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| Product | Description | |
|---|---|---|
| furylfuramide isomerase | Requires NADH. Group: Enzymes. Enzyme Commission Number: EC 5.2.1.6. CAS No. 72561-07-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5449; furylfuramide isomerase; EC 5.2.1.6; 72561-07-0. Cat No: EXWM-5449. |  |
| Furyl phosphoro dichloridate | Furyl phosphoro dichloridate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Phosphorodichloridicacid, 2-furanyl ester, 105262-70-2, Furylphosphorodichloridate, ACMC-20m83b, AGN-PC-00N635, CTK4A3704, AG-D-18539, Phosphorodichloridic acid, 2-furanyl ester. Product Category: Heterocyclic Organic Compound. CAS No. 105262-70-2. Molecular formula: C4H3Cl2O3P. Mole weight: 200.944582 [g/mol]. Purity: 0.96. IUPACName: 2-dichlorophosphoryloxyfuran. Canonical SMILES: C1=COC(=C1)OP(=O)(Cl)Cl. Product ID: ACM105262702. Alfa Chemistry ISO 9001:2015 Certified. Categories: Furan-2-yl phosphorodichloridate. |  |
| Fusacandin A | It is produced by the strain of Fusarium sambucinum. It inhibits (1,3)-β-glucan synthetase and has antifungal properties. Synonyms: D-Glucitol, O-beta-D-galactopyranosyl-(1-2)-O-6-O-((2E,4Z)-1-oxo-2,4-decadienyl)-beta-D-galactopyranosyl-(1-3)-1,5-anhydro-1-C-(2,4-dihydroxy-6-(hydroxymethyl)phenyl)-, 3-((2E,4E,7S,8E,10E)-7-hydroxy-2,4,8,10-hexadecatetraenoate). CAS No. 166407-33-6. Molecular formula: C51H74O21. Mole weight: 1023.12. |  |
| Fusacandin B | It is produced by the strain of Fusarium sambucinum. It inhibits (1,3)-β-glucan synthetase and has antifungal properties. Synonyms: D-Glucitol, O-beta-D-galactopyranosyl-(1-2)-O-beta-D-galactopyranosyl-(1-3)-1,5-anhydro-1-C-(2,4-dihydroxy-6-(hydroxymethyl)phenyl)-, 3-((2E,4E,7S,8E,10E)-7-hydroxy-2,4,8,10-hexadecatetraenoate). CAS No. 166407-34-7. Molecular formula: C41H60O20. Mole weight: 872.90. | |
| Fusapyrone | It is a broad spectrum antifungal metabolite isolated from several species of fusarium. It exhibits low animal-toxicity as evidenced by a lack of toxicity against artemia salina. It is a useful candidate for control of postharvest crop diseases. Synonyms: 3-(4-deoxy-β-xylo-hexopyranosyl)-2-hydroxy-6-[(3E,5E,8Z)-2-hydroxy-7-(hydroxymethyl)-1,1,5,9,11-pentamethyl-3,5,8-heptadecatrien-1-yl]-2H-pyran-2-one; Neofusapyrone. Grade: >95%. CAS No. 156856-31-4. Molecular formula: C34H54O9. Mole weight: 606.79. | |
| Fusarenon X | A mycotoxin produced by Fusarium, having immunosuppressive and carcinogenic properties. Group: Biochemicals. Alternative Names: (3α,4 β,7α)-4-(Acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-trichothec-9-en-8-one; 4 β-Acetoxy-3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one; 3-Acetylnivalenol; 4-Acetylnivalenol; Nivalenol Monoacetate. Grades: Highly Purified. CAS No. 23255-69-8. Pack Sizes: 500ug. US Biological Life Sciences. |  Worldwide |
| Fusaric acid | Fusaric acid is a potent dopamine β-hydroxylase inhibitor. Uses: Scientific research. Group: Natural products. CAS No. 536-69-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-128483. |  |
| Fusaric acid | Fusaric acid. Group: Biochemicals. Alternative Names: 5-Butyl-2-pyridinecarboxylic acid; 5-Butylpicolinic acid. Grades: Highly Purified. CAS No. 536-69-6. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Fusaric acid 99+.9% | Fusaric acid 99+.9%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Fusaricidin A | Fusaricidin A, a new depsipeptide antibiotic, was isolated from the culture broth of Bacillus polymyxa KT-8 obtained from the rhizosphere of garlic suffering from the basal rot caused by Fusarium oxysporum. Fusaricidin A is active against fungi and Gram-positive bacteria. Uses: Fusaricidin a is a cyclic lipopeptide with potent antimicrobial properties that was originally isolated from various strains of the genus bacillus. this natural compound has attracted great interest in drug discovery due to its broad-spectrum antimicrobial activity, low toxicity to human cells, and potential as a new therapeutic agent for drug-resistant pathogens. fusaricidin a is a desirable can. Synonyms: 1-Oxa-4,7,10,13,16-pentaazacyclononadecane-6-acetamide, 18-[[15-[[(Z)-aminoiminomethyl]amino]-3-hydroxy-1-oxopentadecyl]amino]-9-[(1R)-1-hydroxyethyl]-3,19-dimethyl-12,15-bis(1-methylethyl)-2,5,8,11,1 4,17-hexaoxo-, (3R,6R,9R,12S,15R,18S,19R)-. Molecular formula: C41H74N10O11. Mole weight: 883.08. | |
