Antimicrobici

<p>Phleomycin HCl is an antibiotic compound derived from *Streptomyces verticillus*, which is known for its robust DNA-cleaving activity. As an antibiotic, it functions primarily by inducing breaks in DNA strands, thereby inhibiting DNA replication and transcription processes. This mechanism of action is particularly effective in targeting rapidly dividing cells, making Phleomycin a valuable tool in molecular biology.</p>

<p>Dalbavancin is a lipoglycopeptide antibiotic with action against gram-positive bacteria, including MRSA and is used for treating acute bacterial skin and skin structure infections.</p>

<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>

<p>Darunavir is an HIV protease inhibitor that is used in the treatment of HIV-1 infection. This drug inhibits HIV-1 protease from binding and catalyzing by attaching to the enzyme and preventing HIV replication.</p>

<p>A broad-spectrum antibiotic of macrolide class, which inhibits 50S ribosomal subunit and inhibits protein synthesis. Spiramycin is also effective against Gram-positive and gram-negative bacteria as well as protozoal parasite Toxoplasma gondii.</p>

<p>Binds cyclophilin D and inhibits calcineurin; immunosuppressant</p>

<p>Inhibitor of bacterial cell wall biogenesis; cephalosporin</p>

<p>Desfuroyl ceftiofur sodium is a veterinary cephalosporin antibiotic, which is derived from cephalosporin C, a beta-lactam antibiotic produced by the fungus Cephalosporium acremonium. Its mode of action involves the inhibition of bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBPs). This prevents the cross-linking of peptidoglycan layers, leading to cell lysis and bacterial death, particularly effective against Gram-negative and some Gram-positive bacteria.</p>

Neomycin EP impurity C (Neomycin C) trifluoroacetate is a reference standard, which is a meticulously characterized chemical impurity often used in pharmaceutical analysis. This compound is derived from the fermentation of *Streptomyces fradiae*, which produces a complex mixture of aminoglycoside antibiotics, including Neomycin B and Neomycin C.

Lactoferrin is a multifunctional glycoprotein, which is primarily sourced from bovine milk, human milk, and other mammalian secretions. With its high affinity for iron, lactoferrin sequesters iron ions, which inhibits bacterial growth by depriving them of the iron necessary for proliferation. This mechanism enables lactoferrin to exhibit potent antimicrobial properties.

<p>Validoxylamine A is an antibiotic, which is a secondary metabolite produced by certain strains of the Actinomyces species. It functions as a potent inhibitor of the enzyme glucose isomerase, which plays a crucial role in the isomerization of glucose to fructose, an important biochemical reaction in various microbial and plant systems.</p>

<p>Enduracidin hydrochloride is an antimicrobial compound, which is a lipopeptide antibiotic derived from the genus Streptomyces, specifically Streptomyces fungicidicus or Streptomyces roseosporus. The compound exerts its antimicrobial activity by inhibiting the synthesis of bacterial cell walls, primarily targeting the lipid II cycle, a critical precursor in the peptidoglycan synthesis pathway. This inhibition disrupts the construction of peptidoglycan layers, ultimately leading to bacterial cell lysis and death.</p>

<p>Baloxavir marboxil is a selective inhibitor of the cap-dependent endonuclease of RNA polymerase, an acidic protein in influenza A and B viruses. In patients, baloxavir marboxil reduces the time to recovery by alleviating the symptoms of the influenza A and B infection, in both adults and children.</p>

Vulgamycin is a novel antibiotic, which is derived from a specific strain of soil bacteria belonging to the genus *Streptomyces*. This microorganism is known for its prolific secondary metabolite production, enabling the development of unique compounds with therapeutic potential. Vulgamycin operates by inhibiting bacterial cell wall synthesis, a mechanism of action that targets key enzymatic pathways, resulting in effective bactericidal activity against a wide range of Gram-positive bacteria.

<p>Cidofovir is an anti-viral agent that is used to treat Cytomegalovirus (CMV) retinitis in patients with AIDS. This drug suppresses CMV replication by inhibiting viral DNA synthesis.</p>

<p>Lucimycin is an antibiotic, which is derived from the fermentation of specific Streptomyces bacterial strains. This compound exerts its antibacterial effects by binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and effectively halting bacterial growth. Lucimycin is particularly effective against Gram-positive bacteria and some Gram-negative species, making it a valuable tool in both clinical and research settings.</p>

<p>Inhibitor of protein synthesis; aminoglycoside</p>

<p>Inhibitor of protein synthesis; aminoglycoside</p>

<p>Amopyroquine is an antimalarial agent and is used for the treatment of malaria. Its mode of action involves the inhibition of haem polymerase in the parasite, leading to the accumulation of toxic haem</p>

<p>Cephradine is a first-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating bacterial infections like urinary tract infections, respiratory infections, and skin infections.</p>

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.

