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| Product | Description | |
|---|---|---|
| UBP302 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| UBP 302 | UBP 302. Group: Biochemicals. Grades: Purified. CAS No. 745055-91-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| UBP 302 | UBP 302 is a potent and selective GLUK5 (GluR5)-subunit containing kainate receptor antagonist (apparent KD = 402 nM) that displays ~ 260-fold selectivity over AMPA receptors, ~ 90-fold selectivity over recombinant human GLUK6- and GLUK2-containing kainate receptors. It has no activity at NMDA or group I mGlu receptors. UBP 302 was shown to block kainate receptor-mediated LTP induction in rat hippocampal mossy fibers. Synonyms: UBP302, UBP-302, UBP 302; (S)-1-(2-Amino-2-carboxyethyl)-3-(2-carboxybenzyl)pyrimidine-2,4-dione; 2-[[3-[(2S)-2-amino-2-carboxyethyl]-2,6-dioxopyrimidin-1-yl]methyl]benzoic acid. Grades: ≥98% by HPLC. CAS No. 745055-91-8. Molecular formula: C15H15N3O6. Mole weight: 333.3. |  |
| UBP 310 | UBP 310 is a GLUK5 kainate receptor antagonist (IC50 = 130 nM), displaying 12,700-fold selectivity for GLUK5 over GLUK6. It has no activity at mGlu group I or NMDA receptors at concentrations of up to 10 μM. UBP 310 also blocks recombinant homomeric GLUK7 receptors. Synonyms: UBP310, UBP 310, UBP-310; (S)-1-(2-Amino-2-carboxyethyl)-3-(2-carboxy-thiophene-3-yl-methyl)-5-methylpyrimidine-2,4-dione; 3-[[3-(2-amino-2-carboxyethyl)-5-methylidene-2,6-dioxopyrimidin-3-ium-1-yl]methyl]thiophene-2-carboxylic acid. Grades: ≥98% by HPLC. CAS No. 902464-46-4. Molecular formula: C14H15N3O6S. Mole weight: 353.35. | |
| UBP 310 | UBP 310. Group: Biochemicals. Grades: Purified. CAS No. 902464-46-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UBP310 (GluK1/GluK3 Antagonist, UBP310, (S)-1-(2-Amino-2-carboxyethyl)-3-(2-carboxy-thiophene-3-yl-methyl)-5-methylpyrimidine-2,4-dione, UBP-310, UBP 310) | A potent antagonist highly selective for GluK1 (Kb = 10nM), GluK3 (IC50 = 23nM), and GluK1/K5 (Kb = 8nM) subtype kainate receptors. Does not interact with GluK2 and GluK2/K5 receptors. Low affinity to AMPA receptors (Kd = 83uM). Does not interact with mGluR1 ornMDA receptors at concentration less than 10uM. Often used in studying neuronal excitability and synaptic plasticity. Group: Biochemicals. Grades: Highly Purified. CAS No. 902464-46-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| UBP608 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UBP714 | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Ubrogepant | Ubrogepant (MK-1602) is an orally active and selective antagonist of calcitonin gene-related peptide receptor ( CGRP ). Ubrogepant has high affinity for CGRP receptors in human and rhesus monkeys, and can effectively block the cAMP response stimulated by α-CGRP. Ubrogepant can be used in the study of acute migraine [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-1602. CAS No. 1374248-77-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12366. |  |
| Ubrogepant | Ubrogepant is and selective oral calcitonin gene-related peptide (CGRP) receptor antagonist originated by Merck & Co. In Sep 2016, Allergan initiated a phase III extension trial for Migraine in USA. Uses: Migraine. Synonyms: MK-1602; MK 1602; MK1602; Ubrogepant; (3'S)-1',2',5,7-Tetrahydro-N-[(3S,5S,6R)-6-methyl-2-oxo-5-phenyl-1-(2,2,2-trifluoroethyl)-3-piperidinyl]-2'-oxo-spiro[6H-cyclopenta[b]pyridine-6,3'-[3H]pyrrolo[2,3-b]pyridine]-3-carboxamide. Grades: 98%. CAS No. 1374248-77-7. Molecular formula: C29H26F3N5O3. Mole weight: 549.55. | |
