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| Product | Description | |
|---|---|---|
| Unoprostone isopropyl ester | Unoprostone isopropyl ester. Group: Biochemicals. Alternative Names: (5Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-(3-oxodecyl)cyclopenthyl]-5-heptenoic acid isopropyl ester; UF-021; Rescula. Grades: Highly Purified. CAS No. 120373-24-2. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C25H44O5. US Biological Life Sciences. |  Worldwide |
| unsaturated chondroitin disaccharide hydrolase | The enzyme releases 4-deoxy-4,5-didehydro D-glucuronic acid or 4-deoxy-4,5-didehydro L-iduronic acid from chondroitin disaccharides, hyaluronan disaccharides and heparin disaccharides and cleaves both glycosidic (1?3) and (1?4) bonds. It prefers the sulfated disaccharides to the unsulfated disaccharides. Group: Enzymes. Synonyms: UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Enzyme Commission Number: EC 3.2.1.180. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3864; unsaturated chondroitin disaccharide hydrolase; EC 3.2.1.180; UGL (ambiguous); unsaturated glucuronyl hydrolase (ambiguous). Cat No: EXWM-3864. |  |
| Unsaturated Polyester Resin | Unsaturated Polyester Resin. Group: Polymers. |  |
| unsaturated rhamnogalacturonyl hydrolase | The enzyme is part of the degradation system for rhamnogalacturonan I in Bacillus subtilis strain 168. Group: Enzymes. Synonyms: YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Unsaturated rhamnogalacturonyl hydrolase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3855; unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: EXWM-3855. | |
| Unsaturated rhamnogalacturonyl hydrolase 105A from Bacillus subtilis, Recombinant | Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 43.4 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1508. | |
| Unsaturated rhamnogalacturonyl hydrolase 105A from Bacteroides thetaiotaomicron, Recombinant | Unsaturated rhamnogalacturonyl hydrolase (EC 3.2.1.172, YteR, YesR) is an enzyme with systematic name 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose hydrolase. This enzyme catalyses the following chemical reaction: 2-O-(4-deoxy-beta-L-threo-hex-4-enopyranuronosyl)-alpha-L-rhamnopyranose + H2O ? 5-dehydro-4-deoxy-D-glucuronate + L-rhamnopyranose. Group: Enzymes. Synonyms: Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Enzyme Commission Number: EC 3.2.1.172. Purity: >90% as judged by SDS-PAGE. Unsaturated rhamnogalacturonyl hydrolase. Mole weight: 52.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Unsaturated rhamnogalacturonyl hydrolase; EC 3.2.1.172; YteR; YesR. Cat No: NATE-1509. | |
| unspecific monooxygenase | A group of P-450 heme-thiolate proteins, acting on a wide range of substrates including many xenobiotics, steroids, fatty acids, vitamins and prostaglandins; reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, N-, S- and O-dealkylations, desulfation, deamination, and reduction of azo, nitro and N-oxide groups. Together with EC 1.6.2.4, NADPH-hemoprotein reductase, it forms a system in which two reducing equivalents are supplied by NADPH. Some of the reactions attributed to EC 1.14.15.3, alkane 1-monooxygenase, belong here. Group: Enzymes. Synonyms: microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hy. Enzyme Commission Number: EC 1.14.14.1. CAS No. 9038-14-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0906; unspecific monooxygenase; EC 1.14.14.1; 9038-14-6; microsomal monooxygenase; xenobiotic monooxygenase; aryl-4-monooxygenase; aryl hydrocarbon hydroxylase; microsomal P-450; flavoprotein-linked monooxygenase; flavoprotein monooxygenase; substrate,reduced-flavoprotein:oxygen oxidoreductase (RH-hydroxylating or -epoxidizing). Cat No: EXWM-0906. | |
