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| Product | Description | |
|---|---|---|
| Uridine 5'-Triphosphate Tris Salt | As a polyphosphate analogue of the nucleoside Uridine, Uridine 5'-Triphosphate Tris Salt can be used in the preparation of potent and selective agonists at the G-protein-coupled P2Y receptors. Synonyms: UTP. Grades: 95%. CAS No. 108321-53-5. Molecular formula: C9H15N2O15P3 xC4H11NO3. Mole weight: 484.14. |  |
| URIDINE 5-TRIPHOSPHATE TRIS TYPE VI | Heterocyclic Organic Compound. Alternative Names: (2R,5S)-2-(2,4-Dioxo-3,4-dihydro-1(2H)-pyrimidinyl)-5-({[hydroxy( {hydroxy[ (oxophosphino) oxy]phosphoryl}oxy) phosphoryl]oxy}methyl) t etrahydrofuran-3,4-diyl. CAS No. 108321-53-5. Molecular formula: C9H15N2O15P3. Mole weight: 484.14. Purity: 0.96. IUPACName: Uridine 5-triphosphate tris salt. Catalog: ACM108321535. |  |
| 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 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 Choline Ammonium Salt | Uridine Diphosphate Choline Ammonium Salt, a vital biochemical constituent in choline metabolism, not only serves as a precursor for acetylcholine, a neurotransmitter related to cognitive function and memory, but also exerts neuroprotective effects through a host of therapeutic pathways. Notably, studies show that this compound can enhance memory and cognitive performance in people with Alzheimer's disease and dementia while holding potential for treating neurological disorders such as Parkinson's disease and stroke. Synonyms: Uridine 5'-(Trihydrogen Diphosphate) P'-[2-(Trimethylammonio)ethyl] Ester Ammonium Salt. Grades: > 95%. Molecular formula: C14H28N4O12P2. Mole weight: 506.34. | |
| Uridine Diphosphate Choline (UDPC) | Uridine Diphosphate Choline (UDPC) is a fundamental biochemical compound inherent to the human body assuming indispensability in an array of intricate cellular processes. It has biomedical application for studying neurodegenerative afflictions such as Alzheimer's disease, Parkinson's disease and cognitive impairments. Notably, UDPC functions as a precursor, stimulating the production of acetylcholine. Synonyms: Uridine 5'-(Trihydrogen Diphosphate) P'-[2-(TriMethylaMMonio)ethyl] Ester Inner Salt. Grades: > 95%. CAS No. 99492-83-8. Molecular formula: C14H25N3O12P2. Mole weight: 489.32. | |
| Uridine Diphosphate Choline (UDPC) | Uridine Diphosphate Choline (UDPC). Uses: For analytical and research use. Group: Impurity standards. CAS No. 99492-83-8. Molecular Formula: C14H25N3O12P2. Mole Weight: 489.31. Catalog: APB99492838. | |
| Uridine Diphosphate-GlcNaz | Uridine Diphosphate-GlcNaz was tested for recognition by the GlmU uridyltransferase enzyme and for activities as substrates for glycosyltransferase. Synonyms: Uridine 5'-(trihydrogen diphosphate) P'-(2-azido-2-deoxy-α-D-glucopyranosyl) Ester Sodium Salt. CAS No. 1355005-50-3. Molecular formula: C15H21N5Na2O16P2. Mole weight: 635.28. | |
| Uridine diphosphate glucose,[glucose-6-3h] | Heterocyclic Organic Compound. Alternative Names: URIDINE DIPHOSPHATE GLUCOSE, [GLUCOSE-6-3H]. CAS No. 108866-91-7. Molecular formula: C15H22N2O17P2T2. Mole weight: 570.32. Catalog: ACM108866917. | |
| Uridine Diphosphate Glucose (UDP-Glucose) | Uridine Diphosphate Glucose is a derivative of Uridine. Uridine is a nucleoside with a uracil attached to a ribose ring. Uridine is one of the four standard components of RNA. CAS No. 133-89-1. Molecular formula: C15H24N2O17P2. Mole weight: 566.31. | |
| Uridine diphosphocholine sodium salt | Uridine diphosphocholine sodium salt. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1772607-47-2. Molecular Formula: C14H26N3NaO12P2. Mole Weight: 513.31. Catalog: APB1772607472. | |
| 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 7 | Uridine impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 137868-52-1. Molecular Formula: C15H22N2Na2O17P2. Mole Weight: 610.27. Catalog: APB137868521. | |
| Uridine impurity 8 | Uridine impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 154925-95-8. Molecular Formula: C21H39BrN2O5Si2. Mole Weight: 535.63. Catalog: APB154925958. | |
| 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. | |
| Uridylyl(2'-5')adenosine ammonium salt | Heterocyclic Organic Compound. Alternative Names: URIDYLYL(2'-5')ADENOSINE AMMONIUM SALT. CAS No. 108320-81-6. Molecular formula: C19H27N8O12P. Mole weight: 590.44. Catalog: ACM108320816. | |
