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| Product | Description | |
|---|---|---|
| Ergosterol | 5g Pack Size. Group: Analytical Reagents, Bioactive Small Molecules, Biochemicals, Building Blocks, Research Organics & Inorganics. Formula: C28H44O. CAS No. 57-87-4. Prepack ID 90028111-5g. Molecular Weight 396.65. See USA prepack pricing. |  |
| Ergosterol | Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Uses: Scientific research. Group: Natural products. CAS No. 57-87-4. Pack Sizes: 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-N0181. |  |
| Ergosterol | Most important vitamin of the provitamins D. Usually obtained from yeast which synthesizes it from simple sugars such as glucose. Group: Biochemicals. Alternative Names: (3 β,22E)-Ergosta-5,7,22-trien-3 β-ol; (24R)-Ergosta-5,7,22-trien-3 β-ol; 24-Methylcholesta-5,7,22-trien-3 β-ol; 24R-Methylcholesta-5,7,22E-trien-3 β-ol; 24α-Methyl-22E-dehydrocholesterol; 3 β-Hydroxyergosta-5,7,22-triene; Ergosterin; Provitamin D; Provitamin D2. Grades: Highly Purified. CAS No. 57-87-4. Pack Sizes: 10g, 25g, 50g, 100g. US Biological Life Sciences. |  Worldwide |
| Ergosterol | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsnutritional composition compoundseuropean pharmacopoeia (ph. eur.)impurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: (3beta,22E)-Ergosta-5,7,22-trien-3-ol, 24R-Methylcholesta-5,7,22E-trien-3beta-ol, 24alpha-Methyl-22E-dehydrocholesterol, Ergosterin, 3beta-Hydroxyergosta-5,7,22-triene, Provitamin D, 24-Methylcholesta-5,7,22-trien-3beta-ol, Provitamin D2, Ergosta-5,7,22-trien-3-ol, (3beta,22E)-,Ergosterol (8CI), (22E,24R)-Ergosta-5,7,22-trien-3beta-ol, (24R)-Ergosta-5,7,22-trien-3beta-ol. |  |
| Ergosterol acetate | Ergosterol acetate. Group: Biochemicals. Alternative Names: (3b,22E)-Ergosta-5,7,22-trien-3b-ol 3-acetate; Ergosta-5,7,22-trien-3b-ol acetate; Ergosteryl 3b-acetate. Grades: Highly Purified. CAS No. 2418-45-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C30H46O2. US Biological Life Sciences. | Worldwide |
| Ergosterol Impurity 6 | Ergosterol Impurity 6. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-3-((Z)-2-((1R,3aR,7aR)-1-((2R,5R,E)-5,6-dimethylhept-3-en-2-yl)-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl)vinyl)-4-methylcyclohex-3-en-1-yl 3,5-dinitrobenzoate. CAS No. 105620-21-1. Molecular formula: C35H46N2O6. Mole weight: 590.76. Catalog: APB105620211. | |
| Ergosterol peroxide | Ergosterol peroxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2061-64-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C28H44O3. US Biological Life Sciences. | Worldwide |
| Vitamin D2 (Ergocalciferol; Calciferol; Ergosterol) | The synthetic form of Vitamin D. Prepared from ergosterol by UV irradiation in a suitable solvent. Commercial solutions are usually made with propylene glycol or sesame oil. Antirachitic. Group: Biochemicals. Alternative Names: Vitamin D2; Calciferol; Ergosterol; Ergocalciferol; (3 β,5Z,7E,22E)-9,10-Secoergosta-5,7,10(19),22-tetraen-3-ol; Calciferol; Ercalciol; Oleovitamin D2; Radiostol; Radsterin; (+)-Vitamin D2; Viosterol; Vio D; Vitavel-D. Grades: Highly Purified. CAS No. 50-14-6. Pack Sizes: 1g, 5g, 25g. Molecular Formula: C??H??O, Molecular Weight: 396.65. US Biological Life Sciences. | Worldwide |
| 1-(2,6-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Voriconazole Impurity 29; Voriconazole Impurity 16. CAS No. 1157981-64-0. Molecular formula: C10H7F2N3O. Mole weight: 223.18. |  |
| 1-(2-chloro-2-(2,4-difluorophenyl)ethyl)-1H-1,2,4-triazole | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Voriconazole Impurity 28. Grades: 98%. CAS No. 206050-24-0. Molecular formula: C10H8ClF2N3. Mole weight: 243.64. | |
| 1-(4-Chloro-3-methoxyphenyl)-4,4-dimethylpentan-3-one | 1-(4-Chloro-3-methoxyphenyl)-4,4-dimethylpentan-3-one is an intermediate in the synthesis of 5-(3-((1H-1,2,4-Triazol-1-yl)methyl)-3-hydroxy-4,4-dimethylpentyl)-2-chlorophenol (T767575), which is a tebuconazole impurity. Tebuconazole (T013000) is an ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. CAS No. 1539797-51-7. Pack Sizes: 50mg, 100mg. Molecular Formula: C14H19ClO2. US Biological Life Sciences. | Worldwide |
| 1-(6-chloro-5-fluoropyrimidin-4-yl)ethanol | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: 4-Pyrimidinemethanol, 6-chloro-5-fluoro-α-methyl-; Voriconazole Impurity 21. CAS No. 1289559-76-7. Molecular formula: C6H6ClFN2O. Mole weight: 176.58. | |
| 1-Bromo-4-(4-chlorophenyl)butan-2-one | 1-Bromo-4-(4-chlorophenyl)butan-2-one is an intermediate in the synthesis of 5-(4-Chlorophenyl)-2,2-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)-1,3-pentanediol (C377885), which is a hydroxy tebuconazole conjugate. Tebuconazole (T013000) is an ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. CAS No. 143327-55-3. Pack Sizes: 10mg, 50mg. Molecular Formula: C10H10BrClO, Molecular Weight: 261.54. US Biological Life Sciences. | Worldwide |