| Fusaricidin B | Fusaricidins B, a new depsipeptide antibiotic, has been isolated as a minor component from the culture broth of Bacillus polymyxa KT-8 which was obtained from the rhizosphere of garlic suffering from the basal rot caused by Fusarium oxysporum. Fusaricidins B is active against fungi and Gram-positive bacteria almost as well as fusaricidin A. Molecular formula: C42H76N10O11. Mole weight: 897.11. | |
| Fusaricidin C | Fusaricidins C, a new depsipeptide antibiotic, has been isolated as a minor component from the culture broth of Bacillus polymyxa KT-8 which was obtained from the rhizosphere of garlic suffering from the basal rot caused by Fusarium oxysporum. Fusaricidins C is active against fungi and Gram-positive bacteria almost as well as fusaricidin A. Molecular formula: C45H74N10O12. Mole weight: 947.13. | |
| Fusaricidin D | Fusaricidins D, a new depsipeptide antibiotic, has been isolated as a minor component from the culture broth of Bacillus polymyxa KT-8 which was obtained from the rhizosphere of garlic suffering from the basal rot caused by Fusarium oxysporum. Fusaricidins D is active against fungi and Gram-positive bacteria almost as well as fusaricidin A. Molecular formula: C46H76N10O12. Mole weight: 961.15. | |
| Fusarielin A | An antibiotic originally isolated from Fusarium sp. K432. The antifungal spectrum of Fusarielin A is relatively narrow. And the MICs against Kotokococcus and streptococcus were 3.1 μg/mL and 12.5 μg/mL, respectively. Synonyms: 4,6-Heptadiene-1,3-diol, 7-[(1aR,2R,3S,3aS,4aS,5aR,6aR,6bS)-decahydro-1a,5a-dimethyl-2-[(1E)-1-methyl-1-propen-1-yl]naphtho[1,2-b:6,7-b']bisoxiren-3-yl]-2,4-dimethyl-, (2S,3S,4E,6E)-. Molecular formula: C25H38O4. Mole weight: 402.57. | |
| Fusarin C | Fusarin C is produced by the strain of Fusarium moniliforrme which has mutagenicity. Synonyms: CCRIS 4320; HSDB 7078; (2E,3E,5E,7E,9E)-2-Ethylidene-11-[(1R,5a)-4a-hydroxy-4-(2-hydroxyethyl)-2-oxo-6-oxa-3-azabicyclo[3.1.0]hexan-1a-yl]-4,6,10-trimethyl-11-oxo-3,5,7,9-undecatetraenoic acid methyl ester. CAS No. 79748-81-5. Molecular formula: C23H29NO7. Mole weight: 431.48. | |
| fusarinine-C ornithinesterase | Hydrolyses the three ornithine ester bonds in fusarinine C. Also acts on N5-dinitrophenyl-L-ornithine methyl ester. Group: Enzymes. Synonyms: ornithine esterase; 5-N-acyl-L-ornithine-ester hydrolase. Enzyme Commission Number: EC 3.1.1.48. CAS No. 60202-10-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3475; fusarinine-C ornithinesterase; EC 3.1.1.48; 60202-10-0; ornithine esterase; 5-N-acyl-L-ornithine-ester hydrolase. Cat No: EXWM-3475. | |
| Fusarisetin A | It is an unusual pentacyclic metabolite related to equisetin isolated from Fusarium. It is identified from a natural product screen using a three-dimensional matrigel-induced bioassay to study acinar morphogenesis. It is the first inhibitor of acini reported in the literature. Synonyms: (+)-Fusarisetin A; 5H-Benz[4',5']indeno[2',1':3,4]furo[2,3-c]pyrrole-1,12(2H,5aH)-dione,3,3a,5b,7a,8,9,10,11,11a,11b-decahydro-3a-hydroxy-3-(hydroxymethyl)-2,5,9,11b-tetramethyl-, (3S,3aR,5S,5aS,5bS,7aS,9R,11aR,11bS,12aR)-. Grade: >98% by HPLC. CAS No. 1300041-53-5. Molecular formula: C22H31NO5. Mole weight: 389.49. | |
| Fusariumester A1 | Fusariumester A1 is a compelling antifungal compound, showcasing robust inhibitory prowess against fungal pathogens, specifically hailing from the esteemed genus Fusarium. Molecular formula: C36H58O11. Mole weight: 666.84. | |
| Fusariumester A2 | Fusariumester A2 is a compelling fungicidal compound originating from the Fusarium fungus. Its modus operandi encompasses the disruption of fungal cellular barriers, culminating in their demise. Molecular formula: C36H58O11. Mole weight: 666.84. | |
| Fusarochromanone | Produced by the strain of Fusarium equiseti. Fusarochromanone causes Tibial chondrodysplasia in animals and is associated with kashin-Beck's disease in children. Synonyms: Fusarochromenone; 4H-1-Benzopyran-4-one, 5-amino-6-(3-amino-4-hydroxy-1-oxobutyl)-2,3-dihydro-2,2-dimethyl-; 5-Amino-6-(3-amino-4-hydroxy-1-oxobutyl)-2,3-dihydro-2,2-dimethyl-4H-1-benzopyran-4-one. Grade: >98%. CAS No. 104653-89-6. Molecular formula: C15H20N2O4. Mole weight: 292.33. | |
