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| Product | Description | |
|---|---|---|
| Undecamethylenediamine | Undecamethylenediamine. CAS No. 822-08-2. Molecular formula: C11H26N2. Mole weight: 186.34g/mol. Purity: N/A. IUPAC Name: undecane-1,11-diamine. SMILES: C(CCCCCN)CCCCCN. InChI: InChI=1S/C11H26N2/c12-10-8-6-4-2-1-3-5-7-9-11-13/h1-13H2. |  |
| Undecane-[d24] | Undecane-[d24]. Synonyms: n-Undecane-d24. Grade: ≥98% by CP; ≥98% atom D. CAS No. 164858-54-2. Molecular formula: C11D24. Mole weight: 180.46. |  |
| Undecanedioic Acid | OtherSolid;Solid. Alternative Names: Undecane-1,11-dioic acid. CAS No. 1852-04-6. Purity: 97%. Product ID: ACM1852046-1. Molecular formula: C11H20O4. Mole weight: 216.27. IUPAC Name: Undecanedioic acid. Canonical SMILES: C(CCCCC(=O)O)CCCCC(=O)O. ECNumber: 217-440-6. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Undecanedioic Acid | OtherSolid;Solid. Alternative Names: Undecane-1,11-dioic acid. CAS No. 1852-04-6. Molecular formula: C11H20O4. Mole weight: 216.27. Purity: 97%. IUPAC Name: Undecanedioic acid. SMILES: C(CCCCC(=O)O)CCCCC(=O)O. InChI: InChI=1S/C11H20O4/c12-10(13)8-6-4-2-1-3-5-7-9-11(14)15/h1-9H2,(H,12,13)(H,14,15). | |
| Undecanoic acid | Undecanoic acid. Alternative Names: Hendecanoic acid. CAS No. 112-37-8. Molecular formula: C11H22O2. Mole weight: 186.30. Purity: >98%. SMILES: CCCCCCCCCCC(=O)O. InChI: InChI=1S/C11H22O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3,(H,12,13). | |
| Undecanoic acid | Undecanoic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 112-37-8. Pack Sizes: 1kg, 2kg, 5kg, 10kg, 25kg. Molecular Formula: C11H22O2. US Biological Life Sciences. |  Worldwide |
| Undecanoic Acid | Undecanoic acid is a white crystalline solid. Insoluble in water. Specific gravity 0.85. Hence floats on water.;Solid;Solid;colourless crystals/ faint fatty, aldehydic odour. Alternative Names: Hendecanoic Acid. CAS No. 112-37-8. Molecular formula: C11H22O2. Mole weight: 186.29. Purity: 99%. IUPAC Name: undecanoic acid. SMILES: CCCCCCCCCCC(=O)O. InChI: InChI=1S/C11H22O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3,(H,12,13). | |
| Undecanoic acid,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoro- | Undecanoic acid,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoro-. CAS No. 1765-48-6. Product ID: ACM1765486. Molecular formula: C11H2F20O2. Mole weight: 546.13. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecanoic acid,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoro-,ethyl ester | Undecanoic acid,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoro-,ethyl ester. Alternative Names: Ethyl 11H-perfluoroundecanoate, 1649-56-5, Ethyl 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoate, AC1MC6YY, CTK8E8061, MolPort-000-155-333, PC3262, AKOS005256725, AG-E-14619, FT-0625833, A810608, I14-38962, 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-eicosafluoroundecanoic acid ethyl ester, ethyl 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosakis(fluoranyl)undecanoate, ETHYL 11H-PERFLUOROUNDECANOATE;Ethyl 11H-perfluoroundecanoate 97%;Ethyl11H-perfluoroundecanoate97%. CAS No. 1649-56-5. Purity: 96%. Product ID: ACM1649565. Molecular formula: C13H6F20O2. Mole weight: 574.15. IUPAC Name: ethyl 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-icosafluoroundecanoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecanoic acid,2,2-dimethyl- | Undecanoic acid,2,2-dimethyl-. Alternative Names: ALPHA,ALPHA-DIMETHYLUNDECANOIC ACID;2,2-DIMETHYLUNDECANOIC ACID. CAS No. 13005-29-3. Product ID: ACM13005293. Molecular formula: C13H26O2. Mole weight: 214.34. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecanol | Undecanol. Alternative Names: 1-Hendecanol. CAS No. 112-42-5. Molecular formula: C11H24O. Mole weight: 172.30. Purity: 99%+. IUPAC Name: undecan-1-ol. SMILES: CCCCCCCCCCCO. | |
| Undecanone-2 Redistilled | Undecanone-2 Redistilled (Methyl Nonyl Ketone). CAS No. 112-12-9. FEMA No. 3093. Kosher: Y. VIGON Item # 500499. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Undecanoyl chloride | Undecanoyl chloride. CAS No. 17746-05-3. Product ID: ACM17746053. Molecular formula: C11H21ClO. Mole weight: 204.74. Alfa Chemistry - ISO 9001:32057 Certified. | |
