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| Product | Description | |
|---|---|---|
| UK-1 (Antibiotic) | Antibiotic UK-1 is an unusual bis-benzoxazole metabolite isolated from a species of Streptomyces. It exhibits good antitumor activity but is devoid of antimicrobial activity. Antibiotic UK-1 acts as a magnesium ion-dependent DNA binding agent and inhibitor of human topoisomerase II. Group: Biochemicals. Grades: Highly Purified. CAS No. 151271-53-3. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| UK-1 (Antibiotic) (UK1, Methyl 2'-(2-hydroxyphenyl) -[2,4'-bibenzo[d]oxazole]-4-carboxylate, 2'- (2-Hydroxyphenyl)-(2,4'-bibenzoxazole)-4-carboxylic acid methyl ester) | Antibiotic. Antifungal. Topoisomerase II (Topo II) inhibitor. Mg2+- and Zn2+-dependent DNA binding agent. Potent anticancer compound. Group: Biochemicals. Grades: Highly Purified. CAS No. 151271-53-3. Pack Sizes: 250ug, 1mg. US Biological Life Sciences. | Worldwide |
| UK-2A | UK-2A is produced by Streptomyces sp. 517-02. Its antifungal effect is similar to that of Antimycin A3. Molecular formula: C26H30N2O9. Mole weight: 514.52. |  |
| UK-2B | UK-2B is produced by Streptomyces sp. 517-02. Its antifungal effect is similar to that of Antimycin A3. Molecular formula: C27H30N2O9. Mole weight: 526.53. | |
| UK-2C | UK-2C is produced by Streptomyces sp. 517-02. Its antifungal effect is similar to that of Antimycin A3. Molecular formula: C27H32N2O9. Mole weight: 528.55. | |
| UK-2D | UK-2D is produced by Streptomyces sp. 517-02. Its antifungal effect is similar to that of Antimycin A3. Molecular formula: C27H32N2O9. Mole weight: 528.55. | |
| UK 356618 | UK 356618 (Compound 4j) is a potent and selective inhibitor of matrix metalloprotease-3 (MMP-3) with an IC50 of 5.9 nM. UK 356618 is less potent against MMP-1, MMP-2, MMP-9, MMP-13 and MMP-14 compared with MMP-3[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 230961-08-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-107394. |  |
| UK-356618 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| UK-356618 | Potent and selective inhibitor of matrix metalloprotease-3 (MMP-3) (IC50 = 5.9 nM). Displays selectivity over a range of MMPs (IC50 values are 73, 840, 1790, 1900 and 51000 for MMP-13, MMP-9, MMP-2, MMP-14 and MMP-1 respectively). Group: Biochemicals. Alternative Names: (2R) -N1- [ (1S) -2, 2-Dimethyl-1- [ [ [ (1R) -1-phenylethyl] amino] carbonyl] propyl] -N4-hydroxy-2- [3- (2-methyl [1, 1'-biphenyl] -4-yl) propyl] butanediamide; UK 356618;PF-03890101. Grades: Highly Purified. CAS No. 230961-08-7. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| UK 370106 | UK 370106. Group: Biochemicals. Grades: Purified. CAS No. 230961-21-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| UK-371,804 HCl | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UK-383367 | UK-383367 is an orally available pro-collagen C-protease inhibitor (BMP-1) with an IC50 value of 44 nM. UK-383367 can reduce renal fibrosis and inflammation in chronic kidney disease (CKD) and may be used to study postoperative skin scarring[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 348622-88-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13102. | |
| UK-383367 | UK-383367. Group: Biochemicals. Alternative Names: ( βR)-3-(Aminocarbonyl)- β-(3-cyclohexylpropyl)-N-hydroxy-1,2,4-oxadiazole-5-propanamide; 5-[(1R)-4-Cyclohexyl-1-[2-(hydroxyamino)-2-oxoethyl]butyl]-1,2,4-oxadiazole-3-carboxamide; UK 383367; PF-04171426. Grades: Highly Purified. CAS No. 348622-88-8. Pack Sizes: 10mg. Molecular Formula: C15H24N4O4, Molecular Weight: 324.38. US Biological Life Sciences. | Worldwide |
| UK-383,367 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UK-3A | UK-3A is an antifungal antibiotic obtained from the mycelial cake of Streptomyces sp. 517-02. The antifungal spectrum of UK-3A was relatively broad (MICs for yeasts and filamentous fungi: 1.56-6.25 and 0.39-1.56 micrograms/ml, respectively). The cytotoxic activity of UK-3A was weak (IC50: 18-100 micrograms/ml). Synonyms: UK3A; UK 3A. Molecular formula: C25H28N2O8. Mole weight: 484.5. | |
| UK-41637 | UK-41637 is a polyether antibiotic produced by Actinomadura cremea. It exhibits activity against gram-positive bacteria and parasites. Molecular formula: C46H77O15Na. Mole weight: 893.08. | |
