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| Product | Description | |
|---|---|---|
| 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. Alternative Names: 1,3(2H,9bH)-Dibenzofurandione, 2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyl-. CAS No. 125-46-2. Purity: 95%. Product ID: CI-GU-0024. Molecular formula: C18H16O7. Mole weight: 344.3 g/mol. IUPAC Name: 2,6-diacetyl-7,9-dihydroxy-8,9b-dimethyldibenzofuran-1,3-dione. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Usnoflast | Usnoflast is the selective, orally active inhibitor for NLRP3 that blocks the release of IL-1β, and exhibits anti-inflammatory activity[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2455519-86-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-156647. |  |
| USP10-IN-3 | USP10-IN-3 (compound D1) is a potent USP10 inhibitor with an IC50 value of 7.2 μM. USP10-IN-3 inhibits cell proliferation. USP10-IN-3 induces apoptosis and cell cycle arrest at S-phase[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3059565-11-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-163622. | |
| USP15-IN-1 | USP15-IN-1 is a potent USP15 inhibitor with an IC50 value of 3.76 μM. USP15-IN-1 can be used for researching anticancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2260826-16-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148046. | |
| USP1-IN-2 | USP1-IN-2 (Compound I-193) is a potent ubiquitin-specific protease 1 (USP1) inhibitor with an IC50 of less than about 50 nM. USP1-IN-2 can be used for the study of cancers such as osteosarcoma[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2098212-05-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148099. | |
| USP25/28 inhibitor AZ1 | USP25/28 inhibitor AZ1 (AZ1) is an orally active, selective, noncompetitive, dual ubiquitin specific protease (USP) 25/28 inhibitor with IC50s of 0.7 μM and 0.6 μM, respectively. USP25/28 inhibitor AZ1 attenuates colitis and tumorigenesis in the mice model[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZ1. CAS No. 2165322-94-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117370. | |
| USP28-IN-4 | USP28-IN-4 is a USP28 inhibitor (IC50=0.04 μM) with high selectivity over USP2, USP7, USP8, USP9x, UCHL3 and UCHL5. USP28-IN-4 shows cytotoxicity against cancer cells, down-regulates the cellular level of c-Myc through ubiquitin-proteasome system. USP28-IN-4 also decreases the ankyrase-1/2 level in vitro. USP28-IN-4 enhance the sensitivity of colorectal cancer cells to Regorafenib (HY-10331)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2931509-15-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-149230. | |
| USP30 inhibitor 11 | USP30 inhibitor 11 is a selective and potent ubiquitin specific peptidase 30 (USP30) inhibitor with an IC50 of 0.01 μΜ, the example 83 extracted from patent WO2017009650A1. USP30 inhibitor 11 is used for the study of cancer and conditions involving mitochondrial dysfunction[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2067332-64-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111623. | |
| USP5-IN-1 | USP5-IN-1 (compound 64) is a selective competitive inhibitor of USP5 zinc finger ubiquitin binding domain (ZnF-UBD) (KD=2.8 μM). USP5-IN-1 competitively blocks the binding of ubiquitin to ZnF-UBD, inhibits the catalytic activity of USP5, and thus hinders the hydrolysis of ubiquitin chains. USP5-IN-1 can inhibit USP5 cleavage of Lys48-linked diubiquitin substrates in vitro and is a potential USP5 chemical probe and potential inhibitor of USP5-related cancers. Uses: Scientific research. Category: Signaling pathways. CAS No. 2851040-81-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139979. | |
| USP7-797 | USP7-797 (USP7-IN-7) is an orally available, selective USP7 inhibitor (IC50=0.5 nmol/L) with antitumor activity. USP7-797 reduces the level of MDM2, thereby increasing the stability and activity of p53, leading to cell cycle arrest and apoptosis. USP7-797 has low nanomolar cytotoxicity against p53 mutant cancer cell lines, p53 wild-type hematological tumors, and neuroblastoma cell lines[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: USP7-IN-7. CAS No. 2413944-70-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136910. | |
