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| Product | Description | |
|---|---|---|
| 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 glucose,[glucose-6-3h] | Uridine diphosphate glucose,[glucose-6-3h]. Alternative Names: URIDINE DIPHOSPHATE GLUCOSE, [GLUCOSE-6-3H]. CAS No. 108866-91-7. Product ID: ACM108866917. Molecular formula: C15H22N2O17P2T2. Mole weight: 570.32. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Uridine diphosphate glucuronic acid | Uridine diphosphate glucuronic acid (UDP-α-D-glucuronic acid) is a glucuronic acid donor. Uridine diphosphate glucuronic acid transfers its glucuronic acid moiety to acceptor molecules, thereby forming "ether" glucuronides, while being converted into uridine 5'-pyrophosphate. Uridine diphosphate glucuronic acid serves as a substrate for Arabidopsis UDP-GlcA 4-epimerase 1, and undergoes reversible 4-epimerization to generate UDP-α-D-galacturonic acid[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UDP-α-D-glucuronic acid. CAS No. 2616-64-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-125954. |  |
| Uridine diphosphate glucuronic acid ammonium | Uridine diphosphate glucuronic acid ammonium (UDP-α-D-glucuronic acid ammonium) is a glucuronic acid donor. Uridine diphosphate glucuronic acid ammonium transfers its glucuronic acid moiety to acceptor molecules, thereby forming "ether" glucuronides, while being converted into uridine 5'-pyrophosphate. Uridine diphosphate glucuronic acid ammonium serves as a substrate for Arabidopsis UDP-GlcA 4-epimerase 1, and undergoes reversible 4-epimerization to generate UDP-α-D-galacturonic acid[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UDP-α-D-glucuronic acid ammonium. CAS No. 43195-60-4. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-125954A. | |
| Uridine impurity 4 | Uridine impurity 4. Uses: For analytical and research use. CAS No. 122567-97-9. Molecular formula: C17H16N2O5. Mole weight: 328.32. Catalog: APB122567979. |  |
| Uridine impurity 5 | Uridine impurity 5. Uses: For analytical and research use. Molecular formula: C18H18N2O8S. Mole weight: 422.41. Catalog: APB10889. | |
| Uridine impurity 7 | Uridine impurity 7. Uses: For analytical and research use. 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. 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. 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 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. Category: Signaling pathways. Alternative Names: Tri-O-acetyl uridine. CAS No. 4105-38-8. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-14905. | |
| Uridine triphosphate trisodium dihydrate | Uridine triphosphate (trisodium dihydrate) (UTP (trisodium dihydrate); Uridine 5'-triphosphate (trisodium dihydrate)) is a biochemical reagent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: UTP trisodium dihydrate; Uridine 5'-triphosphate trisodium dihydrate. CAS No. 116295-90-0. Pack Sizes: 10 mM * 1 mL in Water; 50 mg; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-107372A. | |
| 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. Category: Signaling pathways. Alternative Names: UTP trisodium salt; Uridine 5'-triphosphate trisodium salt. CAS No. 19817-92-6. Pack Sizes: 10 mM * 1 mL in Water; 50 mg; 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'-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 |
| 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. Category: Signaling pathways. CAS No. 1229582-33-5. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Alternative Names: 2-Propenoic acid, 3-(1H-imidazol-4-yl)-;3-Imidazol-4-ylacrylic acid. CAS No. 104-98-3. Purity: 99%. Product ID: ACM104983. Molecular formula: C6H6N2O2. Mole weight: 138.12. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. 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 |
