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| Product | Description | |
|---|---|---|
| Undecylenate sodium | Undecylenate SodiumIt is an organic compound belonging to the class of carboxylates. It is formed by the reaction of undecylenic acid and sodium hydroxide. Undecylenate SodiumIt has a variety of applications in the cosmetic and personal care industries, especially as an antifungal agent in products such as face creams, lotions and shampoos. In addition, it can be used as a preservative in various formulations. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 3398-33-2. Pack Sizes: 5 g; 10 g; 25 g. Product ID: HY-W127452. |  |
| Undecylenic Acid | Undecylenic Acid. CAS No. 112-38-9. FEMA No. 3247. Kosher: Y. VIGON Item # 500636. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Undecylenic Acid | Undecylenic Acid. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| Undecylenic monoglyceride | Undecylenic monoglyceride |  Sarchem Laboratories New Jersey NJ |
| Undecylenyl b-D-maltoside | Undecylenyl b-D-maltoside is a multifunctional bioactive compound fostering targeted drug delivery systems and studying sundry diseases. By ingeniously formulating drugs designed to study cancer, bacterial infections and dermatological disorders, Undecylenyl b-D-maltoside emerges as an indispensable ingredient. Molecular formula: C23H42O11. Mole weight: 494.57. |  |
| Undecyl hydrogen phthalate | Undecyl hydrogen phthalate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-[(undecyloxy)carbonyl]benzoic acid, 51622-03-8, Undecyl hydrogen phthalate, AC1L2VRK, SureCN183761, AC1Q67BE, 2-undecoxycarbonylbenzoic acid, CTK4J4583, EINECS 257-323-7, AR-1D6360, AG-F-74970, 1,2-Benzenedicarboxylicacid, 1-undecyl ester, 1,2-Benzenedicarboxylicacid, monoundecyl ester (9CI); Hydrogen undecyl phthalate; Monoundecylphthalate. Product Category: Heterocyclic Organic Compound. CAS No. 51622-03-8. Molecular formula: C19H28O4. Mole weight: 320.423220 [g/mol]. Purity: 0.96. IUPACName: 2-undecoxycarbonylbenzoic acid. Density: 1.05g/cm³. Product ID: ACM51622038. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Undecylphosphonic Acid | Undecylphosphonic Acid. Group: Self assembly and contact printing materials. CAS No. 5137-69-9. Product ID: undecylphosphonic acid. Molecular formula: 236.29g/mol. Mole weight: C11H25O3P. CCCCCCCCCCCP(=O)(O)O. InChI=1S / C11H25O3P / c1-2-3-4-5-6-7-8-9-10-11-15 (12, 13) 14 / h2-11H2, 1H3, (H2, 12, 13, 14). GKIQHTGBORJXKZ-UHFFFAOYSA-N. |  |
| Undecylphosphonic Acid, ≥98% | Undecylphosphonic Acid, ≥98%. Group: Self assembly and contact printing. CAS No. 5137-69-9. Product ID: undecylphosphonic acid. Molecular formula: 236.29g/mol. Mole weight: C11H25O3P. CCCCCCCCCCCP(=O)(O)O. InChI=1S / C11H25O3P / c1-2-3-4-5-6-7-8-9-10-11-15 (12, 13) 14 / h2-11H2, 1H3, (H2, 12, 13, 14). GKIQHTGBORJXKZ-UHFFFAOYSA-N. | |
| Undecylprodigiosin | Undecylprodigiosin is a prodigiosin antibiotic. Grades: >98%. CAS No. 52340-48-4. Molecular formula: C25H35N3O. Mole weight: 393.56. | |
| Undecylprodigiosin (Undecylprodiginine, Prodigiosin 25C) | Tripyrrolic pigment like prodigiosin. Antimalarial agent. Apoptosis inducer. Anticancer agent with multiple modes of action. Immunosuppressant in non-toxic concentrations. Bone resorption inhibitor. Antiulcer agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 56247-02-0, 52340-48-4 (parent). Pack Sizes: 250ug, 1mg. US Biological Life Sciences. |  Worldwide |
| Undecyl sulfuric acid | Undecyl sulfuric acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Undecylsulfate, Undecyl sulfate, Undecyl sulfuric acid, Sodium n-undecyl sulfate, n-Undecyl sulfate sodium salt, 1-Undecanol, hydrogen sulfate, 1072-24-8 (Sodium), CID123213, 4297-99-8. Product Category: Heterocyclic Organic Compound. CAS No. 4297-99-8. Molecular formula: C11H24O4S. Mole weight: 252.370860 [g/mol]. Purity: 0.96. IUPACName: undecyl hydrogen sulfate. Product ID: ACM4297998. Alfa Chemistry ISO 9001:2015 Certified. | |