| 2-(2,4-Dichlorophenyl)-2-methyl-4-propyl-1,3-dioxolane | An impurities of Propiconazole. Propiconazole is a triazole fungicide inhibiting fungicide due to its binding with and inhibiting the 14-alpha demethylase enzyme from demethylating a precursor to ergosterol. Synonyms: 2-(2,4-Dichlorophenyl)-2-methyl-4-propyl-1,3-dioxolane; 83833-32-3; EINECS 281-007-8; 1,3-Dioxolane,2-(2,4-dichlorophenyl)-2-methyl-4-propyl-; SCHEMBL8336206; DTXSID10868759; SR-01000390593; SR-01000390593-1. Grades: > 95%. CAS No. 83833-32-3. Molecular formula: C13H16Cl2O2. Mole weight: 275.18. | |
| 2-?[[2-? (Dimethylamino) ?ethyl]?thio]?-acetic Acid | 2-?[[2-? (Dimethylamino) ?ethyl]?thio]?-acetic Acid functions as a co-drugs, and also acts as a reagent for the preparation of hydroxamate-based histone deacetylase inhibitors for enhancing activity of antifungal agents which inhibit a step in the ergosterol synthesis pathway. Group: Biochemicals. Grades: Highly Purified. CAS No. 933682-63-4. Pack Sizes: 1g, 10g. Molecular Formula: C6H13NO2S, Molecular Weight: 163.24. US Biological Life Sciences. | Worldwide |
| 2- (4-Chlorophenyl) hexanenitrile-d9 | 2- (4-Chlorophenyl) hexanenitrile-d9 is an intermediate used in the synthesis of Myclobutanil-d9 (M831402), which is the labeled analogue of Myclobutanil (M831400), which is an fungicide used on a wide range of food crops. Myclobutanil inhibits the biosynthesis of ergosterol, a critical componet of fungal cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C12H5D9ClN, Molecular Weight: 216.75. US Biological Life Sciences. | Worldwide |
| (24S)-3 β-Hydroxyergost-5-en-7-one | (24S)-3 β-Hydroxyergost-5-en-7-one is a secondary metabolite found in the fruiting bodies of Cyttaria johowii. (24S)-3 β-Hydroxyergost-5-en-7-one is a derivative of Ergosterol (E599240) which is the most important of the provitamins D. Ergosterol is usually obtained from yeast, synthesized from simple sugars such as glucose. Group: Biochemicals. Grades: Highly Purified. CAS No. 156767-69-0. Pack Sizes: 1mg, 2mg. Molecular Formula: C28H46O2, Molecular Weight: 414.66. US Biological Life Sciences. | Worldwide |
| (2R,3R)- 2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2,3-butanediol Methanesulfonate | (2R,3R)- 2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2,3-butanediol Methanesulfonate is a useful synthetic intermediate in the synthesis of Efinaconazole (E435070); a topical antifungal for onychomycosis. (2R,3R)- 2-(2,4-Difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-2,3-butanediol Methanesulfonate is also used as a reagent in the synthesis of Ravuconazole (R128000); an ergosterol biosynthesis inhibitor and antifungal. Group: Biochemicals. Grades: Highly Purified. CAS No. 1175536-50-1. Pack Sizes: 5mg, 50mg. Molecular Formula: C13H17F2N3O5S, Molecular Weight: 365.35. US Biological Life Sciences. | Worldwide |
| 2- (tert-Butyl) -2- (4-chloro-3-methoxyphenethyl) oxirane | 2- (tert-Butyl) -2- (4-chloro-3-methoxyphenethyl) oxirane is an intermediate in the synthesis of 5-(3-((1H-1,2,4-Triazol-1-yl)methyl)-3-hydroxy-4,4-dimethylpentyl)-2-chlorophenol (T767575), which is a tebuconazole impurity. Tebuconazole (T013000) is an ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C15H21ClO2. US Biological Life Sciences. | Worldwide |
| (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne | (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne is a byproduct in the synthesis of Terbinafine Hydrochloride (T107500); an orally active, antimycotic allylamine related to Naftifine. It is a specific inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Also antifungal. Group: Biochemicals. Grades: Highly Purified. CAS No. 635708-74-6. Pack Sizes: 10mg, 100mg. Molecular Formula: C?H??Cl, Molecular Weight: 156.65. US Biological Life Sciences. | Worldwide |
| 3-[[ (1, 1-Dimethylethyl) diphenylsilyl]oxy] Ergosta-7,24(28)-diene | 3-[[ (1, 1-Dimethylethyl) diphenylsilyl]oxy] Ergosta-7,24(28)-diene is an intermediate in the synthesis of Episterol which is a compound influencing ergosterol biosynthesis, and thus acting as an antifungal agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 1691234-02-2. Pack Sizes: 500ug, 1mg. Molecular Formula: C44H64OSi. US Biological Life Sciences. | Worldwide |
| 3-((1H-1,2,4-Triazol-1-yl)methyl)-1-(4-chloro-3-methoxyphenyl)-4,4-dimethylpentan-3-ol | 3-((1H-1,2,4-Triazol-1-yl)methyl)-1-(4-chloro-3-methoxyphenyl)-4,4-dimethylpentan-3-ol is an intermediate in the synthesis of 5-(3-((1H-1,2,4-Triazol-1-yl)methyl)-3-hydroxy-4,4-dimethylpentyl)-2-chlorophenol (T767575), which is a tebuconazole impurity. Tebuconazole (T013000) is an ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C17H24ClN3O2. US Biological Life Sciences. | Worldwide |