| unspecific peroxygenase | A heme-thiolate protein (P-450). Enzymes of this type include glycoproteins secreted by agaric basidiomycetes. They catalyse the insertion of an oxygen atom from H2O2 into a wide variety of substrates, including aromatic rings such as naphthalene, toluene, phenanthrene, pyrene and p-nitrophenol, recalcitrant heterocycles such as pyridine, dibenzofuran, various ethers (resulting in O-dealkylation) and alkanes such as propane, hexane and cyclohexane. Reactions catalysed include hydroxylation, epoxidation, N-oxidation, sulfooxidation, O- and N-dealkylation, bromination and one-electron oxidations. They have little or no activity toward chloride. Mechanistically, the catalytic cycle of unspecific (mono)-peroxygenases combines elements of the "shunt" pathway of cytochrome P-450s (a side activity that utilizes a peroxide in place of dioxygen and NAD[P]H) and the classic heme peroxidase cycle. Group: Enzymes. Synonyms: aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Enzyme Commission Number: EC 1.11.2.1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0512; unspecific peroxygenase; EC 1.11.2.1; aromatic peroxygenase; mushroom peroxygenase; haloperoxidase-peroxygenase; Agrocybe aegerita peroxidase. Cat No: EXWM-0512. | |
| Upacicalcet sodium | Upacicalcet sodium is an intravenous calcimimetic agent. Upacicalcet suppresses excessive parathyroid hormone (PTH) secretion, thereby lowering blood PTH levels, by acting directly on parathyroid cell membrane calcium-sensing receptors. Upacicalcet can be used for researching the disease of secondary hyperparathyroidism (SHPT) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2052969-18-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109106A. |  |
| Upadacitinib | Upadacitinib (ABT-494) (ABT-494) is a selective Janus kinase (JAK) 1 inhibitor, which is being studied for the treatment of several autoimmune disorders in the IC50 of 43 nM. CAS No. 1310726-60-3. Product ID: API1310726603. Molecular formula: C17H19F3N6O. |  |
| Upadacitinib | Upadacitinib (ABT-494) is a potent, orally active and selective Janus kinase 1 ( JAK1 ) inhibitor ( IC 50 =43 nM). Upadacitinib (ABT-494) displays approximately 74 fold selective for JAK1 over JAK2 (200 nM) in cellular assays dependent on specific, relevant cytokines. Upadacitinib (ABT-494) can be used for several autoimmune disorders research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-494. CAS No. 1310726-60-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-19569. | |
| Upadacitinib Impurity 63 | Upadacitinib Impurity 63. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: N-(2,2,2-trifluoroethyl)-1H-imidazole-1-carboxamide. CAS No. 1046861-47-5. Molecular formula: C6H6F3N3O. Mole weight: 193.13. Catalog: APB1046861475. |  |
| Upadacitinib Impurity 89 | Upadacitinib Impurity 89. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5H-pyrrolo[2,3-b]pyrazin-2-amine. CAS No. 1504066-86-7. Molecular formula: C6H6N4. Mole weight: 134.14. Catalog: APB1504066867. | |
