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One of the isotope labelled form of Famotidine, which is a histamine H2 receptor antagonist that inhibits stomach acid production. Synonyms: 3-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]-N-(aminosulfonyl)propanimidamide-13C4-d3. Molecular formula: C14[13C]4H16D3Cl2NO4. Mole weight: 391.24.
Felodipine 3,5-dimethyl ester
Felodipine 3,5-dimethyl ester. Group: Biochemicals. Alternative Names: 4-(2,3-Dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid 3,5-dimethyl ester. Grades: Highly Purified. CAS No. 91189-59-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C17H17Cl2NO4. US Biological Life Sciences.
Worldwide
Felodipine EP Impurity B
Felodipine EP Impurity B. Uses: For analytical and research use. Alternative Names: dimethyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. CAS No. 91189-59-2. Molecular formula: C17H17Cl2NO4. Mole weight: 370.23. Catalog: APB91189592.
Felodipine EP Impurity C
Felodipine EP Impurity C. Uses: For analytical and research use. Alternative Names: diethyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. CAS No. 79925-38-5. Molecular formula: C19H21Cl2NO4. Mole weight: 398.28. Catalog: APB79925385.
Felodipine Impurity 1
Felodipine Impurity 1. Uses: For analytical and research use. Molecular formula: C18H18Cl2N2O5. Mole weight: 413.25. Catalog: APB10520.
Felodipine Impurity 10
Felodipine Impurity 10. Uses: For analytical and research use. Alternative Names: 3-ethyl 5-methyl 4-(3,4-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. Molecular formula: C18H19Cl2NO4. Mole weight: 383.07. Catalog: APB06186.
Felodipine Impurity 4
Felodipine Impurity 4. Uses: For analytical and research use. Alternative Names: 4-(2,3-dichlorophenyl)-3-(ethoxycarbonyl)-5-(methoxycarbonyl)-2,6-dimethylpyridine 1-oxide. Molecular formula: C18H17Cl2NO5. Mole weight: 397.05. Catalog: APB06189.
Felodipine Impurity 5
Felodipine Impurity 5. Uses: For analytical and research use. Alternative Names: (Z)-methyl 2-(2,3-dichlorobenzylidene)-3-oxobutanoate. CAS No. 68064-69-7. Molecular formula: C12H10Cl2O3. Mole weight: 272.00. Catalog: APB68064697.
Felodipine Impurity 6
Felodipine Impurity 6. Uses: For analytical and research use. Alternative Names: 4-(2,3-dichlorophenyl)-5-(methoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylic acid. CAS No. 123853-39-4. Molecular formula: C16H15Cl2NO4. Mole weight: 355.04. Catalog: APB123853394.
Felodipine Impurity 7
Felodipine Impurity 7. Uses: For analytical and research use. Alternative Names: 4-(2,3-dichlorophenyl)-5-(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine-3-carboxylic acid. Molecular formula: C17H17Cl2NO4. Mole weight: 369.05. Catalog: APB06188.
Felodipine Impurity 8
Felodipine Impurity 8. Uses: For analytical and research use. Alternative Names: 3-ethyl 5-methyl 4-(2-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. CAS No. 39562-06-6. Molecular formula: C18H20ClNO4. Mole weight: 349.11. Catalog: APB39562066.
Felodipine Impurity 9
Felodipine Impurity 9. Uses: For analytical and research use. Alternative Names: 3-ethyl 5-methyl 4-(2,4-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. Molecular formula: C18H19Cl2NO4. Mole weight: 383.07. Catalog: APB06187.
A metabolite of Felodipine. Felodipine is a calcium channel blocker. Synonyms: 4-(2,3-dichlorophenyl)-5-(ethoxycarbonyl)-2-(hydroxymethyl)-6-methylnicotinic acid. Grade: > 95%. Molecular formula: C17H15Cl2NO5. Mole weight: 384.22.