| Fusarubin | Fusarubin is a metabolite of Fusarium solani. Synonyms: Oxyjavanicin; NSC106193; 1H-Naphtho[2,3-c]pyran-5,10-dione, 3,4-dihydro-3,6,9-trihydroxy-7-methoxy-3-methyl-. CAS No. 1702-77-8. Molecular formula: C15H14O7. Mole weight: 306.27. | |
| Fuscaxanthone C | Fuscaxanthone C. Group: Biochemicals. Alternative Names: NSC 27594; AIDS-011975. Grades: Plant Grade. CAS No. 15404-76-9. Pack Sizes: 10mg. Molecular Formula: C26H30O6, Molecular Weight: 438.512999999999. US Biological Life Sciences. | Worldwide |
| Fuscin | Mycotoxin. Antibacterial agent. ADP transport inhibitor. Human CCR5 receptor antagonist. Anti-HIV compound. Mitochondrial respiration and oxidative phosphorylation inhibitor. Group: Biochemicals. Alternative Names: 3,4,7,9-Tetrahydroxy-6-methyl-1H-phenalen-1-one, 9,10-Dihydro-5-hydroxy-4,8,8-trimethyl-2H,4H-benzo[1,2-b:4,3-c]dipyran-2,6(8H)-dione. Grades: Highly Purified. CAS No. 83-85-2. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C??H??O?. US Biological Life Sciences. | Worldwide |
| Fuscin | Produced by the strain of Oidiodendron fuscum Ag 122 and Camb 111, Fuscin has resistance to gram-positive bacteria and mycobacterium (weak) activity. Fuscin is also an anti-HIV compound and antagonist of CKR-5 (CCR5). Synonyms: 9,10-Dihydro-5-hydroxy-4,8,8-trimethyl-2-H,4-H-benzo(1,2-b-4,3-c)-dipyran-2,6(8H)-dione; 2-Hydroxy-4,8,8-trimethyl-9,10-dihydro-4H-pyrano[3,2-f]isochromene-5,6-dione. Grade: ≥95%. CAS No. 83-85-2. Molecular formula: C15H16O5. Mole weight: 276.28. | |
| Fused Magnesium Oxide (MgO) Powder | Fused Magnesium Oxide (MgO) Powder. Group: Magnetic nanoparticles. Alternative Names: Fused Magnesium Oxide; Fused Magnesia; Electrofused Magnesium Oxide; Electro Fused Magnesium Oxide; Fused Magnesium Oxide; magnesium oxide; magnesium(II) oxide; magnesia; periclase. 99.5%. |  |
| fusicocca-2,10(14)-diene synthase | A multifunctional enzyme with EC 2.5.1.29 farnesyltranstransferase activity. Group: Enzymes. Synonyms: fusicoccadiene synthase; PaFS; PaDC4. Enzyme Commission Number: EC 4.2.3.43. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5202; fusicocca-2,10(14)-diene synthase; EC 4.2.3.43; fusicoccadiene synthase; PaFS; PaDC4. Cat No: EXWM-5202. | |
| Fusicoccin | Fusicoccin (Fusicoccin A), a fungal pytotoxin, is a stabilizer of specific 14-3-3 protein-protein interactions. Fusicoccin sabilizes H + -ATPase/14-3-3 cmplex in pants, maintaining the enzyme in activated state. Fusicoccin also stabilizes 14-3-3 protein interactions with binding partners containing a C-terminal 14-3-3 recognition motif (a mode 3 motif), such as ERα, GPIbα, TASK3, CTFR, and p53. Fusicoccin induces apoptosis in cancer cells and has anticancer activity [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Fusicoccin A. CAS No. 20108-30-9. Pack Sizes: 1 mg. Product ID: HY-122815. | |
| Fusicoccin | Fusicoccin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Fucicoccin; fusicoccin A; 3-[2-(Acetyloxy)-1-methylethyl]-1,2,4,5,6,6a,7,8,9,10a-decahydro-1,5-dihydroxy-9-(methoxymethyl)-6,10a-dimethylcyclopenta[a,d]-dicylo coten-4-yl-6; FUSICOCCIN. Product Category: Heterocyclic Organic Compound. CAS No. 20108-30-9. Molecular formula: C36H56O12. Mole weight: 680.82. Purity: 0.96. IUPACName: fusicoccin. Canonical SMILES: CC1C2CCC(C2=CC3(C(CC(=C3C(C1O)OC4C(C(C(C(O4)COC(C)(C)C=C)O)OC(=O)C)O)C(C)COC(=O)C)O)C)COC. Density: 1.24g/cm³. Product ID: ACM20108309. Alfa Chemistry ISO 9001:2015 Certified. | |
| Fusicoccin H | Fusicoccin H is a metabolite of Fusicoccum amygdali. Synonyms: 1,2,4,5,6,6aβ,7,8,9,10a-Decahydro-5α-hydroxy-9α-hydroxymethyl-6α,10aα-dimethyl-3-isopropyldicyclopenta[a,d]cycloocten-4β-yl α-D-glucopyranoside. CAS No. 50906-51-9. Molecular formula: C26H42O8. Mole weight: 482.61. | |
