Antifungals

Nikkomycin Z (Nikkomycin Z from Streptomyces tendae) is a competitive chitin synthase inhibitor.It inhibitor of the growth of filamentous fungi, insects,

Loflucarban (Fluonilid) is an antimycotic compoud.

FR194738 is an inhibitor of squalene epoxidase with an IC50 of 9.8 nM in HepG2 cell homogenates.

Applications Gliotoxin is a sulfur-containing mycotoxin produced by species of fungi and pathogens of humans. Gliotoxin exhibits inhibitory activities against histone H3K9 methyltransferase, a key enzyme in the regulation of transcriptional activity by writing epigenetic marks. Gliotoxin also exhibits immunosuppressive properties by causing apoptosis of cells of the immune system. In addition, various studies suggests Gliotoxin may also be a potential anti-inflammatory, antibiotic, antifungal and antiviral agent. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Takahashi, M., et al.: J. Antibiotics., 65, 263 (2012); Li., Y.G., et al.: Biochem. Biophy. Rsch. Commun., 422, 85 (2012); Zhang, H.C., et al.: Applied, Mech. Mater., 178, 783 (2012); Scharf, D.H., et al.: Appl. Microbiol. Biotechnol., 93, 467 (2012);

Ceftriaxone: cephalosporin antibiotic, effective against Gram-positive/negative bacteria, with anti-inflammatory/antioxidant properties.

Neoaureothin is a natural antibiotic product, which is derived from marine actinomycetes with a complex polyketide structure. Its mode of action involves the inhibition of bacterial protein synthesis by binding selectively to the ribosomal subunits, thereby obstructing the translation process in susceptible microbial strains. The specificity of its action allows it to target a broad spectrum of Gram-positive bacteria while presenting a lower risk of resistance development compared to traditional antibiotics. Neoaureothin is utilized extensively in research settings to explore novel antibacterial pathways and potential therapeutic applications in combating resistant bacterial strains. Its unique source and mode of action make it a valuable tool in the study of marine-derived antibiotics, offering insights into alternative treatment strategies for bacterial infections. Researchers often employ this compound in experimental assays to gauge inhibition potency, elucidate biological pathways, and refine synthetic analogues for enhanced efficacy.

Pan-histone demethylase inhibitor; anti-fungal; iron-chelator

Applications Labelled Isavuconazole (I777832). It is a new triazole currently undergoing phase III clinical trials. This compound has shown in vitro activity against a large number of clinical important yeasts and molds including Aspergillus spp., Fusarium spp., Scedosporium spp., Candida spp., the Zygomycetes and Cryptococcus spp. References Ohwada, J., et al.: Bioorg. Med. Chem. Lett., 13, 191 (2003), Guinea, J., et al.: Antimicrob. Agents Chemother., 52, 1396 (2008)

Flusilazole (DPX6573) is an organosilicon fungicide with broad spectrum antifungal effects.

Ibrexafungerp (MK 3118) is a β-1,3-glucan synthase inhibitor with antifungal activity.

Rezafungin acetate (Biafungin acetate) is a echinocandin with antibacterial activity, inhibiting 1,3-β-D-glucan synthase.

Butoconazole (1-[4-(4-chlorophenyl)-2-[(2,6-dichlorophenyl)thio]butyl]-1H-imidazole) is an imidazole antifungal agent

Applications A thiadiazole derivative with fungacidal properties. An antitumor agent. References Lu, K. et al.: Cancer Chemother. Pharmacol., 4, 275 (1980); Rauckyte, T. et al.: ECOpole’04, Ksiega Konf./Proc., 139 (2004); Nelson, J.A. et al.: Cancer Res., 36, 1375 (1976);

Bifonazole is an antifungal drug that is used for the treatment of fungal infections. This drug inhibits the production of ergosterol and destabilizes the fungal cytochrome p450 51 enzyme. Bifonazole 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.

2-Methoxy-1,4-naphthoquinone triggers A549 cell apoptosis via JNK/p38 MAPK pathways, independent of cell cycle arrest, due to oxidative DNA damage from ROS.

Antibacterial agent 132 showed antimicrobial activity against C.

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. Terbinafine HCl 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.