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| Product | Description | |
|---|---|---|
| Uridine-5'-triphosphate trisodium salt dihydrate (UTP) | 1g Pack Size. Group: Biochemicals, Building Blocks. Formula: C9H12N2Na3O15P3 · xH2O. CAS No. 19817-92-6. Prepack ID 11038928-1g. Molecular Weight 550.09. See USA prepack pricing. |  |
| Uridine-5'-triphosphate trisodium salt dihydrate (UTP) | 5g Pack Size. Group: Biochemicals, Building Blocks. Formula: C9H12N2Na3O15P3 · xH2O. CAS No. 19817-92-6. Prepack ID 11038928-5g. Molecular Weight 550.09. See USA prepack pricing. | |
| Uridine 5?-triphosphate trisodium salt hydrate | Type IV, ?93.0% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Uridine 5'-Triphosphate Trisodium Salt Hydrate | It is a polyphosphate analogue of the nucleoside uridine, which can be used in the preparation of potent and selective agonists at the G-protein-coupled P2Y receptors. Synonyms: Uridine 5'-(Tetrahydrogen Triphosphate) Trisodium Salt Hydrate; NSC 20260 Hydrate; Trisodium UTP Hydrate; UTP Trisodium Salt Hydrate; Utipina Hydrate. Grade: 95%. Molecular formula: C9H12N2Na3O15P3 xH2O. Mole weight: 550.09. |  |
| Uridine 5'-triphosphate trisodium salt monohydrate | UTP serves as a building block for RNA synthesis and modification, playing a vital role in cellular processes such as gene expression and protein synthesis. It is often utilized in research involving RNA labeling, transcription and RNA structural studies. Synonyms: Uridine 5'-(tetrahydrogen triphosphate), sodium salt, hydrate (1:3:1); Uridine 5'-triphosphate trisodium salt hydrate; UTP sodium salt hydrate; Uridine 5'-triphosphate, sodium salt hydrate. Grade: ≥90% by HPLC. CAS No. 1266569-92-9. Molecular formula: C9H14N2Na3O16P3. Mole weight: 568.10. | |
| Uridine 5?-triphosphate tris salt | Type VI, ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Uridine 98+% | Uridine 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences. |  Worldwide |
| Uridine 99+% (HPLC) | Uridine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 58-96-8. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Uridine-d13 5?-triphosphate disodium salt solution | ?98 atom % D, ?95% (CP), 100 mM (in 5mM Tris / D2O). Group: Fluorescence/luminescence spectroscopy. | |
| uridine diphosphate-α-Dglucose-[1-13C] disodium salt | uridine diphosphate-α-Dglucose-[1-13C] disodium salt. Synonyms: uridine diphosphate-α-D-[1-13C]glucose (disodium salt); ridine diphosphate-alpha-D-[1-13C]glucose (disodium salt); uridine 5'-diphospho-alpha-D-glucose-1-13C, disodium salt; Uridine 5'-(trihydrogendiphosphate),p'-(a-D-glucopyranosyl-1-13c)ester,disodium salt(9ci). CAS No. 478529-38-3. Molecular formula: C14[13C]H22N2Na2O17P2. Mole weight: 611.26. | |
| Uridine Diphosphate-α-D-[UL-13C6]galactose Disodium Salt | Uridine Diphosphate-α-D-[UL-13C6]galactose Disodium Salt. Group: Biochemicals. Alternative Names: UDP-α-D-[UL-13C6]galactose Disodium Salt. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C913C6H22N2Na2O17P2, Molecular Weight: 616.22. US Biological Life Sciences. | Worldwide |
| Uridine Diphosphate Choline Ammonium Salt | Uridine Diphosphate Choline Ammonium Salt. Uses: For analytical and research use. Group: Carbohydrates. Catalog: APS003437. Format: Neat. | |
| Uridine diphosphate glucose,[glucose-14c(u)] | Uridine diphosphate glucose,[glucose-14c(u)]. Uses: Designed for use in research and industrial production. Additional or Alternative Names: URIDINE DIPHOSPHATE GLUCOSE, [GLUCOSE-14C(U)]. Product Category: Heterocyclic Organic Compound. CAS No. 25193-88-8. Molecular formula: C15H24N2O17P2. Mole weight: 578.41. Product ID: ACM25193888. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Uridine impurity 4 | Uridine impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 122567-97-9. Molecular formula: C17H16N2O5. Mole weight: 328.32. Catalog: APB122567979. | |