| Fusidate sodium | Sodium fusidate is a bacteriostatic antibiotic isolated from the fermentation broth of Fusidium coccineum. It suppresses nitric oxide lysis of pancreatic islet cells. It also inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. It is also used to inhibit the replication of gram-positive bacteria including Staphylococcus, Streptococcus, and Corynebacterium species. Uses: Anti-bacterial agents. Synonyms: 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, sodium salt (1:1), (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-; Fucidin; Fucidina; Fucidine; Fusidic acid sodium salt; Fusidin; Sodium fucidate; Sodium fusidate; Sodium fusidin; SQ 16360; ZN 6-Na; Sodium (Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoate. Grade: 98%. CAS No. 751-94-0. Molecular formula: C31H47NaO6. Mole weight: 538.70. | |
| Fusidate Sodium | Sodium fusidate is the more water soluble sodium salt of fusidic acid, a steriodal metabolite of Fusidium coccineum which is a Gram +ve antibiotic. Fusidic acid inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. Fusidic acid has also been shown to suppress nitric oxide lysis of pancreatic islet cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 751-94-0. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Fusidic acid | Fusidic acid (Fusidate) a bacteriostatic antibiotic produced from the Fusidium coccineum fungus, belongs to the class of steroids. Fusidic acid has no corticosteroid effects. Fusidic acid inhibits the growth of bacteria by preventing the release of translation elongation factor G (EF-G) from the ribosome. Fusidic acid holds promise for research in anticancer and anti-infective applications. [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Fusidate; SQ-16603. CAS No. 6990-6-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1350. | |
| Fusidic acid | Fusidic acid is a bacteriostatic steroid antibiotic which targets protein synthesis in gram-positive bacteria. Synonyms: (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, 16-acetate, (Z)-; Flucidin; Foban; Fucithalmic; Fugen; Fusidinic acid; NSC 56192; Optifucin; Phudicin; Ramycin; SQ 16603; Usidin; (Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid. Grade: 98%. CAS No. 6990-6-3. Molecular formula: C31H48O6. Mole weight: 516.72. | |
| Fusidic acid | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C31H48O6. CAS No. 6990-6-3. Prepack ID 30666063-1g. Molecular Weight 516.71. See USA prepack pricing. |  |
| Fusidic Acid | Fusidic acid is a bacteriostatic antibiotic. Fusidic Acid suppresses nitric oxide lysis of pancreatic islet cells. Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. Group: Biochemicals. Alternative Names: (3α, 4α, 8α, 9 β, 11α, 13α, 147 β,167 β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic Acid; Flucidin; Fucithalmic; Fusidinic Acid; NSC 56192; Ramycin; SQ 16603. Grades: Highly Purified. CAS No. 6990-6-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| FUSIDIC ACID | Fusidic acid is a steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum. It has a role as a protein synthesis inhibitor, an EC 2.7.1.33 (pantothenate kinase) inhibitor and an Escherichia coli metabolite. It is a 3alpha-hydroxy steroid, an 11alpha-hydroxy steroid, a sterol ester, a steroid acid, an alpha,beta-unsaturated monocarboxylic acid and a steroid antibiotic. It is a conjugate acid of a fusidate. It derives from a hydride of a 5alpha-cholestane. CAS No. 6990-6-3. Product ID: PAP-0038. Molecular formula: C31H48O6. Category: Antibacterial, anti-inflammatory and antiviral. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; FUSIDIC ACID; PAP-0038; Antibacterial, anti-inflammatory and antiviral; C31H48O6; 6990-06-3. Standard: EP/ BP. Color: White to Off-White. EC Number: 230-256-0. Physical State: neat. Solubility: Practically insoluble in water, freely soluble in ethanol (96 per cent). Storage: Sealed in dry,2-8°C. Applications: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. Boiling Point: 521.49°C (rough estimate). Melting Point: 190-192°C. Density: 1.0389 (rough estimate). Product Description: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. |  |
