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| Product | Description | |
|---|---|---|
| Flucloxacillin Sodium | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopypesticides & metabolitespharma & vet compounds & metabolitespesticides & metabolitespharma & vet compounds & metabolitesbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Flucloxacillin sodium, NSC 277175, Monosodium flucloxacillin,4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)- (9CI), Sodium [3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]penicillin, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-, sodium salt (7CI), Floxapen, Floxapen sodium, Sodium flucloxacillin, Staphylex, Flucloxacillin sodium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-(2?,5?,6?)]-, Floxacillin sodium, BRL-2039. |  |
| Flucloxacillin Sodium | Flucloxacillin, a new semisynthetic penicillin. Group: Biochemicals. Alternative Names: (2S, 5R, 6R) -6- [ [ [3- (2-Chloro-6-fluorophenyl) -5-methyl-4-isoxazolyl] carbonyl] amino] -3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo [3. 2. 0] heptane-2-carboxylic Acid Sodium; Floxacillin Sodium; Floxapen Sodium; Floxapen Sodium; Staphylex Sodium. Grades: Highly Purified. CAS No. 1847-24-1. Pack Sizes: 10mg, 50mg, 100mg, 1g. Molecular Formula: C19H16ClFN3NaO5S, Form: White. US Biological Life Sciences. |  Worldwide |
| Flucloxacillin Sodium Impurity B | An impurity of Flucloxacillin. Flucloxacillin is a narrow-spectrum beta-lactam antibiotic of the penicillin class. Synonyms: 2-[[[[3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]methyl]-5,5-dimethyl-4-thiazolidinecarboxylic Acid. Grades: > 95%. CAS No. 1276016-89-7. Molecular formula: C18H19ClFN3O4S. Mole weight: 427.89. |  |
| Fluconazole | Fluconazole (UK-49858) is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole inhibits C. albicans and Candida kefyr with IC99s range from 0.20 μg/mL to 0.39 μg/mL. Uses: Designed for use in research and industrial production. Additional or Alternative Names: FLUCONAZOLE;FLUCONAZOLE-D4;FLUCONAZOLE-D4 (BISMETHYLENE-D4);diflucan;2,4-DIFLUORO-ALPHA, ALPHA-1-BIS(1H-1,2,4-TRIAZOL-1-YLMETHYL)BENZYL ALCOHOL;2,4-DIFLUORO-,1-BIS(1H-1,2,4-TRIAZOL-1-YLMETHYL)BENZYL ALCOHOL;A-(2,4-DIFLUOROPHENYL)-A-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-1H-1,2,4-TRIAZOL-1-ETHANOL;alpha-(2,4-difluorophenyl)-alpha-(1h-1,2,4-triazol-1-ylmethyl)-1h-1,2,4-triazole-1-ethanol. Product Category: Inhibitors. Appearance: solid. CAS No. 86386-73-4. Molecular formula: C13H12F2N6O. Mole weight: 306.27. Purity: 0.9967. Canonical SMILES: FC1=CC=C(C(O)(CN2C=NC=N2)CN3C=NC=N3)C(F)=C1. Density: 1.05. Product ID: ACM86386734. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Fluconazole | analgesic. Grades: USP. CAS No. 86368-73-4. Product ID: 8-01362. Molecular formula: C13H12F2N6O. Mole weight: 306.27. Properties: Source : |  |
| Fluconazole | Fluconazole (UK-49858) is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole inhibits C. albicans and Candida kefyr with IC 99 s range from 0.20 μg/mL to 0.39 μg/mL [1]. Uses: Scientific research. Group: Natural products. Alternative Names: UK-49858. CAS No. 86386-73-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0101. |  |
| Fluconazole-13C3 solution | 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material. Group: Antifungals standards. | |
