A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Tungsten Tube / Pipe / Ring. Group: Magnetic nanoparticles. Alternative Names: W Tube, W Pipe, Tungsten Tube, Tungsten Pipe.
Tungsten(VI) chloride
Tungsten(VI) chloride. Uses: A precursor to tungsten based carbenes. Group: Electrolytes. Alternative Names: Tungsten chloride, (OC-6-11)-; [WCl6]; RTR-004479; hexachloridotungsten; KSC491C2D; Tungsten(VI) chloride; Hexachlorotungsten; EINECS 236-293-9; CTK3J1121; ARONIS24089. CAS No. 13283-01-7. Product ID: hexachlorotungsten. Molecular formula: 396.54g/mol. Mole weight: WCl6;Cl6W. Cl[W](Cl)(Cl)(Cl)(Cl)Cl. InChI=1S/6ClH.W/h6*1H;/q;;;;;;+6/p-6. KPGXUAIFQMJJFB-UHFFFAOYSA-H.
Tungsten (VI) Chloride
TUNGSTEN (VI) CHLORIDE, 99.9% pure, -8 mesh, (Synonym: Tungsten Hexachloride), Formula: WCl6. CAS No. 13283-01-7. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
Tungsten (VI) Fluoride
TUNGSTEN (VI) FLUORIDE, 99.9% pure, liquid, (Synonym: Tungsten Hexafluoride), Formula: WF6. CAS No. 7783-82-6. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
Texas TX
Tungsten(VI) oxide
100g Pack Size. Group: Inorganic Chemicals, Research Organics & Inorganics. Formula: WO3. CAS No. 1314-35-8. Prepack ID 10584499-100g. Molecular Weight 231.84. See USA prepack pricing.
Tungsten W powder. Uses: Aerospace alloys, alloys for electronic package, alloys for heat sinks, anti-armor alloys, circuit breakers, contacts and electrode materials, contacts in a protective atmosphere, electrodes for gas sensors. Group: Element powders. CAS No. 7440-33-7. Molecular formula: 183.84. Mole weight: W. >99.5%.
Tungsten (W) Sputtering Targets
Tungsten (W) Sputtering Targets. Group: Sputtering targets. Alternative Names: Tungsten (W) Sputtering Targets, W Sputtering Target, W Sputter Target, W Target, Tungsten Sputtering Target, Tungsten Sputter Target, Tungsten Target. CAS No. 12018-22-3. 99.95%, 99.99%, 99.999%.
Tungstosilicic acid hydrate. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences.
Worldwide
Tunicamycin
N-linked glycosylation is a highly regulated post-translational modification that is involved in protein folding and conformation, oligomerization, sorting, cell-cell interactions, and targeting of proteins to sub- or extra-cellular locations. It is initiated in the endoplastic reticulum with the transfer of a carbohydrate moiety to an asparagine residue within a specific amino acid consensus sequence and then further processed in the Golgi whereupon a mature glycoprotein is exported through the secretory machinery to the plasma membrane. Tunicamycin, a mixture of nucleoside antibiotics, is a specific inhibitor of N-linked glycoslylation that blocks the first step of glycoprotein synthesis thereby inducing protein unfolding. At 500 nM, it can impair the function of several receptor tyrosine kinases, including EGFR, ErbB2, ErbB3, and IGF-IR.1 Also at 500 nM, it radiosensitizes U251 glioma and BXPC3 pancreatic adenocarcinoma cells to chemotherapy.1 Tunicamycin impairs ALK phosphorylation Group: Biochemicals. Alternative Names: Streptomyces Iysosuperficus. Grades: Molecular Biology Grade. CAS No. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C39H64N4O16, Molecular Weight: 844.4. US Biological Life Sciences.
Worldwide
Tunicamycin
Tunicamycin is a mixture of homologous nucleoside antibiotic that inhibits N-linked glycosylation and blocks GlcNAc phosphotransferase (GPT). Tunicamycin causes accumulation of unfolded proteins in cell endoplasmic reticulum (ER) and induces ER stress, and causes blocking of DNA synthesis and cell cycle arrest in G1 phase. Tunicamycin inhibits gram-positive bacteria, yeasts, fungi, and viruses and has anti-cancer activity[1][2][3].Tunicamycin increases exosome release in cervical cancer cells[4]. Uses: Scientific research. Group: Natural products. CAS No. 11089-65-9. Pack Sizes: 2 mg; 5 mg; 10 mg. Product ID: HY-A0098.
