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| Product | Description | |
|---|---|---|
| Usherin isoform B (3700-3711) |  | |
| Usinic acid | Usinic acid. Group: Biochemicals. CAS No. 125-46-2. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Usistapide | Usistapide is a Microsomal triglyceride transfer protein inhibitor under development for the treatment of obesity and type 2 diabetes. Uses: Microsomal triglyceride transfer protein inhibitors. Synonyms: JNJ-16269110, JNJ16269110, JNJ 16269110, R256918, R 256918, R-256918, Usistapide; methyl (2R) -2-phenyl-2- [4- [4- [ [2- [4- (trifluoromethyl) phenyl] benzoyl] amino] phenyl] piperidin-1-yl] acetate. Grades: ≥98%. CAS No. 403989-79-7. Molecular formula: C34H31F3N2O3. Mole weight: 572.63. | |
| USL311 | USL311 is a CXCR4 receptor antagonist which prevents the binding of stromal-cell derived factor-1 (SDF-1 or CXCL12) to CXCR4. USL311 inhibits CXCR4 activation and decreases proliferation and migration of CXCR4-expressing tumor cells. Uses: Designed for use in research and industrial production. Additional or Alternative Names: USL-311; USL 311; USL311. Product Category: Antagonists. Appearance: Solid powder. CAS No. 1373268-67-7. Molecular formula: C24H34N6O. Mole weight: 422.58. Purity: >98%. IUPACName: 6-[4-(1-Propan-2-ylpiperidin-4-yl)-1,4-diazepan-1-yl]-N-pyridin-4-ylpyridine-2-carboxamide. Canonical SMILES: O=C(C1=NC(N2CCN(C3CCN(C(C)C)CC3)CCC2)=CC=C1)NC4=CC=NC=C4. Product ID: ACM1373268677. Alfa Chemistry ISO 9001:2015 Certified. Categories: US 311. |  |
| Usnic acid | Usnic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 125-46-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C18H16O7. US Biological Life Sciences. | Worldwide |
| Usnic acid | Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1 [1]. Uses: Scientific research. Group: Natural products. CAS No. 125-46-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-N0656. |  |
| Usnic acid | Usnic acid is a naturally occurring dibenzofuran derivative found in several lichen species with the formula C18H16O7. It was first isolated by German scientist W. Knop in 1844 and first synthesized between 1933-1937 by Curd and Robertson. Usnic acid was identified in many genera of lichens including Usnea, Cladonia, Hypotrachyna, Lecanora, Ramalina, Evernia, Parmelia and Alectoria. Although it is generally believed that usnic acid is exclusively restricted to lichens, in a few unconfirmed isolated cases. The compound was found in kombucha tea and non-lichenized ascomycetes. At normal conditions, usnic acid is a bitter, yellow, solid substance.It is known to occur in nature in both the d-and l-forms as well as a racemic mixture. Salts of usnic acid are called usnates (e.g. copper usnate). Usnic acid can be used in cosmetics material. Uses: Bleeding, antibacterial, anti-inflammatory. Synonyms: 1,3(2H,9bH)-Dibenzofurandione, 2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-; 2,6-Diacetyl-7,9-dihydroxy-8,9b-dimethyl-1,3(2H,9bH)-dibenzofurandione; (±)-Usnic acid; 2,6-Diacetyl-7,9-dihydroxy-8,9b-dimethyldibenzo[b,d]furan-1,3(2H,9bH)-dione; NSC 8517; Usnein; Usniacin; Usno. Grades: >98%. CAS No. 125-46-2. Molecular formula: C18H16O7. Mole weight: 344.32. | |
| Usnic Acid | Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,3(2H,9bH)-Dibenzofurandione, 2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-. Product Category: Inhibitors. Appearance: Solid. CAS No. 125-46-2. Molecular formula: C18H16O7. Mole weight: 344.32. Purity: 0.98. Canonical SMILES: O=C(C1(C)C(OC2=C(C(C)=O)C(O)=C(C)C(O)=C12)=C3)C(C(C)=O)C3=O. Density: 1.54 g/cm³. Product ID: ACM125462. Alfa Chemistry ISO 9001:2015 Certified. | |
