ChemicalBook > CAS DataBase List > ASP5878
ASP5878
- Product Name
- ASP5878
- CAS No.
- 1453208-66-6
- Chemical Name
- ASP5878
- Synonyms
- ASP5878;ASP-5878 (ASP5878;ASP5878, 10 mM in DMSO;ASP5878; ASP 5878; ASP-5878;ASP 5878,Inhibitor,FGFR,ASP5878,Fibroblast growth factor receptor,inhibit;1H-Pyrazole-1-ethanol, 4-[[5-[(2,6-difluoro-3,5-dimethoxyphenyl)methoxy]-2-pyrimidinyl]amino]-;2-(4-((5-((2,6-Difluoro-3,5-dimethoxybenzyl)oxy)pyrimidin-2-yl)amino)-1H-pyrazol-1-yl)ethan-1-ol
- CBNumber
- CB33164874
- Molecular Formula
- C18H19F2N5O4
- Formula Weight
- 407.37
- MOL File
- 1453208-66-6.mol
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ASP5878 Property
- Boiling point:
- 645.3±65.0 °C(Predicted)
- Density
- 1.41±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO : ≥ 250 mg/mL (613.69 mM);Water : < 0.1 mg/mL (insoluble)
- pka
- 14.41±0.10(Predicted)
- form
- Solid
- color
- Light yellow to yellow
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N-Bromosuccinimide Price
TRC
- Product number
- A788595
- Product name
- ASP5878
- Packaging
- 1mg
- Price
- $285
- Updated
- 2021/12/16
TRC
- Product number
- A788595
- Product name
- ASP5878
- Packaging
- 2.5mg
- Price
- $615
- Updated
- 2021/12/16
ChemScene
- Product number
- CS-0017707
- Product name
- ASP5878
- Purity
- 99.71%
- Packaging
- 5mg
- Price
- $450
- Updated
- 2021/12/16
American Custom Chemicals Corporation
- Product number
- INB0009816
- Product name
- ASP-5878
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $454.83
- Updated
- 2021/12/16
ChemScene
- Product number
- CS-0017707
- Product name
- ASP5878
- Purity
- 99.71%
- Packaging
- 10mg
- Price
- $750
- Updated
- 2021/12/16
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ASP5878 Chemical Properties,Usage,Production
Uses
ASP5878 is a selective inhibitor of FGFR1, 2, 3 and 4.
in vivo
ASP5878 (3 mg/kg, orally, once daily) shows antitumor activity in a Hep3B2.1-7 subcutaneous xenograft? and HCC orthotopic xenograft mouse model[1].
?
ASP5878 induces shrinkage of FGF19-expressing HCC xenograft model[1].
| Animal Model: | Four-week-old male nude mice (CAnN.Cg-Foxn1nu/CrlCrlj [nu/nu]) (Hep3B2.1-7 cells inoculated subcutaneously)[1]. |
| Dosage: | 3 mg/kg. |
| Administration: | Orally once daily from days 14 to 52. |
| Result: | Induced tumor regression by 9% and 88% at 1 and 3 mg/kg, respectively, without affecting the body weight for 14 days. Induced the suppression of FGFR4 phosphorylation, mobility shift of FRS2, and suppression of ERK phosphorylation. |
| Animal Model: | HCC orthotopic xenograft model (mouse)[1]. |
| Dosage: | 3 mg/kg. |
| Administration: | Orally once daily for 24 days. |
| Result: | Exhibited a lower tumor burden than vehicle- and sorafenibtreated mice. Induced sustained tumor regression without tumor regrowth. |
IC 50
FGFR1: 0.47 nM (IC50); FGFR2: 0.6 nM (IC50); FGFR3: 0.74 nM (IC50); FGFR4: 3.5 nM (IC50)
ASP5878 Preparation Products And Raw materials
Raw materials
Preparation Products
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