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| Product | Description | |
|---|---|---|
| Ursodeoxycholic acid impurity 55 | Ursodeoxycholic acid impurity 55. Uses: For analytical and research use. CAS No. 69700-82-9. Molecular formula: C26H44O4. Mole weight: 420.63. Catalog: APB69700829. |  |
| Ursodeoxycholic acid methyl ester | Ursodeoxycholic acid methyl ester. Alternative Names: (3α,5β,7β)-3,7-Dihydroxycholan-24-oic Acid. CAS No. 10538-55-3. Product ID: ACM10538553. Molecular formula: C25H42O4. Mole weight: 406.60. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Ursodeoxycholic acid methyl ester | Ursodeoxycholic acid methyl ester. Group: Biochemicals. Alternative Names: (3a,5b,7b)-3,7-Dihydroxycholan-24-oic acid. Grades: Highly Purified. CAS No. 10538-55-3. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C25H42O4. US Biological Life Sciences. |  Worldwide |
| Ursodeoxycholic Acid Methyl Ester-[d5] | Ursodeoxycholic Acid Methyl Ester-[d5]. Uses: A precursor to manufacture udca (ursodeoxycholic acid). Synonyms: Ursodeoxycholic Acid D5 Methyl Ester. Grade: 95% atom D. CAS No. 93701-19-0. Molecular formula: C25H37D5O4. Mole weight: 411.63. |  |
| Ursodeoxycholic acid sodium | Ursodeoxycholic acid (Ursodeoxycholate) sodium is a secondary bile acid issued from the transformation of (cheno)deoxycholic acid by intestinal bacteria, acting as a key regulator of the intestinal barrier integrity and essential for lipid metabolism. Ursodeoxycholic acid sodium acts as signaling molecule, exerting its effects by interacting with bile acid activated receptors, including G-protein coupled bile acid receptor 5 (TGR5, GPCR19) and the farnesoid X receptor (FXR). Ursodeoxycholic acid sodium can be used for the research of a variety of hepatic and gastrointestinal diseases. Orally active[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ursodeoxycholate sodium; Ursodiol sodium; UCDA sodium. CAS No. 2898-95-5. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-13771A. |  |
| Ursodeoxycholic Acid, Sodium Salt | Ursodeoxycholic Acid, Sodium Salt. CAS No: 128-13-2 |  Sarchem Laboratories New Jersey NJ |
| Ursodeoxycholic acid (Standard) | Ursodeoxycholic acid (Standard) is the analytical standard of Ursodeoxycholic acid. This product is intended for research and analytical applications. Ursodeoxycholic acid (Ursodeoxycholate) is a secondary bile acid issued from the transformation of (cheno)deoxycholic acid by intestinal bacteria, acting as a key regulator of the intestinal barrier integrity and essential for lipid metabolism. Ursodeoxycholic acid acts as signaling molecule, exerting its effects by interacting with bile acid activated receptors, including G-protein coupled bile acid receptor 5 (TGR5, GPCR19) and the farnesoid X receptor (FXR). Ursodeoxycholic acid can be used for the research of a variety of hepatic and gastrointestinal diseases. Ursodeoxycholic acid also reduces ACE2 expression and is beneficial for reducing SARS-CoV-2 infection. Orally active[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ursodeoxycholate (Standard); Ursodiol (Standard); UDCA (Standard). CAS No. 128-13-2. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-13771R. | |
| Ursolic acid | Ursolic acid is a natural pentacyclic triterpenoid carboxylic acid displaying antitumor activity. It was shown to downregulate the MMP-2 and uPA expression, and also inhibit Na+/K+-ATPase activity (IC50 = 24.7 μM) as well as NF-κB activation in various cancer cell lines. Ursolic acid can induce apoptosis in cancer cells. Ursolic acid also has obvious antioxidant function, so it is widely used as a raw material for medicine and cosmetics. Uses: Antidepressant. Synonyms: NSC-167406; NSC-4060; NSC167406; NSC4060; NSC 167406; NSC 4060; Malol; Prunol; Urson; 3beta-Hydroxyurs-12-en-28-oic acid. Grade: ≥ 98%. CAS No. 77-52-1. Molecular formula: C30H48O3. Mole weight: 456.711. | |
| Ursolic acid | Ursolic Acid is a Triterpene acid used in cosmetics, that also has STAT3 pathway inhibiting properties.Ursolic acid protects against muscle atrophy and boosts muscle growth (see also tomatidine. Group: Biochemicals. Alternative Names: (3 β)-3-Hydroxy-urs-12-en-28-oic Acid; (+)-Ursolic Acid; Bungeolic Acid; Malol; Merotaine; Neoage UR; Prunol; NSC 167406; NSC 4060; β-Ursolic Acid. Grades: Highly Purified. CAS No. 77-52-1. Pack Sizes: 1g, 5g, 10g. Molecular Formula: C??H??O?, Molecular Weight: 456.7. US Biological Life Sciences. | Worldwide |