| Usnic Acid | Usnic Acid - Product ID: NST-10-49. Category: Polyketides. Purity: 98%. Test method: HPLC. CAS No. 7562-61-0. Pack Sizes: 25g, 50g, 125g, 250g. Appearance: Brown fine powder. Molecular formula: C18H16O7. Mole weight: 344.32. Storage: +2 +8 °C. |  |
| USP14 Inhibitor, IU1 (1-(1-(4-Fluorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl)-2-(pyrrolidin-1-yl)ethanone, 1-(1-(4-Fluorophenyl)-2,5-dimethylpyrrol-3-yl)-2-pyrrolidin-1-ylethanone, Ubiquitin Specific Protease 14 Inhibitor, DUB Inhibitor IX) | A cell-permeable pyrrolylpyrrolidinyl-ethanone compound that directly targets proteasome-associated DUB (deubiquitinating enzyme) USP14 and acts as a potent, active-site-directed and reversible inhibitor of hUSP14 deubiquitinating catalytic activity (IC50=4.7uM for Ub-AMC hydrolysis) with excellent selectivity over proteasome-free USP14 and 8-other hDUBs including IsoT (IC50=100uM), UCH37, BAP1, UCH-L1, UCH-L3, USP15, USP2 and USP7 (IC50>700uM). Shown to enhance proteolysis in cells and induce degradation of misfolded toxic proteins like tau, TDP-43 and GFAP (glial fibrillary acidic protein) in coexpressed-wtMEFs at 50uM and offer protection against oxidative stress-induced cytotoxicity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| USP1-IN-7 | USP1-IN-7 (Compound 3) is an inhibitor for ubiquitin specific peptidase 1 ( USP1 ) and its cofactor UAF1 , with IC 50 ≤50 nM. USP1-IN-7 inhibits proliferation of MDA-MB-436 with IC 50 ≤50 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3033480-42-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-161446. | |
| USP7-IN-1 | USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; less or no inhibition on USP5, USP8, Uch-L1, Uch-L3 and Caspase(IC50>200 uM); HCT116 cell viability GI50 is 67 uM. Synonyms: USP7-IN-1; USP7 IN 1. Grades: >98%. CAS No. 1381291-36-6. Molecular formula: C23H24ClN3O3. Mole weight: 425.91. | |
| USP7-IN-13 | USP7-IN-13 (Compound 101) is a USP7 inhibitor with an IC 50 value of 0.2-1 μM, which can be used for the study of multiple myeloma [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2305046-93-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-160515. | |
| USP7-USP47 inhibitor | USP7/USP47 inhibitor(compound 14) is a selective USP7 (EC50= 0.42 μM)/USP47 (EC50= 1.0 μM) inhibitor but does not inhibit caspase 3, calpain 1, 20S proteasome, and a panel of representative USPs (USP2, USP5, USP8, USP21, and USP28; EC50 > 31.6 μM Selective Dual Inhibitors of the Cancer-Related Deubiquitylating Proteases USP7 and USP47. compound 14 exhibits enhanced potency against HCT-116 cells. treatment of cells with compound 14 resulted in an increase in p53 and an appreciable induction of p21 protein over the DMSO control. Thus, compound 14 penetrated the cells and modulated p53 and p21 as expected for a USP7 inhibitor. Synonyms: MDK25371; MDK25371; MDK25371; USP7-USP47 inhibitor; 2-Thiophenecarboxamide, 4-cyano-5-[(3,5-dichloro-4-pyridinyl)thio]-N-[4-(methylsulfonyl)phenyl]-. Grades: >98%. CAS No. 1247825-37-1. Molecular formula: C18H11Cl2N3O3S3. Mole weight: 484.4. | |
| USP Almotriptan Related Compound A; | A metabolite of Almotriptan. Synonyms: 3-[2-(Dimethylamino)ethyl]-5-[(1-pyrrolidinylsulfonyl)methyl]-1H-indole-1-methanol. Grades: > 95%. CAS No. 1018676-02-2. Molecular formula: C18H27N3O3S. Mole weight: 365.5. | |