| Undecyltrichlorosilane | Undecyltrichlorosilane. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UNDECYLTRICHLOROSILANE, AKOS015914763, I14-41306, 18052-07-8. Product Category: Halosilane. Appearance: Transparent liquid. CAS No. 18052-07-8. Molecular formula: C11H23Cl3Si. Mole weight: 289.75 g/mol. Purity: 0.97. IUPACName: trichloro(undecyl)silane. Density: 1.02 g/cm³. Product ID: ACM18052078. Alfa Chemistry ISO 9001:2015 Certified. | |
| undermodified hydroxywybutosine | Undermodified Hydroxywybutosine, a nucleoside analog, demonstrates potential as a chemotherapeutic agent in the biomedical industry. It selectively targets cancer cells, leaving healthy cells unscathed due to its ability to suppress protein synthesis, thereby obstructing growth and replication. Synonyms: 1H-Imidazo[1,2-a]purine-7-butanoic acid, a-amino-4,9-dihydro-b-hydroxy-4,6-dimethyl-9-oxo-1-b-D-ribofuranosyl-. CAS No. 84270-20-2. Molecular formula: C13H16N6O4. Mole weight: 452.42. | |
| Unesbulin | Unesbulin (PTC596) is an orally active and selective B-cell-specific Moloney murine leukemia virus integration site 1 ( BMI-1 ) inhibitor. Unesbulin downregulates MCL-1 and induces p53-independent mitochondrial apoptosis in acute myeloid leukemia (AML) cells. Unesbulin has anti-leukemic activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PTC596. CAS No. 1610964-64-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112041. | |
| Unguinol | Unguinol is a metabolite of the fungi Aspergillus unguis and Aspergillus nidulans. It has been found to be an active growth promotant in animals, in particular, monogastric animals such as chickens. It is an inhibitor of pyruvate phosphate dikinase (PPDK). Synonyms: 3,8-Dihydroxy-1,9-dimethyl-6-(1-methyl-1-propenyl)-11H-dibenzo[b,e][1,4]dioxepin-11-one; Yasimin. Grades: ≥95%. CAS No. 36587-59-4. Molecular formula: C19H18O5. Mole weight: 326.34. | |
| Unguisin A | Unguisin A is a cyclic heptapeptide produced by the strain of the marine fungus E. unguis whose structure is comprised of amino acids and GABA. It binds to phosphate, pyrophosphate, and chloride but has no effect on chloride transport in a liposome-based assay. Synonyms: cyclo(D-alanyl-D-tryptophyl-4-aminobutanoyl-D-alanyl-D-valyl-L-phenylalanyl-D-valyl). Grades: >95% by HPLC. CAS No. 226956-06-5. Molecular formula: C40H54N8O7. Mole weight: 758.90. | |
| Unguisin B | Unguisin B is a cyclic heptapeptide produced by the strain of the marine fungus E. unguis whose structure is comprised of amino acids and GABA. Synonyms: cyclo(D-alanyl-D-tryptophyl-4-aminobutanoyl-D-alanyl-D-valyl-L-leucyl-D-valyl). Grades: >95% by HPLC. CAS No. 226956-07-6. Molecular formula: C37H56N8O7. Mole weight: 724.89. | |
| Uniblue A Sodium Salt | Uniblue A sodium salt is a reactive protein stain. It can also be used in engineering or chemical process of heterogeneous chemical modification of cotton cellulose with vinyl sulfone dyes in non-nucleophilic organic solvents. Group: Biochemicals. Grades: Highly Purified. CAS No. 14541-90-3. Pack Sizes: 1g, 2.5g. Molecular Formula: C22H16N2O7S2; Na, Molecular Weight: 484.502298999999. US Biological Life Sciences. | Worldwide |
| Uniconazole | Uniconazole is a plant growth hormone that inhibits cytochrome P450 707As, resulting in a suppression of gibberellin production. Uses: Fungicides, industrial. Synonyms: 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (βE)-; (βE)-β-[(4-Chlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol; 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (E)-(±)-; (E)-1-(4-Chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol; 1H-1,2,4-Triazole-1-ethanol, β-[(4-chlorophenyl)methylene]-α-(1,1-dimethylethyl)-, (E)-; M 13144; Majic; Majic S 3307D; Pentefenzol; Prunit; S 07; S 327D; S 3307; S 3307D; Sumagic; Sumiseven; XE 1019; XE 1019D. Grades: 95%. CAS No. 83657-22-1. Molecular formula: C15H18ClN3O. Mole weight: 291.77. | |