| 3-(4-Chloro-3-methoxyphenethyl)-4,4-dimethylpent-1-en-3-ol | 3-(4-Chloro-3-methoxyphenethyl)-4,4-dimethylpent-1-en-3-ol is an intermediate in the synthesis of 5-(3-((1H-1,2,4-Triazol-1-yl)methyl)-3-hydroxy-4,4-dimethylpentyl)-2-chlorophenol (T767575), which is a tebuconazole impurity. Tebuconazole (T013000) is an ergosterol biosynthesis inhibitor. Fungicide. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C16H23ClO2. US Biological Life Sciences. | Worldwide |
| 3-(6-bromo-5-fluoropyrimidin-4-yl)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Voriconazole Impurity 31. CAS No. 1307315-04-3. Molecular formula: C16H13BrF3N5O. Mole weight: 428.21. | |
| 4-amino-1-(2-(2,4-difluorophenyl)-2-oxoethyl)-1H-1,2,4-triazol-4-ium chloride | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Voriconazole Impurity 5; Voriconazole Impurity 30; 1H-1,2,4-Triazolium, 4-amino-1-[2-(2,4-difluorophenyl)-2-oxoethyl]-, chloride (9CI). CAS No. 154534-83-5. Molecular formula: C10H9ClF2N4O. Mole weight: 274.65. | |
| 4-chloro-5-fluoro-6-vinylpyrimidine | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Pyrimidine, 4-chloro-6-ethenyl-5-fluoro-. CAS No. 1403893-61-7. Molecular formula: C6H4ClFN2. Mole weight: 158.56. | |
| 6-Chloro Voriconazole | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: 6-Chloro-α-(2,4-difluorophenyl)-5-fluoro-β-methyl-α-(1H-1,2,4-triazol-1-ylmethyl)-4-pyrimidineethanol; rac-6-Chloro Voriconazole. CAS No. 188416-35-5. Molecular formula: C16H13ClF3N5O. Mole weight: 383.76. | |
| 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B | 8,9-Dideoxy-28,29-dihydro-7,10-dihydroxy-35-O-(2,6-dideoxy-L-ribo-hexopyranosyl)amphotericin B is a highly potent antifungal compound, used in research of a diverse array of fungal infections, such as aspergillosis, candidiasis and cryptococcosis. By selectively binding to ergosterol within the membranes of fungal cells, this compound disrupts their structural integrity, ultimately culminating in profound and irreversible cellular demise. Uses: Anti-bacterial agents. Synonyms: Nystatin A3. CAS No. 62997-67-5. Molecular formula: C53H85NO20. Mole weight: 1056.24. | |
| (αR,βR)-rel-6-Chloro-α-(2,4-difluorophenyl)-5-fluoro-β-methyl-α-(1H-1,2,4-triazol-1-ylmethyl)-4-pyrimidineethanol | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: Voriconazole (2R,3R)-Isomer; Voriconazole 3-Epimer; (2R,3R)-3-(6-chloro-5-fluoropyrimidin-4-yl)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol compound with (2S,3S); Voriconazole Impurity 12. CAS No. 137234-76-5. Molecular formula: C16H13ClF3N5O. Mole weight: 383.76. | |
| Amorolfine hydrochloride | Amorolfine (Ro 14-4767/002) hydrochloride is a potent anti-fungal agent. Amorolfine hydrochloride inhibits ergosterol biosynthesis. Amorolfine hydrochloride has the potential for the research of Neoscytalidium dimidiatum onychomycosis [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Ro 14-4767/002. CAS No. 78613-38-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0238. | |
| Amphotericin B | Amphotericin B is a polyene antifungal agent against a wide variety of fungal pathogens. It binds irreversibly to ergosterol, resulting in disruption of membrane integrity and ultimately cell death. Uses: Scientific research. Group: Natural products. CAS No. 1397-89-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B0221. | |
| Amphotericin B Solution, 100X | Amphotericin B is a polyene antifungal agent for yeast, mold and mycoplasma. It was first isolated by Gold, et a., from Streptomyces nodosus in 1955. It is an amphoteric compound composed of a hydrophilic polyhydroxyl chain along one side and a lipophilic polyene hydrocarbon chain on the other. Amphotericin B is poorly soluble in water. Amphotericin B binds to sterols, preferentially to the primary fungal cell membrane sterol, ergosterol. This binding disrupts osmotic integrity of the fungal membrane, resulting in leakage of intracellular potassium, magnesium, sugars, and metabolites and then cellular death.Used in the preparation of baculoviral stocks.Amphotericin B Solution, 100X is composed of USP grade Amphotericin B in a High pH buffer (NaOH/Na+,H2O). The concentration of Amphotericin B in the final product is 0.25 g/L. Group: Biochemicals. Alternative Names: Abelcet; Abelecet; AmBisome; Ampho-Moronal; Amphocin; Amphozone; Apothecon; Fungilin; Fungizona; Fungizone; Halizon; LNS-AmB; NS 718; NSC 527017. Grades: Cell Culture Grade. CAS No. 1397-89-3. Pack Sizes: 50ml, 100ml. Molecular Formula: C47H73NO17, Molecular Weight: 924.09. US Biological Life Sciences. | Worldwide |