| Fluconazole (a-(2,4-Difluorophenyl)-a-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-triazol-1-ethanol) | Used as an antifungal. Group: Biochemicals. Alternative Names: a-(2,4-Difluorophenyl)-a-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-triazol-1-ethanol. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Fluconazole (anhydrous) | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C13H12F2N6O. CAS No. 86386-73-4. Prepack ID 68611425-1g. Molecular Weight 306.27. See USA prepack pricing. |  |
| Fluconazole Beta-D-Glucuronide | A derivative of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Fluconazole β-D-Glucuronide; 1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)-1-(1H-1,2,4-triazol-1-ylmethyl)ethyl β-D-Glucopyranosiduronic Acid; Fluconazole Glucuronide. Grades: > 95%. CAS No. 136134-23-1. Molecular formula: C20H22F2N6O6. Mole weight: 480.43. | |
| Fluconazole-d4 (a-(2,4-Difluorophenyl)-a-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-triazole-1-ethanol-d4, UK-49858-d4, Biozolene-d4, Diflucan-d4, Elazor-d4, Triflucan-d4) | Used as an antifungal. Group: Biochemicals. Alternative Names: a-(2,4-Difluorophenyl)-a-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-triazole-1-ethanol-d4; UK-49858-d4; Biozolene-d4; Diflucan-d4; Elazor-d4; Triflucan-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Fluconazole EP Impurity E | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: (R)-1-(4,6-difluoro-6-(1H-1,2,4-triazol-1-yl)cyclohexa-1,4-dien-1-yl)ethanone. Grades: > 95%. Molecular formula: C10H9F2N3O. Mole weight: 225.20. | |
| Fluconazole EP Impurity F | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Fluconazole Diol Impurity; 2-(2,4-Difluorophenyl)-3-(1H-1,2,4-triazol-1-yl)-1,2-propanediol. Grades: > 95%. CAS No. 118689-07-9. Molecular formula: C11H11F2N3O2. Mole weight: 255.23. | |
| Fluconazole hydrate | 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 Impurity 1 | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 2-(2,4-Difluorophenyl)-1,2,3-propanetriol. Grades: > 95%. CAS No. 173837-65-5. Molecular formula: C9H10F2O3. Mole weight: 204.18. | |
| Fluconazole Impurity (1-(2,4-Difluorophenyl)-1-(1H-1,2,4-Triazol-1-yl)-2,3-Epoxy Propane Methanesulfonate Salt) | An intermediate of Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 2-[[(2,4-Difluorophenyl)-2-oxiranyl]methyl]-1H-1,2,4-triazole methanesulfonate. Grades: > 95%. CAS No. 86386-77-8. Molecular formula: C11H9F2N3O CH4O3S. Mole weight: 237.21 96.11. | |
| Fluconazole Impurity 17 | Fluconazole Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-(2,4-difluorophenyl)-1,4-di(1H-1,2,4-triazol-1-yl)butan-2-ol. CAS No. 1222655-38-0. Molecular formula: C14H14F2N6O. Mole weight: 320.3. Catalog: APB1222655380. | |
| Fluconazole Impurity 2 | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-3-(4H-1,2,4-triazol-4-yl)propan-2-ol. Grades: > 95%. Molecular formula: C13H12F2N6O. Mole weight: 306.28. | |
| Fluconazole Impurity 29 | Fluconazole Impurity 29. Uses: For analytical and research use. Group: Impurity standards. CAS No. 168479-96-7. Molecular formula: C10H7F2N3O. Mole weight: 223.18. Catalog: APB168479967. | |
| Fluconazole Impurity 3 | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 4-Defluoro-4-(1H-1,2,4-triazol-1-yl) Fluconazole; α-[2-fluoro-4-(1H-1,2,4-triazol-1-yl)phenyl]-α-(1H-1,2,4-triazol-1-ylmethyl)-1H-1,2,4-Triazole-1-ethanol. Grades: > 95%. CAS No. 871550-15-1. Molecular formula: C15H14FN9O. Mole weight: 355.34. | |
| Fluconazole Impurity 4 | Fluconazole Impurity 4 is an impurity of Fluconazole, a distinguished antifungal medication. Grades: > 95%. Molecular formula: C13H13FN6O. Mole weight: 288.29. | |