| UK-427857 | UK-427857 Inhibitor. Uses: Scientific use. Product Category: T6016. CAS No. 376348-65-1. |  |
| UK-432097 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UK-5099 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. | |
| UK-5099 | Inhibitor of plasma membrane monocarboxylate transporters (MCTs) and the mitochondrial pyruvate carrier (MPC). Group: Biochemicals. Alternative Names: 2-Cyano-3-(1-phenyl-1H-indol-3-yl)-2-propenoic Acid; UK 5099; PF-06340678. Grades: Highly Purified. CAS No. 56396-35-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| UK-5099 | UK-5099 (PF-1005023) is a potent inhibitor of the mitochondrial pyruvate carrier ( MPC ). UK-5099 (PF-1005023) inhibits pyruvate-dependent O 2 consumption with an IC 50 of 50 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-1005023. CAS No. 56396-35-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15475. | |
| UK-59811 hydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UK-61732 | UK-61732 is a lactone antibiotic produced by Sacchraropolyspora hirsute 367. It inhibits gram-positive bacteria. Molecular formula: C28H37NO7. Mole weight: 499.59. | |
| UK-63052 | UK-63052 is one antibiotic of UK-63052 complex, which is produced by Streptomyces braegensis subsp. Japonicus. It is effective against some gram-positive bacteria including Staphylococcus aureus. Synonyms: Antibiotic UK-63052. CAS No. 120763-23-7. Molecular formula: C56H68N10O14. Mole weight: 1169.3. | |
| UK-63598 | UK-63598 is one antibiotic of UK-63052 complex, which is produced by Streptomyces braegensis subsp. Japonicus. It is effective against some gram-positive bacteria including Staphylococcus aureus. Synonyms: Antibiotic UK-63598; SW-163D. CAS No. 120796-23-8. Molecular formula: C53H62N10O14. Mole weight: 1127.3. | |
| UK-65662 | UK-65662 is one antibiotic of UK-63052 complex, which is produced by Streptomyces braegensis subsp. Japonicus. It is effective against some gram-positive bacteria including Staphylococcus aureus. Synonyms: Antibiotic UK-65662. CAS No. 120832-02-2. Molecular formula: C55H66N10O14. Mole weight: 1155.3. | |
| UK-69735 | UK-69735 is an antibiotic isolated from Amycolatopsis orientalis with activity against anaerobic bacteria, including clostridium difficile and Treponema hyodysenteriae (MIC = 0.39 and 0.78 μg/mL, respectively). Synonyms: Antibiotic UK-69735. Molecular formula: C58H86N2O18. Mole weight: 1099.3. | |
| UK 78282 hydrochloride | UK 78282 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 136647-02-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| UK-78282 hydrochloride | UK-78282, a novel piperidine, potent and selective Kv1.3 blocker with an IC 50 of 200 nM. UK-78,282 effectively suppresses human T-lymphocyte activation in vitro. UK-78,282 binds to residues at the inner surface of the channel overlapping the site of action of verapamil [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 136647-02-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W013727. | |
| UK-78282 monohydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| UK-78624 | UK 78624 is a melbemycin antibiotic produced by Streptomyces hygroscopicus. It possesses anthelmintic and ectoparasiticidal activity. Synonyms: UK 78624; UK78624. Grade: ≥98%. CAS No. 127346-82-1. Molecular formula: C38H54O10. Mole weight: 670.83. | |
| UK-80694 | UK-80694 is a melbemycin antibiotic produced by Streptomyces hygroscopicus. It possesses anthelmintic and ectoparasiticidal activity. Synonyms: UK 80694. CAS No. 127346-84-3. Molecular formula: C42H60O12. Mole weight: 756.92. | |
| UK-80695 | UK-80695 is a melbemycin antibiotic produced by Streptomyces hygroscopicus. It possesses anthelmintic and ectoparasiticidal activity. Synonyms: UK 80695; Milbemycin B, 5-O-demethyl-28-deoxy-6,28-epoxy-13-(2-methyl-1-oxopropoxy)-25-(1-methyl-1-propenyl)-, (6R,13R,25S)-. CAS No. 127346-86-5. Molecular formula: C38H54O9. Mole weight: 654.83. | |
| UK Chemical Suppliers | United Kingdom Chemical Suppliers Database, Includes: England, Scotland, Wales, Ireland & Northern Ireland | UK Chemical Suppliers United Kingdom |