Felodipine Metabolite Lactone
A metabolite of Felodipine. Felodipine is a calcium channel blocker. Synonyms: Furo[3,?4-b]?pyridine-3-carboxylic acid, 4-(2,?3-dichlorophenyl)?-1,?4,?5,?7-tetrahydro-2-methyl-5-oxo-, ethyl ester. Grade: > 95%. CAS No. 85825-42-9. Molecular formula: C17H13Cl2NO4. Mole weight: 366.20.
Felodipine Related Compound A
Felodipine Related Compound A. Uses: For analytical and research use. CAS No. 96382-71-7. Mole weight: 382.24. Catalog: AP96382717.
Felodipine (Standard)
Felodipine (Standard) is the analytical standard of Felodipine. This product is intended for research and analytical applications. Felodipine, a dihydropyridine, is a potent, vasoselective calcium channel antagonist. Felodipine lowers blood pressure (BP) by selective action on vascular smooth muscle, especially in the resistance vessels. Felodipine, an anti-hypertensive agent, induces autophagy. Felodipine can cross the blood-brain barrier[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 72509-76-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0309R.
Felypressin
Felypressin is a Vasopressin 1 agonist and has effects at all Arginine vasopressin receptor 1As. It is a non-catecholamine vasoconstrictor that is chemically related to vasopressin. It is a synthetic hormone characterized by vasoconstrictor properties and is widely used in dental procedures. It has been added to local anesthetic solutions to increase the duration of the anesthetic effect and decrease the risk of toxicity during dental procedures. It is a vasoconstrictor with reduced antidiuretic activity. Synonyms: Octapressin; Octopressin; Phelypressin; Phenylalanine Lysine Vasopressin; PLV-2; Vasopressin, Phenylalanyl-Lysyl; Vasopressin, 2-L-phenylalanine-8-L-lysine-; 2-L-Phenylalanine-8-L-lysinevasopressin; Oxytocin, 2,3-bis(phenylalanine)-8-lysine-; Vasopressin, 2-(phenylalanine)-8-lysine; 2-Phenylalanine-8-lysine-vasopressin; H-Cys(1)-Phe-Phe-Gln-Asn-Cys(1)-Pro-Lys-Gly-NH2; L-cysteinyl-L-phenylalanyl-L-phenylalanyl-L-glutaminyl-L-asparagyl-L-cysteinyl-L-prolyl-L-lysyl-glycinamide (1->6)-disulfide. Grade: >98%. CAS No. 56-59-7. Molecular formula: C46H65N13O11S2. Mole weight: 1040.22.
Felypressin
Felypressin (PLV-2) is a non-catecholamine vasoconstrictor and a vasopressin 1 agonist. Felypressin is widely used in dental procedures[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PLV-2. CAS No. 56-59-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-A0182.
Felypressin Acetate
Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: Vasopressin, 2-L-phenylalanine-8-L-lysine-, acetate (salt); 2-L-Phenylalanine-8-L-lysinevasopressin Acetate (Salt); 2,3-Bis(phenylalanine)-8-lysineoxytocin Acetate; 2-(Phenylalanine)-8-lysinevasopressin Acetate; 2-Phenylalanine-8-lysine-vasopressin Acetate; L-cysteinyl-L-phenylalanyl-L-phenylalanyl-L-glutaminyl-L-asparagyl-L-cysteinyl-L-prolyl-L-lysyl-glycinamide (1->6)-disulfide acetic acid; H-Cys(1)-Phe-Phe-Gln-Asn-Cys(1)-Pro-Lys-Gly-NH2.CH3CO2H. Grade: ≥95%. CAS No. 914453-97-7. Molecular formula: C46H65N13O11S2.xC2H4O2. Mole weight: 1100.3.
Felypressin Impurity A
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: H-Cys(N-ethylacetamide)-Phe-Phe-Gln-Asn-Cys(N-ethylacetamide)-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C52H77N15O13S2. Mole weight: 1084.47.