| UBX domain-containing protein 11 (447-460) | UBX domain-containing protein 11 (447-460) is a peptide derived from UBX domain-containing protein 11. UBX domain-containing protein 11 is involved in the reorganization of actin cytoskeleton mediated by RND1, RND2 AND RND3. It promotes RHOA activation mediated by GNA12 and GNA13. Synonyms: Colorectal tumor-associated antigen COA-1 (447-460); UBX domain-containing protein 5 (447-460). | |
| UC 112 | UC 112. Group: Biochemicals. Grades: Purified. CAS No. 383392-66-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UC 112 | UC-112 is an IAP inhibitor (IC50 values from 0.7 - 3.4 μM). UC-112 also potently inhibits the growth of P-glycoprotein. Uses: Iap inhibitor. Synonyms: UC-112; UC 112; UC112; 5-((benzyloxy)methyl)-7-(pyrrolidin-1-ylmethyl)quinolin-8-ol; (Z,6R)-2-methyl-6-[(5R,9R,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid. Grades: ≥98%. CAS No. 383392-66-3. Molecular formula: C22H24N2O2. Mole weight: 348.44. | |
| UCA 1064-A | UCA 1064-A is an antitumor antibiotic isolated from Wallemia sebi, which inhibits HeLa S3 cells with IC50 of 12.7 μmol/L, suppresses saccharomyces cerevisiae and gram-positive bacteria with MIC of 0.05 and 40 μg/mL, respectively. Molecular formula: C28H45NO. Mole weight: 411.66. | |
| UCA 1064-B | UCA 1064-B is an antitumor antibiotic isolated from Wallemia sebi, which inhibits HeLa S3 cells with IC50 of 14.8 μmol/L, suppresses saccharomyces cerevisiae and gram-positive bacteria with MIC of 0.39 and 40 μg/mL, respectively. Molecular formula: C28H47NO. Mole weight: 413.68. | |
| Ucar Solution Vinyl Resin 9003-22-9 | Ucar Solution Vinyl Resin - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| UCB 35625 | UCB 35625 is a potent CCR1 and CCR3 antagonist. Synonyms: UCB35625, UCB 35625, UCB-35625; 1,4-TRANS-1-(1-CYCLOOCTEN-1-YLMETHYL)-4-[[(2,7-DICHLORO-9H-XANTHEN-9-YL)CARBONYL]AMINO]-1-ETHYLPIPERIDINIUM IODIDE. CAS No. 301648-08-8. Molecular formula: C30H37Cl2IN2O2. Mole weight: 655.44. | |
| UCB 35625 | UCB 35625. Group: Biochemicals. Grades: Purified. Pack Sizes: 1mg, 10mg. US Biological Life Sciences. | Worldwide |
| UCD38B hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCE1022 | UCE1022 is a cytotoxin with topoisomerase I mediated DNA cleavage activity. Synonyms: UCE-1022; UCE 1022. CAS No. 158243-10-8. Molecular formula: C18H10O10S. Mole weight: 418.3. | |
| UCE 6 | UCE 6 is an antitumor metabolite with topoisomerase I mediated DNA cleavage activity. Synonyms: UCE-6; UCE6. CAS No. 150829-94-0. Molecular formula: C24H20O8. Mole weight: 436.4. | |
| Ucenprubart | Ucenprubart is an anti- CD200R1 human IgG4κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG4 kappa, Isotype Control (HY-P99003). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2414559-57-0. Pack Sizes: 1 mg. Product ID: HY-P990770. | |
