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vu 590 dihydrochloride c24h34cl2n4o7

vu 590 dihydrochloride c24h34cl2n4o7

vu 590 dihydrochloride c24h34cl2n4o7

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VU 590 dihydrochloride | C24H34Cl2N4O7 - PubChemVU 590 dihydrochloride | C24H34Cl2N4O7 | CID 71433535 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological ...

VulcanChem (Page 245) @ ChemBuyersGuide vu 590 dihydrochloride c24h34cl2n4o7, Inc.

vu 0365114 cas:1208222-39-2 vc288261 : vu 0409106 cas:1276617-62-9 vc010089 : vu 0422288 cas:1630936-95-6 vc010109 : vu 0463271 cas:1391737-01-1 vc009849 : vu 0469650 hydrochloride cas:1443748-47-7 vc010111 : vu 1545 cas:890764-63-3 vc009343 : vu 29 cas:890764-36-0 vc009763 : vu 590 dihydrochloride cas:1783987-83-6 vc009543 : vu 591 vu 590 dihydrochloride c24h34cl2n4o7VU590 dihydrochloride | V-130 | Alomone LabsScientific background VU590 dihydrochloride is a synthetic blocker of K ir 1.1 channel with an IC50 of 294nM for K ir 1.1 channel. VU590 also inhibits K ir 7.1 channels at micromolar concentrations whilst having no effect on K ir 2.1 or K ir 4.1 channels. At a voltage of -120mV VU590 inhibits K ir 1.1 currents by 95.3±0.5%. Inhibition of the K ir 1.1 channel is dose dependent. 10 µM of VU590 vu 590 dihydrochloride c24h34cl2n4o7VU 590 dihydrochloride| NaveproteinVU 590 dihydrochloride | Products for research use only! Product Name:VU 590 dihydrochloride Catalog NO.:BCC7803. CAS NO.:313505-85-0 Molecular Formula:C 24 H 32 N 4 O 7.2HCl Molecular Weight:561.46 Chemical Name: 7,13-bis(4-nitrobenzyl)-1,4,10-trioxa-7,13-diazacyclopentadecane dihydrochloride Purify method:HPLC-DAD Purity:>98% as determined by HPLC storage:

VU 590 dihydrochloride, Tocris Bioscience | Fisher Scientific

CAS: 313505-85-0: Molecular Formula: C24H34Cl2N4O7: Molecular Weight (g/mol) 561.457: InChI Key: FRYYSUBAHIUBNJ-UHFFFAOYSA-N: Synonym: vu 590 dihydrochloride,7,13-bis 4-nitrophenyl methyl-1,4,10-trioxa-7,13-diazacyclopentadecane dihydrochloride,7,13-bis 4-nitrophenyl methyl-1,4,10-trioxa-7,13-diazacyclopentadecane-hydrogen chloride 1/2VU 590 dihydrochloride | CAS 313505-85-0 | SCBT - Santa vu 590 dihydrochloride c24h34cl2n4o7VU 590 dihydrochloride has been reported to inhibit the renal, outer medullary potassium channel (ROMK, KIR1.1) while also able to inhibit the inward rectifying potassium channel KIR7.1. This comppound is also reported to not display an effect towards KIR2.1 or KIR4.1 and additionally acts as an intracellular ROMK channel pore blocker.VU 590 dihydrochloride | C24H34Cl2N4O7 - PubChemVU 590 dihydrochloride | C24H34Cl2N4O7 | CID 71433535 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological vu 590 dihydrochloride c24h34cl2n4o7

VU 590 dihydrochloride hydrate (HPLC) | Sigma-Aldrich

VU 590 dihydrochloride hydrate (HPLC) Empirical Formula (Hill Notation) C 24 H 32 N 4 O 7 ·2HCl · xH 2 O . Molecular Weight 561.46 (anhydrous basis) MDL number MFCD16875439. PubChem Substance ID 329829050VU 590 dihydrochloride Supplier | CAS 1783987-83-6 | 2 Citations for VU 590 dihydrochloride. Citations are publications that use Tocris products. Selected citations for VU 590 dihydrochloride include: Yin et al (2018) The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis.VU 590 dihydrochloride (CAS 1783987-83-6): R&D SystemsView and buy high quality VU 590 dihydrochloride. Inhibitor of Kir1.1 (ROMK) and Kir7.1. Cited in 2 publications.

