(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE
(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE Basic information
- Product Name:
- (5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE
- Synonyms:
-
- PDGF RECEPTOR TYROSINE KINASE INHIBITOR II
- PDGFR Tyrosine Kinase Inhibitor II
- D-65476
- [2-(1H-2-INDOLYCARBONYL)-1H-5-INDOLYL]BUTANOATE
- [2-(1H-2-INDOLYLCARBONYL)-1H-5-INDOLYL]BUTANOATE
- (5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE
- Butanoic acid, 2-(1H-indol-2-ylcarbonyl)-1H-indol-5-yl ester
- CAS:
- 249762-74-1
- MF:
- C21H18N2O3
- MW:
- 346.38
- Mol File:
- Mol File
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(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE Chemical Properties
- storage temp.
- 2-8°C
- solubility
- DMSO: 5mg/mL
- form
- solid
- color
- yellow
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(5-BUTANOATE-1H-2-INDOLYL)(1H-2-INDOLYL)-METHANONE Usage And Synthesis
Uses
D-65476 is an inhibitor of type Ⅲ receptor tyrosine kinase (Flt3). In the absence of IL-3, D-65476 inhibits the proliferation of TEL-Flt3 transfected BA/F3 cells (IC50= 0.2 μM), which can be used in the study of Flt3-driven leukemia[1].
Biological Activity
Cell permeable: yes', 'Primary Target
PDGFR in swiss 3T3 cells', 'Product competes with ATP.', 'Reversible: yes', 'Target IC50: 1.1 μM inhibiting PDGFR in swiss 3T3 cells; 6.2 μ M for hPDGFβ-R-mFlt3 and 50 nM in EOL-1 cells
References
[1] Teller S, et al. Bis(1H-2-indolyl)-1-methanones as inhibitors of the hematopoietic tyrosine kinase Flt3. Leukemia. 2002;16(8):1528-1534. DOI:10.1038/sj.leu.2402630