<p>9’-Deoxy-8’,8’-dihydroxyherbicidin is a specialized compound, classified as an antibacterial agent and secondary metabolite, which is naturally derived from microbial sources, specifically certain strains of actinomycetes. These microorganisms are prolific producers of bioactive secondary metabolites, including antibiotics and herbicidins, which exhibit diverse biological activities.</p>

<p>Adefovir is an antiviral drug that is used for the treatment of hepatitis B infections. This drug works by blocking the enzyme reverse transcriptase, therefore preventing the replication of the virus in the body.</p>

<p>Herbicidin H is a naturally occurring microbial herbicide, which is derived from specific strains of soil-borne bacteria. This compound is primarily isolated from Streptomyces species, known for their prolific production of various bioactive secondary metabolites. The mode of action of Herbicidin H involves the disruption of essential cellular processes within plant cells, particularly affecting nucleic acid synthesis. This disruption leads to impaired growth and eventual plant death, making it a potent agent against a range of undesirable plant species.</p>

A derivative of azithromycin, used as an antibiotic

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.

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>Bedaquiline fumarate is the salt form of bedaquiline, a diarylquinoline molecule with an ATP synthetase inhibitory activity. Bedaquiline fumarate is an FDA-approved drug for the oral treatment of multidrug-resistant tuberculosis. Bedaquiline fumarate acts by inhibiting the activity of the ATP synthetase in the pathogenic bacterium Mycobacterium tuberculosis, even in the case of multiple antibiotic resistant strains.</p>

<p>Santonin is a terpenoid compound with action as an anthelmintic by paralyzing parasitic worms and is used for expelling intestinal worms.</p>

2-Methyl-4-isothiazolin-3-one is a biocidal agent, which is a synthetic compound derived from isothiazolinone chemistry. Its primary mode of action involves the inhibition of microbial cell growth by disrupting essential enzyme systems within the cells, leading to cell death. This compound is often supplied as a 50% aqueous solution, facilitating its integration into different mediums.

<p>Ribavirin is a guanosine nucleoside analog with broad-spectrum antiviral properties. Ribavirin gets phosphorylated to ribavirin triphosphate in cells and competes with natural nucleotides for incorporation in a nascent RNA chain, thus interfering with RNA synthesis by inhibiting viral RNA polymerases. Ribavirin is also an inhibitor of inosinate dehydrogenase (IMP), which is involved in the biosynthesis of GTP.</p>

2-[(2-Amino-6-oxo-3H-purin-9-yl)methoxy]ethyl (2S)-2-aminopropanoate is a nucleotide analog, a synthetic compound designed to mimic the structure of natural nucleotides incorporated into DNA. It is derived from chemical synthesis to specifically interfere with viral DNA replication. The compound acts by selectively inhibiting viral DNA polymerase, an enzyme essential for the replication of viral genetic material. This inhibition effectively halts the proliferation of the virus, rendering it unable to reproduce within the host cell.

<p>Gentamicin B is an aminoglycoside antibiotic, which is derived from the bacterium Micromonospora. This derivative exhibits its mode of action by binding to the 30S subunit of the bacterial ribosome, disrupting protein synthesis. As a result, it causes misreading of mRNA, ultimately leading to cell death, thereby exhibiting bactericidal effects.</p>

<p>Oxiconazole is an anti-fungal agent that is used for the treatment of various dermatophyte infections. It can be used to treat athlete’s foot, ringworm and jock itch. This drug inhibits ergosterol biosynthesis and acts to destabilize the fungal cytochrome enzyme P450 51. Additionally, this drug has shown to inhibit DNA synthesis and suppress concentrations of ATP.</p>

<p>Fengycin A analogue is an antifungal lipopeptide, which is a cyclic compound derived from microbial sources, specifically produced by Bacillus subtilis strains. It functions primarily by disrupting the cell membranes of pathogenic fungi, leading to altered membrane permeability and subsequent cell death. The unique structure of fengycin allows it to interact with membrane lipids, compromising membrane integrity and inhibiting fungal growth.</p>

<p>Carbomycin is a macrolide antibiotic, which is derived from the bacterium Streptomyces halstedii. This antibiotic functions by binding to the 50S ribosomal subunit, thereby inhibiting bacterial protein synthesis. Through this mechanism, carbomycin effectively disrupts the growth and replication of susceptible bacterial strains, making it a potent tool in combating bacterial infections.</p>