Felypressin Impurity B
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: H-Cyclo(Cys-Phe-Phe-Gln-Asn-Cys)-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C46H66N12O12S2. Mole weight: 1043.29.
Felypressin Impurity C
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: Cyclo[H-Cyclo(Cys-Phe-Phe-Gln-Asn-Cys)]-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C92H130N26O22S4. Mole weight: 2080.57.
Felypressin Impurity D
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: Cyclo[H-Cyclo(Cys-Phe-Phe-Gln-Asn-Cys)]-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C92H130N26O22S4. Mole weight: 2080.57.
Felypressin Impurity E
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: Aceyl-Cyclo(Cys-Phe-Phe-Gln-Asn-Cys)-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C48H67N13O12S2. Mole weight: 1082.33.
Felypressin Impurity F
An impurity of Felypressin. Felypressin is a non-catecholamine vasoconstrictor that is chemically related to vasopressin, the posterior pituitary hormone. Synonyms: H-Cyclo(Cys-Phe-Phe-Gln-Asn-Cys)-Pro-Lys-Gly-Nh2. Grade: > 95%. Molecular formula: C46H64N12O12S2. Mole weight: 1041.27.
Felzartamab
Felzartamab (MOR-202) is a human monoclonal antibody that targets CD38 and can be used in multiple myeloma research[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: MOR-202. CAS No. 2197112-39-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P99616.
FEMA 4774
FEMA 4774 is a positive allosteric modulator of taste receptors T1R2 and T1R3 and enhancer of sucrose sweetness. Synonyms: FEMA4774; FEMA-4774; Fema No. 4774; S9632; S-9632; S 9632. CAS No. 1359963-68-0. Molecular formula: C19H25N3O4. Mole weight: 359.42.
FeMnCoCr High-Entropy Alloy Spherical Powder
We are engaged in the development, production and sales of FeMnCoCr High Entropy Alloy (HEA) spherical powders and offer personalized customization services for high-quality metal powders. FeMnCoCr high entropy alloy spherical powder is a new type of alloy with very unique properties. The different dimensions and the bonding between the elements lead to an alloy with lattice distortion and slow diffusion effects.
FeMoCoCr High-Entropy Alloy Spherical Powder
We are engaged in the development, production, and sales of FeMoCoCr high entropy alloy spherical powder and provide personalized customization service for high-quality metal powder. FeMoCoCr high entropy alloy spherical powder is a new alloy with very unique properties.
FEN1-IN-1
FEN1-IN-1 (compound 1) is a small molecule flap endonuclease 1 (FEN1) inhibitor with antitumor activity. FEN1-IN-1 binds to the active site of FEN1 and partly achieves inhibition by the co-ordination of Mg2+ ions. FEN1-IN-1 initiaties a DNA damage response and activates the ATM checkpoint signalling pathway, the phosphorylation of histone H2AX and the ubiquitination of FANCD2 in mammalian cells. FEN1-IN-1 is promising for research of cancers[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 824983-91-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-123834.
FEN1-IN-2
FEN1-IN-2 (compound 20) is a flap endonuclease 1 (FEN1) inhibitor, with IC50 values of 3 nM and 226 nM for FEN1 and XPG, respectively[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 824983-94-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122695.
FEN1-IN-4
FEN1-IN-4 (Compound 2) is a human flap endonuclease-1 (hFEN1) inhibitor[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1995893-58-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-136485.
FEN1-IN-4
FEN1-IN-4 is a human flap endonuclease-1 (hFEN1) inhibitor. Synonyms: FEN1 Inhibitor C2; JUN93587; 1-(cyclopropylmethyl)-3-hydroxyquinazoline-2,4(1H,3H)-dione. CAS No. 1995893-58-7. Molecular formula: C12H12N2O3. Mole weight: 232.24.