| Upamostat | Upamostat (WX-671) is a serine protease inhibitor. Upamostat is the orally available prodrug of the WX-UK1, which is a urokinase plasminogen activator (uPA) inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: WX-671. CAS No. 590368-25-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16511. | |
| UPCDC30245 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Upconverting Nanoparticle Quantum Dots | Upconverting Nanoparticle Quantum Dots. Group: Upconverting nanoparticles (ucnps). CAS No. 753489-02-0. 99.9%. | |
| Upconverting Nanoparticles | Upconverting Nanoparticles. Uses: Fluorescence imaging,biodetection, photodynamic therapy, photoactivation of anti-cancer drugs and biomolecules etc. Group: Quantum dots. | |
| Upconverting Nanoparticles | Upconverting Nanoparticles. Uses: Fluorescence imaging,biodetection, photodynamic therapy, photoactivation of anti-cancer drugs and biomolecules etc. Group: other nano materials other quantum dots. | |
| upconverting nanoparticles(green light) | upconverting nanoparticles(green light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| upconverting nanoparticles(near-infrared light) | upconverting nanoparticles(near-infrared light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| upconverting nanoparticles(purple blue light) | upconverting nanoparticles(purple blue light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| Upconverting nanoparticles/Quantum dots | Upconverting nanoparticles/Quantum dots. Group: Upconverting nanoparticles (ucnps). | |
| upconverting nanoparticles(UV light) | upconverting nanoparticles(UV light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| upconverting nanoparticles(yellow-green light) | upconverting nanoparticles(yellow-green light). Uses: Up conversion noparticles have excellent optical stability. they have been widely applied in biomedicine, including in vivo bioimaging, in vivo bioimaging, biodetection, immunohistochemistry, microarray detection, photodymic therapy, and photoactivated drug activation. Group: Upconverting nanoparticles. Pack Sizes: 50 mg. | |
| Upconverting Quantum Dots | Upconverting Quantum Dots. Group: Upconverting nanoparticles (ucnps). CAS No. 753489-02-0. 99.9%. | |
| Uperin-2.1 | Uperin-2.1 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. It has activity against gram-positive bacteria. Synonyms: H-Gly-Ile-Val-Asp-Phe-Ala-Lys-Lys-Val-Val-Gly-Gly-Ile-Arg-Asn-Ala-Leu-Gly-Ile-OH. Grade: >95%. Molecular formula: C88H151N25O23. Mole weight: 1927.3. |  |
| Uperin-2.2 | Uperin-2.2 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: H-Gly-Phe-Val-Asp-Leu-Ala-Lys-Lys-Val-Val-Gly-Gly-Ile-Arg-Asn-Ala-Leu-Gly-Ile-OH. Grade: >96%. Molecular formula: C88H151N25O23. Mole weight: 1927.3. | |
| Uperin-2.3 | Uperin-2.3 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: Gly-Phe-Phe-Asp-Leu-Ala-Lys-Lys-Val-Val-Gly-Gly-Ile-Arg-Asn-Ala-Leu-Gly-Ile-NH2. Grade: >95%. Molecular formula: C92H152N26O22. Mole weight: 1974.39. | |
| Uperin-2.4 | Uperin-2.4 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: H-Gly-Ile-Leu-Asp-Phe-Ala-Lys-Thr-Val-Val-Gly-Gly-Ile-Arg-Asn-Ala-Leu-Gly-Ile-OH. Grade: >97%. Molecular formula: C87H148N24O24. Mole weight: 1914.2. | |