| 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 an agonist of endogenous CRF receptor, with Kis of 0.4, 0.3, and 0.5 nM for hCRF1, rCRF2α and mCRF2β, respectively. Uses: Scientific research. Category: Signaling pathways. 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 is a selective endogenous peptide agonist of type-2 corticotropin-releasing factor (CRF2) receptor. Urocortin II, human has an effect of promoting satiet and neuroprotective effect. Urocortin II, human also has bactericidal, antiparasitic and pro-inflammation activity. Urocortin II, human can activate NF-κB pathway and ERK1/2 MAP kinase. Urocortin II, human can reduce pulmonary arterial hypertension and shows cardiac protection effect. Urocortin II, human can be used for the researches of infection, inflammation, metabolic, neurological and cardiovascular disease[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 351999-18-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-P1752. | |
| 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 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 II, mouse | Urocortin II, mouse is a potent and selective endogenous peptide agonist of type-2 corticotropin-releasing factor (CRF2) receptor with Ki values of 0.66 nM and ?100 nM for CRFR2 and CRFR1, respectively. Urocortin II, mouse activates CRF2 receptors in a cAMP/PKA- and Ca2+/CaMKII-dependent manner.Urocortin II, mouse is expressed in discrete areas of the central nervous system, and activates central neurons involved in the processing of visceral sensory information, and in modulating autonomic outflow[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 330648-32-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2847. | |
| 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. | |
| 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 (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. Category: Signaling pathways. CAS No. 154525-25-4. Pack Sizes: 500 μg; 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 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 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 | 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 |
| 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. Category: Signaling pathways. CAS No. 1143-70-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-100599. | |
| Urolithin A | Urolithin A (3,8-Dihydroxy Urolithin, 2',7-Dihydroxy-3,4-benzocoumarin), a metabolite of ellagitannin, is a first-in-class natural compound that induces mitophagy both in vitro and in vivo following oral consumption. Group: Inhibitors. Alternative Names: 3,8-Dihydroxy Urolithin; 2',7-Dihydroxy-3,4-benzocoumarin. CAS No. 1143-70-0. Pack Sizes: 10mg. Product ID: S5312. Formula: C13H8O4. Smiles: C1=CC2=C(C=C1O)C(=O)OC3=C2C=CC(=C3)O. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| Urolithin A 8-Methyl Ether | Urolithin A 8-Methyl Ether. Alternative Names: 3-Hydroxy-8-methoxy-6H-benzo[c]chromen-6-one. CAS No. 35233-17-1. Purity: 98%. Product ID: ACM35233171. Molecular formula: C14H10O4. Mole weight: 242.23. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. Category: Signaling pathways. CAS No. 1139-83-9. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Category: Signaling pathways. CAS No. 165393-06-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 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 μM. 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. Category: Signaling pathways. Alternative Names: 3,4,8,9-Tetrahydroxy urolithin. CAS No. 131086-98-1. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Category: Signaling pathways. CAS No. 1453297-45-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W746164. | |
| Urolithin M5 | Urolithin M5 (Decarboxyellagic acid) is an orally active influenza virus neuraminidase inhibitor and neuroprotective agent, with IC50 values of 174.8 μM (HK68), 191.5 μM (pdm09), 243.2 μM (WSN) and 257.1 μM (PR8) against four influenza virus neuraminidases, respectively. Urolithin M5 inhibits viral neuraminidase activity, thereby blocking influenza virus replication (including oseltamivir (HY-13317)-resistant strains), protecting infected mammals from death and improving pulmonary edema. Urolithin M5 forms a hydrogen-bond stabilized complex with IGF1R, and binds to MAPK14, AKT1, NFKB1 and EGFR. Urolithin M5 reduces reactive oxygen species production, inhibits neuronal apoptosis, restores mitochondrial transmembrane potential, and promotes neurite outgrowth of damaged neuronal cells. Urolithin M5 can be used in research related to influenza virus infection and Alzheimer's disease[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Decarboxyellagic acid. CAS No. 91485-02-8. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg. Product ID: HY-N7922. | |