FEN1-IN-7
FEN1-IN-7 (compound 16) is a selective inhibitor of Flap endonuclease-1 (FEN1, IC50=18 nM), involving in mammalian cells to repair DNA damage. FEN1-IN-7 also targets to related endonuclease, xeroderma pigmentosum G (XPG) with an IC50 value of 3.04 μM. FEN1-IN-7 increases the cellular sensitivity of cancer cells to potent DNA alkylating agents or methylating agents[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 824983-90-6. Pack Sizes: 1 mg. Product ID: HY-153792.
FEN1-IN-SC13
FEN1-IN-SC13 is a potent DNA fragmentation endonuclease 1 (FEN1) inhibitor with antitumor activity. FEN1-IN-SC13 interferes with DNA replication and repair in vitro and in cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2098776-03-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145758.
Fenaclon
Fenaclon is an anticonvulsant used to treat epilepsy. Synonyms: Propanamide, 3-chloro-N-(2-phenylethyl)-; Propionamide, 3-chloro-N-phenethyl-; 3-Chloro-N-phenethylpropionamide; Fenaclonum; Fenakon; Phenacon; Phenacone; β-Chloro-N-phenethylpropionamide; β-Chloropropio-N-phenylethylamide. Grade: ≥95%. CAS No. 306-20-7. Molecular formula: C11H14ClNO. Mole weight: 211.69.
Fenamidone
Fenamidone is a fungicide effective against Oomycete diseases. Uses: Fungicides, industrial. Synonyms: (S)-1-anilino-4-methyl-2-methylthio-4-phenylimidazolin-5-one. CAS No. 161326-34-7. Molecular formula: C17H17N3OS. Mole weight: 311.4.
Fenamidone Metabolite
It is a metabolite of fennanone. Synonyms: (S)-5-Methyl-5-phenyl-3-phenylamino imidazoli-dine-2,4-dione. CAS No. 332855-88-6. Molecular formula: C16H15N3O2. Mole weight: 281.31.
Fenamiphos
Systemic broad spectrum nematocide with anticholinesterase activity. Nematocide. Group: Biochemicals. Alternative Names: N- (1-Methylethyl) phosphoramidic Acid Ethyl 3-Methyl-4-(methylthio)phenyl Ester; Isopropyl phosphoramidic Acid Ethyl 4-(Methylthio)-m-tolyl Ester; B 68138; BAY 68138; Bayer 68138; Ethyl 3-Methyl-4-(methylthio)phenyl (1-Methylethyl) phosphoramidate; Ethyl 4-(Methylthio)-m-tolyl Isopropyl phosphoramidate; Fenamifos; Fenamithion; Nemacur; Nemacur P; Phenamiphos. Grades: Highly Purified. CAS No. 22224-92-6. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Fenamiphos 90%
Fenamiphos 90%. Group: Biochemicals. Alternative Names: N- (1-Methylethyl) phosphoramidic acid ethyl 3-methyl-4-(methylthio)phenyl ester; Isopropyl phosphoramidic acid ethyl 4-(methylthio)-m-tolyl ester; B 68138. Grades: Highly Purified. CAS No. 22224-92-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C13H22NO3PS. US Biological Life Sciences.
Worldwide
Fenamiphos Sulfone
A toxic metabolite of Fenamiphos, a pesticide in fruits and vegetables. Group: Biochemicals. Alternative Names: N- (1-Methylethyl) phosphoramidic Acid Ethyl 3-Methyl-4-(methylsulfonyl)phenyl Ester; Isopropyl phosphoramidic Acid Ethyl 4-(Methylsulfonyl)-m-tolyl Ester; BAY 68138 Sulfone; O-Ethyl O- [4- (Methylsulfonyl) -m-tolyl] isopropyl phosphoramidate. Grades: Highly Purified. CAS No. 31972-44-8. Pack Sizes: 250mg. US Biological Life Sciences.