| USP7 activator 1 | USP7 activator 1 (compound MS-8) is an activator of USP7 by engaging the allosteric C-terminal binding pocket of USP7[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 868940-26-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-173352. | |
| USP7-IN-11 | USP7-IN-11 is a potent ubiquitin-specific protease 7 (USP7) (Deubiquitinase) inhibitor with an IC50 of 0.37 nM. USP7-IN-11 has anticancer effects (WO2022048498A1; Example 187)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2763872-32-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-148482. | |
| USP7-IN-9 | USP7-IN-9 is a highly potent ubiquitin-specific protease 7 (USP7) inhibitor with an IC50 value of 40.8 nM. USP7-IN-9 can induce apoptosis and arrest cell progression at G0/G1 and S phases in RS4; 11 cells. USP7-IN-9 reduces the protein levels of oncoproteins MDM2 and DNMT1 and increases the protein levels of tumor suppressors p53 and p21[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2444374-01-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-146887. | |
| USP8-IN-1 | USP8-IN-1 is a USP8 inhibitor with an IC50 of 1.9 μM. USP8-IN-1 inhibits H1975 cell growth with a GI50 of 82.04 μM (CN111138358A; U10)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2477650-96-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-147032. | |
| Ustekinumab | Ustekinumab is an anti-IL-12/IL-23 IgG1κ human monoclonal antibody. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CNTO-1275; L04AC05; TT-20. CAS No. 815610-63-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 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. Alternative Names: 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. Alternative Names: [(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 A | Ustusol A is produced by the strain of Aspergillus ustus. Alternative Names: (3S,5S,9R,10S)-3,9,11-trihydroxydrim-7-en-6-one; 3β,9α,11-trihydroxy-6-oxodrim-7-ene; 1(4H)-Naphthalenone, 4a,5,6,7,8,8a-hexahydro-4,7-dihydroxy-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-, (4R,4aS,7S,8aS)-. Grades: 98.0%. CAS No. 1175543-02-8. Molecular formula: C15H24O4. Mole weight: 268.35. | |
| Ustusolate A | Ustusolate A is produced by Aspergillus ustus and exerts weak cytotoxicity against HL-60 and A549 cells with IC50 values of 20.6 and 30.0 microM, respectively. Alternative Names: 6-O-(octa-2E,4E,6E-trienoyl)-12-hydroxy-6-epi-albrassitriol; 2,4,6-Octatrienoic acid, (1R,4S,4aS,8aS)-1,4,4a,5,6,7,8,8a-octahydro-4-hydroxy-3,4-bis(hydroxymethyl)-4a,8,8-trimethyl-1-naphthalenyl ester, (2E,4E,6E)-. Grades: ≥98%. CAS No. 1136611-58-9. Molecular formula: C23H34O5. Mole weight: 390.51. | |
| Ustusolate C | Ustusolate C is produced by Aspergillus ustus. Study shows that it has moderate cytotoxicity against A549 and HL-60 cells. Alternative Names: 9α-hydroxy-6β-(7-hydroxyocta-2E,4E-dienoyloxy)-5α-drim-7-en-11,12-olide; 2,4-Octadienoic acid, 7-hydroxy-, (5R,5aS,9aS,9bS)-1,3,5,5a,6,7,8,9,9a,9b-decahydro-9b-hydroxy-6,6,9a-trimethyl-1-oxonaphtho[1,2-c]furan-5-yl ester, (2E,4E)-. Grades: 97.0%. CAS No. 1188398-15-3. Molecular formula: C23H32O6. Mole weight: 404.50. | |
| Ustusolate E | Ustusolate E is a metabolite of marine-derived fungus Aspergillus ustus 094102. Ustusolate E exhibits cytotoxic activity against A549 and HL-60 cell lines. Alternative Names: 9α-hydroxy-6β-(6-oxohex-2E,4E-dienoyloxy)-5α-drim-7-en-11,12-olide; 2,4-Hexadienoic acid, 6-oxo-, (5R,5aS,9aS,9S)-1,3,5,5a,6,7,8,9,9a,9b-decahydro-9b-hydroxy-6,6,9a-trimethyl-1-oxonaphtho[1,2-c]furan-5-yl ester, (2E,4E)-. Grades: 93.0%. CAS No. 1175543-06-2. Molecular formula: C21H26O6. Mole weight: 374.43. | |
| Ustusol C | Ustusol C is produced by the strain of Aspergillus ustus. Alternative Names: 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 selective and potent androgen receptor (AR) antagonist, with a Ki of 267 nM for UT-155 binding to AR-LBD. Uses: Scientific research. Category: Signaling pathways. CAS No. 2031161-35-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112895. | |
| UT-34 | UT-34 is a potent, selective, orally bioactive second-generation pan-androgen receptor (AR) antagonist and degrader, with IC50 values of 211.7 nM, 262.4 nM, and 215.7 nM for wild-type AR, F876L-AR, and W741L-AR, respectively. UT-34 binds to the ligand-binding domain (LBD) and functional 1 (AF-1) domain of AR and requires the ubiquitin-proteasome pathway for AR degradation. UT-34 has anti-prostate cancer effects. Uses: Scientific research. Category: Signaling pathways. CAS No. 2168525-92-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136242. | |