| Uridine impurity 9 | Uridine impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 10003-93-7. Molecular formula: C18H23N4O14P. Mole weight: 550.37. Catalog: APB10003937. | |
| uridine kinase | Cytidine can act as acceptor; GTP and ITP can act as donors. Group: Enzymes. Synonyms: pyrimidine ribonucleoside kinase; uridine-cytidine kinase; uridine kinase (phosphorylating); uridine phosphokinase. Enzyme Commission Number: EC 2.7.1.48. CAS No. 9026-39-5. 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-3078; uridine kinase; EC 2.7.1.48; 9026-39-5; pyrimidine ribonucleoside kinase; uridine-cytidine kinase; uridine kinase (phosphorylating); uridine phosphokinase. Cat No: EXWM-3078. |  |
| uridine nucleosidase | This enzyme belongs to the family of hydrolases, specifically those glycosylases that hydrolyse N-glycosyl compounds. The systematic name of this enzyme class is uridine ribohydrolase. This enzyme is also called uridine hydrolase. This enzyme participates in pyrimidine metabolism. Group: Enzymes. Synonyms: uridine hydrolase. Enzyme Commission Number: EC 3.2.2.3. CAS No. 9025-47-2. 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-3984; uridine nucleosidase; EC 3.2.2.3; 9025-47-2; uridine hydrolase. Cat No: EXWM-3984. | |
| uridine phosphorylase | The enzyme participates the the pathways of pyrimidine ribonucleosides degradation and salvage. The mammalian enzyme also accepts 2'-deoxyuridine. Group: Enzymes. Synonyms: pyrimidine phosphorylase; UrdPase; UPH; UPase. Enzyme Commission Number: EC 2.4.2.3. CAS No. 9030-22-2. Upase. 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-2657; uridine phosphorylase; EC 2.4.2.3; 9030-22-2; pyrimidine phosphorylase; UrdPase; UPH; UPase. Cat No: EXWM-2657. | |
| Uridine (Standard) | Uridine (Standard) is the analytical standard of Uridine. This product is intended for research and analytical applications. Uses: Scientific research. Group: Natural products. CAS No. 58-96-8. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1449R. |  |
| Uridine triacetate | Uridine triacetate (Tri-O-acetyl uridine) is an orally active proagent of Uridine (HY-B1449). Uridine triacetate is quickly absorbed in the gut, and is rapidly deacetylated in the circulation to yield free uridine. Uridine triacetate is used for the research of 5-fluorouracil (5-FU) and capecitabine toxicity, or early-onset cardiac or central nervous system (CNS) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tri-O-acetyl uridine. CAS No. 4105-38-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-14905. | |
| Uridine triphosphate trisodium salt | Uridine triphosphate (UTP) trisodium salt is a pyrimidine nucleoside triphosphate that is used as a substrate to synthesize RNA or as an energy source in metabolic reactions. Uridine triphosphate trisodium salt activates membrane-bound P2Y2 receptors[1][2]. Uses: Scientific research. Group: Natural products. Alternative Names: UTP trisodium salt; Uridine 5'-triphosphate trisodium salt. CAS No. 19817-92-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W013093. | |
| Uridylyl-2'-5'-uridine ammonium salt | Uridylyl-2'-5'-uridine ammonium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 108321-54-6. Pack Sizes: 1mg, 2mg, 5mg. Molecular Formula: C18H23N4O14P·NH3. US Biological Life Sciences. | Worldwide |
| Uridylyl-3'-5'-adenosine ammonium salt | Uridylyl-3'-5'-adenosine ammonium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. | Worldwide |