<p>Cefditoren acid sodium is an antibacterial agent that belongs to the class of third-generation cephalosporins, which is derived from Acremonium fungus and produced through chemical synthesis. This compound acts by inhibiting bacterial cell wall synthesis, leading to cell lysis and death. It achieves this by binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall. The interruption of peptidoglycan synthesis in the cell wall is crucial for maintaining bacterial cell integrity, and its inhibition results in the bactericidal activity of cefditoren acid sodium. It is effective against a range of Gram-positive and Gram-negative bacteria. The key applications of this compound include the treatment of bacterial infections such as respiratory tract infections, skin infections, and other conditions caused by susceptible bacteria. Its spectrum of activity and pharmacokinetic properties make it suitable for situations where third-generation cephalosporins are indicated. Understanding the specific interaction with PBPs and the resistance mechanisms is crucial for optimizing its clinical use and managing antibiotic resistance.</p>

<p>Ampicillin is a β-lactam antibiotic with a broad spectrum of activity against Gram-positive and Gram-negative bacteria. It is used in the treatment of bacterial infections, including those caused by methicillin-resistant Staphylococcus aureus (MRSA), Streptococcus pneumoniae, and Listeria monocytogenes. Ampicillin binds to penicillin-binding proteins in the bacterial cell wall by competitive inhibition. It prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division.</p>

<p>Cefatrizine is a broad-spectrum antibiotic, which is a semisynthetic cephalosporin derived from cephalosporin C, a natural product originating from the fungus Acremonium chrysogenum. It exerts its mode of action through the inhibition of bacterial cell wall synthesis, a critical component for bacterial growth and replication. Specifically, cefatrizine targets and binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, leading to the inhibition of peptidoglycan synthesis. This disruption results in cell lysis and ultimately bacterial cell death.</p>

<p>Amphotericin B is a macrocycle antibiotic with very potent antifungal effects and resistance very rarely occurs. Amphotericin B is a polyene antifungal that binds to fungal cell membrane, i.e., ergosterol disrupts the membrane permeability leading to leakage of intracellular components. It is often used as an alternative therapy for leishmaniasis and to treat severe mycoses including: systemic Candida, Cryptococcus, blastomycosis, and histoplasmosis.</p>

<p>Cidofovir is an anti-viral agent that is used to treat Cytomegalovirus (CMV) retinitis in patients with AIDS. This drug suppresses CMV replication by inhibiting viral DNA synthesis.</p>

Taurine derivative; used to prevent infection in catheters

<p>Tubulin ligand which promotes microtubule assembly and stabilises microtubule cytoskeleton against depolymerisation. The compound has anti-tumoral activity since its interference with cytoskeleton dynamics affects the assembly of mitotic spindle, segregation of chromosomes, cell division and blocks the cell cycle in G1 or M phase. The compound is also used for the purification of tubulin or microtubule-associated proteins.</p>

<p>Clevudine-d4 is a deuterium-labeled analog of the nucleoside analogue clevudine, which is a synthetic antiviral compound. It is derived from chemical synthesis, specifically designed for research purposes involving the metabolic and pharmacokinetic pathways of clevudine. Clevudine-d4 acts as an inhibitor of the hepatitis B virus (HBV) by interfering with the viral DNA polymerase. It incorporates into viral DNA, leading to chain termination during HBV replication.</p>

Terbinafine is an antifungal drug that is used in the treatment of dermatophyte infections of the toenails and fingernails. Terbinafine also treats other skin infections. This drug works by inhibiting ergosterol synthesis which in return inhibits fungal squalene monooxygenase. This results in a disruption of fungal cell wall synthesis.

<p>rec beta-Defensin 2 (human) is a recombinant peptide, which is a human-derived antimicrobial protein. It is sourced through recombinant DNA technology, enabling the production of a synthetic version of the natural peptide found in epithelial cells. Its mode of action involves disrupting microbial cell membranes, leading to cell lysis, in addition to modulating the immune response by interacting with immune cells and enhancing the production of cytokines.</p>

<p>Bleomycin 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, particularly in regions rich in guanine and cytosine. This leads to inhibition of DNA synthesis and, consequently, cellular replication, making it effective in targeting rapidly dividing cancer cells.</p>

<p>Ceftaroline fosamil is an antibacterial agent used to treat various bacterial infections such as pneumonia. Ceftaroline fosamil binds to the ribosomal RNA of bacteria, preventing the formation of proteins necessary for cell division. Ceftaroline fosamil has been shown to be highly active against Mycobacterium tuberculosis, Mycobacterium avium complex, and fungi such as Candida species.</p>

