Antifungals Standards Suppliers USA
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Product | Description | |
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Cambendazole Quick inquiry Where to buy Suppliers range | analytical standard. Uses: For analytical and research use. Group: Antifungals Standards; Pharma & Vet Compounds & Metabolites; Standards for Environmental Regulatory Methods; Pharma & Vet Compounds & Metabolites. Grades: analytical standard. CAS No. 26097-80-3. Pack Sizes: 10MG. IUPAC Name: propan-2-yl N-[2-(1,3-thiazol-4-yl)-3H-benzimidazol-5-yl]carbamate. Molecular formula: C14H14N4O2S. Mole weight: 302.35. EC Number: 247-459-5. Catalog: APS26097803. SMILES: CC (C)OC (=O)Nc1ccc2nc ([nH]c2c1)c3cscn3. Format: Neat. Shipping: Room Temperature. | |
Fluconazole hydrate Quick inquiry Where to buy Suppliers range | Fluconazole (hydrate) is the hydrate salt form of fluconazole, which is a triazole antifungal intended for oral treatment of superficial and systemic mycoses. In tests done in standard mycological media, the compound had minimal inhibitory concentrations against pathogenic Candida species that were usually in excess of 100 mg/l. Fluconazole inhibited branching and hyphal development in C. albicans at concentrations as low as 10(-6) M (0.3 mg/l), but miconazole and ketoconazole were still active in these tests at concentrations 100 times lower than this. Oral fluconazole was not associated with a significantly increased risk of birth defects overall or of 14 of the 15 specific birth defects of previous concern. Fluconazole exposure may confer an increased risk of tetralogy of Fallot. Fluconazole is predicted to be ineffective against Cryptococcus gattii in the koala as a sole therapeutic agent administered at 10 mg/kg p.o. every 12 h. Synonyms: UK 49858 hydrate; UK49858 hydrate; UK-49858 hydrate. Grades: >98%. CAS No. 155347-36-7. Molecular formula: C13H14F2N6O2. Mole weight: 324.29. | |
Fluconazole mesylate Quick inquiry Where to buy Suppliers range | Fluconazole (mesylate) is the mesylate salt form of fluconazole, which is a triazole antifungal intended for oral treatment of superficial and systemic mycoses. In tests done in standard mycological media, the compound had minimal inhibitory concentrations against pathogenic Candida species that were usually in excess of 100 mg/l. Fluconazole inhibited branching and hyphal development in C. albicans at concentrations as low as 10(-6) M (0.3 mg/l), but miconazole and ketoconazole were still active in these tests at concentrations 100 times lower than this. Oral fluconazole was not associated with a significantly increased risk of birth defects overall or of 14 of the 15 specific birth defects of previous concern. Fluconazole exposure may confer an increased risk of tetralogy of Fallot. Fluconazole is predicted to be ineffective against Cryptococcus gattii in the koala as a sole therapeutic agent administered at 10 mg/kg p.o. every 12 h. Synonyms: UK 49858 mesylate; UK49858 mesylate; UK-49858 mesylate. Grades: >98%. CAS No. 159532-41-9. Molecular formula: C14H16F2N6O4S. Mole weight: 402.38. | |
Lanoconazole Quick inquiry Where to buy Suppliers range | analytical standard. Uses: For analytical and research use. Group: Antifungals Standards; Pharma & Vet Compounds & Metabolites; Pharma & Vet Compounds & Metabolites. Grades: analytical standard. CAS No. 101530-10-3. Pack Sizes: 25MG. IUPAC Name: (2E)-2-[4-(2-chlorophenyl)-1,3-dithiolan-2-ylidene]-2-imidazol-1-ylacetonitrile. Molecular formula: C14H10ClN3S2. Mole weight: 319.83. Catalog: APS101530103. SMILES: Clc1ccccc1C2CS\C (=C (\C#N)/n3ccnc3)\S2. Format: Neat. | |
Miconazole Nitrate Quick inquiry Where to buy Suppliers range | Pharmacopeia & Metrological Institutes Standards; Pharma & Vet Compounds & Metabolites; Pharma & Vet Compounds & Metabolites; API Standards; British Pharmacopoeia; European Pharmacopoeia (Ph. Eur.); Impurity Standards; Pharmaceutical Toxicology; Pharmacopoeial Standards. Uses: For analytical and research use. Group: reagents. Alternative Names: Miconazole Nitrate, Albistat, Fungisdin,1-[(2RS)-2-[(2,4-Dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole Nitrate, Gyno-Daktarin, Epi-Monistat, Dactrine, Vodol, Priconazole, 1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]-, mononitrate (9CI), Dermonistat, R 14889, Deralbine, Zimycan, Conofite, Micotef, NSC 169434, Florid, Lotrimin AF Powder, Hi-Pick, 1-[2-(2,4-Dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]-1H-imidazole nitrate (1:1), (+/-)-Miconazole nitrate, Conoderm, Ecobi, Aflorix, Lotrimin AF Spray Liquid, 1-[2-(2,4-Dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]-1H-imidazole mononitrate, Imidazole, 1-[2,4-dichloro-beta-[(2,4-dichlorobenzyl)oxy]phenethyl]-, mononitrate (8CI), [2, 4-Dichloro-beta- (2, 4-dichlorobenzyloxy) phenethyl]imidazole nitrate, Antifungal Cream, Fungiderm, Andergin, Brentan, Daktacort, Monistat, Isoconazole Nitrate Imp. C (EP) as Nitrate, Miconal, Prilagin, Miconazole nitrate, Monistat Cream and Suppositories, Lotrimin AF Powder Aerosol, Monistat-Derm, Daktar, Zeasorb AF, Miconaz, Loptrimin AF Jock-Itch Powder Aerosol, Gyno-Monistat, Daktarin, Daktarin talc, Micatin. CAS No. 22832-87-7. Pack Sizes: 200MG. IUPAC Name: 1-[2- (2, 4-dichlorophenyl) -2-[ (2, 4-dichlorophenyl) methoxy]ethyl]imidazole; nitric acid. | |
Pyrrole-2-carboxylic acid Quick inquiry Where to buy Suppliers range | Small amphoteric polar metabolite produced by many streptomyces species; An important dereplication standard in discovery, displaying a distinctive UV spectrum and a broad range of biological activities, albeit weak; Demonstrated antiparasitic activity against trypanosomes by selective proline racemase inhibition and has potent antifungal activity against phytophthora. Synonyms: Minaline; 2-Pyrrolecarboxylic Acid. Grades: > 95 % by HPLC. CAS No. 634-97-9. Molecular formula: C5H5NO2. Mole weight: 111.10. |