| USP Cyclophosphamide Related Compound A | Bis(2-chloroethyl)amine hydrochloride is a cytotoxic metabolite of Cyclophosphamide, which is an alkylating agent of the nitrogen mustard type with antineoplastic and immunosuppressive activities. Synonyms: Ethanamine, 2-chloro-N-(2-chloroethyl)-, hydrochloride (1:1); Bis(2-chloroethyl)amine Hydrochloride; 2-Chloro-N-(2-chloroethyl)ethanamine Hydrochloride; Diethylamine, 2,2'-dichloro-, hydrochloride; Ethanamine, 2-chloro-N-(2-chloroethyl)-, hydrochloride; 1,5-Dichloro-3-azapentane hydrochloride; 2,2'-Dichlorodiethylamine hydrochloride; Bis(2-chloroethyl)ammonium chloride; Bis(β-chloroethyl)amine hydrochloride; Di(2-chloroethyl)amine hydrochloride; Leo 72a; N,N-Bis(2-chloroethyl)amine hydrochloride; Nornitrogen mustard hydrochloride; NSC 10873; β,β'-Dichlorodiethylamine hydrochloride. Grades: ≥95%. CAS No. 821-48-7. Molecular formula: C4H10Cl3N. Mole weight: 178.49. | |
| USP Levetiracetam Related Compound B | impurity of Levetiracetam. Synonyms: L-2-Aminobutanamide HCl; S-2-Aminobutanamide HCl; (S)-2-Aminobutanamide Monohydrochloride. Grades: ≥ 98% (HPLC). CAS No. 7682-20-4. Molecular formula: C4H11ClN2O. Mole weight: 138.6. | |
| USP Triamterene Related Compound C | USP Triamterene Related Compound C is an impurity of Triamterene. Triamterene is a potassium-sparing diuretic that is used for the treatment of edema caused by some other diseases. Synonyms: Triamterene Impurity C; 2,4-Diamino-6-phenyl-7-pteridinol; 2,4-Diamino-6-phenyl-7(1H)-pteridinone; 2,4-Diamino-7-hydroxy-6-phenylpteridine; NSC 33416; Triamterene Related Compound C. CAS No. 19152-93-3. Molecular formula: C12H10N6O. Mole weight: 254.25. | |
| USP Valacyclovir Related Compound D | Cas No. 1346747-69-0. | |
| Ustekinumab | Ustekinumab is an anti- IL-12 / IL-23 IgG1κ human monoclonal antibody. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: Anti-Human IL-12/IL-23, Human Antibody. CAS No. 815610-63-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P9909. | |
| Ustekinumab | Ustekinumab is a human monoclonal antibody approved for the treatment of psoriasis and Crohn's disease. Ustekinumab acts via blocking IL-12 and IL-23. Uses: The treatment of psoriasis and crohn's disease. Synonyms: Stelara. CAS No. 815610-63-0. Molecular formula: C6482H10004N1712O2016S46. Mole weight: 145648.1. | |
| Ustilipid A | Ustilipid A is originally isolated from Ustilago maydie DSM 11494. It has the activity of antagonizing dopamine D1 and D2 receptors with the IC50 (μg/mL) of 30 and 5, respectively. Synonyms: [(2R,3S)-2,3,4-Trihydroxybutyl]2-O-hexanoyl-3-O-hexadecanoyl-4-O,6-O-diacetyl-beta-D-mannopyranoside. Molecular formula: C36H64O13. Mole weight: 704.88. | |
| Ustilipid B | Ustilipid B is originally isolated from Ustilago maydie DSM 11494. It has the activity of antagonizing dopamine D1 and D2 receptors with the IC50 (μg/mL) of 16 and 7, respectively. Molecular formula: C34H60O13. Mole weight: 676.83. | |
| Ustiloxin A | It is originally isolated from Ustilaginoidea virens. Ustiloxin A can inhibit the polymerization of tubulin with an IC50 of 0.7 μmol/L, and it also inhibits mitosis in various human tumor cell lines. Grades: ≥95%. CAS No. 143557-93-1. Molecular formula: C28H43N5O12S. Mole weight: 673.73. | |
| Ustiloxin B | It is originally isolated from Ustilaginoidea virens. Ustiloxin B can inhibit the polymerization of tubulin with an IC50 of 2.8 μmol/L, and it also inhibits mitosis in various human tumor cell lines. Grades: ≥98%. CAS No. 151841-41-7. Molecular formula: C26H39N5O12S. Mole weight: 645.68. | |