<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&amp;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>

<p>4-Epichlortetracycline is a metabolite of chlortetracycline, which is derived from the Streptomyces genus of bacteria. It is structurally related to tetracycline antibiotics but differs specifically in its epimerization at the fourth position. This alteration results in a product with significantly reduced antibacterial activity compared to its parent compound. The mechanism of action primarily involves ribosomal binding, inhibiting protein synthesis in susceptible bacteria; however, the epimerization here compromises this efficacy.</p>

<p>A broad-spectrum antibiotic of cephalosporin class, which inhibits bacterial cell wall synthesis by targeting the penicillin-binding protein, involved in peptidoglycan synthesis. This third-generation cephalosporin is very active against Pseudomonas species and can also be used to treat bacterial meningitis as it penetrates in the cerebrospinal fluid.</p>

<p>b-Apo-oxytetracycline is a tetracycline antibiotic and is used for the treatment of bacterial infections. It binds to the 30S ribosomal subunit, inhibiting protein synthesis.</p>

<p>Neospiramycin I is a macrolide antibiotic with action on bacterial ribosomes to inhibit protein synthesis and is used for treating bacterial infections in research applications.</p>

<p>Ceftazidime is a broad-spectrum beta-lactam antibiotic that inhibits bacterial growth by inhibiting penicillin-binding proteins (PBPs). It is used to treat many bacteria infections including pneumonia and septicaemia. It has shown to be effective against some treatment-resistant bacteria such as Pseudomonas aeruginosa.</p>

<p>Flucloxacillin sodium is a beta-lactam antibiotic with action on bacterial cell wall synthesis and is used for treating skin, bone, and respiratory infections.</p>

<p>Capastat sulfate is an antibiotic with action against Mycobacterium tuberculosis by inhibiting protein synthesis and is used for treating tuberculosis.</p>

<p>Anti-viral; inhibits Hepatitis C virus NS3/4a protease</p>

<p>Lamivudine (commonly called 3TC) is a potent nucleoside analogue reverse transcriptase inhibitor. It is one of the front line treatments for HIV.  It is an analogue of cytidine, and can inhibit both types (1 and 2) of HIV reverse transcriptase as well as the reverse transcriptase of hepatitis B. It needs to be phosphorylated to its triphosphate form before it is active.</p>

<p>Lomefloxacin is a fluoroquinolone antibiotic with a mode of action that inhibits bacterial DNA gyrase and topoisomerase IV. It is used for treating bacterial infections like bronchitis and urinary tract infections.</p>

Fosmidomycin sodium hydrate is an antibiotic, which is a natural product derived from Streptomyces lavendulae. This compound specifically inhibits the non-mevalonate pathway of isoprenoid biosynthesis by targeting 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR), an essential enzyme in the pathway. By disrupting this process, fosmidomycin effectively impedes the synthesis of essential isoprenoid precursors, which are crucial for the survival and proliferation of certain bacteria and parasites.

<p>Inhibitor of protein synthesis; glycylcycline class</p>

<p>Tilmicosin is a macrolide antibiotic that is used in veterinary medicine. It is used to treat bovine respiratory disease and inhibits bacterial growth by binding to the 50S ribosomal subunit of the bacteria resulting in reduced protein synthesis.</p>

<p>Saquinavir is a HIV protease inhibitor drug that is used with other antiretroviral drugs for the treatment of HIV-1. As this drug prevents HIV protease activity, it prevents the proteolysis of the Gag polyprotein and thus results in non-infectious virus particles.</p>

Amicoumacin B is a bacterial metabolite, which is derived from *Bacillus subtilis*. This compound exhibits a strong antibacterial function by targeting bacterial ribosomes, thereby inhibiting protein synthesis. As a result, it disrupts the growth and proliferation of bacterial cells, making it effective against a broad spectrum of Gram-positive bacteria.

<p>Geneticin is very efficient against gram-negative bacteria, however it is not applied for treating infections due to high renal toxicity. Geneticin and its resistance genes found application in the selection of transgenic cell lines including yeasts such as P. pastoris and S. serevisiae, other eukaryotic cell lines such as CHO or HEK293, but also plant cells and bacterial cells.</p>

<p>Anti-viral; non-nucleoside reverse transcriptase inhibitor</p>

Antibiotic of anthracycline class; DNA synthesis inhibitor

<p>Exalamide is an arenecarboxamide antifungal agent with action on fungal growth inhibition and is used for research on fungal infections.</p>

Butoconazole nitrate is an antifungal agent and is used for the treatment of vaginal yeast infections. It inhibits the synthesis of ergosterol, disrupting the fungal cell membrane.