| uronate dehydrogenase | Requires Mg2+. The enzyme, characterized from the bacterium Agrobacterium fabrum, participates in oxidative degradation pathways for galacturonate and glucuronate. The enzyme can only accept the β anomeric form of the substrate. The 1,5-lactone product is rather stable at cytosolic pH and does not hydrolyse spontaneously at a substantial rate. Group: Enzymes. Synonyms: uronate:NAD-oxidoreductase; uronic acid dehydrogenase. Enzyme Commission Number: EC 1.1.1.203. CAS No. 37250-98-9. Uronate dehydrogenase. 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-0108; uronate dehydrogenase; EC 1.1.1.203; 37250-98-9; uronate:NAD-oxidoreductase; uronic acid dehydrogenase. Cat No: EXWM-0108. | |
| Uronate dehydrogenase from Agrobacterium tumefaciens, Recombinant | In enzymology, an uronate dehydrogenase (EC 1.1.1.203) is an enzyme that catalyzes the chemical reaction: D-galacturonate + NAD+ + H2O ? D-galactarate + NADH + H+. The 3 substrates of this enzyme are D-galacturonate, NAD+, and H2O, whereas its 3 products are D-galactarate, NADH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: uronate:NAD+ 1-oxidoreductase; uronate: NAD-oxidoreductase; uronic acid dehydrogenase; EC 1.1.1.203. Enzyme Commission Number: EC 1.1.1.203. CAS No. 37250-98-9. Purity: >95% as judged by SDS-PAGE. Uronate dehydrogenase. Mole weight: 31.14 kDa. Activity: 3000 U/ml. Storage: Uronate dehydrogenase should be stored at 4 °C or and will remain stable up to 3 years if stored as specified. Form: 3.2 M ammonium sulphate. Source: E. coli. Species: Agrobacterium tumefaciens. uronate:NAD+ 1-oxidoreductase; uronate: NAD-oxidoreductase; uronic acid dehydrogenase; EC 1.1.1.203. Cat No: NATE-1575. | |
| uronolactonase | This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. The systematic name of this enzyme class is D-glucurono-6,2-lactone lactonohydrolase. This enzyme is also called glucuronolactonase. This enzyme participates in ascorbate and aldarate metabolism. Group: Enzymes. Synonyms: glucuronolactonase. Enzyme Commission Number: EC 3.1.1.19. CAS No. 9025-93-8. 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-3444; uronolactonase; EC 3.1.1.19; 9025-93-8; glucuronolactonase. Cat No: EXWM-3444. | |
| Uroporphyrin III octamethyl ester | Uroporphyrin III octamethyl ester. Alternative Names: 3,8,13,17-Tetrakis(2-methoxy-2-oxoethyl)-21H,23H-porphyrin-2,7,12,18-tetrapropanoic acid tetramethyl ester. CAS No. 15435-60-6. Purity: 98%. Product ID: ACM15435606-2. Molecular formula: C48H54N4O16. Mole weight: 942.96. IUPAC Name: methyl 3-[3,7,13,17-tetrakis(2-methoxy-2-oxoethyl)-8,12,18-tris(3-methoxy-3-oxopropyl)-21,24-dihydroporphyrin-2-yl]propanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Uroporphyrin i,octamethyl ester | Uroporphyrin i,octamethyl ester. Alternative Names: Uroporphyrin I octamethyl ester, U3253_ALDRICH, U3253_SIGMA, CID66288, NSC89197, EINECS 233-444-0, NSC 89197, 10170-03-3, 21H,23H-Porphine-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetrakis(2-methoxy-2-oxoethyl)-, tetramethyl ester, 21H,23H-Porphine-2,7,12,17-tetraacetic acid, 3,8,13,18-tetrakis(3-methoxy-3-oxopropyl)-, 2,7,12,17-tetramethyl ester, Tetramethyl 3,8,13,18-tetrakis(2-methoxy-2-oxoethyl)-21H,23H-porphine-2,7,12,17-tetrapropionate. CAS No. 10170-03-3. Purity: 96%. Product ID: ACM10170033. Molecular formula: C48H54N4O16. Mole weight: 942.96. IUPAC Name: methyl 3-[3,8,13,18-tetrakis(2-methoxy-2-oxoethyl)-7,12,17-tris(3-methoxy-3-oxopropyl)-21,22-dihydroporphyrin-2-yl]propanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| uroporphyrinogen decarboxylase | Acts on a number of porphyrinogens. Group: Enzymes. Synonyms: uroporphyrinogen III decarboxylase; porphyrinogen carboxy-lyase; porphyrinogen decarboxylase; uroporphyrinogen-III carboxy-lyase. Enzyme Commission Number: EC 4.1.1.37. CAS No. 9024-70-8. 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-4781; uroporphyrinogen decarboxylase; EC 4.1.1.37; 9024-70-8; uroporphyrinogen III decarboxylase; porphyrinogen carboxy-lyase; porphyrinogen decarboxylase; uroporphyrinogen-III carboxy-lyase. Cat No: EXWM-4781. | |