| Ucf-101 | Ucf-101 is a selective and competitive inhibitor of pro-apoptotic protease Omi/HtrA2 , with an IC 50 of 9.5 μM for His-Omi. Ucf-101 exhibits very little activity against various other serine proteases (IC 50 >200 μM). Ucf-101 has a natural red fluorescence at 543 nm that is used to monitor its ability to enter mammalian cells. Ucf-101 has a significant cardioprotective effect against MI/R injury and also has certain neuroprotective effect [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 313649-08-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-125959. | |
| UCF 101 | UCF 101 is an Omi/HtrA2 protease inhibitor with IC50 value of 9.5 μM. Omi/HtrA2 is a mitochondria serine protease released in response to apoptotic stimuli. UCF 101 is naturally fluorescent enabling the visualization of its entry into cells. Synonyms: RT-014861; 5-({5-[2-(Dihydroxyamino)phenyl]furan-2-yl}methylidene)-1,3-diphenyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione. Grades: ≥98%. CAS No. 313649-08-0. Molecular formula: C27H17N3O5S. Mole weight: 495.5. | |
| UCF-101 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCF116-A | UCF116-A is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C37H48N2O8. Mole weight: 648.78. | |
| UCF116-B | UCF116-B is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C36H48N2O8. Mole weight: 636.77. | |
| UCF116-C | UCF116-C is a metabolite produced by Steptomyces sp. It is inactive for Ftase. Molecular formula: C34H46N2O8. Mole weight: 610.74. | |
| UCF76-A | UCF76-A is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C19H20O7. Mole weight: 360.36. | |
| UCF76-B | UCF76-B is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C18H16O7. Mole weight: 344.31. | |
| UCF76-C | UCF76-C is a FTase inhibitor produced by Steptomyces sp. Molecular formula: C18H16O6. Mole weight: 328.32. | |
| UCH9 | UCH9 is an antitumor antibiotic produced Streptomyces. II. It exhibits bacteriophage and gram-positive bacteria activity. Synonyms: UCH-9; UCH 9. Molecular formula: C55H82O24. Mole weight: 1127.2. | |
| UCHL1, His tagged human | recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| UCH-L1 Inhibitor - CAS 668467-91-2 | The UCH-L1 Inhibitor, also referenced under CAS 668467-91-2, controls the biological activity of UCH-L1. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Group: Fluorescence/luminescence spectroscopy. | |
| UCHL3 active human | recombinant, expressed in baculovirus infected Sf9 cells, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| UCL 1684 | UCL 1684 is a potent and nonpeptidic blocker of the apamin-sensitive Ca2+-activated K+ channel (KCa2.1) (IC50 = 3 nM in rat sympathetic neurons). UCL 1684 was shown to block hKCa2.1 and rKCa2.2 channels expressed in HEK 293 cells (IC50 = 762 and 364 pM, respectively). Synonyms: UCL-1684 Dibromide; UCL 1684 Dibromide; UCL1684 Dibromide; UCL-1684 Br; UCL 1684 Br; UCL1684 Br; 6,12,19,20,25,26-Hexahydro-5,27:13,18:21,24-trietheno-11,7-metheno-7H-dibenzo [b,n] [1,5,12,16]tetraazacyclotricosine-5,13-diium dibromide. Grades: ≥97% by HPLC. CAS No. 199934-16-2. Molecular formula: C34H30Br2N4. Mole weight: 654.44. | |
| UCL 2077 | UCL 2077 is a slow afterhyperpolarization (sAHP) channel blocker that reduces sAHP in hippocampal slice preparations. UCL 2077 exhibits no effect on Ca2+ currents or the time course of sAHP/sIAHP. It also inhibits KCNQ1 and KCNQ2. Synonyms: UCL2077, UCL 2077, UCL-2077; N-Trityl-3-pyridinemethanamine; (3-Triphenylmethylaminomethyl)pyridine. Grades: ≥99% by HPLC. CAS No. 918311-87-2. Molecular formula: C25H22N2. Mole weight: 350.46. | |