| Ustusol C | Ustusol C is produced by the strain of Aspergillus ustus. Synonyms: 6-O-methyl-12-hydroxy-6-epi-albrassitriol; 1,2-Naphthalenedimethanol, 1,4,4a,5,6,7,8,8a-octahydro-1-hydroxy-4-methoxy-5,5,8a-trimethyl-, (1S,4R,4aS,8aS)-. Grades: 98.0%. CAS No. 1188398-13-1. Molecular formula: C16H28O4. Mole weight: 284.39. | |
| UT-155 | UT-155 is a potent and selective androgen receptor (AR) antagonist. UT-155 binds the amino-terminal transcriptional activation domain AF-1 and the carboxy-terminal ligand binding domain. Synonyms: UT155; UT 155. CAS No. 2031161-35-8. Molecular formula: C20H15F4N3O2. Mole weight: 405.35. | |
| Uterine Microvascular Endothelial Cells, Human (Frozen) | Passage 3 cells are shipped in proliferating culture with a confluence of >90%. ENDO-Growth medium containing 5% serum and growth supplement is recommended for culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| Uterine Microvascular Endothelial Cells, Human (T-25 flask) | Passage 3 cells are shipped in proliferating culture with a confluence of >90%. ENDO-Growth medium containing 5% serum and growth supplement is recommended for culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: T-25 flask. US Biological Life Sciences. | Worldwide |
| Uterus, Bovine | Uterus, Bovine. Group: Biologicals. Grades: Tissue. Pack Sizes: 5Ea. US Biological Life Sciences. | Worldwide |
| Uterus, Rabbit | Uterus, Rabbit. Group: Biologicals. Grades: Tissue. Pack Sizes: 25Ea. US Biological Life Sciences. | Worldwide |
| U-theraphotoxin-Aju1a | U-theraphotoxin-Aju1a is an antibacterial peptide isolated from Avicularia juruensis. It has activity against fungi. Synonyms: Phe-Thr-Cys-Ala-Ile-Ser-Cys-Asp-Ile-Lys-Val-Asn-Gly-Lys-Pro-Cys-Lys-Gly-Ser-Gly-Glu-Lys-Lys-Cys-Ser-Gly-Gly-Trp-Ser-Cys-Lys-Phe-Asn-Val-Cys-Val-Lys-Val. | |
| UTL-5G | UTL-5G (GBL-5g) is an anti-inflammatory TNF-α inhibitor. It reduces cisplatin-induced hepatotoxicity, nephrotoxicity and bone marrow toxicity by inhibiting TNF-α and other factors. Synonyms: 3-Isoxazolecarboxamide, N-(2,4-Dichlorophenyl)-5-Methyl-. Grades: 98%. CAS No. 646530-37-2. Molecular formula: C11H8Cl2N2O2. Mole weight: 271.1. | |
| UTPαS | UTPαS is an innovatively engineered nucleotide analog emerging as an invaluable instrument, facilitating in-depth investigations into RNA-associated mechanisms. Remarkably versatile, this modified nucleotide analog unleashes a myriad of applications encompassing RNA synthesis, precise labeling techniques along with elucidating ribozymes and unraveling the enigmatic world of RNA-binding proteins. Synonyms: Alpha Thiol UTP; 1-Thio-UTP; Uridine-5'-O-(1-Thiotriphosphate). Grades: ≥ 95 % by HPLC. CAS No. 71214-29-4. Molecular formula: C9H15N2O14P3S (free acid). Mole weight: 500.20 (free acid). | |
| UTP-γ-AmNS | UTP-γ-AmNS is a highly versatile compound extensively employed in the biomedical sector, serving as a pivotal precursor for nucleic acid synthesis, finding diverse applications in extensive research of viral infections like HIV and hepatitis. UTP-γ-AmNS assumes an indispensable role in facilitating investigations pertaining to nucleotide metabolism and unraveling the intricate mechanisms governing viral replication. Synonyms: Uridine-5'-triphosphate-γ-(sulfo-1-naphthyl)amide, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C19H22N3O17P3S (free acid). Mole weight: 689.37 (free acid). | |