| undecaprenol kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. This enzyme participates in peptidoglycan biosynthesis. Group: Enzymes. Synonyms: isoprenoid alcohol kinase; isoprenoid alcohol phosphokinase; C55-isoprenoid alcohol phosphokinase; isoprenoid alcohol kinase (phosphorylating); C55-isoprenoid alcohol kinase; C55-isoprenyl alcohol phosphokinase; polyisoprenol kinase. Enzyme Commission Number: EC 2.7.1.66. CAS No. 9068-22-8. 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-3097; undecaprenol kinase; EC 2.7.1.66; 9068-22-8; isoprenoid alcohol kinase; isoprenoid alcohol phosphokinase; C55-isoprenoid alcohol phosphokinase; isoprenoid alcohol kinase (phosphorylating); C55-isoprenoid alcohol kinase; C55-isoprenyl alcohol phosphokinase; polyisoprenol kinase. Cat No: EXWM-3097. |  |
| undecaprenyl-diphosphate phosphatase | Isolated from the bacteria Micrococcus lysodeikticus, Escherichia coli and Bacillus subtilis. The product of the reaction, ditrans,octacis-undecaprenyl phosphate, is essential for cell wall polysaccharide biosynthesis in these strains. Group: Enzymes. Synonyms: C55-isoprenyl diphosphatase; C55-isoprenyl pyrophosphatase; isoprenyl pyrophosphatase (ambiguous); undecaprenyl pyrophosphate phosphatase; undecaprenyl pyrophosphate pyrophosphatase; UPP phosphatase; Und-PP pyrophosphatase; UppP (ambiguous); BacA; undecaprenyl-diphosphate phosphohydrolase; undecaprenyl-diphosphatase. Enzyme Commission Number: EC 3.6.1.27. CAS No. 9077-80-9. 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-4611; undecaprenyl-diphosphate phosphatase; EC 3.6.1.27; 9077-80-9; C55-isoprenyl diphosphatase; C55-isoprenyl pyrophosphatase; isoprenyl pyrophosphatase (ambiguous); undecaprenyl pyrophosphate phosphatase; undecaprenyl pyrophosphate pyrophosphatase; UPP phosphatase; Und-PP pyrophosphatase; UppP (ambiguous); BacA; undecaprenyl-diphosphate phosphohydrolase; undecaprenyl-diphosphatase. Cat No: EXWM-4611. | |
| undecaprenyldiphospho-muramoylpentapeptide β-N-acetylglucosaminyltransferase | The enzyme also works when the lysine residue is replaced by meso-2,6-diaminoheptanedioate (meso-2,6-diaminopimelate, A2pm) combined with adjacent residues through its L-centre, as it is in Gram-negative and some Gram-positive organisms. The undecaprenol involved is ditrans,octacis-undecaprenol (for definitions, click here). Group: Enzymes. Synonyms: MurG transferase; UDP-N-acetyl-D-glucosamine:N-acetyl-α-D-muramyl(oyl-L-Ala-γ-D-Glu-L-Lys-D-Ala-D-Ala)-diphosphoundecaprenol β-1,4-N-acetylglucosaminlytransferase. Enzyme Commission Number: EC 2.4.1.227. CAS No. 60976-26-3. 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-2456; undecaprenyldiphospho-muramoylpentapeptide β-N-acetylglucosaminyltransferase; EC 2.4.1.227; 60976-26-3; MurG transferase; UDP-N-acetyl-D-glucosamine:N-acetyl-α-D-muramyl(oyl-L-Ala-γ-D-Glu-L-Lys-D-Ala-D-Ala)-diphosphoundecaprenol β-1,4-N-acetylglucosaminlytransferase. Cat No: EXWM-2456. | |
| undecaprenyl-diphosphooligosaccharide-protein glycotransferase | A bacterial enzyme that has been isolated from Campylobacter jejuni and Campylobacter lari. It forms a glycoprotein by the transfer of a glucosyl-N-acetylgalactosaminyl-N,N'-diacetylbacillosamine (GalNAc2(Glc)GalNAc3diNAcBac) polysaccharide and related oligosaccharides to the side-chain of an L-asparagine residue in the sequence -Asp/Glu-Xaa-Asn-Xaa'-Ser/Thr- (Xaa and Xaa' not Pro) in nascent polypeptide chains. Requires Mn2+ or Mg2+. Occurs on the external face of the plasma membrane. The polyprenol involved is normally tritrans,heptacis-undecaprenol but a decaprenol is used by some species. Group: Enzymes. Synonyms: PglB. Enzyme Commission Number: EC 2.4.99.19. 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-2703; undecaprenyl-diphosphooligosaccharide-protein glycotransferase; EC 2.4.99.19; PglB. Cat No: EXWM-2703. | |
| undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase | The enzyme shows no activity with UDP-4-amino-4-deoxy-β-L-arabinose. Group: Enzymes. Synonyms: undecaprenyl-phosphate Ara4FN transferase; Ara4FN transferase; polymyxin resistance protein PmrF; UDP-4-amino-4-deoxy-α-L-arabinose:ditrans,polycis-undecaprenyl phosphate 4-amino-4-deoxy-α-L-arabinosyltransferase. Enzyme Commission Number: EC 2.4.2.53. 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-2683; undecaprenyl-phosphate 4-deoxy-4-formamido-L-arabinose transferase; EC 2.4.2.53; undecaprenyl-phosphate Ara4FN transferase; Ara4FN transferase; polymyxin resistance protein PmrF; UDP-4-amino-4-deoxy-α-L-arabinose:ditrans,polycis-undecaprenyl phosphate 4-amino-4-deoxy-α-L-arabinosyltransferase. Cat No: EXWM-2683. | |
| undecaprenyl-phosphate galactose phosphotransferase | This enzyme belongs to the family of transferases, specifically those transferring non-standard substituted phosphate groups. Group: Enzymes. Synonyms: poly(isoprenol)-phosphate galactose phosphotransferase; poly(isoprenyl)phosphate galactosephosphatetransferase; undecaprenyl phosphate galactosyl-1-phosphate transferase; UDP-galactose:undecaprenyl-phosphate galactose phosphotransferase. Enzyme Commission Number: EC 2.7.8.6. CAS No. 37278-29-8. 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-3344; undecaprenyl-phosphate galactose phosphotransferase; EC 2.7.8.6; 37278-29-8; poly(isoprenol)-phosphate galactose phosphotransferase; poly(isoprenyl)phosphate galactosephosphatetransferase; undecaprenyl phosphate galactosyl-1-phosphate transferase; UDP-galactose:undecaprenyl-phosphate galactose phosphotransferase. Cat No: EXWM-3344. | |
| undecaprenyl-phosphate glucose phosphotransferase | The enzyme is involved in biosynthesis of xanthan. Group: Enzymes. Synonyms: GumD; undecaprenylphosphate glucosylphosphate transferase. Enzyme Commission Number: EC 2.7.8.31. 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-3330; undecaprenyl-phosphate glucose phosphotransferase; EC 2.7.8.31; GumD; undecaprenylphosphate glucosylphosphate transferase. Cat No: EXWM-3330. | |
| undecaprenyl-phosphate mannosyltransferase | Requires phosphatidylglycerol. Group: Enzymes. Synonyms: guanosine diphosphomannose-undecaprenyl phosphate mannosyltransferase; GDP mannose-undecaprenyl phosphate mannosyltransferase; GDP-D-mannose:lipid phosphate transmannosylase. Enzyme Commission Number: EC 2.4.1.54. CAS No. 37277-62-6. 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-2600; undecaprenyl-phosphate mannosyltransferase; EC 2.4.1.54; 37277-62-6; guanosine diphosphomannose-undecaprenyl phosphate mannosyltransferase; GDP mannose-undecaprenyl phosphate mannosyltransferase; GDP-D-mannose:lipid phosphate transmannosylase. Cat No: EXWM-2600. | |
| undecaprenyl phosphate N,N'-diacetylbacillosamine 1-phosphate transferase | Isolated from Campylobacter jejuni. Part of a bacterial N-linked glycosylation pathway. Group: Enzymes. Synonyms: PglC. Enzyme Commission Number: EC 2.7.8.36. 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-3335; undecaprenyl phosphate N,N'-diacetylbacillosamine 1-phosphate transferase; EC 2.7.8.36; PglC. Cat No: EXWM-3335. | |
| Undecavertol | Undecavertol. CAS No. 81782-77-6. VIGON Item # 500944. Categories: Speciality Ingrdients Suppliers, Fragrances, violet decenol, Perfumers. | America & Internationally |
| Undecenoic acid | Undecenoic acid. Group: Biochemicals. Alternative Names: Undecylenic acid. Grades: Highly Purified. CAS No. 112-38-9. Pack Sizes: 100g, 250g, 500g. Molecular Formula: C11H20O2. US Biological Life Sciences. | Worldwide |
| Undecenoic acid,3-methylbutyl ester | Undecenoic acid,3-methylbutyl ester. Alternative Names: Undecenoicacid, isopentyl ester (8CI); Isoamyl undecylenate. CAS No. 12262-03-2. Product ID: FFC-AR-12262032. Molecular formula: C16H30O2. Mole weight: 254.41. IUPAC Name: 3-methylbutyl (E)-undec-6-enoate. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecenoic Acid BP/USP | Undecenoic Acid BP/USP. CAS No. 112-38-9. |  |