| Amphotericin B, USP | Amphotericin B is a polyene antifungal agent for yeast, mold and mycoplasma. It was first isolated by Gold, et a., from Streptomyces nodosus in 1955. It is an amphoteric compound composed of a hydrophilic polyhydroxyl chain along one side and a lipophilic polyene hydrocarbon chain on the other. Amphotericin B is poorly soluble in water. Amphotericin B binds to sterols, preferentially to the primary fungal cell membrane sterol, ergosterol. This binding disrupts osmotic integrity of the fungal membrane, resulting in leakage of intracellular potassium, magnesium, sugars, and metabolites and then cellular death.Used in the preparation of baculoviral stocks. Group: Biochemicals. Alternative Names: Abelcet; Abelecet; AmBisome; Ampho-Moronal; Amphocin; Amphozone; Apothecon; Fungilin; Fungizona; Fungizone; Halizon; LNS-AmB; NS 718; NSC 527017. Grades: USP. CAS No. 1397-89-3. Pack Sizes: 1g, 10g, 25g, 100g. Molecular Formula: C47H73NO17, Molecular Weight: 924.09. US Biological Life Sciences. | Worldwide |
| Arasertaconazole | Arasertaconazole is the (R)-enantiomer of Sertaconazole, an imidazole antifungal agent that inhibits the synthesis of ergosterol, an essential cell wall component of fungi. Synonyms: (R)-Sertaconazole; 1-[(2R)-2-[(7-Chlorobenzo[b]thien-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl]-1H-Imidazole. Grades: > 95%. CAS No. 583057-48-1. Molecular formula: C20H15Cl3N2OS. Mole weight: 437.78. | |
| Brassicasterol | Brassicasterol, a metabolite of Ergosterol, plays a role in the inhibitory effect on bladder carcinogenesis promotion via androgen signaling. Brassicasterol shows dual anti-infective properties against HSV-1 (IC50=1.2 μM) and Mycobacterium tuberculosis, and cardiovascular protective effect. Brassicasterol exerts an anti-cancer effect by dual-targeting AKT and androgen receptor signaling in prostate cancer. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ergosta-5,22E-dien-3beta-ol; (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(E,1R,4R)-1,4,5-trimethylhex-2-enyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol. Product Category: Inhibitors. Appearance: Cryst. CAS No. 474-67-9. Molecular formula: C28H46O. Mole weight: 398.66. Purity: 0.98. IUPACName: (3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol. Canonical SMILES: CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C. Product ID: ACM474679-1. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Brassicasterol | Brassicasterol is a metabolite of Ergosterol and has cardiovascular protective effects. Brassicasterol exerts anticancer effects in prostate cancer through dual targeting of AKT and androgen receptor signaling pathways. Brassicasterol inhibits HSV-1 ( IC 50 =1.2 μM) and Mycobacterium tuberculosis. Brassicasterol also inhibits sterol δ 24-reductase , slowing the progression of atherosclerosis. Brassicasterol is also a cerebrospinal fluid biomarker for Alzheimer's disease [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. CAS No. 474-67-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-113289. | |
| Calmodulin Antagonist W-13 (N-(4-aminobutyl)-5-chloro-2-naphthalenesulfonamide hydrochloride) | An Ergosterol Biosynthesis inhibitor. Group: Biochemicals. Alternative Names: N-(4-aminobutyl)-5-chloro-2-naphthalenesulfonamide hydrochloride. Grades: Molecular Biology Grade. CAS No. 88519-57-7. Pack Sizes: 5mg, 25mg. US Biological Life Sciences. | Worldwide |
| Candicidin complex | Candicidin complex is a group of macrocycloheptene antifungal compounds produced by Streptomyces griseus. The candicidin complex contains analogues A, B, C and D, of which candicidin D is the main component. It has antifungal activity against fungi, especially Candida albicans, and is clinically used to treat vaginal candidiasis by combining with ergosterol and destroying the fungal membrane. Synonyms: Levorin. Grades: >95% by HPLC. CAS No. 1403-17-4. Molecular formula: C59H84N2O18 (for Candicidin D). Mole weight: 1109.30. | |
| Ciclopirox-D11 D-glucuronide | Ciclopirox-D11 D-glucuronide is a renowned pharmaceutical compound manifesting its exceptional proclivity towards research of an assortment of fungal infections owing to its robust antifungal attributes. By obstructing the development of ergosterol within the cell membrane of fungi, this compound demonstrates inhibitory efficacy in eradicating afflictions attributable to Aspergillus, Candida and dermatophyte species in a laudable manner. Molecular formula: C18H14NO8D11. Mole weight: 394.47. | |