| Ularitide | Urodilatin is a hormone that is involved in regulating blood pressure and the excretion of water and sodium from the kidneys. Synonyms: Urodilatin; Urodilatin ularitide. Grade: ≥98% by HPLC. CAS No. 115966-23-9. Molecular formula: C145H234N52O44S3. Mole weight: 3505.93. | |
| Ulcine-d3 Bromide | Ulcine-d3 Bromide. Group: Biochemicals. Alternative Names: Ulcudexter-d3 Bromide; Uldumont-d3 Bromide; Vagamin-d3 Bromide; Vagantin-d3 Bromide; Xanteline-d3 Bromide; β-Diethylaminoethyl Xanthene-9-carboxylate-d3 Methobromide-d3; Asabaine-d3; Avagal-d3; Banthin-d3; Banthine-d3; Banthine-d3 Bromide; Doladene-d3; Frenogastrico-d3; Gastron-d3; Gastrosedan-d3; MTB 51-d3; Mantheline-d3; Metantyl-d3; Metanyl-d3; Metaxan-d3; Methanide-d3; Methantheline-d3 Bromide; Methanthelinium-d3 Bromide; Methanthine-d3 Bromide; Methelina-d3; Resobantin-d3; SC 2910-d3; N, N-diethyl-N-methyl-2-[ (9H-xanthen-9-ylcarbonyl) oxy]ethanaminium-d3 Bromide; Diethyl (2-hydroxyethyl) methylammonium-d3 Bromide, Xanthene-9-carboxylate; N, N-diethyl-N-methyl-2-[ (9H-xanthen-9-ylcarbonyl) oxy]ethanaminium-d3 Bromide. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C21H23D3BrNO3, Molecular Weight: 423.36. US Biological Life Sciences. | Worldwide |
| Ulefnersen | Ulefnersen (ION363) is an Antisense Oligonucleotide (ASO) directed against the 6th intron of the fused-in sarcoma (FUS) transcript to silence FUS in a non-allele-specific manner. Ulefnersen can reduce postnatal levels of FUS protein in the brain and spinal cord in disease-relevant mouse model of ALS-FUS , delaying motor neuron degeneration. Ulefnersen can be used in the research of Amyotrophic Lateral Sclerosis (ALS) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ION-363. CAS No. 2589926-25-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-147410. | |
| Ulifloxacin | A metabolite of Prulifloxacin. Ulifloxacin is a new quinolone antibiotic and it is effective against pneumonia. Group: Biochemicals. Alternative Names: 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-1H,4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic Acid. Grades: Highly Purified. CAS No. 112984-60-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Ulifloxacin | Ulifloxacin is a broad-spectrum quinolone antibiotic. Ulifloxacin is the active metabolite of Prulifloxacin (HY-B0024). Ulifloxacin has anti-bacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 112984-60-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108279. | |
| Ulifloxacin-[d8] | Ulifloxacin-[d8] is a labelled metabolite of Prulifloxacin. Ulifloxacin is a quinolone antibiotic used for the treatment of pneumonia. Synonyms: Ulifloxacin d8; 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl-d8)-1H,4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic Acid. Grade: 95% by HPLC; 98% atom D. CAS No. 1246820-95-0. Molecular formula: C16H8D8FN3O3S. Mole weight: 357.43. | |
| Uliledlimab | Uliledlimab is a potent against CD73 humanizedized monoclonal antibody. Uliledlimab inhibits the conversion of extracellular adenosine monophosphate (AMP) to adenosine. Uliledlimab can be used in research of cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: TJ004309. CAS No. 2378407-27-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99169. | |
| Ulimorelin | Ulimorelin (TZP-101) is a ghrelin receptor (GRLN) agonist with an EC 50 of 29 nM and a K i of 16 nM. Ulimorelin is a prokinetic agent and causes vasorelaxation through competitive antagonist action at α1-adrenoceptors. Ulimorelin stimulates intestinal motility and is used for malnutrition [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TZP-101. CAS No. 842131-33-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-14903. | |
| Ulinastatin | Ulinastatin (Uristatin) is a trypsin and serine protease inhibitor. Ulinastatin is the main protein binding inhibitor of various trypsin, chymotrypsin, and various pancreatic proteases. Ulinastatin shows neuroprotective, anti-inflammatory, anti-apoptotic, anti-oxidant effects [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Uristatin. CAS No. 80449-31-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-134616. | |