| Fluconazole Impurity A | A stereoisomer of Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Iso Fluconazole; (2RS)-(2,4-Difluorophenyl)-α-(4H-1,2,4-triazol-4-ylmethyl)-1H-1,2,4-triazole-1-ethanol. Grades: > 95%. CAS No. 89429-59-4. Molecular formula: C13H12F2N6O. Mole weight: 306.28. | |
| Fluconazole Impurity C | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 1,1'-(1,3-Phenylene)bis-1H-1,2,4-triazole; 1,1'-(1,3-Phenylene)di-1H-1,2,4-triazole. Grades: > 95%. CAS No. 514222-44-7. Molecular formula: C10H8N6. Mole weight: 212.22. | |
| Fluconazole Impurity E | | |
| Fluconazole Impurity G | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Fluconazole Epoxide Impurity ; 1-[[(2RS)-2-(2,4-Difluorophenyl)oxiran-2-yl]methyl]-1H-1,2,4-triazole. Grades: > 95%. CAS No. 86386-76-7. Molecular formula: C12H11F2N3O4S. Mole weight: 331.30. | |
| Fluconazole Impurity I | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Fluconazole Amino Impurity ; 4-Amino-1-[(2RS)-2-(2,4-difluorophenyl)-2-hydroxy-3(1H-1,2,4-triazol-1-yl)propyl]-4H-1,2,4-triazolium bromide. Grades: > 95%. CAS No. 150168-54-0. Molecular formula: C13H14F2N7O. Br. Mole weight: 402.2. | |
| Fluconazole Impurity K | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: 2-(2-fluorophenyl)-1,3-di(1H-1,2,4-triazol-1-yl)propan-2-ol. CAS No. 1348664-75-4. Molecular formula: C13H13FN6O. Mole weight: 288.28. | |
| Fluconazole mesylate | 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. | |
| Fluconazole N-Oxide | An impurity of the antifungal agent Fluconazole. Fluconazole is a triazole antifungal agent that is effective against most Candida strains. Synonyms: Fluconazole mono-N-Oxide. Grades: > 95%. Molecular formula: C13H12F2N6O2. Mole weight: 322.28. | |
| Fluconazole solution | 2.0 mg/mL in methanol, ampule of 1 mL, certified reference material. Group: Antifungals standards. | |
| Flucycloxuron | analytical standard, mixture of (E) and (Z) isomers. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. Alternative Names: UBI-A 1335, N-[[[4-[[[[(4-Chlorophenyl)cyclopropylmethylene]amino]oxy]methyl]phenyl]amino]carbonyl]-2,6-difluorobenzamide, PH 70-23, DU 319722, OMS 3041,A 1335, Andalin, Flucycloxuron, Andalin DC 25, N-[[[4-[[[[(4-chlorophenyl)cyclopropylmethylene]amino]oxy]methyl]phenyl]amino]carbonyl]-2,6-difluoro-Benzamide. | |
| Flucythrinate | analytical standard, mixture of stereo isomers. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Flucytosine | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Flucytosine | Flucytosine (5-Fluorocytosine) is an antifungal compound with oral activity. Flucytosine is a widely used cytotoxic drug that, after further metabolism, produces fluorinated ribonucleotides and deoxyribonucleotides, inhibits DNA and protein synthesis, and has multiple effects such as inhibiting candida and candida neoplasm infection and producies cytotoxicity to cancer cells [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Fluorocytosine; NSC 103805; Ro 2-9915. CAS No. 2022-85-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0139. | |
| Flucytosine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardseuropean pharmacopoeia (ph. eur.)impurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Flucytosine. | |
| Flucytosine (5-Fluorocytosine) | 1g Pack Size. Group: Bioactive Small Molecules, Biochemicals, Fluorinated Products. Formula: C4H4FN3O. CAS No. 2022-85-7. Prepack ID 33980289-1g. Molecular Weight 129.09. See USA prepack pricing. | |
| Flucytosine Glucuronide | Flucytosine Glucuronide is a metabolite of the antifungal/antimicrobial agent, 5-Fluorocytosine. Synonyms: 5-Fluoro Cytosine O-β-D-Glucuronide; 4-Amino-5-fluoro-2-pyrimidinyl β-D-Glucopyranosiduronic Acid. Grades: > 95%. CAS No. 150494-26-1. Molecular formula: C10H12FN3O7. Mole weight: 305.22. | |