| Citronellol | Citronellol ((±)-Citronellol) is an orally active inducer of apoptosis. Citronellol can prevent oxidative stress, mitochondrial dysfunction, and apoptosis in the SH-SY5Y cell Parkinson's disease model induced by 6-OHDA by regulating the ROS-NO , MAPK/ERK , and PI3K/Akt signaling pathways. Citronellol can induce necroptosis in human lung cancer cells through the TNF-α pathway and accumulation of ROS. Citronellol can reduce the levels of LC-3 and p62 to regulate the autophagy pathway, inhibit oxidative stress and neuroinflammation, and thus have neuroprotective effects on Parkinson's rats. Citronellol exhibits anti- fungal activity against Trichophyton rubrum by inhibiting ergosterol synthesis [2] [4] [6] [7]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-Citronellol; (±)-β-Citronellol. CAS No. 106-22-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W010201. | |
| Destriazolyl Bromo Propiconazole (Mixture of Diastereomers) | An impurities of Propiconazole. Propiconazole is a triazole fungicide inhibiting fungicide due to its binding with and inhibiting the 14-alpha demethylase enzyme from demethylating a precursor to ergosterol. Synonyms: 2-(Bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane; 2-Bromomethyl-2-(2,4-dichlorophenyl)-4-propyldioxolane. Grades: > 95%. CAS No. 60207-89-8. Molecular formula: C13H15BrCl2O2. Mole weight: 354.07. | |
| Efinaconazole | Efinaconazole is a triazole antifungal. It is approved for use in Canada and the USA as a 10% topical solution for the treatment of onychomycosis (fungal infection of the nail). Efinaconazole acts as a 14α-demethylase inhibitor. Efinaconazole inhibits fungal lanosterol 14α-demethylase involved in the biosynthesis of ergosterol, a constituent of fungal cell membranes. Efinaconazole has been shown to be active against isolates of the following microorganisms, both in vitro and in clinical infections. Efinaconazole exhibits in vitro minimum inhibitory concentrations (MICs) of 0.06 μg/mL or less against most ( ≥ 90%) isolates of the following microorganisms: Trichophyton rubrum; Trichophyton mentagrophytes. Synonyms: KP103; KP-103; KP 103; CTK5J2975; AGJ95634; KB145948; AGJ 95634; KB 145948; AGJ-95634; KB-145948; Efinaconazole; trade name: Jublia. Grades: >98%. CAS No. 164650-44-6. Molecular formula: C18H22F2N4O. Mole weight: 348.39. | |
| Efinaconazole | Efinaconazole is a triazole antifungal. It is approved for use in Canada and the USA as a 10% topical solution for the treatment of onychomycosis (fungal infection of the nail). Efinaconazole acts as a 14α-demethylase inhibitor. Efinaconazole inhibits fungal lanosterol 14α-demethylase involved in the biosynthesis of ergosterol, a constituent of fungal cell membranes. Efinaconazole has been shown to be active against isolates of the following microorganisms, both in vitro and in clinical infections. Efinaconazole exhibits in vitro minimum inhibitory concentrations (MICs) of 0.06 μg/mL or less against most ( ≥ 90%) isolates of the following microorganisms: Trichophyton rubrum; Trichophyton mentagrophytes. Uses: Designed for use in research and industrial production. Additional or Alternative Names: KP103; KP-103; KP 103; CTK5J2975; AGJ95634; KB145948; Efinaconazole; trade name: Jublia. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 164650-44-6. Molecular formula: C18H22F2N4O. Mole weight: 348.39. Purity: >98%. IUPACName: (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol. Canonical SMILES: C[C@@H](N1CCC(CC1)=C)[C@@](O)(C2=CC=C(F)C=C2F)CN3N=CN=C3. Product ID: ACM164650446. Alfa Chemistry ISO 9001:2015 Certified. | |
| Epoxiconazole | Epoxiconazole, a fungicide, is a demethylation inhibitor of the Ergosterol biosynthesis pathway. Epoxiconazole exhibits strong inhibitory effects on both carbendazim-resistant and phenamacril-resistant isolates, and can be used for controlling many crop diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 133855-98-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119683. | |
| Fenpropimorph | Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 67564-91-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-128033. | |
| Fenticonazole Nitrate | Fenticonazole Nitrate is an antifungal imidazole ring derivative. Fenticonazole Nitrate operates via hindering ergosterol integration, and sequentially destructing the cytoplasmatic outer membrane. Fenticonazole Nitrate is effective against Gram-positive bacteria, mycoses, and vaginal candidiasis [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: REC 15-1476. CAS No. 73151-29-8. Pack Sizes: 10 mM * 1 mL; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0359. | |