| Uridylyl-(3'->5')-adenylyl-(3'->5')-guanosine | Uridylyl-(3'->5')-adenylyl-(3'->5')-guanosine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 221-174-6, Uridylyl-(3.5)-adenylyl-(3.5)-guanosine, 3022-36-4. Product Category: Heterocyclic Organic Compound. CAS No. 3022-36-4. Molecular formula: C29H36N12O19P2. Mole weight: 918.612664 [g/mol]. Purity: 0.96. IUPACName: [3-[[5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)-4-hydroxyoxolan-2-yl]methyl [5-(2,4-dioxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate. Product ID: ACM3022364. Alfa Chemistry ISO 9001:2015 Certified. | |
| Uridylyl-3'-5'-cytidine ammonium salt | Uridylyl-3'-5'-cytidine ammonium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. | Worldwide |
| Uridylyl-3'-5'-guanosine ammonium salt | Uridylyl-3'-5'-guanosine ammonium salt. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg. US Biological Life Sciences. | Worldwide |
| Uridylyl(5'->3')uridylyl(5'->3')adenosine | Uridylyl(5'->3')uridylyl(5'->3')adenosine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 213-906-8, Uridylyl(5.3)uridylyl(5.3)adenosine, 1066-10-0. Product Category: Heterocyclic Organic Compound. CAS No. 1066-10-0. Molecular formula: C28H35N9O20P2. Mole weight: 879.573324 [g/mol]. Purity: 0.96. IUPACName: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3-[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-4-hydroxyoxolan-2-yl]methyl hydrog. Product ID: ACM1066100. Alfa Chemistry ISO 9001:2015 Certified. | |
| Urine, Human, Ethanol & Drug Free | SOURCE: Group: Biologicals. Pack Sizes: 1L. US Biological Life Sciences. | Worldwide |
| Urine, Human, Female, Single Donor | Human Urine is collected from normal healthy female donors. Group: Biologicals. Pack Sizes: 50ml, 10x50ml. US Biological Life Sciences. | Worldwide |
| Urine, Human, Male, Single Donor | Urine is a liquid product of the body that is secreted by the kidneys by a process called urination and excreted through the urethra. Cellular metabolism generates numerous waste compounds, many rich in nitrogen, that require elimination from the bloodstream. This waste is eventually expelled from the body in a process known as micturition, the primary method for excreting water-soluble chemicals from the body. These chemicals can be detected and analyzed by urinalysis. Urine contains a range of substances that vary with what is introduced into the body. Aside from water, urine contains an assortment of inorganic salts and organic compounds, including proteins, hormones, and a wide range of metabolites. Group: Biologicals. Pack Sizes: 50ml. US Biological Life Sciences. | Worldwide |
| Urine, Normal | Human Urine formation helps to maintain the balance of minerals and other substances in the body. For example, excess of calcium is normally eliminated through the urine. Urine also excretes ammonia, the build-up of which is harmful to the body. Human urine is the result of a mechanism that maintains the appropriate amount of water in the body. When it leaves the body, Human urine is usually around pH 6, though it may be as low as 4.5 or as high as 8.2. As urea, the compound which accounts for 75-90% of the nitrogen in urine begins to decay, hydroxide ions form, raising the pH as high as 9-9.3. The decay of urea into carbon dioxide is catalyzed by urease. Group: Biologicals. Pack Sizes: 1L. US Biological Life Sciences. | Worldwide |
| URMC-099 | URMC-099 is an orally bioavailable and potent mixed lineage kinase type 3 (MLK3) (IC50=14 nM) inhibitor with with excellent blood-brain barrier penetration properties. Uses: Scientific research. Group: Signaling pathways. CAS No. 1229582-33-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12599. | |