| Undecoylium Chloride Iodine | Undecoylium Chloride Iodine. CAS No. 1338-54-1. Product ID: ACM1338541. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecyl acetate | Undecyl acetate. Alternative Names: N-undecyl acetate. CAS No. 1731-81-3. Purity: 99%+. Product ID: ACM1731813-1. Molecular formula: C13H26O2. Mole weight: 214.34. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Undecyl-beta-D-glucopyranoside | 250mg Pack Size. Group: Biochemicals, Building Blocks, Carbohydrates. Formula: C17H34O6. CAS No. 70005-86-6. Prepack ID 72880752-250mg. Molecular Weight 334.44826. See USA prepack pricing. |  |
| Undecyl chloride | Undecyl chloride. CAS No. 2473-3-2. Molecular formula: C11H23Cl. Mole weight: 190.75g/mol. IUPAC Name: 1-chloroundecane. SMILES: CCCCCCCCCCCCl. InChI: InChI=1S/C11H23Cl/c1-2-3-4-5-6-7-8-9-10-11-12/h2-11H2,1H3. | |
| Undecyl cyanide | Undecyl cyanide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2437-25-4. Pack Sizes: 10g, 25g. Molecular Formula: C12H23N. US Biological Life Sciences. | Worldwide |
| Undecylenic Acid | Undecylenic Acid. Alternative Names: Undec-10-enoic acid, 10-Undecenoic acid. CAS No. 112-38-9. Purity: 95%. Product ID: CI-GU-0184. Molecular formula: C11H20O2. Mole weight: 184.27 g/mol. IUPAC Name: undec-10-enoic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. |  US and Canada |
| 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 monoglyceride | Undecylenic monoglyceride |  Sarchem Laboratories New Jersey NJ |
| Undecylphosphonic Acid | Undecylphosphonic Acid. CAS No. 5137-69-9. Molecular formula: C11H25O3P. Mole weight: 236.29g/mol. IUPAC Name: undecylphosphonic acid. SMILES: CCCCCCCCCCCP(=O)(O)O. InChI: 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). | |
| Undecylphosphonic Acid, ≥98% | Undecylphosphonic Acid, ≥98%. CAS No. 5137-69-9. Molecular formula: C11H25O3P. Mole weight: 236.29g/mol. IUPAC Name: undecylphosphonic acid. SMILES: CCCCCCCCCCCP(=O)(O)O. InChI: 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). | |
| Undecylprodigiosin | Undecylprodigiosin is a prodigiosin antibiotic. Grade: >98%. CAS No. 52340-48-4. Molecular formula: C25H35N3O. Mole weight: 393.56. | |
| UNEP OC Pesticide ECD Internal Standard Mixture PCB-112/155/198 5 μg/mL in isooctane | UNEP OC Pesticide ECD Internal Standard Mixture PCB-112/155/198 5 μg/mL in isooctane. Uses: For analytical and research use. Purity: 98%. Catalog: APB12557. |  |
| 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. Category: Signaling pathways. Alternative Names: PTC596. CAS No. 1610964-64-1. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Grade: ≥95%. CAS No. 36587-59-4. Molecular formula: C19H18O5. Mole weight: 326.34. | |
| 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 |
| Uniform Polystyrene Microspheres (blue) | Uniform Polystyrene Microspheres (blue). | |
| 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). | |
| Uniform Polystyrene Microspheres (red) | Uniform Polystyrene Microspheres (red). | |
| Uniform Polystyrene Microspheres (yellow) | Uniform Polystyrene Microspheres (yellow). | |
| UniPR129 | UniPR129 is a potent and orally active Eph/ephrin antagonist. UniPR129 can inhibit EphA2-ephrin-A1 interaction with an IC50 of 945 nM and a Ki of 370 nM. UniPR129 can inhibit angiogenesis and show antitumor and neuroprotective effect. UniPR129 can be used for the researches of cancer and neurological disease, such as colorectal cancer and optic neuropathy[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1639159-47-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-123607. | |
| UniPR1331 | UniPR1331 is an orally active 3β-hydroxy-Δ5-choline acid derivative that inhibits Eph-ephrin interactions. UniPR1331 blocks the interaction of VEGFR2 with its natural ligand vascular endothelial growth factor and inhibits subsequent autophosphorylation, signaling, and pro-angiogenic activation of endothelial cells. UniPR1331 exhibits anti-angiogenesis, anti-cancer and anti-inflammation effects. UniPR1331 can be used for the researches of cancer and inflammation, such as glioma and colitis[1][2][3]. Uses: Scientific research. Category: 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. | |