| Hydroxy Terbinafine | A metabolite of Terbinafine, an orally active, antimycotic allylamine related to naftifine. A specfic inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Isavuconazole | Isavuconazole (BAL-4815) is a triazole proagent with antifungal activity against yeasts, molds, and dimorphic fungi. Isavuconazole inhibits ergosterol biosynthesis and results in the disruption of fungal membrane structure and function. Isavuconazole is a moderate inhibitor of CYP3A4. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Isavuconazole;4-[2-[(1R,2R)-2-(2,5-Difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-4-thiazolyl]benzonitrile;2R,3R)-3-[4-(4-Cyanophenyl)thiazol-2-yl]-2-(2,5-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol;BAL 4815;RO 0094815;Isavuconazolep;4-[2-[(1R,2R)-2-(2,5-Difluorophenyl)-2-hydroxy-1-Methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-4-thiazolyl]benzonitrile;NaMe:Isavuconazole;4-[2-[(2R,3R)-3-(2,5-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)butan-2-yl]-1,3-thiazol-4-yl]benzonitrile. Product Category: Inhibitors. CAS No. 241479-67-4. Molecular formula: C22H17F2N5OS. Mole weight: 437.4650864. Purity: 0.9997. Density: 1.38. Product ID: ACM241479674. Alfa Chemistry ISO 9001:2015 Certified. | |
| Isavuconazole | Isavuconazole (BAL-4815) is a triazole proagent with antifungal activity against yeasts, molds, and dimorphic fungi. Isavuconazole inhibits ergosterol biosynthesis and results in the disruption of fungal membrane structure and function. Isavuconazole is a moderate inhibitor of CYP3A4. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAL-4815; RO-0094815. CAS No. 241479-67-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-14273. | |
| Itraconazole | Itraconazole (R51211) is a triazole antifungal agent and a potent and orally active Hedgehog (Hh) signaling pathway antagonist with an IC 50 of ~800 nM. Itraconazole potently inhibits lanosterol 14α-demethylase ( cytochrome P450 enzyme ), thereby inhibits the oxidative conversion of lanosterol to ergosterol. Itraconazole has anticancer and antiangiogenic effects. Itraconazole is a oxysterol-binding protein ( OSBP ) inhibitor [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: R51211. CAS No. 84625-61-6. Pack Sizes: 100 mg; 500 mg. Product ID: HY-17514. | |
| Itraconazole | Itraconazole (R51211) is a triazole antifungal agent and a potent and orally active Hedgehog (Hh) signaling pathway antagonist with an IC50 of ~800 nM. Itraconazole potently inhibits lanosterol 14α-demethylase (cytochrome P450 enzyme), thereby inhibits the oxidative conversion of lanosterol to ergosterol. Itraconazole has anticancer and antiangiogenic effects. Itraconazole is a oxysterol-binding protein (OSBP) inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3H-1,2,4-Triazol-3-one, 4-(4-(4-(4-((2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl)methoxy)phenyl)-1-piperazinyl)phenyl)-2,4-dihydro-2-(1-methylpropyl)-;(+-)-1-sec-Butyl-4-(p-(4-(p-(((2R*,4S*)-2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl)methoxy)phenyl)-1-piperazinyl)phenyl)-delta(sup 2)-1,2,4-triazolin-5-one. Product Category: Inhibitors. Appearance: Off-white crystalline solid. CAS No. 84625-61-6. Molecular formula: C35H38Cl2N8O4. Mole weight: 705.63. Purity: 0.9981. Canonical SMILES: ClC1=C(C=CC(Cl)=C1)[C@@]2(O[C@@H](COC3=CC=C(N4CCN(C5=CC=C(N(C=NN6C(C)CC)C6=O)C=C5)CC4)C=C3)CO2)CN7C=NC=N7. Density: 1.4 g/cm³. ECNumber: 283-347-2. Product ID: ACM84625616. Alfa Chemistry ISO 9001:2015 Certified. | |
| Lanoconazole | Lanoconazole is a potent and orally active imidazole antifungal agent, shows a broad spectrum of activity against fungi in vitro and in vivo. Lanoconazole interferes with ergosterol biosynthesis by inhibiting sterol 14-alpha demethylase and blocking fungal membrane ergosterol biosynthesis. Lanoconazole can be used for the investigation of dermatophytosis and onychomycosis. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 101530-10-3. Molecular formula: C14H10ClN3S2. Mole weight: 319.84. Purity: 0.98. Canonical SMILES: N#C/C(N1C=CN=C1)=C2SC(C(C=CC=C3)=C3Cl)CS\2.[(E)]. Product ID: ACM101530103. Alfa Chemistry ISO 9001:2015 Certified. | |
| Luliconazole | Luliconazole is an azole antifungal drug. Its mechanism of action involves inhibition of ergosterol biosynthesis by inhibition of sterol 14α-demethylase. Group: Biochemicals. Alternative Names: [R-(E)]-α-[4-(2,4-Dichlorophenyl)-1,3-dithiolan-2-ylidene]-1H-imidazole-1-acetonitrile; Lulicon; NND 502. Grades: Highly Purified. CAS No. 187164-19-8. Pack Sizes: 500mg, 1g. Molecular Formula: C??H?Cl?N?S?, Molecular Weight: 354.28. US Biological Life Sciences. | Worldwide |
| Lumisterol | Lumisterol (9β,10α-Ergosterol), a steroid compound, is the (9β,10α)-stereoisomer of Ergosterol (HY-N0181). Lumisterol is a photoprotective agent against UVB-induced DNA damage and anti-proliferative activities [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 9β,10α-Ergosterol. CAS No. 474-69-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0181A. | |