| urocanate hydratase | Contains tightly bound NAD+. Group: Enzymes. Synonyms: urocanase; 3-(5-oxo-4,5-dihydro-3H-imidazol-4-yl)propanoate hydro-lyase. Enzyme Commission Number: EC 4.2.1.49. CAS No. 9014-58-8. 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-5038; urocanate hydratase; EC 4.2.1.49; 9014-58-8; urocanase; 3-(5-oxo-4,5-dihydro-3H-imidazol-4-yl)propanoate hydro-lyase. Cat No: EXWM-5038. | |
| urocanate reductase | The enzyme from the bacterium Shewanella oneidensis MR-1 contains a noncovalently-bound FAD and a covalently-bound FMN. It functions as part of an anaerobic electron transfer chain that utilizes urocanate as the terminal electron acceptor. The activity has been demonstrated with the artificial donor reduced methyl viologen. Group: Enzymes. Synonyms: urdA (gene name). Enzyme Commission Number: EC 1.3.99.33. 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-1435; urocanate reductase; EC 1.3.99.33; urdA (gene name). Cat No: EXWM-1435. | |
| Urocanic acid | Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). Uses: Scientific research. Group: Natural products. CAS No. 104-98-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-113008. | |
| Urocanic acid | Urocanic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 104-98-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C6H6N2O2. US Biological Life Sciences. | Worldwide |
| Urocanic acid | It is produced by the strain of Bac. subtilis var. theronophilus. Urocanic acid has an inhibitory effect on Eichner's ascites pain in animals. Synonyms: 4-imidazoleacrylic acid; trans-Urocanic acid; 5-Imidazoleacrylic acid; (2E)-3-(1H-IMIDAZOL-4-YL)ACRYLIC ACID; 3-(1H-Imidazol-4-yl)-2-propenoic acid; NSC 66357. Grade: 99%. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. | |
| Urocanic acid | Urocanic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Propenoic acid, 3-(1H-imidazol-4-yl)-;3-Imidazol-4-ylacrylic acid. Product Category: Imidazoles. Appearance: White to Off-White Powder. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. Purity: 0.99. Product ID: ACM104983. Alfa Chemistry ISO 9001:2015 Certified. | |
| Urocortin (human) | Urocortin (human) is a neuropeptide hormone that acts as an endogenous CRF agonist (Ki = 0.4, 0.3 and 0.5 nM for hCRF1, rCRF2α and mCRF2β, respectively). Synonyms: Human urocortin; Human urocortin 1; Human urocortin I. CAS No. 176591-49-4. Molecular formula: C204H337N63O64. Mole weight: 4696.29. | |
| Urocortin, human | Urocortin, human, a 40-aa neuropeptide, acts as a selective agonist of endogenous CRF 2 receptor , with K i s of 0.4, 0.3, and 0.5 nM for hCRF 1 , rCRF 2α and mCRF 2β , respectively. Uses: Scientific research. Group: Peptides. Alternative Names: Urocortin (human); Human urocortin; Human urocortin 1; Human urocortin I. CAS No. 176591-49-4. Pack Sizes: 500 μg; 1 mg; 5 mg. Product ID: HY-P1295. | |
| Urocortin II, human | Urocortin II (human), a new member of the corticotropin-releasing-factor (CRF) family, is a selective endogenous peptide agonist of type-2 corticotropin-releasing factor (CRF2) receptor. Molecular formula: C194H339N63O54S. Mole weight: 4450.28. | |
| Urocortin II (human) trifluoroacetate salt | Urocortin II is a neuropeptide hormone that is a member of the corticotropin-releasing factor (CRF) family. Urocortin II is a highly selective agonist of the CRF2 receptor and does not show affinity for the CRF binding protein. Synonyms: PD080645. Grade: ≥95%. CAS No. 398001-88-2. Molecular formula: C196H340F3N63O56S. Mole weight: 4564.23. | |