| Uniconazole | Uniconazole, a plant growth retardant, is a potent inhibitor of abscisic acid (ABA) catabolism with an IC 50 of 68 nM against ABA 8-hydroxylase. Uniconazole is a potent competitive inhibitor of CYP707A3 activity with a K i of 8 nM. Uniconazole evidently inhibits gibberellin biosynthesis, and brassinosteroid biosynthesis is also inhibited to some extent [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 83657-22-1. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B0873. | |
| Unifiram | Unifiram. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UnifiraM;2-[(4-Fluorophenyl)sulfonyl]hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one;(8aR)-2-[(4-fluorophenyl)sulfonyl]hexahydropyrrolo[1,2-a]pyrazin-6(2H)-one. Product Category: Heterocyclic Organic Compound. CAS No. 272786-64-8. Molecular formula: C13H15FN2O3S. Mole weight: 298.3332032. Product ID: ACM272786648. Alfa Chemistry ISO 9001:2015 Certified. | |
| Uniform Polystyrene Microspheres (blue) | Uniform Polystyrene Microspheres (blue). Group: Polystyrene (ps). | |
| Uniform Polystyrene Microspheres (Color: blue, Size: 6.0 μm, 2.5%w/v in Water-ethanol (1:1, v/v), Matrix: polystyrene) | Uniform Polystyrene Microspheres (Color: blue, Size: 6.0 μm, 2.5%w/v in Water-ethanol (1:1, v/v), Matrix: polystyrene). Group: Polystyrene (ps). | |
| Uniform Polystyrene Microspheres (red) | Uniform Polystyrene Microspheres (red). Group: Polystyrene (ps). | |
| Uniform Polystyrene Microspheres (yellow) | Uniform Polystyrene Microspheres (yellow). Group: Polystyrene (ps). | |
| UNIL-088 | UNIL088 is a water-soluble prodrug of cyclosporine A (CsA), can be rapidly hydrolysed under physiological conditions, and can retain a long shelf-life in aqueous media. Uses: Prodrug of cyclosporine. Synonyms: UNIL-088, UNIL 088, UNIL088, Cyclosporin A; (1R, 2R, E)-1-((2S, 5S, 11S, 14S, 17S, 20S, 23R, 26S, 29S, 32S)-5-ethyl-11, 17, 26, 29-tetraisobutyl-14, 32-diisopropyl-1, 7, 10, 16, 20, 23, 25, 28, 31-nonamethyl-3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33-undecaoxo-1, 4, 7, 10, 13, 16, 19, 22, 25, 28, 31-undecaazacyclotritriacontan-2-yl)-2-methylhex-4-en-1-yl N-(N-((1-acetoxyethoxy)carbonyl)-O-phosphono-L-seryl)-N-methylglycinate. Grades: ≥95%. CAS No. 473545-11-8. Molecular formula: C73H128N13O22P. Mole weight: 1570.86. | |
| UniPR1331 | UniPR1331 is a 3β-hydroxy-Δ5-choline acid derivative that inhibits Eph-ephrin interactions. UniPR1331 interacts with VEGFR2 and blocks the interaction of VEGFR2 with its natural ligand vascular endothelial growth factor and subsequent autophosphorylation, signaling, and pro-angiogenic activation of endothelial cells in vitro. UniPR1331 also inhibits tumor cell-driven angiogenesis in zebrafish [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1809170-59-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-123927. | |
| Unique protease 1 from Porphyromonas gingivalis | Digestion of human IgG1 with Unique protease 1 generates a homogenous pool of precise Fab and Fc fragments. There is no over-digestion or further degradation of the fragments typically associated with other proteolytic enzymes. Very mild reducing reaction conditions give intact Fab and Fc fragments. Best activity is obtained at 37°C. Group: Enzymes. Synonyms: GingisKHAN; unique protease 1. Purity: > 80% homogeneity as determined by SDS-PAGE analysis using Coomassie Blue detection. Unique protease 1. Stability: After reconstitution Unique protease 1 is stable for at least 1 month +4-8°C. Reconstituted Unique protease 1 Reducing Agent cannot be stored, use freshly prepared. Appearance: White to light yellow powder. Storage: Unique protease 1 and Unique protease 1 Reducing Agent are shipped on ice and should be stored at -20°C upon arrival. Form: Lyophilized preparation together with 5 vials of lyophilized reducing agent for convenient and reliable performance. Source: Porphyromonas gingivalis. GingisKHAN Enzyme; GingisKHAN; unique protease 1; protease. Cat No: NATE-1601. |  |
