Company Name: |
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788 |
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jkinfo@jkchemical.com |
Products Intro: |
Product Name:AZ 11645373 CAS:227088-94-0 Package:100Mg,10Mg,50Mg,5Mg
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Company Name: |
3B Pharmachem (Wuhan) International Co.,Ltd.
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Tel: |
821-50328103-801 18930552037 |
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3bsc@sina.com |
Products Intro: |
Product Name:AZ 11645373;3-[1-[[(3'-Nitro[1,1'-biphenyl]-4-yl)oxy]Methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione CAS:227088-94-0 Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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| 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione Basic information |
Product Name: | 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione | Synonyms: | 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione;AZ11645373;1'-BIPHENYL]-4-YL)OXY]METHYL]-3-(4-PYRIDINYL)PROPYL]-2;3-[1-[[(3'-NITRO[1;4-THIAZOLIDINEDIONE;2,4-Thiazolidinedione, 3-[1-[[(3'-nitro[1,1'-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-;3-(1-((3'-nitro-[1,1'-biphenyl]-4-yl)oxy)-4-(pyridin-4-yl)butan-2-yl)thiazolidine-2,4-dione;3-(1-((3'-nitro-[1,1'-biphenyl]-4-yl)oxy)-4-(pyridin-4-yl)butan-2-yl)thiazolidine-2,4-dione | CAS: | 227088-94-0 | MF: | C24H21N3O5S | MW: | 463.512 | EINECS: | | Product Categories: | Aromatics, Heterocycles, Neurochemicals | Mol File: | 227088-94-0.mol | |
| 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione Chemical Properties |
Boiling point | 689.1±65.0 °C(Predicted) | density | 1.362±0.06 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | DMSO: ≥10mg/mL | form | solid | pka | 5.95±0.10(Predicted) | color | tan |
Hazard Codes | Xi | Risk Statements | 37/38-41 | Safety Statements | 26-39 | WGK Germany | 3 |
| 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione Usage And Synthesis |
Uses | A selective P2X7 receptor antagonist. | Biological Activity | Potent and selective human P2X 7 antagonist (K B values are 5 - 7 and > 10,000 nM at hP2X 7 and rP2X 7 respectively) that is completely without effect at all other P2X subtypes. Inhibits BzATP-mediated calcium influx and inhibits ATP-mediated IL-1 β release in vitro (K B values are 15 and 92 nM respectively). | storage | Store at +4°C | references | 1. stokes l, jiang lh, alcaraz l, et al. characterization of a selective and potent antagonist of human p2x(7) receptors, az11645373. british journal of pharmacology. 2006;149(7):880-887. |
| 3-[1-[[(3μ-nitro[1,1μ-biphenyl]-4-yl)oxy]methyl]-3-(4-pyridinyl)propyl]-2,4-thiazolidinedione Preparation Products And Raw materials |
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