| Metconazole | Metconazole is an conazole based fungicide used for the control of black sigatoka disease on banana. Metconazole acts primarily as an inhibitor of ergosterol biosynthesis which interferes with the synthesis of fungal cell membranes. Group: Biochemicals. Alternative Names: 5-[ (4-chlorophenyl) methyl]-2, 2-dimethyl-1- (1H-1, 2, 4-triazol-1-ylmethyl) cyclopentanol; Caramba, Quash. Grades: Highly Purified. CAS No. 125116-23-6. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| methyl 2-fluoro-3-oxopentanoate | One of the impurities of Voriconazole, which has been found to be an ergosterol biosynthesis inhibitor and could be used as an antifungal agent. Synonyms: pentanoic acid, 2-fluoro-3-oxo-, methyl ester; Voriconazole Impurity 23. CAS No. 180287-02-9. Molecular formula: C6H9FO3. Mole weight: 148.13. | |
| Miconazole | Antifungal (topical). Miconazole is an imidazole antifungal agent commonly applied topically to the skin or to mucous membranes to cure fungal infections. It works by inhibiting the synthesis of ergosterol, a critical component of fungal cell membranes. It can also be used against certain species of Leishmania protozoa which are a type of unicellular parasites that also contain ergosterol in their cell membranes. In addition to its antifungal and antiparasitic actions, it also has some antibacterial properties. Group: Biochemicals. Alternative Names: 1-[2,4-Dichloro- β - [ (2, 4-dichlorobenzyl) oxy] phenethyl] imidazole; (±)-Miconazole; Daktanol; Daktarin IV; Florid-F; Lauriad; MJR 1762; Miconazole; Monistat IV; NSC 170986; R 18134; Zimybase. Grades: Highly Purified. CAS No. 22916-47-8. Pack Sizes: 1g, 2g, 5g, 10g. Molecular Formula: C??H??Cl?N?O, Molecular Weight: 416.13. US Biological Life Sciences. | Worldwide |
| Miconazole | Miconazole is an imidazole antifungal agent, developed by Janssen Pharmaceutica, commonly applied topically to the skin or to mucous membranes to cure fungal infections. It works by inhibiting the synthesis of ergosterol, a critical component of fungal cell membranes. Synonyms: NSC 169434; NSC169434; NSC-169434; Daktarin IV. Grades: >98%. CAS No. 22916-47-8. Molecular formula: C18H14Cl4N2O. Mole weight: 416.13. | |
| Miconazole nitrate | Miconazole nitrate is an imidazole antifungal agent that blocks ergosterol biosynthesis. It is commonly used as a topical drug for skin infections. It promotes the differentiation of mature oligodendrocytes from progenitor cells. Uses: 14-alpha demethylase inhibitors. Synonyms: Albistat; Andergin; Aflorix; 1-[2- (2, 4-dichlorophenyl) -2-[ (2, 4-dichlorophenyl) methoxy]ethyl]imidazole nitrate; [2, 4-Dichloro-β - (2, 4-dichlorobenzyloxy) phenethyl]imidazole Nitrate; Brentan; Conoderm; Conofite; Daktacort; Florid; Fungiderm; Fungisdin; Micatin; Miconal; Zimycan. Grades: >98%. CAS No. 22832-87-7. Molecular formula: C18H15Cl4N3O4. Mole weight: 479.14. | |
| Myclobutanil | Myclobutanil is an fungicide used on a wide range of food crops. Myclobutanil inhibits the biosynthesis of ergosterol, a critical componet of fungal cell membranes. Group: Biochemicals. Alternative Names: Nova; Nova (pesticide); Nova 40W; Nova W; Nu-Flow M; RH 3866; Rally; Spectracide Immunox Multi-Purpose Fungicide; Systhane; Systhane 12E; Systhane 40W; Systhane 6 Flo; (±)-Myclobutanil; Deccotanil; Eagle; HOE 39304F; α-butyl-α-(4-Chlorophenyl)-1H-1,2,4-triazole-1-propanenitrile. Grades: Highly Purified. CAS No. 88671-89-0. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Natamycin | Pimaricin is a macrocyclic tetraene originally isolated from Streptomyces natalensis in 1957. Pimaricin exhibits broad spectrum antifungal activity against yeast and filamentous fungi by binding specifically to ergosterol to block fungal growth. Unlike the related polyenes, nystatin and filipin, pimaricin does not change the permeability of the plasma membrane. Pimaricin is used in the food industry for surface treatment of cheeses as a mould inhibitor. Group: Biochemicals. Alternative Names: Pimaricin; Antibiotic A 5283; Tennecetin; Cl-12625; Mycophyt; Myprozine; Natacyn; Synogil. Grades: Highly Purified. CAS No. 7681-93-8. Pack Sizes: 100mg. Molecular Formula: C??H??NO??, Molecular Weight: 665.73. US Biological Life Sciences. | Worldwide |
| Nystatin | Nystatin is a mixture of the byproducts of Streptomyces noursei. Nystatin belongs to the group of medicines called antifungals. Nystatin works by binding to a substance called ergosterol, which is a component of fungal cell membranes. Binding to ergosterol disrupts the cell membrane and causes holes to appear. Group: Biochemicals. Alternative Names: Nystatin A1; Mycostatin; Fungicidin. Grades: USP. CAS No. 1400-61-9. Pack Sizes: 10MU, 25MU, 100MU, 250MU. Molecular Formula: C??H??NO??, Molecular Weight: 962.1. US Biological Life Sciences. | Worldwide |