| Fludalanine | Fludalanine, an analogue of D-alanine that irreversibly inactivates the racemase, inhibits the synthetase. Uses: Antibacterial. Synonyms: MK641; MK641; MK641; Fludalanine; 3-Fluoro-D-(2-2H)alanine;(S)-2-amino-3-fluoropropanoic-2-d acid. Grades: ≥98%. CAS No. 35523-45-6. Molecular formula: C3H6FNO2. Mole weight: 108.09. | |
| Fludarabine | 9H-Purin-6-amine,9-b-D-arabinofuranosyl-2-fluoro-. CAS No. 21679-14-1. Product ID: 8-04718. Molecular formula: C10H12FN5O4. Mole weight: 285.23. Purity: 0.98. | |
| Fludarabine | Fludarabine. Group: Biochemicals. Grades: Purified. CAS No. 21679-14-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Fludarabine | Fludarabine (NSC 118218) is a DNA synthesis inhibitor and a fluorinated purine analogue with antineoplastic activity in lymphoproliferative malignancies. Fludarabine inhibits the cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal resting or activated lymphocytes [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: F-ara-A; NSC 118218. CAS No. 21679-14-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0069. | |
| Fludarabine (9-b-D-Arabinofuranosyl-2-fluoro-9H-purin-6-amine, 2-F-araA) | Used as an antineoplastic. Group: Biochemicals. Alternative Names: 9-b-D-Arabinofuranosyl-2-fluoro-9H-purin-6-amine, 2-F-araA. Grades: Highly Purified. CAS No. 21679-14-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Fludarabine-Cl | Fludarabine-Cl has an inhibitory effect on RNA adenosine deaminase 1 ( ADAR1 ) with an IC 50 of 0.87 μM and can be used to prevent and/or study cancer or tumor-related diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2734853-80-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-145443. | |
| Fludarabine phosphate | Fludarabine (phosphate) is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NSC 118218 phosphate. CAS No. 75607-67-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0028. | |
| Fludarabine phosphate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Fludarabine phosphate, 2-Fluoro-9-(5-O-phosphono-?-D-arabinofuranosyl)-9H-purin-6-amine. | |
| Fludarabine phosphate | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C10H13FN5O7P. CAS No. 75607-67-9. Prepack ID 56054450-1g. Molecular Weight 365.21. See USA prepack pricing. | |
| Fludarabine phosphate | Fludarabine phosphate. Group: Biochemicals. Alternative Names: 9-b-D-Arabinofuranosyl-2-fluoroadenine 5-phosphate. Grades: Highly Purified. CAS No. 75607-67-9. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C10H13FN5O7P. US Biological Life Sciences. | Worldwide |
| Fludarabine Phosphate | Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis. Uses: Antimetabolites, antineoplastic. Synonyms: Fludarabine 5'-monophosphate; 2-Fluoro-ARA AMP; Fludarabine monophosphate; FAMP; NSC-312887; 2-Fluoro-9-(5-O-phosphono-beta-D-arabinofuranosyl)-9H-purin-6-amine; 2-Fluoroadenine arabinoside 5'-monophosphate; ((2R,3S,4S,5R)-5-(6-amino-2-fluoro-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate; 9-beta-Arabinofuranosyl-2-fluoroadenine-5'-phosphate. Grades: ≥98% by HPLC. CAS No. 75607-67-9. Molecular formula: C10H13FN5O7P. Mole weight: 365.21. | |
| Fludarabine Phosphate | 9-b-D-Arabinofuran-2-fluoroadenine-5 '-phosphate. CAS No. 75607-67-9. Product ID: 8-04906. Molecular formula: C10H13FN5O7P. Mole weight: 365.21. Properties: topical antimicrobial agent. | |