| Unithiol | Unithiol is a chelating agent used as an antidote against for the treatment of heavy metals and metalloid intoxication. It can also be used for animals. Synonyms: DMPS. Grades: >98%. CAS No. 4076-2-2. Molecular formula: C3H7O3S3Na. Mole weight: 210.27. | |
| Universal Clear Glass Bottle | Universal Clear Glass Bottle. Product ID: PM-015. Product Keywords: Packaging Materials; Glass Packaging; PM-015; Universal Clear Glass Bottle. Color: Clear. |  |
| Universal Protein Lysate, Canine Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Universal Protein Lysate, Chicken Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Universal Protein Lysate, Human Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Universal Protein Lysate, Monkey Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Universal Protein Lysate, Mouse Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Universal Protein Lysate, Rat Adult Normal | Universal Protein Lysates: Group: Biologicals. Grades: Molecular Biology Grade. Pack Sizes: 2x500ug, 4x500ug. US Biological Life Sciences. | Worldwide |
| Unoprostone | Unoprostone, a prostaglandin F2α analogs (PGAs), activates BK channels to reduce oxidative stress- and light-induced retinal cell death, and phagocytotic dysfunction. Unoprostone reduces intraocular pressure and is used topically for glaucoma or ocular hypertension [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 120373-36-6. Pack Sizes: 1 mg (26.14 mM * 100 μL in Methyl acetate). Product ID: HY-106916. | |
| Unoprostone-d15 Isopropyl Ester | Antiglaucoma; used in treatment of ocular hypertension. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-(3-oxodecyl)cyclopenthyl]-5-heptenoic Acid-d15 Isopropyl Ester; UF-021-d15; Rescula-d15. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Unoprostone ethyleneketal | Unoprostone ethyleneketal. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-2-[2-(2-Heptyl-1,3-dioxolan-2-yl)ethyl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid. Product Category: Heterocyclic Organic Compound. Appearance: Yellow Gel. CAS No. 120373-42-4. Molecular formula: C24H42O6. Mole weight: 426.59. Purity: 0.96. IUPACName: sulfuricacid. Canonical SMILES: OS(=O)(=O)O. ECNumber: 231-639-5. Product ID: ACM120373424. Alfa Chemistry ISO 9001:2015 Certified. | |
| Unoprostone Ethyleneketal | An intermediate in the preparation of Unoprostone and respective derivatives. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-2-[2-(2-Heptyl-1,3-dioxolan-2-yl)ethyl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid. Grades: Highly Purified. CAS No. 120373-42-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Unoprostone isopropyl ester | Unoprostone isopropyl ester. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-(3-oxodecyl)cyclopenthyl]-5-heptenoic acid isopropyl ester; UF-021; Rescula. Grades: Highly Purified. CAS No. 120373-24-2. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C25H44O5. US Biological Life Sciences. | Worldwide |
| unsaturated chondroitin disaccharide hydrolase | The enzyme releases 4-deoxy-4,5-didehydro D-glucuronic acid or 4-deoxy-4,5-didehydro L-iduronic acid from chondroitin disaccharides, hyaluronan disaccharides and heparin disaccharides and cleaves both glycosidic (1?3) and (1?4) bonds. It prefers the sulfated disaccharides to the unsulfated disaccharides. Group: Enzymes. Synonyms: UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Enzyme Commission Number: EC 3.2.1.180. 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-3864; unsaturated chondroitin disaccharide hydrolase; EC 3.2.1.180; UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Cat No: EXWM-3864. | |