| Fusidic acid, 97.5-101.0% | Fusidic acid, 97.5-101.0%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Fusidic acid acyl glucuronide | Fusidic acid acyl glucuronide is a metabolite originating from fusidic acid, acting as an efficacious antimicrobial compound employed for studying diverse bacterial ailments. It manifestly demonstrates amplified pharmacokinetic attributes encompassing heightened bioavailability and metabolic steadfastness. Synonyms: Fusidic acid, β-D-glucopyranuronosyl ester; 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, β-D-glucopyranuronosyl ester, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-; Fusidic Acid Acyl β-D-Glucuronide; (2S,3S,4S,5R,6S)-6-(((Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoyl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid. Grade: ≥95%. CAS No. 13013-66-6. Molecular formula: C37H56O12. Mole weight: 692.83. | |
| Fusidic Acid-d6 | Fusidic acid is a bacteriostatic antibiotic. Fusidic Acid suppresses nitric oxide lysis of pancreatic islet cells. Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA. Group: Biochemicals. Alternative Names: (3α, 4α, 8α, 9 β, 11α, 13α, 147 β,167 β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic Acid-d6; Flucidin-d6; Fucithalmic-d6; Fusidinic Acid-d6; NSC 56192-d6; Ramycin-d6; SQ 16603-d6. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Fusidic Acid EP Impurity A | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(24SR,17Z)-16α-(Acetyloxy)-3β,11β,24,25-tetrahydroxy-4β,8,14-trimethyl-18-nor-5β,10αcholest-17(20)-en-21-oic acid; 24,25-Dihydro-24,25-dihydroxyfusidic acid; Fusidic Acid Impurity A; Sodium Fusidate EP Impurity A. Grade: ≥95%. Molecular formula: C31H50O8. Mole weight: 550.73. | |
| Fusidic Acid EP Impurity B | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6SR)-6-hydroxy-7,7-dimethyl-2-oxooxepan-3-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; 24,25-Dihydro-24,25-dihydroxyfusidic acid 21,25-lactone; Fusidic Acid Impurity B; Sodium Fusidate EP Impurity B; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-dihydroxy-17-((SR)-6-hydroxy-7,7-dimethyl-2-oxooxepan-3-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate. Grade: ≥95%. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity C | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6S)-6-(1-hydroxy-1-methylethyl)-2-oxodihydro-2H-pyran-3(4H)-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; (24R)-24,25-Dihydro-24,25-dihydroxyfusidic acid 21,24-lactone; Fusidic Acid Impurity C; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-Dihydroxy-17-((R)-6-(2-hydroxypropan-2-yl)-2-oxodihydro-2H-pyran-3(4H)-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate; Sodium Fusidate EP Impurity C. Grade: ≥95%. CAS No. 3054708-75-4. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity D | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6R)-6-(1-hydroxy-1-methylethyl)-2-oxodihydro-2H-pyran-3(4H)-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; (24S)-24,25-Dihydro-24,25-dihydroxyfusidic acid 21,24-lactone; Fusidic Acid Impurity D; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-Dihydroxy-17-((S)-6-(2-hydroxypropan-2-yl)-2-oxodihydro-2H-pyran-3(4H)-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate; Sodium Fusidate EP Impurity D. Grade: ≥95%. CAS No. 3054708-76-5. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity E | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z,24EZ)-16α-(Acetyloxy)-3β,11β,26-trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 26-Hydroxyfusidic acid; Sodium Fusidate EP Impurity E; Fusidic Acid Impurity E; (3α,4α,5α,11α,16β,17Z)-16-(Acetyloxy)-3,11,26-trihydroxy-4,8,14-trimethyl-18-norcholesta-17(20),24-dien-21-oic acid; 26-Hydroxy Fusidic Acid; (2Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-7-hydroxy-6-methylhept-5-enoic acid. Grade: ≥95%. CAS No. 2802408-15-5. Molecular formula: C31H48O7. Mole weight: 532.71. | |
| Fusidic acid EP Impurity F | Fusidic acid EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (2Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-acetoxy-3,11-dihydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methyl-7-oxohept-5-enoic acid. CAS No. 1415035-94-7. Molecular formula: C31H46O7. Mole weight: 530.69. Catalog: APB1415035947. |  |