| Fludarabine phosphate impurity A | Fludarabine phosphate impurity A is an impurity of Fludarabine phosphate, the salient therapeutic recourse for chronic lymphocytic leukemia. Grades: > 95%. Molecular formula: C10H14N5O8P. Mole weight: 363.23. | |
| Fludarabine phosphate impurity B | Fludarabine phosphate impurity B isan impurity of Fludarabine phosphate, a chemotherapy drug primarily used to treat chronic lymphocytic leukemia. Grades: > 95%. CAS No. 149297-79-0. Molecular formula: C5H5N5O. Mole weight: 151.13. | |
| Fludarabine Phosphate Impurity C | Fludarabine Phosphate Impurity C is an impurity of Fludarabine Phosphate with pronounced application in the therapy of diverse malignancies such as chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma (NHL). Grades: > 95%. Molecular formula: C10H14FN5O10P2. Mole weight: 445.20. | |
| Fludarabine Phosphate Impurity D | Fludarabine Phosphate Impurity D is an impurity of Fludarabine Phosphate, a well-established therapeutic agent efficacious in treating B-cell chronic lymphocytic leukemia (CLL). Grades: > 95%. Molecular formula: C5H4FN5. Mole weight: 153.12. | |
| Fludarabine Phosphate Impurity F | Fludarabine Phosphate Impurity F is a byproduct found in the manufacturing process of the chemotherapy drug Fludarabine Phosphate, which is used to treat B-cell chronic lymphocytic leukemia and lymphoma. Its exact role in the biomedical industry is not well understood and further research is needed. Synonyms: [(2R,3S,4S,5R)-5-(6-amino-2-ethoxypurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate. Grades: > 95%. CAS No. 159002-28-5. Molecular formula: C12H18N5O8P. Mole weight: 391.28. | |
| Fludarabine Phosphate USP | 9H-Purin-6-amine,2-fluoro-9-(5-O-phosphono-b-D-arabinofuranosyl)-. Grades: USP. CAS No. 75607-67-9. Product ID: 8-04494. Molecular formula: C10H13N5O7FP. Mole weight: 365.22. | |
| Fludarabine triphosphate trisodium | Fludarabine triphosphate (F-ara-ATP) trisodium, the active metabolite of (HY-B0069), is a potent, noncompetitive and specific inhibitor of DNA primase, with an IC50 of 2.3 ?M and a Ki of 6.1 ?M. Fludarabine triphosphate trisodium inhibits DNA synthesis by blocking DNA primase and primer RNA formation. Fludarabine triphosphate trisodium inhibits ribonucleotide reductase and DNA polymerase and ultimately leads to cellular apoptosis[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: F-ara-ATP trisodium. Pack Sizes: 5 mg (100 mM * 84.59 ?L in Water); 10 mg (100 mM * 169.17 ?L in Water); 25 mg (100 mM * 422.93 ?L in Water); 50 mg (100 mM * 845.85 ?L in Water); 100 mg (100 mM * 1.69 mL in Water). Product ID: HY-136650A. | |
| Fludeoxyglucose | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Fludeoxyglucose Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Fludeoxyglucose Related Compound B | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Fludioxonil | 250mg Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C12H6F2N2O2. CAS No. 131341-86-1. Prepack ID 89981214-250mg. Molecular Weight 248.19. See USA prepack pricing. | |
| Fludioxonil | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Fludioxonil | Fludioxonil (CGA-173506) is a phenylpyrrole-type fungicide with oral activity that can inhibit the growth of S. sclerotiorum. Fludioxonil promotes tumor growth and metastasis, and induces cardiac toxicity. Fludioxonil causes cytoskeletal disruption, DNA damage, and apoptosis in mouse glioma cells [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CGA-173506. CAS No. 131341-86-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-W021040. | |