| Oxiconazole Nitrate | Oxiconazole nitrate is a broad-spectrum imidazole antifungal agent. It is used to treat skin infections such as jock itch, athlete's foot and ringworm. It is also used to treat the skin rash known as tinea versicolor caused by systemic yeast overgrowth. It inhibits a broad spectrum of pathogenic yeasts and molds, including C. neoformans, A. fumigatus, C. albicans, and T. mentagrophytes by inhibiting ergosterol biosynthesis. Uses: Antifungal agents. Synonyms: Ro 13-8996; (Z)-1-[2-(2,4-dichlorophenyl)-2-[[(2,4-dichlorophenyl)oxy]imino]ethyl]-1H-imidazole mononitrate; Myfungar; Oceral; Oxistat; (1Z)-N-[(2,4-dichlorobenzyl)oxy]-1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanimine nitrate; Ethanone, 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-, O-[(2,4-dichlorophenyl)methyl]oxime, (1Z)-, nitrate (1:1). Grades: 98%. CAS No. 64211-46-7. Molecular formula: C18H13Cl4N3O. Mole weight: 492.14. | |
| PF-1163A | PF-1163A is an antibiotic isolated from Penicillium species. It exhibits growth inhibitory activity against pathogenic fungal strain Candida albicans and inhibits the ergosterol biosynthesis in Candida albicans. Synonyms: (3S,10R,13S)-3-[[4-(2-Hydroxyethoxy)phenyl]methyl]-13-[(2S)-2-hydroxypentyl]-4,10-dimethyl-1-oxa-4-azacyclotridecane-2,5-dione. Grades: ≥95%. CAS No. 258871-59-9. Molecular formula: C27H43NO6. Mole weight: 477.6. | |
| PF-1163B | PF-1163B is an antibiotic isolated from Penicillium species. It exhibits growth inhibitory activity against pathogenic fungal strain Candida albicans and inhibits the ergosterol biosynthesis in Candida albicans. Synonyms: Antibiotic PF-1163B; (-)-PF 1163B; 3S-[[4-(2-hydroxyethoxy)phenyl]methyl]-4,10R-dimethyl-13R-pentyl-1-oxa-4-azacyclotridecane-2,5-dione. Grades: ≥95%. CAS No. 258871-60-2. Molecular formula: C27H43NO5. Mole weight: 461.63. | |
| Posaconazole | Anti-fungal agent; sterol α-demethylase inhibitor. Posaconazole is a highly potent broadspectrum antifungal drug. It blocks the synthesis of ergosterol by inhibiting of the enzyme lanosterol 14α-demethylase resulting in accumulation of methylated sterol precursors. In contrast to other antifungal azoles, posaconazole has been reported not to induce the efflux pump mechanism. Posaconazole was able to produce a parasitological cure in a mouse model of the chronic stage of Chagas disease. Group: Biochemicals. Alternative Names: 2, 5-Anhydro-1, 3, 4-trideoxy-2-C- (2, 4-difluorophenyl) -4- [ [4- [4- [4- [1- [ (1S, 2S) -1-ethyl-2-hydroxypropyl] -1, 5-dihydro-5-oxo-4H-1, 2, 4-triazol-4-yl] phenyl] -1-piperazinyl] phenoxy] methyl] -1- (1H-1, 2, 4-triazol-1-yl) -D-threo-pentitol; Noxafil; Sch 56592. Grades: Highly Purified. CAS No. 171228-49-2. Pack Sizes: 250mg, 500mg, 1g, 5g. Molecular Formula: C??H??F?N?O?, Molecular Weight: 700.78. US Biological Life Sciences. | Worldwide |
| Posaconazole Diastereoisomer 1 | A diastereoisomer of Posaconazole which is an inhibitor of 14-alpha-demethylase and prevents the conversion of lanosterol to ergosterol, an important component of the fungal cell wall. Grades: > 95%. Molecular formula: C37H42F2N8O4. Mole weight: 700.8. | |
| Posaconazole hydrate | Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity. Posaconazole strongly inhibits 14-alpha demethylase, a cytochrome P450-dependent enzyme. Posaconazole is a sterol C14? demethylase inhibitor with an IC50 of 0.25 nM. Inhibition of 14-alpha-demethylase prevents the conversion of lanosterol to ergosterol, an important component of the fungal cell wall. Inhibition of ergosterol synthesis changes the fungal cell membrane composition and integrity, alters membrane permeability and eventually leads to fungal cell lysis. Compared to other azole antifungals, posaconazole is a significantly more potent inhibitor of sterol 14-alpha demethylase. Posaconazole is the most advanced candidate for the treatment of Chagas disease. Posaconazole has entered in a phase II clinical trial in the treatment of mycoses. Synonyms: SCH56592 hydrate; SCH-56592 hydrate; SCH 56592 hydrate. Grades: >98%. CAS No. 1198769-38-8. Molecular formula: C37H44F2N8O5. Mole weight: 718.79. | |
| Propiconazole-4H-1,2,4-triazole (Mixture of Diastereomers) | An impurities of Propiconazole. Propiconazole is a triazole fungicide inhibiting fungicide due to its binding with and inhibiting the 14-alpha demethylase enzyme from demethylating a precursor to ergosterol. Synonyms: 4-[[2-(2,4-Dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl]methyl]-4H-1,2,4-triazole. Grades: > 95%. CAS No. 221132-58-7. Molecular formula: C15H17Cl2N3O2. Mole weight: 342.23. | |
| Ravuconazole | Ergosterol biosynthesis inhibitor. Antifungal. Group: Biochemicals. Alternative Names: 4- [2- [ (1R, 2R) -2- (2, 4-Difluorophenyl) -2-hydroxy-1-methyl-3- (1H-1, 2, 4-triazol-1-yl) propyl] -4-thiazolyl] benzonitrile; [R-(R*,R*)]-. Grades: Highly Purified. CAS No. 182760-06-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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