| Urocortin III, mouse | Urocortin III a neuropeptide hormone and a member of the corticotropin-releasing factor (CRF) family, is a highly selective agonist of the CRF2 receptor and does not show affinity for the CRF binding protein. Synonyms: STRESSCOPIN (3-40) (MOUSE). CAS No. 357952-10-4. Molecular formula: C186H312N52O52S2. Mole weight: 4172.97. | |
| Urocortin III, mouse TFA | Urocortin III, mouse TFA is a corticotropin-releasing factor (CRF)-related peptide. Urocortin III preferentially binds and activates CRF-R2[1]. Urocortin III (Ucn3) is a known component of the behavioral stress response system. Urocortin III and CRF-R2 in the medial amygdala regulate complex social dynamics[2]. Uses: Scientific research. Group: Peptides. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1858A. | |
| Urocortin II (mouse) | Urocortin II (mouse) shows considerably high affinity for two splice variants of type 2 CRF receptor (CRF-R2) compared to CRF-R1. It activates CRF-R2α and CRF-R2β with almost the same potency as urocortin (rat). Synonyms: Ucn II (mouse); H-Val-Ile-Leu-Ser-Leu-Asp-Val-Pro-Ile-Gly-Leu-Leu-Arg-Ile-Leu-Leu-Glu-Gln-Ala-Arg-Tyr-Lys-Ala-Ala-Arg-Asn-Gln-Ala-Ala-Thr-Asn-Ala-Gln-Ile-Leu-Ala-His-Val-NH2. Grade: ≥95%. CAS No. 330648-32-3. Molecular formula: C187H320N56O50. Mole weight: 4152.95. | |
| Urocortin (rat) | Urocortin (rat) is a neuropeptide hormone that acts as an endogenous CRF agonist (Ki = 13, 1.5 and 0.97 nM for hCRF1, rCRF2α and mCRF2β, respectively). Synonyms: Urocortin (Rattus norvegicus); Rat urocortin. CAS No. 171543-83-2. Molecular formula: C206H338N62O64. Mole weight: 4707.31. | |
| Urodilatin human | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Uroguanylin | Uroguanylin belongs to the guanylin family of cyclic guanosine monophosphate (cGMP) regulatory peptides. Uroguanylin activates the guanylate cyclase-C/cyclic guanosine monophosphate pathway to induce analgesic effects in colonic hypersensitive animal models, revealing a new approach for the treatment of abdominal pain. Synonyms: Uroguanylin Topoisomer A (human); UGN Topoisomer A (human); H-Asn-Asp-Asp-Cys-Glu-Leu-Cys-Val-Asn-Val-Ala-Cys-Thr-Gly-Cys-Leu-OH (Disulfide bridge: Cys4-Cys12, Cys7-Cys15); UGN (human); L-asparagyl-L-alpha-aspartyl-L-alpha-aspartyl-L-cysteinyl-L-alpha-glutamyl-L-leucyl-L-cysteinyl-L-valyl-L-asparagyl-L-valyl-L-alanyl-L-cysteinyl-L-threonyl-glycyl-L-cysteinyl-L-leucine (4->12),(7->15)-bis(disulfide); L-Asparaginyl-L-α-aspartyl-N-{(1R,4S,7S,10S,13S,16R,19S,22S,25R,32S,38R)-10-(2-amino-2-oxoethyl)-22-(2-carboxyethyl)-38-{[(1S)-1-carboxy-3-methylbutyl]carbamoyl}-32-[(1R)-1-hydroxyethyl]-19-isobutyl-7,13-diisopropyl-4-methyl-3,6,9,12,15,18,21,24,30,33,36-undecaoxo-27,28,40,41-tetrathia-2,5,8,11,14,17,20,23,31,34,37-undecaazabicyclo[14.13.13]dotetracont-25-yl}-L-α-asparagine. Grade: ≥90% by HPLC. CAS No. 154525-25-4. Molecular formula: C64H102N18O26S4. Mole weight: 1667.86. | |
| Uroguanylin | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Uroguanylin (human) | Uroguanylin (human) is a natural ligand for the Guanylyl Cyclase (GCC) receptor expressed in metastatic colorectal cancer tumors. Uroguanylin (human) has anti-tumor actions in an animal model for human colon cancer[1][2]. Uses: Scientific research. Group: Peptides. CAS No. 154525-25-4. Pack Sizes: 500 ?g; 1 mg; 5 mg. Product ID: HY-P3099. | |