| Ulipristal | Ulipristal (CDB 3236) is a selective progesterone receptor modulator (SPRM). Ulipristal binds to the progesteron receptor, thereby inhibiting PR-mediated gene expression, and interfering with progesterone activity in the reproductive system [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CDB-3236; Deacetyl CDB-2914. CAS No. 159811-51-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14959. | |
| Ulipristal | Ulipristal is a selective progesterone receptor modulator. Ulipristal is used as an emergency contraceptive. Group: Biochemicals. Grades: Highly Purified. CAS No. 159811-51-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Ulipristal acetate | Ulipristal acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ulipristal acetate; [(8S,11R,13S,14S,17R)-17-acetyl-11-[4-(dimethylamino)phenyl]-13-methyl-3-oxo-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate; Ella; VA2914. Product Category: Steroidal Compounds. CAS No. 126784-99-4. Molecular formula: C30H37NO4. Mole weight: 475.62. Purity: 0.98. IUPACName: ulipristal acetate. Density: 1.19 g/cm³. Product ID: ACM126784994. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Ulipristal acetate | Ulipristal acetate (CDB-2914) is an orally active, selective progesterone receptor modulator (SPRM). Ulipristal acetate stimulates the autophagic response selectively in leiomyoma cells. Ulipristal acetate has the potential for benign gynecological conditions treatment, such as uterine myoma [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CDB-2914. CAS No. 126784-99-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16508. | |
| Ulipristal Acetate | Ulipristal acetate is a selective progesterone receptor modulator. Group: Biochemicals. Alternative Names: (11 β)-17-(Acetyloxy)-11-[4-(dimethylamino)phenyl]-19-norpregna-4,9-diene-3,20-dione; 17α-Acetoxy-11 β-(4-dimethylaminophenyl)-19-norpregna-4,9-dien-3,20-dione; CDB 2914; EllaOne; HRP 2000; RTI 3021-012; RU 44675; VA 2914. Grades: Highly Purified. CAS No. 126784-99-4. Pack Sizes: 100mg, 500mg. US Biological Life Sciences. | Worldwide |
| Ulipristal Acetate-[d6] | Ulipristal Acetate-[d6] is the labelled analogue of Ulipristal Acetate. Ulipristal Acetate is a selective progesterone receptor modulator (SPRM) used for emergency contraception and uterine fibroid. Synonyms: Ulipristal Acetate D6; 17-(acetyloxy)-11beta-[4-[di(methyl-d3)amino]phenyl]-19-norpregna-4,9-diene-3,20-dione. Grade: 95% by HPLC; 98% atom D. CAS No. 1621894-64-1. Molecular formula: C30H31D6NO4. Mole weight: 481.65. | |
| Ulipristal-[d3] | An isotope labelled derivative of Ulipristal acetate. Ulipristal acetate is a medication used for emergency birth control and uterine fibroids. Synonyms: (11β)-11-[4-(Dimethylamino)phenyl]-17-hydroxy-19-norpregna-4,9-diene-3,20-dione D3. Grade: 95% by HPLC; 98% atom D. Molecular formula: C28H32D3NO3. Mole weight: 436.61. | |
| Ulixacaltamide | Ulixacaltamide (Z944) is an orally available T-type calcium channel antagonist that can slow the progression of epilepsy. Ulixacaltamide effectively reduces tremor in a normal alkaline tremor animal model. Ulixacaltamide reverses thermal hyperalgesia and mediates pain relief [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Z944; PRAX-944. CAS No. 1199236-64-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120546. | |
| Ulixertinib | Ulixertinib (BVD-523; VRT752271) is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC 50 of <0.3 nM against ERK2. Ulixertinib (BVD-523; VRT752271) inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BVD-523; VRT752271. CAS No. 869886-67-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-15816. | |
| Ulixertinib hydrochloride | Ulixertinib hydrochloride (BVD-523 hydrochloride) is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC 50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BVD-523 hydrochloride; VRT752271 hydrochloride. CAS No. 1956366-10-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15816A. | |
| ULK-101 | ULK-101 is a potent and selective ULK1 inhibitor, with IC 50 values of 1.6 nM and 30 nM for ULK1 and ULK2, respectively. ULK-101 suppresses autophagy and sensitizes cancer cells to nutrient stress [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2443816-45-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-114490. | |