| Uperin-2.5 | Uperin-2.5 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: H-Gly-Ile-Val-Asp-Phe-Ala-Lys-Gly-Val-Leu-Gly-Lys-Ile-Lys-Asn-Val-Leu-Gly-Ile-NH2. Grade: >97%. Molecular formula: C91H158N24O22. Mole weight: 1940.41. | |
| Uperin-2.7 | Uperin-2.7 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: H-Gly-Ile-Ile-Asp-Ile-Ala-Lys-Lys-Leu-Val-Gly-Gly-Ile-Arg-Asn-Val-Leu-Gly-Ile-OH. Grade: >98%. Molecular formula: C90H163N25O23. Mole weight: 1963.45. | |
| Uperin-2.8 | Uperin-2.8 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: H-Gly-Ile-Leu-Asp-Val-Ala-Lys-Thr-Leu-Val-Gly-Lys-Leu-Arg-Asn-Val-Leu-Gly-Ile-OH. Grade: >98%. Molecular formula: C90H163N25O24. Mole weight: 1979.4. | |
| Uperin-3.1 | Uperin-3.1 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: Gly-Val-Leu-Asp-Ala-Phe-Arg-Lys-Ile-Ala-Thr-Val-Val-Lys-Asn-Val-Val-NH2. Grade: >96%. Molecular formula: C84H146N24O21. Mole weight: 1828.24. | |
| Uperin-3.5 | Uperin-3.5 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: Gly-Val-Gly-Asp-Leu-Ile-Arg-Lys-Ala-Val-Ser-Val-Ile-Lys-Asn-Ile-Val-NH2. Grade: >98%. Molecular formula: C80H146N24O21. Mole weight: 1780.1. | |
| Uperin 3.6 | Uperin 3.6 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: NH2-Gly-Val-Ile-Asp-Ala-Ala-Lys-Lys-Trp-Asn-Val-Leu-Lys-Asn-Leu-Phe-NH2. Grade: >97%. Molecular formula: C86H139N23O20. Mole weight: 1815.2. | |
| Uperin-4.1 | Uperin-4.1 is a broad-spectrum antibiotic peptide isolated from Uperoleia mjobergii. Synonyms: Gly-Val-Gly-Ser-Phe-Ile-His-Lys-Val-Val-Ser-Ala-Ile-Lys-Asn-Val-Ala-NH2. Grade: >96%. Molecular formula: C79H133N23O20. Mole weight: 1725. | |
| Uperin-7.1 | Uperin-7.1 is a broad-spectrum antibiotic peptide isolated from Litoria ewingii. Synonyms: Gly-Trp-Phe-Asp-Val-Val-Lys-His-Ile-Ala-Ser-Ala-Val-NH2. Molecular formula: C68H102N18O16. Mole weight: 1427.6. | |
| UPF 1069 | UPF 1069. Group: Biochemicals. Alternative Names: 5-(2-Oxo-2-phenylethoxy)-1(2H)-isoquinolinone. Grades: Highly Purified. CAS No. 1048371-03-4. Pack Sizes: 1mg. Molecular Formula: C17H13NO3, Molecular Weight: 279.29. US Biological Life Sciences. | Worldwide |
| UPF 1069 | UPF 1069 is a PARP inhibitor, with IC50s of 8 and 0.3 ?M for PARP-1 and PARP-2, respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 1048371-03-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14478. | |
| UPF-1069 | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Upidosin | Upidosin (Rec 15/2739) is an α-1 adrenoceptor ( α-1 AR ) antagonist. Upidosin shows moderate selectivity for the α-1A AR subtype. Upidosin shows uroselectivity in urethra and prostate with a K b value of 2-3 nM higher than in ear artery and aorta with a K b value of 20-100 nM. Upidosin inhibits [3H]prazosin binding to cloned human α-1A adrenergic receptor. Upidosin can be used for the research of urethral obstruction [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Rec 15/2739; Recordati 15/2739; SB 216469. CAS No. 152735-23-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106954. | |
| Upifitamab | Upifitamab is an ADC Antibody (a naked antibody of upifitamab rilsodotin), which can be used for antibody-coupled agent (ADC) synthesis. Upifitamab rilsodotin is an ADC targeting NaPi2b and is used in ovarian cancer research, particularly in platinum-resistant recurrent ovarian cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2254118-43-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99229. | |
