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Submit ReviewGTP 14564
Description: Class III receptor tyrosine kinase (RTK) inhibitor
Chemical Name: 3-Phenyl-1H-benzofuro[3,2-c]pyrazole
Purity: ≥99% (HPLC)
Biological Activity for GTP 14564
GTP 14564 is a potent, selective inhibitor of class III receptor tyrosine kinases (IC50 values are 0.3 μM for c-Fms, c-Kit, FLT3 and ITD-FLT3 and 1 μM for PDGFRβ). Displays no activity against ERK1, ERK2, EGFR, MEK1, HER2, Src, Abl, PKC, PKA and Akt (IC50 > 10 μM). Inhibits FL-dependent proliferation in BaF/ITD-FLT3 cells more potently than BaF/wt-FLT3 cells; anti-leukemic.
Technical Data for GTP 14564
| M. Wt | 234.26 |
| Formula | C15H10N2O |
| Storage | Store at +4°C |
| Purity | ≥99% (HPLC) |
| CAS Number | 34823-86-4 |
| PubChem ID | 3385203 |
| InChI Key | DZQLVVLATXPWBK-UHFFFAOYSA-N |
| Smiles | N1N=C(C2=C1C1=C(O2)C=CC=C1)C1=CC=CC=C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Product Datasheets for GTP 14564
References for GTP 14564
References are publications that support the biological activity of the product.
Murata et al (2003) Selective cytotoxic mechanism of GTP-14564, a novel tyrosine kinase inhibitor in leukemia cells expressing a constitutively active Fms-like tyrosine kinase 3 (FLT3). J.Biol.Chem. 278 32892 PMID: 12815052
Yao et al (2005) Human leukemias with mutated FLT3 kinase are synergistically sensitive to FLT3 and Hsp90 inhibitors: the key role of the STAT5 signal transduction pathway. Leukemia 19 1605 PMID: 16034464
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Keywords: GTP 14564, GTP 14564 supplier, Class, III, receptor, tyrosine, kinase, RTKs, inhibitors, inhibits, Receptors, GTP14564, Other, 2086, Tocris Bioscience
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