| Utapenem USP Impurity A1 | Utapenem USP Impurity A1. Uses: For analytical and research use. Molecular formula: C23H25N3O9S. Mole weight: 519.3. Catalog: APB10426. |  |
| Utapenem USP Impurity B | Utapenem USP Impurity B. Uses: For analytical and research use. Molecular formula: C12H14N2O4. Mole weight: 250.25. Catalog: APB10395. | |
| Utapenem USP Impurity C | Utapenem USP Impurity C. Uses: For analytical and research use. Molecular formula: C22H27N3O8S. Mole weight: 493.53. Catalog: APB10425. | |
| Utapenem USP Impurity G | Utapenem USP Impurity G. Uses: For analytical and research use. Molecular formula: C44H50N6O14S2. Mole weight: 951.03. Catalog: APB10397. | |
| Utapenem USP Impurity H | Utapenem USP Impurity H. Uses: For analytical and research use. Molecular formula: C23H29N3O8S. Mole weight: 507.56. Catalog: APB10396. | |
| Utapenem USP Impurity I | Utapenem USP Impurity I. Uses: For analytical and research use. Molecular formula: C44H48N6O13S2. Mole weight: 933.02. Catalog: APB10398. | |
| Utapenem USP Impurity J | Utapenem USP Impurity J. Uses: For analytical and research use. Molecular formula: C45H52N6O14S2. Mole weight: 965.06. Catalog: APB10399. | |
| Utapenem USP Impurity K | Utapenem USP Impurity K. Uses: For analytical and research use. Molecular formula: C23H29N3O8S. Mole weight: 507.56. Catalog: APB10400. | |
| Utapenem USP Impurity L | Utapenem USP Impurity L. Uses: For analytical and research use. Molecular formula: C34H39N5O10S2. Mole weight: 741.83. Catalog: APB10402. | |
| Utapenem USP Impurity M | Utapenem USP Impurity M. Uses: For analytical and research use. Molecular formula: C44H48N6O13S2. Mole weight: 933.02. Catalog: APB10401. | |
| Utapenem USP Impurity P | Utapenem USP Impurity P. Uses: For analytical and research use. Molecular formula: C24H30N4O6S. Mole weight: 502.59. Catalog: APB10406. | |
| Utapenem USP Impurity Q | Utapenem USP Impurity Q. Uses: For analytical and research use. Molecular formula: C24H30N4O6S. Mole weight: 502.59. Catalog: APB10403. | |
| Utapenem USP Impurity R | Utapenem USP Impurity R. Uses: For analytical and research use. Molecular formula: C19H21N3O3S. Mole weight: 371.46. Catalog: APB10404. | |
| U-theraphotoxin-Aju1a | U-theraphotoxin-Aju1a is an antibacterial peptide isolated from Avicularia juruensis. It has activity against fungi. Alternative Names: 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. | |
| Utidelone | Utidelone (Epothilone D) is a potent microtubule stabilizer. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Epothilone D; UTD1; KOS 862. CAS No. 189453-10-9. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15278. | |
| U-TOM-CE Phosphoramidite | U-TOM-CE phosphoramidite is a phosphoramidite used in oligonucleotide synthesis. It features the TOM (triisopropylsilyloxymethyl) protecting group at the 2'-hydroxyl position and a cyanoethyl (CE) protecting group on the phosphoramidite at the 3' position. The TOM group provides protection during synthesis and can be removed under mild conditions, making this reagent useful for synthesizing RNA oligonucleotides. This phosphoramidite reagent enhances the stability and efficiency of oligonucleotide synthesis, which is crucial for applications in molecular biology, diagnostics, and therapeutic development. Alternative Names: 5'-Dimethoxytrityl-Uridine, 2'-O-triisopropylsilyloxymethyl-3'-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite; 2'-O-[(Triisopropylsilyloxy)methyl]-3'-O-[diisopropylamino(2-cyanoethoxy)phosphino]-5'-O-(4,4'-dimethoxytrityl)uridine; (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-(((triisopropylsilyl)oxy)methoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[[[tris(1-methylethyl)silyl]oxy]methyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; 2'-O-TOM-U-3'-CE Phosphoramidite. Grades: ≥95%. CAS No. 220230-62-6. Molecular formula: C49H69N4O10PSi. Mole weight: 933.17. | |