| UCL 2077 | UCL 2077. Group: Biochemicals. Grades: Purified. CAS No. 918311-87-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UCL 2077 | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| UCLA GP130 2 | UCLA GP130 2 is a brain-penetrant gp130 agonist, protecting against NMDA-induced toxicity in primary hippocampal neurons in vitro, and increasing STAT3 phosphorylation in SH-SY5Y cells. Synonyms: N-(4-Fluorophenyl)-4-phenyl-2-thiazolamine. Grades: ≥98% by HPLC. CAS No. 339303-87-6. Molecular formula: C15H11FN2S. Mole weight: 270.32. | |
| UCM53 | UCM53 is an inhibitor of bacterial cell division that binds to the GTP site of the cell division protein FtsZ. It inhibits the growth of clinical isolates of antibiotic-resistant Staphylococcus aureus and Enterococcus faecalis. Synonyms: [4-(3-Chloro-4-hydroxybenzoyl)oxynaphthalen-2-yl] 3,4-dihydroxybenzoate. Grades: ≥98%. CAS No. 1449468-52-3. Molecular formula: C24H15ClO7. Mole weight: 450.8. | |
| UCM 707 | UCM 707 is a potent endocannabinoid transport inhibitor (IC50 = 0.8 and 30 μM for inhibition of the anandamide transporter and FAAH, respectively). UCM 707 potentiates hypokinetic and antinociceptive effects of anandamide in vivo. Synonyms: UCM 707; UCM707; UCM-707; (5Z,8Z,11Z,14Z)-N-(3-Furanylmethyl)-5,8,11,14-eicosatetraenamide; N-(furan-3-ylmethyl)icosa-5,8,11,14-tetraenamide. CAS No. 390824-20-1. Molecular formula: C25H37NO2. Mole weight: 383.57. | |
| UCM 707 | UCM 707. Group: Biochemicals. Grades: Purified. CAS No. 390824-20-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UCM710 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCN-01 | KRX-0601, also known as UCN-01, is a synthetic derivative of staurosporine with antineoplastic activity. It inhibits many phosphokinases, including the serine/threonine kinase AKT, calcium-dependent protein kinase C, and cyclin-dependent kinases. This agent arrests tumor cells in the G1/S of the cell cycle and prevents nucleotide excision repair by inhibiting the G2 checkpoint kinase chk1, resulting apoptosis. Uses: Antineoplastic agents. Synonyms: Antibiotic UCN 01; UCN01; Staurosporine; 7-hydroxystaurosporine; KW-2401; KW 2401; KW2401; (3R,9S,10R,11R,13R)-2,3,10,11,12,13-Hexahydro-3-hydroxy-10-methoxy-9-methyl-11-(methylamino)-9,13-epoxy-1H,9H-diindolo[1,2,3-gh:3',2',1'-lm]pyrrolo[3,4-j][1,7]benzodiazonin-1-one; (+)-UCN-01; KRX 0601; NSC 638850. Grades: >99% by HPLC. CAS No. 112953-11-4. Molecular formula: C28H26N4O4. Mole weight: 482.53. | |
| UCN-02 | UCN-02 is an indolocarbazole isolated from a high staurosporine-producing Streptomyces culture with antineoplastic activity. It inhibits many phosphokinases, including the serine/threonine kinase AKT, calcium-dependent protein kinase C, and cyclin-dependent kinases. Synonyms: Antibiotic UCN 02; UCN02; GNF-Pf-3072; 7-hydroxy-staurosporine; 7-epi-Hydroxystaurosporine; (3S,9S,10R,11R,13R)-2,3,10,11,12,13-Hexahydro-3-hydroxy-10-methoxy-9-methyl-11-(methylamino)-9,13-epoxy-1H,9H-diindolo[1,2,3-gh:3',2',1'-lm]pyrrolo[3,4-j][1,7]benzodiazonin-1-one; [3S-(3α, 9α, 10β, 11β, 13α)]-2, 3, 10, 11, 12, 13-Hexahydro-3-hydroxy-10-methoxy-9-methyl-11-(methylamino)-9, 13-epoxy-1H, 9H-diindolo[1, 2, 3-gh:3', 2', 1'-lm]pyrrolo[3, 4-j][1, 7]benzodiazonin-1-one. Grades: >95% by HPLC. CAS No. 121569-61-7. Molecular formula: C28H26N4O4. Mole weight: 482.53. | |