| Fusidic Acid EP Impurity F | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z,24EZ)-16α-(Acetyloxy)-3β,11β-dihydroxy-4β,8,14-trimethyl-26-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 26-Oxofusidic acid; 27-oxo-Fusidic Acid; (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-26-oxo-29-nordammara-17(20),24-dien-21-oic acid; Sodium Fusidate EP Impurity F; Fusidic Acid Impurity F; (2Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methyl-7-oxohept-5-enoic acid. Grade: ≥95%. CAS No. 1415035-94-7. Molecular formula: C31H46O7. Mole weight: 530.70. | |
| Fusidic Acid EP Impurity G | A metabolite of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: A metabolite of fusidic acid. Synonyms: (Z)-2-((4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-11-hydroxy-4,8,10,14-tetramethyl-3-oxohexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; 3-Ketofusidic acid; ent-(17Z)-16α-(Acetyloxy)-11β-hydroxy-4β,8,14-trimethyl-3-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 3-Didehydrofusidic acid; (4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-11-hydroxy-3-oxo-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 11α,16β-dihydroxy-3-oxo-, 16-acetate, (Z)-; 3-Oxofusidic acid; 3-Keto Fusidic Acid; Fusidic Acid Impurity G; Sodium Fusidate EP Impurity G. Grade: ≥95%. CAS No. 4680-37-9. Molecular formula: C31H46O6. Mole weight: 514.69. | |
| Fusidic acid EP Impurity H | Fusidic acid EP Impurity H. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-acetoxy-3-hydroxy-4,8,10,14-tetramethyl-11-oxododecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methylhept-5-enoic acid. CAS No. 16711-91-4. Molecular formula: C31H46O6. Mole weight: 514.69. Catalog: APB16711914. | |
| Fusidic Acid EP Impurity H | A metabolite of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: A metabolite of fusidic acid. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-11-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 11-Didehydrofusidic acid; 11-Keto fusidic acid; 11-Monoketofusidic acid; (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-11-oxo-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,16β-dihydroxy-11-oxo-, 16-acetate, (Z)-; 11-Ketofusidic acid; 11-Oxofusidic acid; Fusidic Acid Impurity H; (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethyl-11-oxohexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; Sodium Fusidate EP Impurity H. Grade: ≥95%. CAS No. 16711-91-4. Molecular formula: C31H46O6. Mole weight: 514.69. | |
| Fusidic Acid EP Impurity I | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β,16β-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 16-epi-Deacetylfusidic acid; (3α,4α,8α,9β,11α,13α,14β,16α,17Z)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid; Deacetyl-16-epifusidic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16α-trihydroxy-, (Z)-; 16-Epideacetylfusidic acid; NSC 319631; Fusidic Acid Impurity I; (Z)-6-Methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16R)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoic acid; Sodium Fusidate EP Impurity I. Grade: ≥95%. CAS No. 5951-83-7. Molecular formula: C29H46O5. Mole weight: 474.68. | |
| Fusidic Acid EP Impurity J | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dieno-21(16β)-lactone; 16-epi-Deacetylfusidic acid 21,16-lactone; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16α-trihydroxy-, γ-lactone; Deacetyl-16-epifusidic acid γ-lactone; (3α,4α,8α,9β,11α,13α,14β,16α)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid, γ-lactone; Fusidic Acid Impurity J; (2aS,3S,4R,6aS,6bS,7R,8aR,11aR,12aS,12bS)-4,7-Dihydroxy-3,6a,12a,12b-tetramethyl-9-(4-methylpent-3-en-1-yl)-1,2,2a,3,4,5,6,6a,6b,7,8,8a,11a,12,12a,12b-hexadecahydro-10H-naphtho[2',1':4,5]indeno[2,1-b]furan-10-one; Sodium Fusidate EP Impurity J. Grade: ≥95%. CAS No. 13011-12-6. Molecular formula: C29H44O4. Mole weight: 456.66. | |
| Fusidic Acid EP Impurity K | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, γ-lactone; 16-Deacetylfusidic acid γ-lactone; ent-(17Z)-3β,11β-dihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dieno-21(16α)-lactone; Deacetylfusidic acid 21,16-lactone; 16-O-Deacetylfusidic acid lactone; (3α,4α,8α,9β,11α,13α,14β,16β)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid, γ-lactone; (2aS,3S,4R,6aS,6bS,7R,8aR,11aS,12aS,12bS)-4,7-Dihydroxy-3,6a,12a,12b-tetramethyl-9-(4-methylpent-3-en-1-yl)-1,2,2a,3,4,5,6,6a,6b,7,8,8a,11a,12,12a,12b-hexadecahydro-10H-naphtho[2',1':4,5]indeno[2,1-b]furan-10-one; Sodium Fusidate EP Impurity K; Fusidic Acid Impurity K. Grade: ≥95%. CAS No. 4701-54-6. Molecular formula: C29H44O4. Mole weight: 456.66. | |