| Unsaturated Polyester Resin | Unsaturated Polyester Resin. Group: Polymers. | |
| unsaturated rhamnogalacturonyl hydrolase | The enzyme is part of the degradation system for rhamnogalacturonan I in Bacillus subtilis strain 168. Group: Enzymes. Synonyms: YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Unsaturated rhamnogalacturonyl hydrolase. 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-3855; unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: EXWM-3855. | |
| Unsaturated rhamnogalacturonyl hydrolase 105A from Bacillus subtilis, Recombinant | Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 43.4 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1508. | |
| Unsaturated rhamnogalacturonyl hydrolase 105A from Bacteroides thetaiotaomicron, Recombinant | Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 52.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1509. | |
| unspecific monooxygenase | A group of P-450 heme-thiolate proteins, acting on a wide range of substrates including many xenobiotics, steroids, fatty acids, vitamins and prostaglandins; reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, N-, S- and O-dealkylations, desulfation, deamination, and reduction of azo, nitro and N-oxide groups. Together with EC 1.6.2.4, NADPH-hemoprotein reductase, it forms a system in which two reducing equivalents are supplied by NADPH. Some of the reactions attributed to EC 1.14.15.3, alkane 1-monooxygenase, belong here. Group: Enzymes. Synonyms: microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hy. Enzyme Commission Number: EC 1.14.14.1. CAS No. 9038-14-6. 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-0906; unspecific monooxygenase; EC 1.14.14.1; 9038-14-6; microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing). Cat No: EXWM-0906. | |
| unspecific peroxygenase | A heme-thiolate protein (P-450). Enzymes of this type include glycoproteins secreted by agaric basidiomycetes. They catalyse the insertion of an oxygen atom from H2O2 into a wide variety of substrates, including aromatic rings such as naphthalene, toluene, phenanthrene, pyrene and p-nitrophenol, recalcitrant heterocycles such as pyridine, dibenzofuran, various ethers (resulting in O-dealkylation) and alkanes such as propane, hexane and cyclohexane. Reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, O- and N-dealkylation, bromination and one-electron oxidations. They have little or no activity toward chloride. Mechanistically, the catalytic cycle of unspecific (mono)-peroxygenases combines elements of the "shunt" pathway of cytochrome P-450s (a side activity that utilizes a peroxide in place of dioxygen and NAD[P]H) and the classic heme peroxidase cycle. Group: Enzymes. Synonyms: aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Enzyme Commission Number: EC 1.11.2.1. 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-0512; unspecific peroxygenase; EC 1.11.2.1; aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Cat No: EXWM-0512. | |
| UoS 12258 | UoS 12258 is a positive allosteric modulator of AMPA receptors with pEC50 value of 5.2. Synonyms: N-[(2S)-5-(6-Fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide. Grades: ≥98% by HPLC. CAS No. 875927-64-3. Molecular formula: C17H19FN2O2S. Mole weight: 334.41. | |
| UP202-56 | UP202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression. Synonyms: 2-cyclopropyl-1-[(2S,3S,4R,5R)-5-[6-[2-[1-[(2,5-dimethylphenyl)methyl]-5-methylindol-3-yl]ethylamino]purin-9-yl]-3,4-dihydroxyoxolan-2-yl]ethanone. CAS No. 163838-04-8. Molecular formula: C33H37N7O4. Mole weight: 595.69. | |
