SolidPeso molecular:1557.5Antibacterial agent 159
CAS:<p>Compound 6d (Antibacterial agent 159) is an antibiotic effective against impetigo and Clostridium difficile infection (CDI), with no observed recurrence for CDI</p>Fórmula:C51H50N16O10S6Pureza:98%Cor e Forma:SolidPeso molecular:1239.43SDH-IN-3
CAS:<p>SDH-IN-3 is a succinate dehydrogenase (SDH) inhibitor, demonstrating potent antifungal activity with an inhibition concentration (IC50) of 7.2 μg/mL and an</p>Fórmula:C15H11F2N3OSPureza:98%Cor e Forma:SolidPeso molecular:319.33Caerulomycin A
CAS:<p>Caerulomycin A (Caerulomycin) (Cerulomycin; Caerulomycin) is an antifungal compound.</p>Fórmula:C12H11N3O2Pureza:99.28%Cor e Forma:SolidPeso molecular:229.23β-Lactamase-IN-2
CAS:<p>β-Lactamase-IN-2 is an inhibitor of β-Lactamase with anti-microbial and anti-bacterial effects.</p>Fórmula:C11H9FO3Pureza:99.52%Cor e Forma:SolidPeso molecular:208.19