| Fusidic Acid EP Impurity L | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-9(11),17(20),24-trien-21-oic acid; 9,11-Anhydrofusidic acid; (3α,4α,8α,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordammara-9(11),17(20),24-trien-21-oic acid; (Z)-2-((3R,4S,5S,8R,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethyl-1,2,3,4,5,6,7,8,10,12,13,14,15,16-tetradecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; 9,11-Anhydro Fusidic Acid; Fusidic Acid Impurity L; Sodium Fusidate EP Impurity L. Grade: ≥95%. CAS No. 74048-41-2. Molecular formula: C31H46O5. Mole weight: 498.70. | |
| Fusidic acid EP Impurity M | Fusidic acid EP Impurity M. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-acetoxy-3-hydroxy-4,8,10,14-tetramethyldodecahydro-1H-cyclopenta[a]phenanthren-17(2H,10H,14H)-ylidene)-6-methylhept-5-enoic acid. CAS No. 1013937-16-0. Molecular formula: C31H48O5. Mole weight: 500.71. Catalog: APB1013937160. | |
| Fusidic Acid EP Impurity M | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 11-Deoxyfusidic acid; (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordammara-17(20),24-dien-21-oic acid; 11-Deoxy Fusidic Acid; Fusidic Acid Impurity M; (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; Sodium Fusidate EP Impurity M. Grade: ≥95%. CAS No. 1013937-16-0. Molecular formula: C31H48O5. Mole weight: 500.71. | |
| Fusidic Acid EP Impurity O | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β,16α-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; Deacetylfusidic acid; 16-O-Deacetylfusidic acid; Fusidic Acid Impurity O; Sodium Fusidate EP Impurity O; (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, (Z)-; 16-Desacetylfusidic acid; (Z)-6-Methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoic acid. Grade: ≥95%. CAS No. 13090-91-0. Molecular formula: C29H46O5. Mole weight: 474.67. | |
| Fusidic Acid EP Impurity O sodium salt | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: An impurity of fusidic acid. Synonyms: 29-Nordammara-17(20),24-dien-21-oic acid, 3,11,16-trihydroxy-, monosodium salt, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-; 16-Deacetyl fusidic acid sodium salt; Sodium Fusidate EP Impurity O; Fusidic Acid EP Impurity O sodium salt; Sodium (Z)-6-methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoate; ent-(17Z)-3β,11β,16α-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid sodium salt; Deacetylfusidic acid sodium salt; 16-O-Deacetylfusidic acid sodium salt. Grade: ≥95%. CAS No. 55601-53-1. Molecular formula: C29H45NaO5. Mole weight: 496.65. | |
| Fusidic Acid Hemihydrate | Fusidic Acid Hemihydrate. Uses: For analytical and research use. Group: Api standards; pharmaceutical toxicology. Alternative Names: Fusidic acid hemihydrate,Fenoprofen 1,3-Butylene Glycol Esters (Mixture of Regio- and Stereoisomers), ent-(17Z)-16alpha-(Acetyloxy)-3beta,11beta-dihydroxy-4beta,8,14-trimethyl-18-nor-5beta,10alpha-cholesta-17(20),24-dien-21-oic acid hemihydrate, 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-3,11-dihydroxy-, hydrate (2:1), (3alpha,4alpha,8alpha,9beta,11alpha,13alpha,14beta,16beta,17Z)-. CAS No. 172343-30-5. IUPAC Name: (2Z)-2-[(3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12,13,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ylidene]-6-methylhept-5-enoic acid;hydrate. Molecular formula: 2C31H48O6.H2O. Mole weight: 1051.43. Catalog: APS172343305. SMILES: O.C[C@@H]1[C@H](O)CC[C@@]2(C)[C@H]1CC[C@@]3(C)[C@H]2[C@H](O)C[C@H]4\C(=C(/CCC=C(C)C)\C(=O)O)\[C@H](C[C@]34C)OC(=O)C.C[C@@H]5[C@H](O)CC[C@@]6(C)[C@H]5CC[C@@]7(C)[C@H]6[C@H](O)C[C@H]8\C(=C(/CCC=C(C)C)\C(=O)O)\[C@H](C[C@]78C)OC(=O)C. Format: Neat. Shipping: Room Temperature. | |
| Fusidic acid sodium salt | ?98% (TLC). Group: Fluorescence/luminescence spectroscopy. | |
| Fusidic acid sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C31H47NaO6. CAS No. 751-94-0. Prepack ID 71875523-1g. Molecular Weight 538.69. See USA prepack pricing. | |