| Uplarafenib | Uplarafenib (B-Raf IN 10) (Compound C09) is a BRAF inhibitor with an IC 50 between 50 and 100 nM. Uplarafenib shows antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: B-Raf IN 10. CAS No. 1425485-87-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148059. | |
| u-plasminogen activator | Formed from the inactive precursor by action of plasmin or plasma kallikrein. Differs in structure from t-plasminogen activator (EC 3.4.21.68), and does not bind to fibrin. In peptidase family S1 (trypsin family). Formerly included in EC 3.4.21.31 and EC 3.4.99.26. Group: Enzymes. Synonyms: urokinase; urinary plasminogen activator; cellular plasminogen activator; urokinase-type plasminogen activator; double-chain urokinase-type plasminogen activator; two-chain urokinase-type plasminogen activator; urokinase plasminogen activator; uPA; u-PA; abbokinase; urinary esterase A. Enzyme Commission Number: EC 3.4.21.73. CAS No. 9039-53-6. uPA. 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-4165; u-plasminogen activator; EC 3.4.21.73; 9039-53-6; urokinase; urinary plasminogen activator; cellular plasminogen activator; urokinase-type plasminogen activator; double-chain urokinase-type plasminogen activator; two-chain urokinase-type plasminogen activator; urokinase plasminogen activator; uPA; u-PA; abbokinase; urinary esterase A. Cat No: EXWM-4165. | |
| Uprifosbuvir | Uprifosbuvir is an antiviral agent. Uprifosbuvir is a NS5b inhibitor developed for the research of chronic hepatitis C virus [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IDX21437; MK-3682. CAS No. 1496551-77-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103487. | |
| Uprosertib | Uprosertib (GSK2141795) is a potent and selective pan-Akt inhibitor with IC 50 values of 180/328/38 nM for Akt1/Akt2/Akt3, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GSK2141795. CAS No. 1047634-65-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15965. | |
| UR-144 5-Hydroxypentyl metabolite-D5 (indole-D5) solution | 100 ?g/mL in methanol, ampule of 1 mL, certified reference material. Group: Cannabinoids standards. | |
| UR-144 5-Hydroxypentyl metabolite solution | 100 ?g/mL in methanol, ampule of 1 mL, certified reference material. Group: Cannabinoids standards. | |
| UR-144 5-Pentanoic acid metabolite solution | 100 ?g/mL in methanol, ampule of 1 mL, certified reference material. Group: Cannabinoids standards. | |
| UR-144 N-(5-Hydroxypentyl) | UR-144 N-(5-Hydroxypentyl). Group: Biochemicals. Alternative Names: [1- (5-hydroxypentyl) -1H-indol-3-yl] (2, 2, 3, 3-tetramethylcyclopropyl ) methanone. Grades: Highly Purified. CAS No. 895155-95-0. Pack Sizes: 5mg. Molecular Formula: C21H29NO2, Molecular Weight: 327.459999999999. US Biological Life Sciences. | Worldwide |
| UR-144 N-(5-Hydroxypentyl) β-D-Glucuronide | UR-144 N-(5-Hydroxypentyl) β-D-Glucuronide. Group: Biochemicals. Alternative Names: (1-Pentyl-1H-indol-3-yl) (2, 2, 3, 3-tetramethylcyclopropyl ) methanone N-(5-Hydroxypentyl) β-D-Glucuronide. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H37NO8, Molecular Weight: 503.58. US Biological Life Sciences. | Worldwide |
| UR-144 N-(5-Hydroxypentyl)-d10 | UR-144 N-(5-Hydroxypentyl)-d10. Group: Biochemicals. Alternative Names: XLR11 N-(5-Hydroxypentyl) Metabolite-d10; [1- (5-Hydroxypentyl) -1H-indol-3-yl] (2, 2, 3, 3-tetramethylcyclopropyl ) -methanone-2, 4, 5, 6, 7-d10. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C21H19D10NO2, Molecular Weight: 337.52. US Biological Life Sciences. | Worldwide |