| 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 mRNA Lipofection Reagent (LNP) | This product is a universal transfection reagent based on LNPs, designed specifically for delivering mRNA. It is suitable for transfection of eukaryotic cells such as HEK293T, WRL-68, HFL-1, A549, MCF7, Capan-2 cells, etc. It has the advantages of high transfection rate, low cytotoxicity, good reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents. |  |
| Universal siRNA Lipofection Reagent (LNP) | This product is a universal transfection reagent based on LNPs, designed specifically for delivering siRNA. It is suitable for transfection of eukaryotic cells such as HEK293T, WRL-68, HFL-1, A549, MCF7, Capan-2 cells, etc. It has the advantages of high transfection rate, low cytotoxicity, good reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents. | |
| Unlabeled FXX489 | Unlabeled FXX489 (NNS309) is a fibroblast activation protein (FAP)-targeting ligand. Unlabeled FXX489 can be labeled with 68Ga and 177Lu and shows anticancer effects. Unlabeled FXX489 can be used for the study of pancreatic ductal adenocarcinoma (PDAC), non-small cell lung cancer (NSCLC), breast cancer (BC), and colorectal cancer (CRC)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NNS309. CAS No. 3076330-05-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P10944. | |
| 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. | |
| 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. | |
| UP12 | UP12 is an ATPase activity activator that activates the ATPase activity of valosin-containing protein (VCP), with an EC50 of 1.24 μM. UP12 is applicable to research related to multisystem proteinopathies[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 443353-87-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-168325. | |
| UP158 | UP158 enhances the activity of ATPase, and activates valosin-containing protein (VCP) with an EC50 of 2.57 μM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 489402-33-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-168324. | |
| UP163 | UP163 enhances the activity of ATPase, and activates valosin-containing protein (VCP) with an EC50 of 9.0 μM. UP163 reduces MG-132 (HY-13259)-induced TDP-43 aggregates[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 591242-60-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-168323. | |
| Upacicalcet sodium | Upacicalcet sodium is a non-peptide calcimimetic that acts as a CaSR agonist (EC50 = 10.8 nM). Upacicalcet sodium reduces serum intact parathyroid hormone (iPTH) and serum Ca2+ levels, reducing hypocalcemia and gastrointestinal complications. Upacicalcet sodium sodium improves vascular calcification and bone disorders in the Adenine (HY-B0152)-induced secondary hyperparathyroidism (SHPT) rat model. Upacicalcet sodium sodium inhibits cortical pore formation and reduces bone fibrosis in rats with chronic kidney disease (CKD). Upacicalcet sodium is useful for studying SHPT[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SK-1403; AJT240; PLS240. CAS No. 2052969-18-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109106A. | |
| Upadacitinib | Upadacitinib (ABT-494) is a potent, orally active and selective Janus kinase 1 (JAK1) inhibitor (IC50=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. Category: Signaling pathways. Alternative Names: ABT-494. CAS No. 1310726-60-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg; 1 g. Product ID: HY-19569. | |
| Upadacitinib | Upadacitinib is a potent and selective JAK inhibitor. Upadacitinib is approximately 74 fold selective for Jak1 over Jak2 in cellular assays dependent on specific, relevant cytokines. Upadacitinib demonstrates efficacy in rat arthritis models. Category: Active pharmaceutical ingredients. CAS No. 1607431-21-9. Product ID: API1607431219. Molecular formula: C21H33F3N6O11. Mole weight: 602.521. |  |
| Upadacitinib Impurity 1 | Upadacitinib Impurity 1. Uses: For analytical and research use. 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 10 | Upadacitinib Impurity 10. Uses: For analytical and research use. Alternative Names: (3S,4R)-3-ethyl-4-(3-(hydroxymethyl)-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide. Molecular formula: C18H21F3N6O2. Mole weight: 410.39. Catalog: APB02092. | |
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