Tunicamycin is a mixture of homologous nucleoside antibiotic that inhibits N-linked glycosylation and blocks GlcNAc phosphotransferase (GPT). Tunicamycin causes accumulation of unfolded proteins in cell endoplasmic reticulum (ER) and induces ER stress, and causes blocking of DNA synthesis and cell cycle arrest in G1 phase. Tunicamycin inhibits gram-positive bacteria, yeasts, fungi, and viruses and has anti-cancer activity.Tunicamycin increases exosome release in cervical cancer cells. Uses: Designed for use in research and industrial production. Additional or Alternative Names: tunicamycin, Tunicamycin A1, CID5607, 11089-65-9. Product Category: Inhibitors. Appearance: White to off-white powder. CAS No. 11089-65-9. Molecular formula: C37H60N4O16. Mole weight: 816.89. Purity: 98%+. IUPACName: N-[2-[3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[2-[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl]-4,5-dihydroxyoxan-3-yl]-12-methyltridec-2-enamide. Canonical SMILES: CC(C)CCCCCCCCC=CC(=O)NC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)NC(=O)C)CC(C3C(C(C(O3)N4C=CC(=O)NC4=O)O)O)O)O)O. Density: 1.57g/cm³. Product ID: ACM11089659. Alfa Chemistry ISO 9001:2015 Certified.
Tunicamycin
Tunicamycin, a mixture of homologous nucleoside antibiotics, has been used to study the effect of N-linked glycosylation of human proton-coupled folate transporter (HsPCFT) in HeLa cells. Tunicamycin blocks the formation of N-glycosidic linkages by inhibiting the first step in glycoprotein synthesis. It exhibits a range of biological activities, including antimicrobial, antivirus, and antitumor effects. It is produced by certain bacteria, including Streptomyces lysosuperficus and Streptomyces chartreusis. Grade: ≥98%. CAS No. 11089-65-9.
Tunicamycin D
Tunicamycin D is a member of the tunicamycin group of nucleoside antibiotics, which are known for their antibacterial, antiviral, and antitumor activities. These activities are primarily due to the inhibition of bacterial phospho-N-acetylmuramyl-pentapeptide transferase (MraY), an enzyme crucial for the biosynthesis of peptidoglycan, which is a major component of bacterial cell walls. Tunicamycins also inhibit the human enzyme UDP-N-acetylglucosamine-dolichyl phosphate N-acetylglucosamine-phosphotransferase (GPT), which is involved in the first step of N-linked glycosylation of proteins in the endoplasmic reticulum. This inhibition can lead to the prevention of N-glycan attachment to proteins, affecting their proper folding, trafficking, and function, and ultimately inducing cellular stress and apoptosis. Synonyms: 2,4(1H,3H)-Pyrimidinedione, 1-[(11S)-11-O-[2-(acetylamino)-2-deoxy-α-D-glucopyranosyl]-6,10-dideoxy-10-[[(2E)-15-methyl-1-oxo-2-hexadecen-1-yl]amino]-L-galacto-β-D-allo-undecodialdo-1,4-furanose-11,7-pyranos-1-yl]-; 1-[(11S)-11-O-[2-(Acetylamino)-2-deoxy-α-D-glucopyranosyl]-6,10-dideoxy-10-[[(2E)-15-methyl-1-oxo-2-hexadecen-1-yl]amino]-L-galacto-β-D-allo-undecodialdo-1,4-furanose-11,7-pyranos-1-yl. Grade: ≥95%. CAS No. 66081-38-7. Molecular formula: C40H66N4O16. Mole weight: 858.98.
Tunicamycin Ready Made Solution
5 mg/mL in DMSO, from Streptomyces sp. Group: Fluorescence/luminescence spectroscopy.
Tunlametinib
Tunlametinib, an antineoplastic agent, is a MEK1/2 inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HL-085. CAS No. 1801756-06-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-132844.
Tupichinol A
Tupichinol A is a natural compound isolated from the underground parts of Tupistra chinensis. Synonyms: (2R,3R)-2-(4-hydroxyphenyl)-7-methoxy-8-methyl-3,4-dihydro-2H-chromen-3-ol. Grade: 98.5%. CAS No. 497142-88-8. Molecular formula: C17H18O4. Mole weight: 286.32.
Turanose
Turanose is an isomer of Sucrose that naturally exists in honey. Turanose has anti-inflammatory and regulates adipogenesis effect. Turanose has potential for obesity and related chronic diseases research [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 547-25-1. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-113334.