| Uroguanylin Topoisomer B (human) | Uroguanylin is a short peptide containing two disulfide bonds that can form interconversion topological isomers with the same disulfide connectivity. In the case of uroguanylin (UGN), both are relatively stable, separable, and slow to transform into each other. Different topoisomers have different biological activities: UGN A topomer can effectively activate the guanylate cyclase C receptor, mainly found in the intestine. The B topomer is a very weak agonist of this receptor. UGN B has strong natriuretic activity in the kidney. Synonyms: UGN Topoisomer B (human); H-Asn-Asp-Asp-Cys-Glu-Leu-Cys-Val-Asn-Val-Ala-Cys-Thr-Gly-Cys-Leu-OH (Disulfide bridge: Cys4-Cys12, Cys7-Cys15). Grade: ≥95%. Molecular formula: C64H102N18O26S4. Mole weight: 1667.88. | |
| Urokinase | 25mg Pack Size. Group: Analytical Reagents, Biochemicals. Formula: -. CAS No. 9039-53-6. Prepack ID 13187505-25mg. Molecular Weight -. See USA prepack pricing. | |
| Urokinase from Human, recombinant | Urokinase or Urokinase-type plasminogen activator (uPA) is a serine protease (EC 3.4.21.73). It is secreted as a single-chain zymogen, pro-Urokinase, possessing little or no intrinsic enzymatic activity. The single chain zymogen is converted into the active two chain enzyme (tcuPA) by cleavage of the bond between Lys157 and Ile158. After activation, Urokinase specifically cleaves the proenzyme plasminogen to form the active enzyme plasmin. The active plasmin then catalyzes the breakdown of fibrin polymers of blood clots. Urokinase is involved in a number of biological functions including fibrinolysis, embryogenesis, cell migration, tissue remodeling, ovulation, and wound healing. Additionally, it is a potent marker of invasion and metastasis in a variety of human cancers associated with breast, stomach, colon, bladder, ovary, brain and endometrium. Group: Enzymes. Synonyms: Two chain urokinase-type plasminogen acti. Enzyme Commission Number: EC 3.4.21.73. Purity: > 90% by SDS-PAGE. uPA. Mole weight: 49.3 kDa. Activity: >1500 mU/mg. Storage: Stable at -80°C for at least 1 year as supplied. Store reconstituted aliquots at -80°C. Avoid repeated freeze and thaw cycles. Form: Lyophilized powder. Source: E. coli. Species: Human. Two chain urokinase-type plasminogen activator; tcuPA; PLAU; ATF; UPA; URK; u-PA; BDPLT5; QPD; Urokinase. Cat No: NATE-1690. | |
| Urokinase from human urine | lyophilized powder, ?500 units/mg protein. Group: Fluorescence/luminescence spectroscopy. | |
| Urokinase, Human urine | Urokinase (peptidolytic) (EC 3.4.21.73) is a serine protease, an inactive form (zymogen) of the serine protease plasminogen. Activation of plasmin triggers a proteolytic cascade reaction, which in turn participates in thrombolysis or extracellular matrix degradation, implicated in vascular disease and cancer-related research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Urokinase-type plasminogen activator; Uronase; Win 22005; Win-Kinase. CAS No. 9039-53-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-108904. | |
| Urokinase light yellow powder | 100mg Pack Size. Group: Biochemicals. Formula: N/A. CAS No. 9039-53-6. Prepack ID 90029023-100mg. See USA prepack pricing. | |
| Urokinase Substrate III, Fluorogenic | Suitable for the quantitative direct fluorescent assay of urokinase. Group: Fluorescence/luminescence spectroscopy. | |
| Urolithin A | Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis , suppresses cell cycle progression, and inhibits DNA synthesis [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1143-70-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100599. | |
| Urolithin A | Urolithin A is a urolithin, a type of microflora human metabolite of dietary ellagic acid derivatives, such as ellagitannins.During intestinal metabolism by bacteria, ellagitannins and punicalagins are converted to urolithins, which have unknown biological activity in vivo.Urolithin A glucuronide is found in plasma at low concentrations. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Uro-A;pyran-6-one.html >3,8-Dihydroxy-6H-dibenzo | |