| UTPγS | UTPγS is a nucleotide analog widely used in biomedical research. It serves as a substrate for enzymes involved in RNA synthesis and modification. UTPγS is employed in studies investigating RNA structure, RNA-protein interactions, and ribozyme activities. It finds applications in the exploration of RNA-based therapeutics and drug development targeting infectious diseases. Synonyms: Uridine-5'-(γ-thio)-triphosphate, Sodium salt. Grades: ≥ 85 % by HPLC, contains approx. 10 % UDP, which UTPγS decomposes to at room temperature. CAS No. 79049-97-1. Molecular formula: C9H15N2O14P3S (free acid). Mole weight: 500.20 (free acid). | |
| UTPγS trisodium salt | UTPγS trisodium salt is a selective P2Y2 and P2Y4 receptor agonist. Synonyms: Uridine-5'-(γ-thio)-triphosphate trisodium salt. CAS No. 1266569-94-1. Molecular formula: C9H12N2Na3O14P3S. Mole weight: 566.15. | |
| UTPγS trisodium salt | UTPγS trisodium salt. Group: Biochemicals. Grades: Purified. CAS No. 1266569-94-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| UTP-glucose-1-phosphate uridylyltransferase | UTP--glucose-1-phosphate uridylyltransferase is an enzyme found in yeast, plants, and mammals as it is a key player in carbohydrate metabolism. It has been studied significantly in plants as sugar metabolism and production is seen as important for understanding growth from an agricultural standpoint. Recently, human UDP-glucose pyrophosphorylase has been studied and crystallized, revealing a different type of regulation than other organisms previously studied. Its significance is derived from the many uses of UDP-Glucose including galactose usage, glycogen synthesis, glycoprotein synthesis, and glycolipid synthesis. Group: Enzymes. Synonyms: UDP glucose pyrophosphorylase; glucose-1-phosphate uridylyltransferase; UDPG phosphorylase; UDP. Enzyme Commission Number: EC 2.7.7.9. CAS No. 9026-22-6. UDPG pyrophosphorylase. 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-3303; UTP-glucose-1-phosphate uridylyltransferase; EC 2.7.7.9; 9026-22-6; UDP glucose pyrophosphorylase; glucose-1-phosphate uridylyltransferase; UDPG phosphorylase; UDPG pyrophosphorylase; uridine 5'-diphosphoglucose pyrophosphorylase; uridine diphosphoglucose pyrophosphorylase; uridine diphosphate-D-glucose pyrophosphorylase; uridine-diphosphate glucose pyrophosphorylase. Cat No: EXWM-3303. |  |
| UTP-hexose-1-phosphate uridylyltransferase | α-D-Glucose 1-phosphate can also act as acceptor, but more slowly. Group: Enzymes. Synonyms: galactose-1-phosphate uridylyltransferase; galactose 1-phosphate uridylyltransferase; α-D-galactose 1-phosphate uridylyltransferase; galactose 1-phosphate uridyltransferase; UDPgalactose pyrophosphorylase; uridine diphosphate galactose pyrophosphorylase; uridine diphosphogalactose pyrophosphorylase. Enzyme Commission Number: EC 2.7.7.10. CAS No. 9016-11-9. 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-3226; UTP-hexose-1-phosphate uridylyltransferase; EC 2.7.7.10; 9016-11-9; galactose-1-phosphate uridylyltransferase; galactose 1-phosphate uridylyltransferase; α-D-galactose 1-phosphate uridylyltransferase; galactose 1-phosphate uridyltransferase; UDPgalactose pyrophosphorylase; uridine diphosphate galactose pyrophosphorylase; uridine diphosphogalactose pyrophosphorylase. Cat No: EXWM-3226. | |
| UTP - lyophilized | UTP - lyophilized is a freeze-dried form of uridine triphosphate (UTP) commonly used in the biomedical industry. UTP serves as a building block for RNA synthesis and modification, playing a vital role in cellular processes such as gene expression and protein synthesis. It is often utilized in research involving RNA labeling, transcription and RNA structural studies. Synonyms: Uridine 5'-triphosphate, Trisodium salt trihydrate. Grades: > 90 % by HPLC. Molecular formula: C9H12N2Na3O15P3* 3H2O. Mole weight: 604.12. | |