| UR-144 N-(5-Hydroxypentyl)-d5 | UR-144 N-(5-Hydroxypentyl)-d5. Group: Biochemicals. Alternative Names: XLR11 N-(5-Hydroxypentyl) Metabolite-d5; [1- (5-Hydroxypentyl) -1H-indol-3-yl] (2, 2, 3, 3-tetramethylcyclopropyl ) -methanone-2, 4, 5, 6, 7-d5. Grades: Highly Purified. Pack Sizes: 500ug. Molecular Formula: C21H24D5NO2, Molecular Weight: 332.49. US Biological Life Sciences. | Worldwide |
| Urabrelimab | Urabrelimab (SRF231) is a fully human anti-CD47 monoclonal antibody that blocks the CD47-SIRP interaction[1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: SRF-231; SRF231. CAS No. 2249722-58-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99533. | |
| Uracil | Uracil is a pyrimidine derivative and one of the four nucleobases in the nucleic acid of RNA. Uracil is a frequently occurring DNA base damage that results from the spontaneous or chemically induced deamination of cytosine and is mutagenic at the level of replication. Uracil could potentially alter transcriptional fidelity, resulting in production of mutant proteins [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 66-22-8. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g; 10 g. Product ID: HY-I0960. | |
| Uracil | Uracil is one of the four nucleobases in the nucleic acid of RNA, and can be used for drug delivery and as a pharmaceutical. Synonyms: Cytarabine Impurity D; Pyrimidin-2,4(1H,3H)-dione; 2,4(1H,3H)-Pyrimidinedione; 2,4-Dioxopyrimidine; 2,4-Pyrimidinedione; Pirod; Pyrod; Fluorouracil Impurity C; 1,2,3,4-Tetrahydropyrimidine-2,4-dione; 2,4-Dihydroxypyrimidine; 2,4-Pyrimidinediol; 4-Hydroxyuracil; Hybar X; NSC 3970; Lamivudine EP Impurity F; Fluorouracil EP Impurity C; Cytarabine EP Impurity D. Grade: >98%. CAS No. 66-22-8. Molecular formula: C4H4N2O2. Mole weight: 112.09. | |
| Uracil | Uracil. CAS No: 66-22-8 |  Sarchem Laboratories New Jersey NJ |
| Uracil | Uracil is a pyrimidine derivative. Applications: A pyrimidine derivative. Group: Coenzymes. Synonyms: 2,4(1H,3H)-Pyrimidinedione; 2,4-Dihydroxypyrimidine; 2,4-Pyrimidinediol. CAS No. 66-22-8. Mole weight: 112.1. Form: Solid. 2,4(1H,3H)-Pyrimidinedione; 2,4-Dihydroxypyrimidine; 2,4-Pyrimidinediol; Uracil; 66-22-8. Cat No: COEC-027. | |
| Uracil | Nitrogenous base on RNA nucleosides. Group: Biochemicals. Alternative Names: 2,4-Dihydroxypyrimidine; 2,4-Dioxopyrimidine; 2,4-Pyrimidinediol; 2,4(1H,3H)-Pyrimidinedione; 2,4-Pyrimidinedione; 4-Hydroxyuracil; Hybar X; NSC 3970; Pirod; Pyrod. Grades: Cell Culture Grade. CAS No. 66-22-8. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg. Molecular Formula: C?H?N?O?, Molecular Weight: 112.09. US Biological Life Sciences. | Worldwide |
| Uracil | 100g Pack Size. Group: Analytical Reagents, Biochemicals. Formula: C4H4N2O2. CAS No. 66-22-8. Prepack ID 31200749-100g. Molecular Weight 112.09. See USA prepack pricing. |  |
| Uracil-[13C,15N2] | Uracil-[13C,15N2] is the labelled analogue of Uracil, which is a nitrogenous base of RNA nucleosides. Synonyms: Uracil-2-13C,15N2; Uracil-13C,15N2; 2,4(1H,3H)-Pyrimidinedione-13C,15N2; 2,4-Dihydroxypyrimidine-13C,15N2; 2,4-Dioxopyrimidine-13C,15N2; 2,4-Pyrimidinediol-13C,15N2; 2,4-Pyrimidinedione-13C,15N2; 4-Hydroxyuracil-13C,15N2; Hybar X-13C,15N2. Grade: 99% by CP; 99% atom 13C; 98% atom 15N. CAS No. 181517-11-3. Molecular formula: C3[13C]H4[15N]2O2. Mole weight: 115.07. | |