Tocris-- |

Tocris--: Tocris page 1 >> 1 2 3 4 5 6 7 8 9 10 11 : : : : 3642-10MG: Src I1: 10 mg: Tocris vu 590 dihydrochloride c24h34cl2n4o7Tocris-- | Tocris--: Tocris page 1 >> 1 2 3 4 5 6 7 8 9 10 11 : : : : 3642-10MG: Src I1: 10 mg: Tocris vu 590 dihydrochloride c24h34cl2n4o7Reengineering an Antiarrhythmic Drug Using Patient hiPSC vu 590 dihydrochloride c24h34cl2n4o7McKeithan et al. used large-scale functional screening of hiPSC cardiomyocytes carrying a mutation that causes an electrophysiological disorder (long QT syndrome type 3) to direct the chemical optimization of mexiletine, an antiarrhythmic drug used to treat the disease. Four new analogs have greater potency and less proarrhythmic liability relative to mexiletine.

Muscarinic receptors 2 and 5 regulate bitter response of vu 590 dihydrochloride c24h34cl2n4o7

Jan 17, 2018 · We have recently identified a novel cholinergic component in sensory control of bladder function, that is, a specialized cholinergic epithelial cell in the urethra, termed the urethral brush cell (UBC) (1, 2).UBCs are polymodal chemosensory cells that express both canonical bitter and umami receptors and their common downstream channel, transient receptor potential cation channel Muscarinic receptors 2 and 5 regulate bitter response of vu 590 dihydrochloride c24h34cl2n4o7Jan 17, 2018 · We have recently identified a novel cholinergic component in sensory control of bladder function, that is, a specialized cholinergic epithelial cell in the urethra, termed the urethral brush cell (UBC) (1, 2).UBCs are polymodal chemosensory cells that express both canonical bitter and umami receptors and their common downstream channel, transient receptor potential cation channel Muscarinic receptor control of pyramidal neuron membrane vu 590 dihydrochloride c24h34cl2n4o7Sep 10, 2015 · VU 0255035, 5 M) muscarinic receptor blockers and was not affected in the presence of a nicotinic receptor blocker (c. mecamylamine hydrochloride, 10 M). (d) Average amplitude of CCh-dependent depolarization evoked by the application of CCh alone (100 M, control, n = 33), pirenzepine dihydrochloride (2 M, n = 6), VU 0255035 (5 M, n vu 590 dihydrochloride c24h34cl2n4o7

Most effective Weight loss lymphatic drainage vu 590 dihydrochloride c24h34cl2n4o7

vu 590 dihydrochloride; molecular weight: 336.02; bitumens, extracts of steam-refined and air-refined, steam-refined, cracking-residue and air-refined bitumens; acetic acid ethenyl ester,polymer with oxirane,minimum number average molecular weight (in amu),17,000Marina Yu. Dvorko's research works | A.E. Favorsky vu 590 dihydrochloride c24h34cl2n4o7Marina Yu. Dvorko's 48 research works with 348 citations and 1,120 reads, including: Synthesis of Uniquely Functionalized Pyrrolines from HydroxypyrrolinesKCC2 - K-Cl co-transporter - AOBIOUS, INCML077 (VU0255011) CAS No: 1135304-61-8 Chemical Name: N-Methyl-N-(4-methyl-1,3-thiazol-2-yl)-2-(6-phenylpyridazin-3-yl)sulfanylacetamide; ML-077; CID-25067404; VU0255011 AOBIOUS launched this product in 2014 CITATIONS - Publications That Use AOBIOUS Product 1) Sci Rep. 2017; 7: 1732.