Worldwide
Fenamiphos Sulfoxide
A toxic metabolite of Fenamiphos, a pesticide in fruits and vegetables. Group: Biochemicals. Alternative Names: N- (1-Methylethyl) phosphoramidic Acid Ethyl 3-Methyl-4-(methylsulfinyl)phenyl Ester; Isopropyl phosphoramidic Acid Ethyl 4-(Ethylsulfinyl)-m-tolyl Ester; Bay 68138 Sulfoxide; O-Ethyl O- [4- (Methylsulfinyl) -m-tolyl] isopropyl phosphoramidate. Grades: Highly Purified. CAS No. 31972-43-7. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
Fe nanopowder
Fe nanopowder. Purity: 99.5 %.
Fenazaquin
Fenazaquin. Group: Biochemicals. Alternative Names: GWN 1708; Magister; Magus; Phenazaquin; Pride Ultra; XDE 436; EL 436; Fenaza; Fenazachin; 4- [2- [4- (1, 1-Dimethylethyl) phenyl] ethoxy] quinazoline. Grades: Highly Purified. CAS No. 120928-09-8. Pack Sizes: 250mg. Molecular Formula: C20H22N2O, Molecular Weight: 306.399999999999. US Biological Life Sciences.
Worldwide
Fenazox
Amfenac is a COX inhibitor with IC50 of 0.25 and 0.15 μM for COX-1 and COX-2, respectively. Synonyms: Amfenac sodium hydrate; Sodium 2-(2-amino-3-benzoylphenyl)acetate hydrate. Grade: 98.0%. CAS No. 61618-27-7. Molecular formula: C15H12NO3·H2O·Na. Mole weight: 295.26.
Fe-Nb Alloy Powder
This product is a binary alloy powder of ferrum and niobium.
Fenbendazole. Group: Biochemicals. Alternative Names: N-[6-(Phenylthio)-1H-benzimidazol-2-yl]carbamic acid methyl ester. Grades: Highly Purified. CAS No. 43210-67-9. Pack Sizes: 10g, 25g, 50g, 100g. Molecular Formula: C15H13N3O2S, Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures. US Biological Life Sciences.
Worldwide
Fenbendazole
Fenbendazole is a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites with an IC50 of about 0.01 μg/ml. Uses: Antinematodal agents. Synonyms: fenbendazole; 43210-67-9; Panacur; Fenbendazol; Phenbendasol; Fenbendazolum; Hoe 881v; Safe-Guard; Methyl 5-(phenylthio)-2-benzimidazolecarbamate; Safe-quard; Panacur aquasol; HOE-881v; 2-(Methoxycarbonylamino)-5-(phenylthio)benzimidazole; Fenbendazole (Panacur); CCRIS 7309; methyl (6-(phenylthio)-1H-benzo[d]imidazol-2-yl)carbamate; Fenbendazol [INN-Spanish]; Fenbendazolum [INN-Latin]; EINECS 256-145-7; methyl [5-(phenylsulfanyl)-1H-benzimidazol-2-yl]carbamate; methyl N-(6-phenylsulfanyl-1H-benzimidazol-2-yl)carbamate; NSC-757824; UNII-621BVT9M36; Fenbendazole for veterinary use; HOE-881Y; DTXSID0040672; methyl N-[5-(phenylsulfanyl)-1H-1,3-benzodiazol-2-yl]carbamate; CHEBI:77092; Carbamic acid, (5-(phenylthio)-1H-benzimidazol-2-yl)-, methyl ester; Methyl (5-(phenylthio)-1H-benzimidazol-2-yl)carbamate; 621BVT9M36; 5-(phenylthio)-2-benzimidazolecarbamic acid methyl ester; Fenbendazole (USP/INN); 2-Benzimidazolecarbamic acid, 5-(phenylthio)-, methyl ester. Grade: >98%. CAS No. 43210-67-9. Molecular formula: C15H13N3O2S. Mole weight: 299.35.
Fenbendazole
5g Pack Size. Group: Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C15H13N3O2S. CAS No. 43210-67-9. Prepack ID 10896222-5g. Molecular Weight 299.35. See USA prepack pricing.