| Fludrocortisone | Fludrocortisone. Group: Biochemicals. Grades: Highly Purified. CAS No. 127-31-1. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C21H29FO5. US Biological Life Sciences. | Worldwide |
| Fludrocortisone | Fludrocortisone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (11β)-. Product Category: Steroidal Compounds. Appearance: White Solid. CAS No. 127-31-1. Molecular formula: C21H29FO5. Mole weight: 380.45. Purity: 0.95. IUPACName: fludrocortisone. Density: 1.3g/cm³. Product ID: ACM127311. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fludrocortisone | Fludrocortisone is a synthetic corticosteroid with moderate glucocorticoid potency and much greater mineralocorticoid potency. It is used for its mineralocorticoid activity and not for its glucocorticoid activity. It has anti-inflammatory activity. Uses: Fludrocortisone could be used against cerebral salt wasting syndrome for behaving the role as a anti-inflammatory agent. Synonyms: (11β)-9-Fluoro-11,17,21-trihydroxypregn-4-ene-3,20-dione; 9α-Fluorohydrocortisone; 9α-Fluoro-17-hydroxycorticosterone; NSC 11318; 9α-Fluorcortisol; 17,21-trihydroxy-20-dion(11beta)-pregn-4-ene-9-fluoro-11; 9-fluoro-11-beta,17,21-trihydroxy-pregn-4-ene-20-dione. Grades: > 95%. CAS No. 127-31-1. Molecular formula: C21H29FO5. Mole weight: 380.46. | |
| Fludrocortisone | Fludrocortisone, a synthetic mineralocorticoid with anti-inflammatory activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 9α-Fludrocortisone; 9α-Fluorcortisol. CAS No. 127-31-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-B1203. | |
| Fludrocortisone (9a-Fluoro-17-hydroxycorticosterone, Fluohydrisone, Astonin H) | Source: Synthetic. Group: Biochemicals. Alternative Names: 9a-Fluoro-17-hydroxycorticosterone, Fluohydrisone, Astonin H. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Fludrocortisone acetate | Fludrocortisone acetate (9α-Fludrocortisone acetate) is an orally active synthetic mineralocorticoid. Fludrocortisone acetate can effectively control sodium retention. Fludrocortisone acetate is used in studies of cardiac injury, adrenal insufficiency and orthostatic hypotension [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 9α-Fludrocortisone acetate; 9α-Fluorcortisol acetate. CAS No. 514-36-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1203A. | |
| Fludrocortisone Acetate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Fludrocortisone acetate, Scherofluron, U 4845, 9alpha-Fluorocortisol 21-acetate, Cortineff, 9alpha-Fluorocortisol acetate, 9-Fluoro-11beta,17-dihydroxy-3,20-dioxopregn-4-en-21-yl acetate, NSC 15186, 9alpha-Fluorohydrocortisone 21-acetate, 9alpha-Fluoro-11beta,17alpha,21-trihydroxypregn-4-ene-3,20-dione 21-acetate, 9alpha-Fluorohydrocortisone acetate, 9-Fluorohydrocortisone acetate, Pregn-4-ene-3,20-dione, 9-fluoro-11beta,17,21-trihydroxy-, 21-acetate (7CI,8CI), Corticosterone, 9-fluoro-17-hydroxy-, 21-acetate (6CI), Alflorone acetate, Fluorocortisol acetate, Fluorohydrocortisone acetate, Fludrocortisone 21-acetate. | |
| Fludrocortisone Acetate | Fludrocortisone acetate is a synthetic corticosteroid with more mineralocorticoid than glucocorticoid activity. Uses: A mineralocorticoid. Synonyms: 17-dihydroxy-20-dion(11-beta)-pregn-4-ene-21-(acetyloxy)-9-fluoro-11; 20-dione,9-fluoro-11-beta,17,21-trihydroxy-pregn-4-ene-21-acetate; 9-fluoro-11-beta,17,21-trihydroxypregn-4-ene-3,20-dione21-acetate; 9-fluoro-17-hydroxy-corticosteron21-acetate; (11β)-21-(. Grades: > 95%. CAS No. 514-36-3. Molecular formula: C23H31FO6. Mole weight: 422.50. | |
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