| uroporphyrinogen-III C-methyltransferase | This enzyme catalyses two sequential methylation reactions, the first forming precorrin-1 and the second leading to the formation of precorrin-2. It is the first of three steps leading to the formation of siroheme from uroporphyrinogen III. The second step involves an NAD+-dependent dehydrogenation to form sirohydrochlorin from precorrin-2 (EC 1.3.1.76, precorrin-2 dehydrogenase) and the third step involves the chelation of Fe2+ to sirohydrochlorin to form siroheme (EC 4.99.1.4, sirohydrochlorin ferrochelatase). In Saccharomyces cerevisiae, the last two steps are carried out by a single bifunctional enzyme, Met8p. In some bacteria, steps 1-3 are catalysed by a single mult.(incorrect). Enzyme Commission Number: EC 2.1.1.107. CAS No. 125752-76-3. 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-1705; uroporphyrinogen-III C-methyltransferase; EC 2.1.1.107; 125752-76-3; uroporphyrinogen methyltransferase; uroporphyrinogen-III methyltransferase; adenosylmethionine-uroporphyrinogen III methyltransferase; S-adenosyl-L-methionine-dependent uroporphyrinogen III methylase; uroporphyrinogen-III methylase; SirA; CysG; CobA [ambiguous - see EC 2.5.1.17] SUMT; uroporphyrin-III C-methyltransferase (incorrect); S-adenosyl-L-methionine:uroporphyrin-III C-methyltransferase. | |
| uroporphyrinogen-III synthase | In the presence of EC 2.5.1.61, hydroxymethylbilane synthase, the enzyme forms uroporphyrinogen III from porphobilinogen. Group: Enzymes. Synonyms: porphobilinogenase; uroporphyrinogen isomerase; uroporphyrinogen III cosynthase; URO-synthase; hydroxymethylbilane hydro-lyase (cyclizing). Enzyme Commission Number: EC 4.2.1.75. CAS No. 37340-55-9. 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-5059; uroporphyrinogen-III synthase; EC 4.2.1.75; 37340-55-9; porphobilinogenase; uroporphyrinogen isomerase; uroporphyrinogen III cosynthase; URO-synthase; hydroxymethylbilane hydro-lyase (cyclizing). Cat No: EXWM-5059. | |
| Urosodeoxycholic Acid EP Impurity A | Urosodeoxycholic Acid EP Impurity A. Uses: For analytical and research use. CAS No. 474-25-9. Molecular formula: C24H40O4. Mole weight: 392.58. Catalog: APB474259. | |
| Urosodeoxycholic Acid EP Impurity B | Urosodeoxycholic Acid EP Impurity B. Uses: For analytical and research use. CAS No. 81-25-4. Molecular formula: C24H40O5. Mole weight: 408.58. Catalog: APB81254. | |
| Urosodeoxycholic Acid EP Impurity C | Urosodeoxycholic Acid EP Impurity C. Uses: For analytical and research use. CAS No. 434-13-9. Molecular formula: C24H40O3. Mole weight: 376.58. Catalog: APB434139. | |
| Urosodeoxycholic Acid EP Impurity D | Urosodeoxycholic Acid EP Impurity D. Uses: For analytical and research use. CAS No. 2955-27-3. Molecular formula: C24H40O5. Mole weight: 408.58. Catalog: APB2955273. | |
| Urosodeoxycholic Acid EP Impurity E | Urosodeoxycholic Acid EP Impurity E. Uses: For analytical and research use. CAS No. 83-44-3. Molecular formula: C24H40O4. Mole weight: 392.58. Catalog: APB83443. | |
| Urosodeoxycholic Acid EP Impurity F (Obeticholic Acid Intermediate 1) | Urosodeoxycholic Acid EP Impurity F (Obeticholic Acid Intermediate 1). Uses: For analytical and research use. CAS No. 4651-67-6. Molecular formula: C24H38O4. Mole weight: 390.56. Catalog: APB4651676. | |
| Urosodeoxycholic Acid EP Impurity G | Urosodeoxycholic Acid EP Impurity G. Uses: For analytical and research use. CAS No. 10538-55-3. Molecular formula: C25H42O4. Mole weight: 406.61. Catalog: APB10538553. | |
| Urosodeoxycholic Acid EP Impurity H | Urosodeoxycholic Acid EP Impurity H. Uses: For analytical and research use. CAS No. 78919-26-3. Molecular formula: C24H40O4. Mole weight: 392.58. Catalog: APB78919263. | |
| Urosodeoxycholic Acid EP Impurity I | Urosodeoxycholic Acid EP Impurity I. Uses: For analytical and research use. CAS No. 130593-75-8. Molecular formula: C24H42O3. Mole weight: 378.6. Catalog: APB130593758. | |
| Urosodeoxycholic Acid EP Impurity J (Obeticholic Acid Impurity 17) | Urosodeoxycholic Acid EP Impurity J (Obeticholic Acid Impurity 17). Uses: For analytical and research use. CAS No. 4185-00-6. Molecular formula: C24H38O4. Mole weight: 390.56. Catalog: APB4185006. | |
| Urosodeoxycholic Acid EP Impurity K | Urosodeoxycholic Acid EP Impurity K. Uses: For analytical and research use. CAS No. 566-24-5. Molecular formula: C24H40O4. Mole weight: 392.58. Catalog: APB566245. | |
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