<p>Closantel sodium dihydrate is a salicylanilide antiparasitic agent with action on flukes, nematodes, and arthropods and is used for veterinary treatment of parasitic infections.</p>

<p>Dihydrostreptomycin B is an aminoglycoside antibiotic, which is derived from the bacterium Streptomyces griseus. This antibiotic operates by binding to the 30S subunit of the bacterial ribosome, leading to the inhibition of protein synthesis. The binding disrupts the decoding site, causing misreading of mRNA and ultimately resulting in bactericidal activity.</p>

Oritavancin diphosphate is a lipoglycopeptide antibiotic with action on bacterial cell wall synthesis and is used for treating acute bacterial skin and skin structure infections.

<p>Inhibitor of protein synthesis; streptogramin</p>

<p>Triclabendazole is a benzimidazole anthelmintic with action on liver flukes by disrupting their microtubule formation and is used for treating fascioliasis in humans and animals.</p>

<p>Raltegravir is an antiretroviral agent that is used for the treatment of HIV infections. It inhibits HIV integrase in order to prevent viral genome from being inserted into the human genome. It binds to the active site of the enzyme and prevents it from binding to a target sequence on the viral DNA. This drug is metabolized by glucuronidation.</p>

<p>N-Boc-protected -Guanidino Oseltamivir is a fine chemical that belongs to the group of versatile building blocks. It is a complex compound that has been used in research as a reagent and speciality chemical. N-Boc-protected -Guanidino Oseltamivir is an important intermediate for the synthesis of a variety of useful compounds, such as pharmaceuticals and natural products. This compound is also used as a reaction component in organic syntheses, especially for the preparation of high quality and useful scaffolds.</p>

<p>Tylosin tartrate is a macrolide antibiotic with action on bacterial protein synthesis inhibition and is used for treating bacterial infections in livestock and poultry.</p>

<p>Clofazimine is a phenazine dye antibiotic with action on bacterial DNA interference and is used for treating leprosy and erythema nodosum leprosum.</p>

<p>Inhibitor of protein synthesis; macrolide class</p>

<p>Inhibitor of hepatitis C viral enzyme NS3-4A serine protease</p>

<p>N-Demethyl roxithromycin is a metabolite of roxithromycin with action on bacterial protein synthesis inhibition and is used for research on macrolide antibiotics.</p>

Fenbendazole is a benzimidazole anthelmintic with action on microtubule formation in parasites and is used for treating gastrointestinal parasites in animals.

<p>Anti-retroviral; HIV protease inhibitor</p>

Piperaquine tetraphosphate tetrahydrate is an antimalarial compound with action on Plasmodium parasites by disrupting DNA synthesis and is used for treating malaria in combination therapies.

<p>Anti-fungal; glucan synthase inhibitor</p>

Fenticonazole nitrate is an imidazole antifungal agent with action on fungal cell membrane disruption and is used for treating fungal infections like vaginal thrush and athlete's foot.

<p>Inhibits chaperone protein HSP90; anti-proliferative; antineoplastic</p>

<p>Doxorubicin (DOX) is an antineoplastic chemotherapy drug used to treat breast, ovarian and pancreatic cancers. It is an antitumor antibiotic that inhibits DNA topoisomerase II. DOX interferes with the topoisomerase II-mediated repair of DNA causing accumulation of mutations. It also leads to the generation of reactive oxygen species (ROS), which further damage DNA as well as proteins and membranes. However, the compound presents with a risk of developing cardiomyopathy as well as drug resistance. Pegylated liposomal doxorubicin has also been developed to treat breast and ovarian cancers, myeloma, and HIV-related Kaposi’s sarcoma.</p>

<p>Temocillin disodium is a beta-lactamase-resistant penicillin antibiotic with action on bacterial cell wall synthesis and is used for treating infections caused by multidrug-resistant gram-negative bacteria.</p>

<p>Pimodivir is a non-nucleoside-derived inhibitor of the polymerase basic protein 2 (PB2) subunit found in the polymerase complex of the influenza A virus. In general, pimodivir is indicated for the treatment of patients with severe influenza although knowledge about possible rise of resistance is not available.</p>

<p>Dihydrostreptomycin sesquisulfate, EP is an aminoglycoside antibiotic, structurally derived from Streptomyces griseus. This compound originates from microbial biosynthesis, a method which harnesses the natural antibiotic-producing capabilities of microbial cultures. The mode of action of dihydrostreptomycin sesquisulfate involves binding to the 30S subunit of bacterial ribosomes, which interrupts the process of protein synthesis, ultimately leading to bacterial cell death.</p>