| URIDYLYL (2-5) GUANOSINE AMMONIUM | Heterocyclic Organic Compound. CAS No. 108321-59-1. Molecular formula: C11H9N3O3S. Mole weight: 263.27246;g/mol. Purity: 0.96. IUPACName: 6-hydroxy-4-oxo-N-phenyl-2-sulfanylidene-1H-pyrimidine-5-carboxamide. Canonical SMILES: C1=CC=C (C=C1)NC (=O)C2=C (NC (=S)NC2=O)O. Catalog: ACM108321591. | |
| Uridylyl-2'-5'-uridine ammonium salt | Uridylyl-2'-5'-uridine ammonium salt is an indispensable and pivotal biomolecule within the biomedical sector, involved in the intricate orchestration of RNA sequence synthesis and modification. Its indispensable functionality encompasses the research of cellular wholeness and the orchestration of gene expression. Synonyms: D-Uridylyl-2'-5'-uridine ammonium salt. Grades: 95%. CAS No. 108321-54-6. Molecular formula: C18H23N4O14P·NH3. Mole weight: 567.41. | |
| 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(2'->5')uridine ammonium salt | Heterocyclic Organic Compound. Alternative Names: 108321-54-6, Uridylyl(2 inverted exclamation marka inverted exclamation marku5 inverted exclamation marka)uridine ammonium salt. CAS No. 108321-54-6. Molecular formula: C18H26N5O14P. Mole weight: 567.4. Purity: 0.96. IUPACName: azane;[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl [2-(2,4-dioxopyrimidin-1-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate. Catalog: ACM108321546. | |
| Uridylyl-(3'-5')-adenosine | Uridylyl-(3'-5')-adenosine, an indispensable enzyme in the field of biomedicine, holds immense significance owing to its pivotal role in nucleotide metabolism. Its involvement in the synthesis of flavin adenine dinucleotide (FAD), a fundamental coenzyme for diverse enzymatic reactions, further amplifies its importance. Prominently employed for investigating FAD-dependent enzymes and their potential implications in a wide array of ailments like cancer, cardiovascular disorders, and neurodegenerative conditions, this product emerges as a scholarly tool in scientific exploration. Synonyms: UpA RNA Dinucleotide (5'-3'); Uridylyladenosine; Uridine-3',5'-adenosine phosphate; (3',5')-Uridylyladenosine. Grades: ≥95% by AX-HPLC. CAS No. 3256-24-4. Molecular formula: C19H24N7O12P. Mole weight: 573.40. | |
| 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'-adenosine ammonium salt | Uridylyl-3'-5'-adenosine ammonium salt is a pivotal compound extensively employed in diverse applications. Notably, it emerges as a fundamental player in enzymatic cascades, serving as a substrate for essential RNA editing enzymes. Moreover, it assumes a vital role in the synthesis of cyclic adenosine monophosphate (cAMP), a critical secondary messenger intricately involved in cellular responses. Molecular formula: C19H27N8O12P. Mole weight: 590.44. | |
| Uridylyl-(3'-5')-cytidine | Uridylyl-(3'-5')-cytidine, a pivotal enzyme central to the biomedicine sector, exhibits invaluable utility for combatting select viral infections and malignancies. Its significance lies in RNA synthesis, bolstering cellular functionality and resilience. Synonyms: UpC RNA Dinucleotide (5'-3'); Cytidylyl-(5',3')-uridine. Grades: ≥95% by AX-HPLC. CAS No. 3013-97-6. Molecular formula: C18H24N5O13P. Mole weight: 549.40. | |
| Uridylyl-3'-5'-cytidine ammonium salt | Uridylyl-3'-5'-cytidine ammonium salt is an exceptional biomedical compound, extensively employed in studying viral infections such as hepatitis C, influenza and respiratory syncytial virus. Representing a formidable nucleotide analogue, it displays remarkable antiviral efficacy against diverse RNA viruses. Molecular formula: C18H27N6O13P. Mole weight: 566.41. | |
| 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 | Uridylyl-(3'-5')-guanosine, an essential nucleoside, proves indispensable in RNA capping that fortifies mRNA stability and translation initiation. Acting as a potent substrate, it employs the services of viral RNA polymerases and guanylyltransferases as its aides. In addition, studies have shown its successful repulsion against RNA viruses - from hepatitis C, to yellow fever and dengue viruses. Synonyms: UpG RNA Dinucleotide (5'-3') ; Uridylyl-(3',5')-guanosine. Grades: ≥95% by AX-HPLC. CAS No. 3474-4-2. Molecular formula: C19H24N7O13P. Mole weight: 589.40. | |