| Ucph 101 | Ucph 101. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UCPH 101. Product Category: Heterocyclic Organic Compound. CAS No. 1118460-77-7. Molecular formula: C27H22N2O3. Mole weight: C27H22N2O3. Purity: >98 %. IUPACName: 2-amino-4-(4-methoxyphenyl)-7-naphthalen-1-yl-5-oxo-4,6,7,8-tetrahydrochromene-3-carbonitrile. Canonical SMILES: COC1=CC=C(C=C1)C2C(=C(OC3=C2C(=O)CC(C3)C4=CC=CC5=CC=CC=C54)N)C#N. Product ID: ACM1118460777. Alfa Chemistry ISO 9001:2015 Certified. Categories: UCPH-101. |  |
| UCPH 101 | UCPH 101 is a selective non-substrate inhibitor of EAAT1 (IC50 = 660, >300000 and >300000 nM for EAAT1, EAAT2 and EAAT3, respectively). UCPH 101 selectively inhibits anion currents in tsA201 cells expressing human EAAT1 (Kd = 0.34 μM) over rat EAAT4 and mouse EAAT5 at concentrations up to 10 μM. Synonyms: UCPH-101, UCPH 101, UCPH101; 2-Amino-5,6,7,8-tetrahydro-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-4H-chromene-3-carbonitrile. Grades: ≥98% by HPLC. CAS No. 1118460-77-7. Molecular formula: C27H22N2O3. Mole weight: 422.48. | |
| UCPH-102 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCS1025 A | UCS1025 A is an antitumor antibiotic isolated from Acremonium sp. KY4917. It exhibits activity against gram-positive bacteria including Staphylococcus and Enterococcus, and proteusbacillus vulgaris. It also inhibits cell proliferation. Synonyms: UCS 1025A. Molecular formula: C22H29NO5. Mole weight: 387.47. | |
| UCS1025 B | UCS1025 B is an antitumor antibiotic isolated from Acremonium sp. KY4917. It exhibits activity against gram-positive bacteria including Staphylococcus and Enterococcus, and proteusbacillus vulgaris. It also inhibits cell proliferation. The activity of B is much weaker than that of A. Synonyms: UCS 1025B. Molecular formula: C22H29NO6. Mole weight: 403.47. | |
| UCSF924NC | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UCT 1072M1 | UCT 1072M1 is a topoisomerase II poison isolated from Aspergillus sp. KY4919, which is toxic to HeLa S3 and Lu-65 cells. Synonyms: UCT1072M1; UCT-1072M1. Molecular formula: C18H12O8. Mole weight: 356.28. | |
| UCT 1072M2 | UCT 1072M2 is a topoisomerase II poison isolated from Aspergillus sp. KY4919, which is toxic to HeLa S3 and Lu-65 cells. Synonyms: UCT1072M2; UCT-1072M2. Molecular formula: C20H16O7. Mole weight: 368.34. | |
| UCT 1072M3 | UCT 1072M3 is a topoisomerase II poison isolated from Aspergillus sp. KY4919, which is toxic to HeLa S3 and Lu-65 cells. UCT 1072M3 is a diastereomer of UCT 1072M2. Synonyms: UCT1072M3; UCT-1072M3. Molecular formula: C20H16O7. Mole weight: 368.34. | |
| UCT4B | UCT4B is an antitumor antibiotic produced by Streptomyces sp. It exhibits topoisomerase II mediated DNA cleavage activity. It suppresses gram-positive bacteria and Klebsiella pneumoniae with MIC of 4.1 and 2.1 μg/mL, respectively. Synonyms: UCT 4B. CAS No. 143200-52-6. Molecular formula: C20H28O7. Mole weight: 380.4. | |
| UD-014 | UD-014 is a selective and long-acting inhibitor of semicarbazide-sensitive amine oxidase (SSAO; VAP-1) (IC50 = 3.2 nM), which shows a therapeutic effect of diabetic nephropathy in a streptozotocin rat model. Uses: The treatment of diabetic nephropathy. Synonyms: UD 014; UD014. | |