| Utomilumab | Utomilumab (PF 05082566) is a fully human IgG2 agonist monoclonal antibody that selectively binds to 4-1BB/CD137. Utomilumab can be used in the research of tumors such as follicular and other CD20+ non-Hodgkin lymphomas[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PF 05082566. CAS No. 1417318-27-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99056. | |
| UTPαS (Sp isomer) | 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. Alternative Names: Alpha Thiol UTP (Sp isomer); 1-Thio-UTP (Sp isomer); Uridine-5'-O-(1-Thiotriphosphate) Sp-isomer; Uridine, 5'→P''-ester with [P''(S)]-thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(O)(OH)(SH)); Uridine, 5'→P''-ester with thiotriphosphoric acid ((HO)2P(O)OP(O)(OH)OP(S)(OH)2), (S)-; Sp-UTP-αS. Grades: ≥95% by HPLC. CAS No. 71214-29-4. Molecular formula: C9H15N2O14P3S. Mole weight: 500.21. | |
| 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. Alternative Names: 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. Alternative Names: Uridine-5'-(γ-thio)-triphosphate; Uridine-5'-O-(γ-Thio)-triphosphate; UTP-γS; Uridine 5'-(trihydrogen diphosphate), P'-anhydride with phosphorothioic acid; UTP-Gamma-S; Uridine 5'-O-(3-thiotriphosphate). Grades: ≥95% by HPLC. CAS No. 79049-97-1. Molecular formula: C9H15N2O14P3S. Mole weight: 500.20. | |
| 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-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-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. | |
| Utreloxastat | Utreloxastat (PTC857) is an orally active and blood-brain barrier-permeable 15-lipooxygenase inhibitor. Utreloxastat is a weak inhibitor of CYP1A2 and 2B6 with an IC50 of >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. Category: Signaling pathways. Alternative Names: PTC857. CAS No. 1213269-96-5. Pack Sizes: 10 mM * 1 mL in DMSO; 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. Alternative Names: 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-T02 | UU-T02 is a novel potent, selective small-molecule inhibitor of β-Catenin/T-cell factor protein-protein interaction (β-catenin/Tcf PPI) with a Ki of 1.36 μM[1]. UU-T02 inhibits canonical Wnt signaling and the growth of colorectal cancer cells[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1500080-17-0. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-117233. | |
| UV-0 | UV-0. CAS No. 131-56-6. Molecular formula: C13H10O3. Mole weight: 214.22g/mol. IUPAC Name: (2,4-dihydroxyphenyl)-phenylmethanone. SMILES: C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2)O)O. InChI: 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. |  |
| UV-1084 | UV-1084. CAS No: 14516-71-3 |  Sarchem Laboratories New Jersey NJ |
| UV1130 | UV1130. CAS No. 104810-47-1. Purity: 36-40%. Product ID: ACM104810471. Molecular formula: C20H23N3O3. Mole weight: 353.42. Alfa Chemistry - ISO 9001:32057 Certified. | |
| UV-1164 | DryPowder; PelletsLargeCrystals;Solid. CAS No. 2725-22-6. Molecular formula: C33H39N3O2. Mole weight: 509.7g/mol. IUPAC Name: 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-octoxyphenol. SMILES: 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: 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. | |
| UV1173 | Liquid. CAS No. 7473-98-5. Molecular formula: C10H12O2. Mole weight: 164.2g/mol. IUPAC Name: 2-hydroxy-2-methyl-1-phenylpropan-1-one. SMILES: CC(C)(C(=O)C1=CC=CC=C1)O. InChI: InChI=1S/C10H12O2/c1-10(2,12)9(11)8-6-4-3-5-7-8/h3-7,12H,1-2H3. | |
| UV-1577 | UV-1577. CAS No: 147315-50-2 | Sarchem Laboratories New Jersey NJ |
| UV184 | DryPowder; Liquid; OtherSolid; PelletsLargeCrystals, Liquid. CAS No. 947-19-3. Molecular formula: C13H16O2. Mole weight: 204.26g/mol. IUPAC Name: (1-hydroxycyclohexyl)-phenylmethanone. SMILES: C1CCC(CC1)(C(=O)C2=CC=CC=C2)O. InChI: 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. | |
| UV-234 | UV-234. CAS No: 70321-86-7 | Sarchem Laboratories New Jersey NJ |
| 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 |
| UV-400 | UV-400. Alternative Names: TINUVIN 400; 3-benzenediol,4-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-reaction; hyl]derivs.; productswith[(dodecyloxy)methyl]oxiraneandoxiranemono[(c10-16-alkyloxy)met; 2-[4-[2-HYDROXY-3-TRIDECYL OXYPROPYL]OXY]-2-HYDROXYPHENYL]-4,6-BIS(2,4-DIMETHYLPH. CAS No. 153519-44-9. Molecular formula: C81H108N6O8. Mole weight: 1293.76. | |
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