| Uracil-13C,15N2 | Compound useful in organic synthesis. Group: Biochemicals. Alternative Names: 2,4(1H,3H)-Pyrimidinedione-13C,15N2; 2,4-Dihydroxypyrimidine-13C,15N2; 2,4-Dioxopyrimidine-13C,15N2; 2,4-Pyrimidinediol-13C,15N2; 2,4-Pyrimidinedione-13C,15N2; 4-Hydroxyuracil-13C,15N2; Hybar X-13C,15N2. Grades: Highly Purified. CAS No. 181517-11-3. Pack Sizes: 5mg. Molecular Formula: C313CH415N2O2, Molecular Weight: 115.07. US Biological Life Sciences. | Worldwide |
| Uracil-1,3-d2 | Uracil-1,3-d2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,4(1H,3H)-Pyrimidinedione-1,3-d2. Product Category: Heterocyclic Organic Compound. CAS No. 20666-60-8. Molecular formula: C4H2D2N2O2. Mole weight: 114.1. Purity: 98 atom % D. IUPACName: 1,3-dideuteriopyrimidine-2,4-dione. Product ID: ACM20666608. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Uracil-[15N2] | Uracil-[15N2] is an isotope form of Uracil. Uracil is one of the four nucleobases in the nucleic acid of RNA that can be used for drug delivery and as a pharmaceutical. Synonyms: 2,4(1H,3H)-Pyrimidinedione-1,3-15N2. Grade: 98% atom 15N. CAS No. 5522-55-4. Molecular formula: C4H4[15N]2O2. Mole weight: 114.07. | |
| Uracil 1-ß-D-arabinofuranoside 99+% (HPLC) | Uracil 1-ß-D-arabinofuranoside 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Uracil-4-acetic acid | Uracil-4-acetic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidineaceticaci;6-CARBOXYMETHYLURACIL;URACIL-4-ACETIC ACID;1,2,3,6-Tetrahydro-2,6-dioxo-4-pyrimidineacetic acid;2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-6-acetic acid;2,6-Dioxo-1,2,3,6-tetrahydro-4-pyrimidineacetic acid;2. Product Category: Heterocyclic Organic Compound. CAS No. 4628-39-1. Molecular formula: C6H6N2O4. Mole weight: 170.12. Product ID: ACM4628391. Alfa Chemistry ISO 9001:2015 Certified. | |
| Uracil-[5,6-d2] | Uracil-[5,6-d2] is the labelled analogue of Uracil. Uracil is one of the four nucleobases in the nucleic acid of RNA which can be used for drug delivery and as a pharmaceutical. Synonyms: Uracil (5,6-D2); 2,4-Dihydroxypyrimidine-d2; 2,4(1H,3H)-Pyrimidinedione-5,6-d2; pyrimidine-2,4(1H,3H)-dione-5,6-d2; 2,4-Dioxopyrimidine-5,6-d2; 2,4-Pyrimidinedione-5,6-d2; pyrimidine-2,4-diol-5,6-d2; Pirod-5,6-d2; Uracil-5,6-d2. Grade: 98%; 98% atom D. CAS No. 24897-52-7. Molecular formula: C4H2D2N2O2. Mole weight: 114.10. | |
| Uracil-5-boronic acid | AldrichCPR. Group: Organometallic reagents. | |
| Uracil-5-boronic acid | Uracil-5-boronic acid. Group: Salt. Product ID: (2,4-dioxo-1H-pyrimidin-5-yl)boronic acid. Molecular formula: 155.91g/mol. Mole weight: C4H5BN2O4. B(C1=CNC(=O)NC1=O)(O)O. InChI=1S/C4H5BN2O4/c8-3-2 (5 (10)11)1-6-4 (9)7-3/h1, 10-11H, (H2, 6, 7, 8, 9). PVEJOCQTIVCDNO-UHFFFAOYSA-N. | |
| uracil-5-carboxylate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. Group: Enzymes. Synonyms: uracil-5-carboxylic acid decarboxylase; uracil-5-carboxylate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.66. CAS No. 59299-01-3. 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-4813; uracil-5-carboxylate decarboxylase; EC 4.1.1.66; 59299-01-3; uracil-5-carboxylic acid decarboxylase; uracil-5-carboxylate carboxy-lyase. Cat No: EXWM-4813. | |
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