| Udenafil | An oral phosphodiesterase 5 inhibitor used for the treatment of erectile dysfunction. Group: Biochemicals. Alternative Names: 3- (6, 7-Dihydro-1-methyl-7-oxo-3-propyl -1H-pyrazolo [4, 3-d] pyrimidin-5-yl) -N- [2- (1-methyl-2-pyrrolidinyl) ethyl] -4-propoxy Benzene sulfonamide; DA 8159; Zydena. Grades: Highly Purified. CAS No. 268203-93-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Udenafil | Udenafil is an oral PDE5 inhibitor. Udenafil significantly increased cAMP and cGMP levels and were more highly distributed in the prostate than plasma. The T/P ratio of udenafil was higher than tadalafil. These findings may help in the assessment of the feasibility of using PDE5 Is to concurrently treat both LUTS and erectile dysfunction. After 12 weeks of treatment, the patients treated with udenafil showed significantly greater change from baseline in the IIEF-EF domain score compared with placebo (placebo, 0.20; 100-mg udenafil, 7.52; and 200-mg udenafil, 9.93, respectively) (P < 0.0001). udenafil significantly enhanced the rates of successful penetration (SEP Q2) and maintenance of erection (SEP Q3) (P < 0.0001). Synonyms: DA-8159, DA 8159, DA8159, Udenafil, Zydena. Grades:>98%. CAS No. 268203-93-6. Molecular formula: C25H36N6O4S. Mole weight: 516.66. | |
| Udenafil | Udenafil (DA8159) is a potent, selective and orally active phosphodiesterase type 5 (PDE5) inhibitor. Udenafil also inhibits cGMP hydrolysis and can be used for erectile dysfunction research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA8159. CAS No. 268203-93-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18253. | |
| UDM-002555 | UDM-002555 is a small-molecule and selective antagonist of protease-activated receptor-4 (PAR-4). It can suppress the activation of platelet in dose manner. In combination with aspirin, it inhibited arterial thrombosis with limited impact on hemostasis in cynomolgus monkeys. Uses: The potential treatment of arterial thrombosis. Synonyms: UDM-002555; UDM 002555; UDM002555. | |
| Udonitrectag | Udonitrectag (REC 0559), a low molecular weight compound that mimics NGF, aims to address the issue of NGF stability [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: REC 0559. CAS No. 1458063-04-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109194. | |
| UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of the B-band lipopolysaccharide of Pseudomonas aeroginosa serotype O5 and of the band-A trisaccharide of Bordetella pertussis, both important respiratory pathogens. The enzyme is highly specific as UDP-α-D-GlcNAc, UDP-α-D-GlcNAcA (UDP-2-acetamido-2-deoxy-α-D-glucuronic acid) and UDP-α-D-GlcNAc3NAc (UDP-2,3-diacetamido-2,3-dideoxy-α-D-glucose) cannot act as substrates. Group: Enzymes. Synonyms: UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Enzyme Commission Number: EC 5.1.3.23. 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-5409; UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase; EC 5.1.3.23; UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Cat No: EXWM-5409. |  |