International Laboratory (IL) (Page 606) @ ChemBuyersGuide vu 590 dihydrochloride c24h34cl2n4o7

VU 590 DIHYDROCHLORIDE CAS:1783987-83-6 Formula: C24H32N4O7 2(HCl) 25mg : VU 591 HYDROCHLORIDE CAS:1315380-70-1 Formula: C16H12N6O5 HCl 50mg : vu 590 dihydrochloride c24h34cl2n4o7 Formula: C24H34Cl2N4O7 50mg : VU590 DIHYDROCHLORIDE CAS:313505-85-0 Formula: C24H34Cl2N4O7 100mg : VUF 11222 CAS:1414376-84-3 Formula: C25H31BrIN 2.5mg : VUF 11222 CAS:1414376-84-3International Laboratory (IL) (Page 606) @ ChemBuyersGuide vu 590 dihydrochloride c24h34cl2n4o7VU 590 DIHYDROCHLORIDE CAS:1783987-83-6 Formula: C24H32N4O7 2(HCl) 25mg : VU 591 HYDROCHLORIDE CAS:1315380-70-1 Formula: C16H12N6O5 HCl 50mg : vu 590 dihydrochloride c24h34cl2n4o7 Formula: C24H34Cl2N4O7 50mg : VU590 DIHYDROCHLORIDE CAS:313505-85-0 Formula: C24H34Cl2N4O7 100mg : VUF 11222 CAS:1414376-84-3 Formula: C25H31BrIN 2.5mg : VUF 11222 CAS:1414376-84-3Inhibition of HMG-CoA Reductase by Atorvastatin Decreases vu 590 dihydrochloride c24h34cl2n4o763 Zhang ZJ, Sniderman AD, Kalant D, Vu H, Monge JC, Tao Y, Cianflone K. The role of amino acids in apoB100 synthesis and catabolism in human HepG2 cells. J Biol Chem. 1993; 268:26920-26926. Medline Google Scholar; 64 Dashti N. The effect of low density lipoproteins, cholesterol, and 25-hydroxycholesterol on apolipoprotein B gene expression in vu 590 dihydrochloride c24h34cl2n4o7

Imatinib Analogs as Potential Agents for PET Imaging of vu 590 dihydrochloride c24h34cl2n4o7

Jan 01, 2014 · 8.2.10 4-(4-Methylpiperazinomethyl)benzoyl chloride dihydrochloride (10a) 24. To 20 g (0.065 mol) of 4-(4-methylpiperazinomethyl)benzoic acid dihydrochloride 9a under a nitrogen atmosphere, 119 mL of thionyl chloride (194 g, 1.625 mol) was added to form a beige-white suspension. The reaction mixture was refluxed for 24 h and then cooled to room vu 590 dihydrochloride c24h34cl2n4o7Form 8-K - SEC0001193125-17-005328.txt : 20170109 0001193125-17-005328.hdr.sgml : 20170109 20170109105608 accession number: 0001193125-17-005328 conformed submission type: 8-k public document count: 26 conformed period of report: 20170109 item information: regulation fd disclosure item information: financial statements and exhibits filed as of date: 20170109 date as of change: 20170109 filer: company data vu 590 dihydrochloride c24h34cl2n4o7CAS 69563-88-8 GI 530159 - BOC SciencesBoc Sciences offers 69563-88-8 GI 530159 in bulk, please inquire us to get a quote for 69563-88-8 GI 530159.

CAS 18711-16-5 NS309 - BOC Sciences

Boc Sciences offers 18711-16-5 NS309 in bulk, please inquire us to get a quote for 18711-16-5 NS309.CAS 1783987-83-6 VU 590 dihydrochloride - BOC SciencesVU 590 dihydrochloride - CAS 1783987-83-6 Catalog number: 1783987-83-6 VU 590 dihydrochloride is a selective renal outer medullary potassium channel (Kir1.1, ROMK) inhibitor (IC50 = 294 nM). VU 590 displays no effect upon Kir2.1 or Kir4.1.Browse Products by Product Name: (V) | Tocris BioscienceVU 10010: Selective positive allosteric modulator of M 4 receptors: 3383: VU 152100: Positive allosteric modulator of M 4 receptors: 3325: VU 1545: Positive allosteric modulator of mGlu 5 receptors: 4458: VU 29: Potent positive allosteric modulator of mGlu 5 receptors: 3891: VU 590 dihydrochloride: Inhibitor of K ir 1.1 (ROMK) and K ir 7.1 vu 590 dihydrochloride c24h34cl2n4o7