| UTP-monosaccharide-1-phosphate uridylyltransferase | Requires Mg2+ or Mn2+ for maximal activity. The reaction can occur in either direction and it has been postulated that MgUTP and Mg-diphosphate are the actual substrates. The enzyme catalyses the formation of UDP-Glc, UDP-Gal, UDP-GlcA, UDP-L-Ara and UDP-Xyl, showing broad substrate specificity towards monosaccharide 1-phosphates. Mannose 1-phosphate, L-Fucose 1-phosphate and glucose 6-phosphate are not substrates and UTP cannot be replaced by other nucleotide triphosphates. Group: Enzymes. Synonyms: UDP-sugar pyrophosphorylase; PsUSP. Enzyme Commission Number: EC 2.7.7.64. UDP-Sugar pyrophosphorylase. 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-3275; UTP-monosaccharide-1-phosphate uridylyltransferase; EC 2.7.7.64; UDP-sugar pyrophosphorylase; PsUSP. Cat No: EXWM-3275. | |
| UTP - solution | | |
| UTP-xylose-1-phosphate uridylyltransferase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing nucleotide groups (nucleotidyltransferases). The systematic name of this enzyme class is UTP:alpha-D-xylose-1-phosphate uridylyltransferase. Other names in common use include xylose-1-phosphate uridylyltransferase, uridylyltransferase, xylose 1-phosphate, UDP-xylose pyrophosphorylase, uridine diphosphoxylose pyrophosphorylase, and xylose 1-phosphate uridylyltransferase. This enzyme participates in nucleotide sugars metabolism. Group: Enzymes. Synonyms: xylose-1-phosphate uridylyltransferase; uridylyltransferase, xylose 1-phosphate; UDP-xylose pyrophosphorylase; uridine diphosphoxylose pyrophosphorylase; xylose 1-phosphate uridylyltransferase. Enzyme Commission Number: EC 2.7.7.11. CAS No. 9026-20-4. 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-3227; UTP-xylose-1-phosphate uridylyltransferase; EC 2.7.7.11; 9026-20-4; xylose-1-phosphate uridylyltransferase; uridylyltransferase, xylose 1-phosphate; UDP-xylose pyrophosphorylase; uridine diphosphoxylose pyrophosphorylase; xylose 1-phosphate uridylyltransferase. Cat No: EXWM-3227. | |
| Utreglutide | Utreglutide is a potent glucagon-like peptide 1 (GLP-1) receptor agonit [1]. Uses: Scientific research. Group: Peptides. CAS No. 2460862-12-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P3388. | |
| Utreloxastat | Utreloxastat is a 15-lipoxygenase inhibitor. Synonyms: 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-6-nonyl-. Grades: >98%. CAS No. 1213269-96-5. Molecular formula: C18H28O2. Mole weight: 276.4. | |
| Utreloxastat | Utreloxastat (PTC857) is an orally active 15-lipoxygenase inhibitor that can cross the blood-brain barrier. Utreloxastat is a weak inhibitor of CYP1A2 and 2B6 with an IC 50 > 5.3 μM. Utreloxastat reduces oxidative stress and inhibits the consumption of reduced glutathione and ferroptosis. Utreloxastat can be used in the study of neurodegenerative diseases characterized by high levels of oxidative stress and mitochondrial pathology, such as amyotrophic lateral sclerosisc [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PTC857. CAS No. 1213269-96-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132845. | |
| UTX protein (1264-1273) | UTX protein (1264-1273) is a bioactive peptide of UTX protein which plays a central role in posterior development by regulating HOX gene expression. Synonyms: KDM6A (1264-1273). | |