| Urolithin A | Urolithin A is a metabolite of ellagic acid. It has been demonstrated to stimulate mitophagy and improve muscle health in old animals and in preclinical models of aging. Alternative Names: 3,8-dihydroxy-6H-benzo[c]chromen-6-one. 3,8-Dihydroxyurolithin. 6H-Dibenzo[b,d]pyran-6-one, 3,8-dihydroxy-. CAS No. 1143-70-0. Product ID: API1143700. Molecular formula: C13H8O4. Mole weight: 228.2. EINECS: 881-478-5. SMILES: C1=CC2=C(C=C1O)C(=O)OC3=C2C=CC(=C3)O. Appearance: Solid. Category: Other APIs. |  |
| Urolithin A | Urolithin A Inhibitor. Uses: Scientific use. Product Category: T7174. CAS No. 1143-70-0. |  |
| Urolithin A | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Urolithin A | Urolithin A is a major metabolite of ellagitannin and exhibits anti-inflammatory and antioxidant properties. Group: Biochemicals. Alternative Names: 3,8-Hydroxydibenzo-α-pyrone; 3,8-Dihydroxyurolithin; 2,7-Dihydroxy-3,4-benzocoumarin; δ-Lactone 2,4,4-Trihydroxy-2-biphenylcarboxylic Acid. Grades: Highly Purified. CAS No. 1143-70-0. Pack Sizes: 50mg. Molecular Formula: C??H?O?. US Biological Life Sciences. | Worldwide |
| Urolithin A | Urolithin A is a secondary metabolite of ellagitannins by the gut bacteria. It exhibits anti-inflammatory, antioxidant and antiproliferative effects. Urolithin A can cross the blood brain barrier thus has the potential therapeutic effect against Alzheimer's Disease. Synonyms: 3,8-dihydroxy-6H-benzo[c]chromen-6-one; 3,8-Dihydroxy-6H-dibenzo(b,d)pyran-6-one; 6H-Dibenzo[b,d]pyran-6-one, 3,8-dihydroxy-. Grade: ≥98% by HPLC. CAS No. 1143-70-0. Molecular formula: C13H8O4. Mole weight: 228.20. | |
| Urolithin A 8-Methyl Ether | Urolithin A 8-Methyl Ether. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-Hydroxy-8-methoxy-6H-benzo[c]chromen-6-one. Appearance: Light Beige to Very Dark Orange Solid. CAS No. 35233-17-1. Molecular formula: C14H10O4. Mole weight: 242.23. Purity: 0.98. Product ID: ACM35233171. Alfa Chemistry ISO 9001:2015 Certified. | |
| Urolithin B | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Urolithin B | Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK , ERK and Akt 's oxidation, and increases AMPK 's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 1139-83-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-126307. | |
| Urolithin C | Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2]. Uses: Scientific research. Group: Natural products. CAS No. 165393-06-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-135897. | |
| Urolithin D | Urolithin D (3,4,8,9-Tetrahydroxy urolithin) is a colonic metabolite of Ellagitannins and a competitive, reversible, and selective antagonist of the EphA receptor. Urolithin D inhibits EphA2-ephrin-A1 binding with an IC50 of 0.9 ?M. Urolithin D is also a potent antioxidant that scavenges free radicals and repairs oxidized DNA damage. Additionally, Urolithin D suppresses triglyceride accumulation and promotes fatty acid oxidation by activating the AMPK signaling pathway. Urolithin D can be used for research on tumors, metabolic, and inflammatory diseases[1][2][3]. Uses: Scientific research. Group: Natural products. Alternative Names: 3,4,8,9-Tetrahydroxy urolithin. CAS No. 131086-98-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133178. | |
| Urolithin E | Urolithin E is a biological molecule. Uses: Scientific research. Group: Signaling pathways. CAS No. 1453297-45-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W746164. | |
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