| URIDYLYL(3-5)GUANOSINE AMMONIUM | Heterocyclic Organic Compound. Alternative Names: 108320-85-0, Uridylyl(3 inverted exclamation marka inverted exclamation marku5 inverted exclamation marka)guanosine ammonium salt. CAS No. 108320-85-0. Molecular formula: C19H27N8O13P. Mole weight: 606.437242 [g/mol]. Purity: 0.96. IUPACName: [5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [5-(2,4-dioxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate;azane. Canonical SMILES: C1=CN (C (=O)NC1=O)C2C (C (C (O2)CO)OP (=O) (O)OCC3C (C (C (O3)N4C=NC5=C4NC (=NC5=O)N)O)O)O. N. Catalog: ACM108320850. | |
| 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-3'-5'-guanosine ammonium salt | Uridylyl-3'-5'-guanosine ammonium salt is a fundamental constituent, renowned for its indispensability in pharmacological research of ameliorating diverse afflictions such as neoplastic growths and viral entanglements. Molecular formula: C19H24N7O13P·Xnh3. Mole weight: 589.41 (free acid). | |
| Uridylyl-(5'->3')-inosine | Heterocyclic Organic Compound. CAS No. 10021-57-5. Molecular formula: C19H23N6O13P. Purity: 0.96. Catalog: ACM10021575. | |
| Uridylyl (5'->3')uridylyl (5'->3')adenosine | Heterocyclic Organic Compound. Alternative Names: EINECS 213-906-8, Uridylyl(5.3)uridylyl(5.3)adenosine, 1066-10-0. 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. Catalog: ACM1066100. | |
| 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, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively. MLK3 activation is associated with many of the pathologic hallmarks of HAND and therefore represents a prime target for adjunctive therapy based on small-molecule kinase inhibition. Synonyms: URMC099; URMC 099; URMC-099. Grades: 98%. CAS No. 1229582-33-5. Molecular formula: C27H27N5. Mole weight: 421.55. | |
| Urobilinogen | Heterocyclic Organic Compound. CAS No. 11000-27-4. Purity: 0.96. Catalog: ACM11000274. | |
| 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. 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. Grades: 99%. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. | |
| 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 | Imidazoles. Alternative Names: 2-Propenoic acid, 3-(1H-imidazol-4-yl)-;3-Imidazol-4-ylacrylic acid. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. Appearance: White to Off-White Powder. Purity: 0.99. Catalog: ACM104983. | |
| 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) 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. Grades: ≥95%. CAS No. 398001-88-2. Molecular formula: C196H340F3N63O56S. Mole weight: 4564.23. | |
| Urocortin III (human) trifluoroacetate salt | Urocortin III is a neuropeptide hormone and a member of the corticotropin-releasing factor (CRF) family. Urocortin III is a highly selective agonist of the CRF2 receptor and does not show affinity for the CRF binding protein. Grades: ≥95%. Molecular formula: C185H307N53O50S2·xCF3COOH. Mole weight: 4137.88. | |
| 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) trifluoroacetate salt | Urocortin III is a neuropeptide hormone and a member of the corticotropin-releasing factor (CRF) family. Urocortin III is a highly selective agonist of the CRF2 receptor and does not show affinity for the CRF binding protein. Grades: ≥95%. Molecular formula: C186H311N51O53S2·xCF3COOH. Mole weight: 4173.90. | |
| 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. Grades: ≥95%. CAS No. 330648-32-3. Molecular formula: C187H320N56O50. Mole weight: 4152.95. | |
| Urocortin II (mouse) 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. Grades: ≥95%. Molecular formula: C187H320N56O50·xCF3COOH. Mole weight: 4152.89. | |
| 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 | Heterocyclic Organic Compound. CAS No. 115966-23-9. Molecular formula: C145H234N52O44S3. Mole weight: 3505.93. Catalog: ACM115966239. | |
| 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. Grades: ≥90% by HPLC. CAS No. 154525-25-4. Molecular formula: C64H102N18O26S4. Mole weight: 1667.86. | |
| 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). Grades: ≥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, 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. | |
| 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 Inhibitor. Uses: Scientific use. Product Category: T7174. CAS No. 1143-70-0. |  |
| 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 |
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