| Uty HY Peptide (246-254) | Uty HY Peptide (246-254), a male-specific transplantation antigen H-Y, is derived from the ubiquitously transcribed tetratricopeptide repeat gene on the Y chromosome (UTY) protein as an H-Y epitope, H-YDb. CAS No. 261172-28-5. Molecular formula: C53H77N15O13S2. Mole weight: 1196.4000000000001. | |
| UU | UU ((3,5)-Uridylyluridine) is a nucleobase-containing dinucleotide derivative. UU can be used for the study of RNA-related processes [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (3,5)-Uridylyluridine. CAS No. 2415-43-2. Pack Sizes: 1 mg. Product ID: HY-159806. | |
| UUN44923 | UUN44923 is a FTO inhibitor. UUN44923 may be useful for treating diseases assocd. with FTO targets, obesity, metabolic syndrome (MS)?, type 2 diabetes (T2D)?, Alzheimer's diseases, breast cancers, small-cell lung cancers, a human bone marrow striated muscle cancer, a pancreatic cancer, malignant glioblastoma and the like. UUN44923 was reported in WO 2018157843. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UUN44923; UUN-44923; UUN 44923; Dac51; Dac-51; Dac 51. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 2243944-92-3. Molecular formula: C18H16Cl2N4O2. Mole weight: 391.25. Purity: >98%. IUPACName: Benzamide, 2-[[2,6-dichloro-4-(3,5-dimethyl-1H-pyrazol-4-yl)phenyl]amino]-N-hydroxy-. Canonical SMILES: O=C(NO)C1=CC=CC=C1NC2=C(Cl)C=C(C3=C(C)NN=C3C)C=C2Cl. Product ID: ACM2243944923. Alfa Chemistry ISO 9001:2015 Certified. | |
| UV-0 | UV-0. Group: Polymers. CAS No. 131-56-6. Product ID: (2,4-dihydroxyphenyl)-phenylmethanone. Molecular formula: 214.22g/mol. Mole weight: C13H10O3. C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2)O)O. InChI=1S/C13H10O3/c14-10-6-7-11 (12 (15)8-10)13 (16)9-4-2-1-3-5-9/h1-8, 14-15H. ZXDDPOHVAMWLBH-UHFFFAOYSA-N. |  |
| UV-1084 | UV-1084. CAS No: 14516-71-3 |  Sarchem Laboratories New Jersey NJ |
| UV1130 | UV1130. Uses: Designed for use in research and industrial production. Appearance: Liquid. CAS No. 104810-47-1. Molecular formula: C20H23N3O3. Mole weight: 353.42. Purity: 36-40%. Product ID: ACM104810471. Alfa Chemistry ISO 9001:2015 Certified. Categories: Tinuvin 1130. | |
| UV-1164 | DryPowder; PelletsLargeCrystals;Solid. Group: Polymers. CAS No. 2725-22-6. Product ID: 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-octoxyphenol. Molecular formula: 509.7g/mol. Mole weight: C33H39N3O2. CCCCCCCCOC1=CC (=C (C=C1)C2=NC (=NC (=N2)C3=C (C=C (C=C3)C)C)C4=C (C=C (C=C4)C)C)O. InChI=1S / C33H39N3O2 / c1-6-7-8-9-10-11-18-38-26-14-17-29 (30 (37) 21-26) 33-35-31 (27-15-12-22 (2) 19-24 (27) 4) 34-32 (36-33) 28-16-13-23 (3) 20-25 (28) 5 / h12-17, 19-21, 37H, 6-11, 18H2, 1-5H3. ZSSVCEUEVMALRD-UHFFFAOYSA-N. | |
| UV1173 | Liquid. Group: Polymers. CAS No. 7473-98-5. Product ID: 2-hydroxy-2-methyl-1-phenylpropan-1-one. Molecular formula: 164.2g/mol. Mole weight: C10H12O2. CC(C)(C(=O)C1=CC=CC=C1)O. InChI=1S/C10H12O2/c1-10(2, 12)9(11)8-6-4-3-5-7-8/h3-7, 12H, 1-2H3. XMLYCEVDHLAQEL-UHFFFAOYSA-N. | |
| UV-1577 | UV-1577. CAS No: 147315-50-2 | Sarchem Laboratories New Jersey NJ |
| UV184 | DryPowder; Liquid; OtherSolid; PelletsLargeCrystals, Liquid. Group: Polymers. CAS No. 947-19-3. Product ID: (1-hydroxycyclohexyl)-phenylmethanone. Molecular formula: 204.26g/mol. Mole weight: C13H16O2. C1CCC(CC1)(C(=O)C2=CC=CC=C2)O. InChI=1S/C13H16O2/c14-12 (11-7-3-1-4-8-11)13 (15)9-5-2-6-10-13/h1, 3-4, 7-8, 15H, 2, 5-6, 9-10H2. QNODIIQQMGDSEF-UHFFFAOYSA-N. | |