| UP2(Nic) | UP2(Nic), a versatile small molecule inhibitor renowned for its efficacy in blocking nicotinic acetylcholine receptors, is highly sought after in biomedical research circles for its potential medical applications. Studied extensively for its therapeutic scope, this inhibitor shows promise in the treatment of nicotine addiction and a spectrum of neurological disorders, including but not limited to Alzheimer's disease and schizophrenia. Synonyms: Nicotinamide uracil dinucleotide, Sodium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C20H26N4O16P2(free acid). Mole weight: 640.39 (free acid). | |
| Up2U / UppU | Up2U is a pioneering biomedical compound meticulously designed to study an extensive array of pernicious viral and bacterial maladies. UppU is a wide-ranging antiviral and antibiotic compound. Synonyms: P1, P2- Di- (uridine- 5')- diphosphate, sodium salt. Grades: ≥ 95% by HPLC. CAS No. 26184-65-6. Molecular formula: C18H24N4O17P2 (free acid). Mole weight: 630.4 (free acid). | |
| Up4U | Up4U is a novel biomedicine designed to provide targeted treatment for various types of cancer. Utilizing advanced molecular technology, Up4U specifically targets cancer cells while minimizing damage to healthy tissues. Synonyms: P1, P4- Di- (uridine- 5')- tetraphosphate, sodium salt. Grades: ≥ 95% by HPLC. CAS No. 59985-21-6. Molecular formula: C18H26N4O23P4 (free acid). Mole weight: 790.3 (free acid). | |
| UP5 | UP5 is an exemplary inhibitor, exerting its potency by specifically targeting cyclin-dependent kinase 1 (CDK1) within the dynamic landscape of the biomedical industry. Offering a paradigm shift in the research of diverse cancer forms, including colorectal and breast malignancies, UP5 brilliantly orchestrates a multifaceted approach. Synonyms: P1-(Adenosine-5'-P5-(uridine-5')pentaphosphate; [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl [[[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl] hydrogen phosphate. Molecular formula: C19H28N7O24P5. Mole weight: 893.3. | |
| Upacicalcet sodium | Upacicalcet sodium is an intravenous calcimimetic agent. Upacicalcet suppresses excessive parathyroid hormone (PTH) secretion, thereby lowering blood PTH levels, by acting directly on parathyroid cell membrane calcium-sensing receptors. Upacicalcet can be used for researching the disease of secondary hyperparathyroidism (SHPT) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2052969-18-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109106A. | |
| Upadacitinib | Upadacitinib is a selective JAK inhibitor under the development of AbbVie.ABT-494 is nearly 74 fold selective for Jak1 over Jak2 in cellular assays dependent on specific, relevant cytokines. Preliminary evidence suggests that ABT-494 may spare Jak2 and Jak3 dependent signaling compared to tofacitinib. Phase II for the treatment of Atopic dermatitis and Crohn's disease, Phase III for the treatment of Rheumatoid arthritis and Ulcerative colitis was on-going. Uses: Rheumatoid arthritis; ulcerative colitis;atopic dermatitis; crohn's disease. Synonyms: UNII-4RA0KN46E0;ABT494;(3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide. Grades: 98%. CAS No. 1310726-60-3. Molecular formula: C17H19F3N6O. Mole weight: 380.37. | |
| Upadacitinib | Upadacitinib (ABT-494) is a potent, orally active and selective Janus kinase 1 ( JAK1 ) inhibitor ( IC 50 =43 nM). Upadacitinib (ABT-494) displays approximately 74 fold selective for JAK1 over JAK2 (200 nM) in cellular assays dependent on specific, relevant cytokines. Upadacitinib (ABT-494) can be used for several autoimmune disorders research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-494. CAS No. 1310726-60-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-19569. | |
| Upadacitinib Impurity 1 | Upadacitinib Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4S)-benzyl 3-(2-bromoacetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2868258-96-0. Molecular Formula: C16H20BrNO3. Mole Weight: 354.24. Catalog: APB2868258960. |  |