| UDP-2,3-diacylglucosamine diphosphatase | The enzyme catalyses a step in the biosynthesis of lipid A. Group: Enzymes. Synonyms: UDP-2,3-diacylglucosamine hydrolase; UDP-2,3-diacylglucosamine pyrophosphatase; ybbF (gene name); lpxH (gene name); UDP-2,3-bis[(3R)-3-hydroxymyristoyl]-α-D-glucosamine 2,3-bis[(3R)-3-hydroxymyristoyl]-β-D-glucosaminyl 1-phosphate phosphohydrolase (incorrect). Enzyme Commission Number: EC 3.6.1.54. 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-4626; UDP-2,3-diacylglucosamine diphosphatase; EC 3.6.1.54; UDP-2,3-diacylglucosamine hydrolase; UDP-2,3-diacylglucosamine pyrophosphatase; ybbF (gene name); lpxH (gene name); UDP-2,3-bis[(3R)-3-hydroxymyristoyl]-α-D-glucosamine 2,3-bis[(3R)-3-hydroxymyristoyl]-β-D-glucosaminyl 1-phosphate phosphohydrolase (incorrect). Cat No: EXWM-4626. | |
| UDP-2,4-diacetamido-2,4,6-trideoxy-β-L-altropyranose hydrolase | The enzyme is involved in biosynthesis of pseudaminic acid. Group: Enzymes. Synonyms: PseG; UDP-6-deoxy-AltdiNAc hydrolase; Cj1312; UDP-2,4-bis(acetamido)-2,4,6-trideoxy-β-L-altropyranose hydrolase. Enzyme Commission Number: EC 3.6.1.57. 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-4629; UDP-2,4-diacetamido-2,4,6-trideoxy-β-L-altropyranose hydrolase; EC 3.6.1.57; PseG; UDP-6-deoxy-AltdiNAc hydrolase; Cj1312; UDP-2,4-bis(acetamido)-2,4,6-trideoxy-β-L-altropyranose hydrolase. Cat No: EXWM-4629. | |
| UDP-2-Acetamido-2,4-dideoxy-4-fluorogalactose | UDP-2-Acetamido-2,4-dideoxy-4-fluorogalactose is an indispensable compound assuming a pivotal status in the intricate domain of glycoconjugate synthesis. By serving as a formidable substrate for a plethora of enzymes actively participating in glycosylation processes, this remarkable compound effectively facilitates the intricate modification of proteins and lipids. Synonyms: Uridine 5'-(2-acetamido-2,4-dideoxy-4-fluoro-a-D-galactopyranosyl)diphosphate; dilithium,[(2R,3R,4R,5R,6R)-3-acetamido-5-fluoro-4-hydroxy-6-(hydroxymethyl)oxan-2-yl][[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate; Uridine 5'-(trihydrogen diphosphate),P'-(2-(acetylamino)-2,4-dideoxy-4-fluoro-alpha-D-galactopyranosyl) ester, dilithium salt; Udp-adfg. CAS No. 120596-20-5. Molecular formula: C17H24FLi2N3O16P2. Mole weight: 621.21. | |
| UDP-2-acetamido-2,6-β-L-arabino-hexul-4-ose reductase | Part of the biosynthesis of UDP-N-acetyl-L-fucosamine. Isolated from the bacteria Pseudomonas aeruginosa and Staphylococcus aureus. Group: Enzymes. Synonyms: WbjC; Cap5F. Enzyme Commission Number: EC 1.1.1.367. 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-0284; UDP-2-acetamido-2,6-β-L-arabino-hexul-4-ose reductase; EC 1.1.1.367; WbjC; Cap5F. Cat No: EXWM-0284. | |
| UDP-2-acetamido-2-deoxy-5-thio-D-glucopyranose | | |
| UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase | A pyridoxal 5'-phosphate protein. This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. The enzymes from Pseudomonas aeruginosa serotype O5 and Thermus thermophilus form a complex with the previous enzyme in the pathway, EC 1.1.1.335 (UDP-N-acetyl-2-amino-2-deoxyglucuronate oxidase). Group: Enzymes. Synonyms: WbpE; WlbC. Enzyme Commission Number: EC 2.6.1.98. 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-2939; UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase; EC 2.6.1.98; WbpE; WlbC. Cat No: EXWM-2939. | |
| UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. Group: Enzymes. Synonyms: WbpD; WlbB. Enzyme Commission Number: EC 2.3.1.201. 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-2146; UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase; EC 2.3.1.201; WbpD; WlbB. Cat No: EXWM-2146. | |
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