Alexidine dihydrochloride | 22573-93-9 suppliers vu 590 dihydrochloride c24h34cl2n4o7

Finetech Industry Limited is a company in England,which specializing in developing, manufacturing and marketing fine organic compounds and intermediates for the pharmaceutical industry. Finetech Industry Limited is supplier for Alexidine dihydrochloride. Most of our products were exported to the North America, Europe and Oceania.VU 590 dihydrochloride| NaveproteinVU 590 dihydrochloride | Products for research use only! Product Name:VU 590 dihydrochloride Catalog NO.:BCC7803. CAS NO.:313505-85-0 Molecular Formula:C 24 H 32 N 4 O 7.2HCl Molecular Weight:561.46 Chemical Name: 7,13-bis(4-nitrobenzyl)-1,4,10-trioxa-7,13-diazacyclopentadecane dihydrochloride Purify method:HPLC-DAD Purity:>98% as determined by HPLC storage:Potassium Channel - Membrane Transporter/Ion vu 590 dihydrochloride c24h34cl2n4o7 - BioCrickBCC7803 VU 590 dihydrochloride; BCC7806 JNJ 303 Potent and selective I Ks blocker; BCC7872 NS 5806 K V 4.3 channel activator; BCC7911 ICA 069673 K V 7.2/K V 7.3 channel opener; BCC7914 GW 542573X Selective activator of K Ca 2.1 channels; BCC7927 Psora 4 Potent K V 1.3 channel blocker; BCC7957 Penitrem A

Potassium Channel Modulators | SCBT - Santa Cruz

VU 590 dihydrochloride VU 590 dihydrochloride is an inhibitor of the renal, outer medullary potassium channel, KIR7.1 313505-85-0 sc-358792 sc-358792A : 10 mg 50 mg: $109.00 $440.00 0 (0) CP-339818 CP-339818 is a vu 590 dihydrochloride c24h34cl2n4o7Membrane Transporter/Ion Channel Compound Library vu 590 dihydrochloride c24h34cl2n4o7The products in the BioCrick screening libraries are all from plants. The biological activities or pharmacological activities of all the BioCrick products are derived from the databases of all over the world the latest literatures, patent reports and clinical validation, you can according to the product manuals on our website to access the relevant literatures, hope that our informations can vu 590 dihydrochloride c24h34cl2n4o7Inward Rectifier Potassium Channel Blockers Products: View our 15 Inward Rectifier Potassium Channel Blockers products for your research including Inward Rectifier Potassium Channel Blockers Small Molecules and Inward Rectifier Potassium Channel Blockers Peptides.

GW2580 | CFMS kinase/CSF-1R inhibitor,selective and ATP vu 590 dihydrochloride c24h34cl2n4o7

GW2580 is a selective and orally bioavailable inhibitor of Colony-stimulating-factor-1 receptor (CSF-1R) with IC50 value of 30nM [1] GW2580 has been demonstrated to be an extremely selective inhibitor for CSF-1R and has been hypothesized to bind to the DFG-out mode of CSF-1R, which might lock it into an inactive conformation [2] GW2580 has shown to inhibit epithelial cell-associated CSF-1 vu 590 dihydrochloride c24h34cl2n4o7590-36-3 chemical query, 590-36-3 melting point boiling vu 590 dihydrochloride c24h34cl2n4o7VU 590 dihydrochloride. CAS No: 313505-85-0; Molecular Weight: 561.457; Molecular Formula:C 24 H 34 CL 2 N 4 O 7; Boiling Point:642.5±50.0 °C(Predicted) Melting Point: Properties Safety and Handling MSDS Computational chemical data 2 Suppliers590-36-3 chemical query, 590-36-3 melting point boiling vu 590 dihydrochloride c24h34cl2n4o7VU 590 dihydrochloride. CAS No: 313505-85-0; Molecular Weight: 561.457; Molecular Formula:C 24 H 34 CL 2 N 4 O 7; Boiling Point:642.5±50.0 °C(Predicted) Melting Point: Properties Safety and Handling MSDS Computational chemical data 2 Suppliers

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