| Ursolic acid | Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Prunol; Urson; Malol. CAS No. 77-52-1. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 200 mg. Product ID: HY-N0140. | |
| Ursolic acid | Ursolic acid. Alternative Names: 3β-Hydroxy-12-ursen-28-oic Acid. CAS No. 77-52-1. Purity: >90.0%. Product ID: FFC-AR-77521. Molecular formula: C30H48O3. Mole weight: 456.7. IUPAC Name: (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ursolic Acid | Ursolic Acid. CAS No: 77-52-1 | Sarchem Laboratories New Jersey NJ |
| Ursolic acid acetate | Ursolic acid acetate (Acetylursolic acid) is a triterpenoid compound and an inhibitor of Plasmodium falciparum heat shock protein 90 (PfHsp90) with a KD of 8.16 μM. Ursolic acid acetate is cytotoxic to KB cells, with an IC50 value of 8.4 μM. Ursolic acid acetate can be used in tumor and antimalarial research[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Acetylursolic acid; 3-Acetylursolic acid. CAS No. 7372-30-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N2815. | |
| Ursolic Acid-d3 | Ursolic Acid-d3 is labelled Ursolic Acid(U850100) which is a Triterpene acid used in cosmetics. It also has STAT3 pathway inhibiting properties. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C30H45D3O3, Molecular Weight: 459.72. US Biological Life Sciences. | Worldwide |
| Ursolic aldehyde | Ursolic aldehyde. CAS No. 19132-81-1. Product ID: FFC-AR-19132811. Molecular formula: C30H48O2. Mole weight: 400.7. IUPAC Name: (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carbaldehyde. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Ursonic acid | Ursolic acid is a naturally occurring triterpenoid that has orally active. Ursolic acid induces the apoptosis of human cancer cells through multiple signaling pathways. Ursolic acid has anti-inflammatory and anticarcinogenic activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 3-Ketoursolic acid. CAS No. 6246-46-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1486. | |
| US EPA Method 8276 Toxaphene Composite Stock Standard in nonane | US EPA Method 8276 Toxaphene Composite Stock Standard in nonane. Uses: For analytical and research use. Purity: 98%. Catalog: APB12575. | |
| Usherin isoform B (3700-3711) | Usherin isoform B (3700-3711). | |
| Usinic acid | Usinic acid. Group: Biochemicals. CAS No. 125-46-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Usmarapride | Usmarapride (SUVN-D4010) (Example 3)is a potent, selective, orally active and brain penetrant 5-HT4 receptor partial agonist (EC50=27.5 nM). Usmarapride (SUVN-D4010) can be used for the research of cognitive deficits associated with Alzheimer's disease[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: SUVN-D4010. CAS No. 1428862-33-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-116565. | |
| 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. | |
| 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. Grade: ≥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. Grade: ≥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. Synonyms: (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)-. Grade: 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. Synonyms: 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)-. Grade: ≥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. Synonyms: 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)-. Grade: 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. Synonyms: 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)-. Grade: 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. 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)-. Grade: 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. 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. | |
| 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. | |
| 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. | |
| 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. Synonyms: KDM6A (1264-1273). | |
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