| ULK1 (1-649), active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| ULK2 (1-631), active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| ULK3, active, His tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| ULK Active human | recombinant, ?40% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Ulocuplumab | Ulocuplumab (Anti-Human CXCR4 Recombinant Antibody/BMS-936564/MDX1338) is a fully human IgG4 anti- CXCR4 antibody. Ulocuplumab induces apoptosis and inhibits CXCL12 mediated CXCR4 activation-migration of chronic lymphocytic leukemia (CLL). Ulocuplumab exhibits antitumor activity in established tumors including acute myeloid leukemia (AML), non-Hodgkin lymphoma (NHL), and multiple myeloma xenograft models [1] [2]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: BMS 936564; MDX 1338; Anti-Human CXCR4 Recombinant Antibody. CAS No. 1375830-34-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99272. | |
| Ulodesine | Ulodesine, also known as BCX4208, is a purine nucleoside phosphorylase (PNP) inhibitor in development as a once-daily oral, chronic treatment for gout. Ulodesine is currently being developed by Biocryst. Ulodesine acts upstream of xanthine oxidase in the purine metabolism pathway to reduce the production of serum uric acid (sUA). Ulodesine has an IC(50) of 0.5 nM to PNP. BCX-4208 is currently undergoing early clinical investigation in psoriasis and gout. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BCX4208, BCX 4208, BCX-4208, Ulodesine, DADMe-immucillin H. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 548486-59-5. Molecular formula: C12H16N4O3. Mole weight: 264.28. Purity: >98%. IUPACName: 7-(((3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl)methyl)-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one. Canonical SMILES: O=C1C(NC=C2CN3C[C@H](O)[C@@H](CO)C3)=C2N=CN1. Product ID: ACM548486595. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ulp1 peptidase | The enzyme from Saccharomyces cerevisiae can also recognize small ubiquitin-like modifier 1 (SUMO-1) from human as a substrate in both SUMO-processing (α-linked peptide bonds) and SUMO-deconjugation (ε-linked peptide bonds) reactions. Ulp1 has several functions, including an essential role in chromosomal segregation and progression of the cell cycle through the G2/M phase of the cell cycle. Belongs in peptidase family C48. Group: Enzymes. Synonyms: Smt3-protein conjugate proteinase; Ubl-specific protease 1; Ulp1; Ulp1 endopeptidase; Ulp1 protease. Enzyme Commission Number: EC 3.4.22.68. 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-4244; Ulp1 peptidase; EC 3.4.22.68; Smt3-protein conjugate proteinase; Ubl-specific protease 1; Ulp1; Ulp1 endopeptidase; Ulp1 protease. Cat No: EXWM-4244. |  |
| Ultra-Conductive Graphene Sheet, 0.001" Thick, 8" Wide, 8" Long | Ultra-Conductive Graphene Sheet, 0.001" Thick, 8" Wide, 8" Long. Uses: Designed for use in research and industrial production. Product ID: ACMA00064479. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ultra Dispersed Diamond - P-L | Ultra Dispersed Diamond - P-L. Group: Elements nanoparticles. >96%. |  |
| Ultra Dispersed Diamond Powder-DC | Ultra Dispersed Diamond Powder-DC. Group: Elements nanoparticles. >98.5%. | |
| Ultra Dispersed Diamond Powder - P | Ultra Dispersed Diamond Powder - P. Group: Elements nanoparticles. 97%+. | |
| Ultra Dispersed Diamond - WC-DC | Ultra Dispersed Diamond - WC-DC. Group: Elements nanoparticles. >98.5%. | |
| Ultra Dispersed Diamond - WS | Ultra Dispersed Diamond - WS. Group: Elements nanoparticles. >98.5%. | |
| Ultrahigh capacitance porous carbon activated carbon | Ultrahigh capacitance porous carbon activated carbon. Group: Carbon compounds. | |
| Ultra High Molecular Weight Polyethylene(UHMW-PE) | UHMW-PE is a fine material with spherical particles for use in coatings, lubricants, and polyolefin and polyamide compounding. This material contributes to improved dispersion when mixed with other fillers, and adds improved lubrication, scratch and impact resistance to the final polymeric compound. Uses: Fiber, medical, building & construction, automotive. Group: other plastics. | |
| Ultrapure alpha-Alumina (Al2O3) Nano Powder | Ultrapure alpha-Alumina (Al2O3) Nano Powder. Group: Oxides nanoparticles. 99.99%. | |
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