| Fusidienol A | Fusidienol A is produced by the strain of Phoma spp. and Fusidium griseum. It is a Ras Farnesyl protein transferase inhibitor. Molecular formula: C16H12O6. Mole weight: 300.26. | |
| Fusion Inhibitory Peptide | Fusion Inhibitory Peptide (Z-D-Phe-Phe-Gly-OH, FIP, Virus Replication Inhibitory Peptide) is a potent inhibitor of the virus replication, by inhibiting the membrane fusing activity of a viral glycoprotein [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Z-D-Phe-Phe-Gly-OH; FIP; Virus Replication Inhibitory Peptide. CAS No. 75539-79-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-114437. | |
| Fusion PLA 3D Printing Filament | Fusion PLA 3D Printing Filament. Group: 3d printing materials. | |
| Fustin | Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone) is a potent amyloid β (Aβ) inhibitor. Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone) increases the expression of acetylcholine (ACh) levels, choline acetyltransferase (ChAT) activity, and ChAT gene induced by Aβ (1-42). Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone) decreases in acetyl cholinesterase (AChE) activity and AChE gene expression induced by Aβ (1-42). Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone) increases muscarinic M1 receptor gene expression and muscarinic M1 receptor binding activity. Fustinis ((±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone) can be used for Alzheimer's disease research [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-Fustin; 3,7,3',4'-Tetrahydroxyflavanone. CAS No. 20725-03-5. Pack Sizes: 1 mg. Product ID: HY-N8376. | |
| Futalosine | A new nucleoside analog, was isolated from a fermentation broth of Streptomyces sp. MK359-NF1. An antibiotic cancer inhibitor. Synonyms: 3-[1,5,6-Trideoxy-1-(1,6-dihydro-6-oxo-9H-purin-9-yl)-β-D-ribo-heptofuranuronoyl]benzoic Acid. CAS No. 210644-32-9. Molecular formula: C19H18N4O7. Mole weight: 414.37. | |
| Futalosine | A new nucleoside analog, was isolated from a fermentation broth of Streptomyces sp. MK359-NF1. Group: Biochemicals. Alternative Names: 3-[1,5,6-Trideoxy-1-(1,6-dihydro-6-oxo-9H-purin-9-yl)- β -D-ribo-heptofuranuronoyl] benzoic Acid. Grades: Highly Purified. CAS No. 210644-32-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| futalosine hydrolase | This enzyme, which is specific for futalosine, catalyses the second step of a novel menaquinone biosynthetic pathway that is found in some prokaryotes. Group: Enzymes. Synonyms: futalosine nucleosidase; MqnB. Enzyme Commission Number: EC 3.2.2.26. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3980; futalosine hydrolase; EC 3.2.2.26; futalosine nucleosidase; MqnB. Cat No: EXWM-3980. | |
| Futibatinib | Futibatinib (TAS-120) is an orally bioavailable, highly selective, and irreversible FGFR inhibitor, with IC 50 s of 3.9, 1.3, 1.6, and 8.3 nM for FGFR 1-4, respectively. Futibatinib inhibits mutant and wild-type FGFR2 with similar IC 50 s (wild-type FGFR2=0.9?nM; V5651=1-3?nM; N550H=3.6?nM; E566G=2.4?nM) [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAS-120. CAS No. 1448169-71-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100818. | |
| Futibatinib | Futibatinib is an orally bioavailable, selective and irreversible inhibitor of fibroblast growth factor receptors (FGFRs), displaying antineoplastic activity. It inhibits FGFR-mediated signal transduction and tumor cell proliferation. Synonyms: 1-[(3S)-3-[4-amino-3-[2-(3,5-dimethoxyphenyl)ethynyl]-1-pyrazolo[3,4-d]pyrimidinyl]-1-pyrrolidinyl]-2-propen-1-one; 1-[(3S)-3-[4-amino-3-[2-(3,5-dimethoxyphenyl)ethynyl]pyrazolo[3,4-d]pyrimidin-1-yl]pyrrolidin-1-yl]prop-2-en-1-one. Grade: ≥ 98 %. CAS No. 1448169-71-8. Molecular formula: C22H22N6O3. Mole weight: 418.45. | |
| Futoquinol | Futoquinol is a neolignan isolated from the dried aerial parts of Piper kadsura (Piperaceae). Futoquinol potently inhibits NO production in microglia cells. Futoquinol has anti-neuroinflammatory activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 28178-92-9. Pack Sizes: 1 mg. Product ID: HY-N3915. | |
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