Fenbendazole
Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent and acts on helminthes primarily by binding to tubulin and disrupting the tubulin microtubule equilibrium. Fenbendazole stabilizes the transcriptional activator HIF-1α. Fenbendazole possesses an efficient anti-proliferative activity and induces apoptosis. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 43210-67-9. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 500 mg. Product ID: HY-B0413.
Fenbendazoleamine
A derivative of Fenbendazole. Fenbendazole is an anthelmintic agent. Fenbendazole reduces plasma total oxidant status and alters precursor B lymphocytes and splenic cell proliferation. Synonyms: 5-(Phenylthio)-1H-benzo[d]imidazol-2-amine; 5-Phenylthio-2-aminobenzimidazole; Fbz-NH2; Fenbendazole Impurity 1. Grade: 95%. CAS No. 53065-28-4. Molecular formula: C13H11N3S. Mole weight: 241.31.
Fenbendazole-amine hydrochloride
Fenbendazole-amine hydrochloride is an impurity of Fenbendazole. Fenbendazole is an anthelmintic agent that reduces plasma total oxidant status and alters precursor B lymphocytes and splenic cell proliferation. Synonyms: 5-Phenylsulfanyl-1H-benzoimidazol-2-ylamine hydrochloride. CAS No. 1448346-29-9. Molecular formula: C13H12ClN3S. Mole weight: 277.77.
Fenbendazole-amine Hydrochloride
Fenbendazole-amine Hydrochloride is a derivative of Fenbendazole (F246750) which is an anthelmintic. Group: Biochemicals. Grades: Highly Purified. CAS No. 1448346-29-9. Pack Sizes: 10mg, 100mg. Molecular Formula: C13H13ClN4S, Molecular Weight: 292.79. US Biological Life Sciences.
Worldwide
Fenbendazole-Amine Sulfoxide
Fenbendazole-Amine Sulfoxide is a highly effective inhibitor of the helminth-specific enzyme, fumarate reductas in Ascaris suum. Also, it inhibits the polymerization of tubulin into microtubules in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 69489-26-5. Pack Sizes: 10mg, 25mg. Molecular Formula: C13H11N3OS, Molecular Weight: 257.31. US Biological Life Sciences.
Worldwide
Fenbendazole-d3
Fenbendazole-d3. Uses: For analytical and research use. CAS No. 1228182-47-5. Mole weight: 302.37. Catalog: AP1228182475.
Fenbendazole-d3
Fenbendazole-d3 is a deuterium labeled Fenbendazole. Fenbendazole-d3 is a HIF-1α agonist and activates the HIF-1α-related GLUT1 pathway. Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1228182-47-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-B0413S.
Fenbendazole-[d3]
Fenbendazole-[d3] is the labelled analogue of Fenbendazole. Fenbendazole is an anthelmintic agent that reduces plasma total oxidant status and alters precursor B lymphocytes and splenic cell proliferation. Synonyms: Fenbendazole-D3; (5-Phenylsulfanyl-1H-benzoimidazol-2-yl)-carbamic acid methyl-D3 ester; N-[6-(Phenylthio)-1H-benzimidazol-2-yl]carbamic Acid Methyl-d3 Ester; 2-[(Methoxy-d3)carbonylamino]-5-(phenylthio)benzimidazole; Axilur-d3; Fenbendazol-d3; Fenbion-d3; (Methyl-d3) 5-(Phenylthio)-2-benzimidazolecarbamate; Methyl-d3 [5-(Phenylthio)-1H-benzimidazol-2-yl]carbamate; Panacur-d3. Grade: ≥98%; ≥99% atom D. CAS No. 1228182-47-5. Molecular formula: C15H10D3N3O2S. Mole weight: 302.37.
Fenbendazole Hydroxide
Fenbendazole Hydroxide is an impurity of Fenbendazole. Fenbendazole is an anthelmintic agent that reduces plasma total oxidant status and alters precursor B lymphocytes and splenic cell proliferation. Synonyms: methyl N-[6-(4-hydroxyphenyl)sulfanyl-1H-benzimidazol-2-yl]carbamate. CAS No. 72447-64-4. Molecular formula: C15H13N3O3S. Mole weight: 315.347.