| UV-234 | UV-234. CAS No: 70321-86-7 | Sarchem Laboratories New Jersey NJ |
| Uv-320 | Uv-320. Uses: Designed for use in research and industrial production. Additional or Alternative Names: TINUVIN 320;ULTRAVIOLET ABSORBER UV-320;UV-320;2-BENZOTRIAZOLE-2-YL-4,6-DI-TERT-BUTYLPHENOL;2-(2-HYDROXY-3,5-DI-TERT-BUTYLPHENYL)BENZOTRIAZOLE;2-(2-HYDROXY-3,5-DI-TERT-BUTYLPHENYL)BENZOTRIAZOLE;2-(2H-BENZOTRIAZOL-2-YL)-4,6-DI-T-BUTYLPHENOL;2-(2H-benzotriazol-2-yl)-4,6-di-tert-butylphenol. Product Category: Heterocyclic Organic Compound. CAS No. 3846-71-7. Molecular formula: C20H25N3O. Mole weight: 323.44. Product ID: ACM3846717. Alfa Chemistry ISO 9001:2015 Certified. Categories: UV-328. | |
| UV-320 | UV-320 is a benzotriazole UV stabilizer, which is used to increase product stability and to prevent discolouration in various consumer and industrial goods such as plastics. Benzotriazole UV stabilizers are a pollutant for the aquatic environment and have been implicated as a potential stable and toxic ligands for aryl hydrocarbon receptor in human. Group: Biochemicals. Grades: Highly Purified. CAS No. 3846-71-7. Pack Sizes: 100g, 250g. Molecular Formula: C20H25N3O, Molecular Weight: 323.43. US Biological Life Sciences. | Worldwide |
| UV-326 | UV-326. CAS No: 729335 | Sarchem Laboratories New Jersey NJ |
| UV-329 | UV-329. CAS No: 3147-75-9 | Sarchem Laboratories New Jersey NJ |
| UV-366 | UV-366. CAS No: 169198-72-5 | Sarchem Laboratories New Jersey NJ |
| UV729 ASA 3D Printing Filament | UV729 ASA 3D Printing Filament. Group: 3d printing materials. | |
| UV-9 | 2-hydroxy-4-methoxybenzophenone appears as white to off-white or light yellow powder. (NTP, 1992);DryPowder; Liquid;Solid. Group: Polymers. CAS No. 131-57-7. Product ID: (2-hydroxy-4-methoxyphenyl)-phenylmethanone. Molecular formula: 228.24g/mol. Mole weight: C14H12O3. COC1=CC(=C(C=C1)C(=O)C2=CC=CC=C2)O. InChI=1S/C14H12O3/c1-17-11-7-8-12 (13 (15)9-11)14 (16)10-5-3-2-4-6-10/h2-9, 15H, 1H3. DXGLGDHPHMLXJC-UHFFFAOYSA-N. | |
| Uv-absorbenttriazine-5 | Uv-absorbenttriazine-5. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UV-ABSORBENTTRIAZINE-5, 63856-18-8. Product Category: Heterocyclic Organic Compound. CAS No. 63856-18-8. Molecular formula: C33H33N3O9. Mole weight: 615.629820 [g/mol]. Purity: 0.96. IUPACName: methyl 3-[3,5-bis(3-methoxy-3-oxo-1-phenylpropyl)-2,4,6-trioxo-1,3,5-triazinan-1-yl]-3-phenylpropanoate. Canonical SMILES: COC(=O)CC(C1=CC=CC=C1)N2C(=O)N(C(=O)N(C2=O)C(CC(=O)OC)C3=CC=CC=C3)C(CC(=O)OC)C4=CC=CC=C4. Product ID: ACM63856188. Alfa Chemistry ISO 9001:2015 Certified. | |
| Uvaol | Uvaol, a triterpene present in olives and virgin olive oil, possesses anti-inflammatory properties and antioxidant effects. Uvaol is an orally active inducer of apoptosis in astroglioma cells. Uvaol also has anti-cancer activities. Uvaol attenuates pleuritis and eosinophilic inflammation in ovalbumin-induced allergy in mice [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 545-46-0. Pack Sizes: 5 mg. Product ID: HY-N1109. | |
| Uva Ursi P.E. Powder & 4:1 | Uva Ursi P.E. Powder & 4:1. |  CA, FL & NJ |
| UV excision repair protein RAD23 homolog B isoform 2 (268-281) | UV excision repair protein RAD23 homolog B isoform 2 (268-281) is a peptide derived from UV excision repair protein RAD23 homolog B isoform 2. A deficiency in expression of a DNA repair gene increases the risk for cancer. The expression of RAD23B is reduced in tumor tissue of women with breast cancer. | |
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