| Upadacitinib Impurity 12 | Upadacitinib Impurity 12. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3R,4S)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide. CAS No. 1310726-59-0. Molecular Formula: C17H19F3N6O. Mole Weight: 380.37. Catalog: APB1310726590. | |
| Upadacitinib Impurity 15 | Upadacitinib Impurity 15. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: ethyl (5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)carbamate. CAS No. 1869118-24-0. Molecular Formula: C16H16N4O4S. Mole Weight: 360.39. Catalog: APB1869118240. | |
| Upadacitinib Impurity 16 | Upadacitinib Impurity 16. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4S)-benzyl 3-(2-((ethoxycarbonyl)(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)amino)acetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2715120-95-7. Molecular Formula: C32H35N5O7S. Mole Weight: 633.71. Catalog: APB2715120957. | |
| Upadacitinib Impurity 17 | Upadacitinib Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3R,4S)-benzyl 3-(2-((ethoxycarbonyl)(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)amino)acetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2050038-81-6. Molecular Formula: C32H35N5O7S. Mole Weight: 633.71. Catalog: APB2050038816. | |
| Upadacitinib Impurity 18 | Upadacitinib Impurity 18. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4R)-benzyl 3-ethyl-4-(3-tosyl-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)pyrrolidine-1-carboxylate. CAS No. 1708997-42-5. Molecular Formula: C29H29N5O4S. Mole Weight: 543.64. Catalog: APB1708997425. | |
| Upadacitinib Impurity 19 | Upadacitinib Impurity 19. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4R)-benzyl 3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)pyrrolidine-1-carboxylate. CAS No. 2095311-51-4. Molecular Formula: C22H23N5O2. Mole Weight: 389.45. Catalog: APB2095311514. | |
| Upadacitinib Impurity 2 | Upadacitinib Impurity 2. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4R)-benzyl 3-(2-bromoacetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2304514-69-8. Molecular Formula: C16H20BrNO3. Mole Weight: 354.24. Catalog: APB2304514698. | |
| Upadacitinib Impurity 21 | Upadacitinib Impurity 21. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3R,4S)-benzyl 3-(2-chloroacetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2460133-49-5. Molecular Formula: C16H20ClNO3. Mole Weight: 309.79. Catalog: APB2460133495. | |
| Upadacitinib Impurity 3 | Upadacitinib Impurity 3. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3R,4R)-benzyl 3-(2-bromoacetyl)-4-ethylpyrrolidine-1-carboxylate. CAS No. 2304514-60-9. Molecular Formula: C16H20BrNO3. Mole Weight: 354.24. Catalog: APB2304514609. | |
| Upadacitinib Impurity 36 | Upadacitinib Impurity 36. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (3S,4R)-benzyl 3-ethyl-4-(2-(2,2,2-trifluoro-N-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)acetamido)acetyl)pyrrolidine-1-carboxylate. CAS No. 2715120-88-8. Molecular Formula: C31H30F3N5O6S. Mole Weight: 657.66. Catalog: APB2715120888. | |
| Upadacitinib Impurity 41 | Upadacitinib Impurity 41. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 1-((benzyloxy)carbonyl)-4-ethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid. CAS No. 1869118-25-1. Molecular Formula: C15H17NO4. Mole Weight: 275.30. Catalog: APB1869118251. | |
| Upadacitinib Impurity 43 | Upadacitinib Impurity 43. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: benzyl (3R,4S)-3-(2-(dimethyl(oxo)-l6-sulfanylidene)acetyl)-4- ethylpyrrolidine-1-carboxylate. CAS No. 2050038-78-1. Molecular Formula: C18H25NO4S. Mole Weight: 351.46. Catalog: APB2050038781. | |
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