Fenbendazole Related Compound B
Fenbendazole Related Compound B. Uses: For analytical and research use. CAS No. 20367-38-8. Mole weight: 225.63. Catalog: AP20367388.
Fenbendazole Sulfone
A derivative of Fenbendazole. Fenbendazole is an anthelmintic agent. Reduces plasma total oxidant status and alters precursor B lymphocytes and splenic cell proliferation. Synonyms: [5-(Phenylsulfonyl)-1H-benzimidazol-2-yl]carbamic Acid Methyl Ester. Grade: > 95%. CAS No. 54029-20-8. Molecular formula: C15H13N3O4S. Mole weight: 331.35.
Fenbendazole Sulfone
Source: Synthetic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Fenbendazole sulfone-d3
Fenbendazole sulfone-d3. Uses: For analytical and research use. CAS No. 1228182-49-7. Mole weight: 334.36. Catalog: AP1228182497.
Fenbendazole sulfone-[d3]
Fenbendazole sulfone-[d3] is the labelled analogue of Fenbendazole sulfone, which is a metabolite of Fenbendazole. Synonyms: (5-Benzenesulfonyl-1H-benzoimidazol-2-yl)-carbamic acid methyl-D3 ester; Fenbendazole sulfone-D3. Grade: 95% by HPLC; 98% atom D. CAS No. 1228182-49-7. Molecular formula: C15H10D3N3O4S. Mole weight: 334.36.
Anti-inflammatory. Group: Biochemicals. Alternative Names: γ-Oxo[1,1-biphenyl]-4-butanoic Acid; 3- (4-Phenylbenzoyl) propionic Acid; 4-(Biphenyl-4-yl)-4-oxobutanoic Acid; Bufemid; CL 82204; Cinopal; Cinopol; Lederfen; Napanol. Grades: Highly Purified. CAS No. 36330-85-5. Pack Sizes: 10mg, 100mg, 1g. Molecular Formula: C16H14O3, Form: White. US Biological Life Sciences.
Worldwide
Fenbufen
Fenbufen is a non-steroidal anti-inflammatory synthetic active reagent. Uses: A non-steroidal anti-inflammatory drug. Synonyms: 4-oxo-4-(4-phenylphenyl)butanoic acid. Grade: > 98 %. CAS No. 36330-85-5. Molecular formula: C16H14O3. Mole weight: 254.28.
Fenbufen-d9
Anti-inflammatory. Group: Biochemicals. Alternative Names: γ-Oxo[1,1'-biphenyl-d9]-4-butanoic Acid; 3-(4-Phenylbenzoyl-d9)propionic Acid; 4-(Biphenyl-d9-4-yl)-4-oxobutanoic Acid; Bufemid-d9; CL 82204-d9; Cinopal-d9; Cinopol-d9; Lederfen-d9; Napanol-d9. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Fenbutrazate
Fenbutrazate is a derivative of Phenmetrazine. Fenbutrazate is a psychostimulant used as an anorexigen (appetite suppressant). Group: Biochemicals. Alternative Names: 2-Phenylbutyric Acid 2-(3-Methyl-2-phenylmorpholino)ethyl Ester; Fenbutrazatum; Nethanol; Phenbutrazate; Phenbutrazatum; 2-(3-Methyl-2-phenylmorpholino)ethyl 2-Phenylbutyrate; α-Ethylbenzeneacetic Acid 2-(3-Methyl-2-phenyl-4-morpholinyl)ethyl Ester. Grades: Highly Purified. CAS No. 4378-36-3. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Fenchlorphos
Fenchlorphos is an acetylcholinesterase inhibitor used as an organophosphorus pesticide. Synonyms: Fenchlorfos. CAS No. 299-84-3. Molecular formula: C8H8Cl3O3PS. Mole weight: 321.55.