ZD-4190 manufacturers
- ZD-4190
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- $46.00
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2026-07-27
- CAS:413599-62-9
- Purity: 99.42%
- Supply Ability: 10g
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| | ZD-4190 Basic information |
| Product Name: | ZD-4190 | | Synonyms: | ZD-4190;ZD-4190;ZD 4190;ZD4190;4-Quinazolinamine, N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[2-(1H-1,2,3-triazol-1-yl)ethoxy]-;Inhibitor,inhibit,Vascular endothelial growth factor receptor,VEGFR,Epidermal growth factor receptor,EGFR,ZD 4190,ErbB-1,HER1,ZD-4190,ZD4190;7-(2-(1H-1,2,3-Triazol-1-yl)ethoxy)-N-(4-bromo-2-fluorophenyl)-6-methoxyquinazolin-4-amine;ZD-4190, 10 mM in DMSO;ZD-4190 ，S6543 | | CAS: | 413599-62-9 | | MF: | C19H16BrFN6O2 | | MW: | 459.27 | | EINECS: | | | Product Categories: | | | Mol File: | 413599-62-9.mol |  |
| | ZD-4190 Chemical Properties |
| storage temp. | Store at -20°C | | solubility | DMSO : 20.83 mg/mL (45.35 mM);Water : < 0.1 mg/mL (insoluble) | | form | Solid | | color | White to off-white |
| | ZD-4190 Usage And Synthesis |
| Uses | ZD-4190 is a potent, orally available inhibitor of the vascular endothelial cell growth factor receptor 2 (VEGFR2) and of epidermal growth factor receptor (EGFR) signalling, used for the treatment of cancer. | | in vivo | ZD4190 (100 mg/kg, p.o.) effectively delays MDA-MB-435 tumor growth in mice. In ZD4190-treated tumors, 18F-FPPRGD2 uptake has decreased significantly relative to baseline by 26.74±8.12% (p<0.05) on day 1 and by 41.19±6.63% (p<0.01) on day 3, then has returned to baseline on day 7. Tumor uptake of 18F-FLT has also decreased on both day 1 and day 3 after initiation of ZD4190 treatment. However, ZD4190 does not significantly change 18F-FDG uptake in tumors, compared with the control group[1]. ZD4190 (50mg/kg, p.o.) prevents outgrowth of residual tumour in a muscle model of minimal residual carcinoma[2]. ZD4190 (12.5-100 mg/kg, p.o.) produces a dose-dependent reduction in K(trans) in PC-3 prostate tumors. At 100 mg/kg, ZD4190 reduces K(trans) in PC-3 tumors by 31% following 2 doses and by 53% following 8 doses[3]. | | IC 50 | EGFR; VEGFR2 | | References | [1] Yang M, et al. PET imaging of early response to the tyrosine kinase inhibitor ZD4190. Eur J Nucl Med Mol Imaging. 2011 Jul;38(7):1237-47. doi: 10.1007/s00259-011-1742-z. Epub 2011 Mar 1. DOI:10.1007/s00259-011-1742-z
[2] Gaballah K, et al. The antiangiogenic agent ZD4190 prevents tumour outgrowth in a model of minimal residual carcinoma in deep tissues. Br J Cancer. 2009 Aug 4;101(3):418-23. doi: 10.1038/sj.bjc.6605092. Epub 2009 Jul 21. DOI:10.1038/sj.bjc.6605092
[3] Checkley D, et al. Dynamic contrast-enhanced MRI of vascular changes induced by the VEGF-signalling inhibitor ZD4190 in human tumour xenografts. Magn Reson Imaging. 2003 Jun;21(5):475-82. DOI:10.1016/s0730-725x(02)00644-6 |
| | ZD-4190 Preparation Products And Raw materials |
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