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ChemicalBook--->CAS DataBase List--->627536-09-8

627536-09-8

627536-09-8 Structure

627536-09-8 Structure
IdentificationBack Directory
[Name]

SD-208
[CAS]

627536-09-8
[Synonyms]

SD-208
CS-2295
SCI 208
SD-208 10MG
SD-208 (SD 208
ALK5 Inhibitor V
SD-208 USP/EP/BP
TGF-β RI Kinase Inhibitor V
SD-208;SD 208; SD208; SCI 208
SD 208;SD208;TGF-Β RI KINASE INHIBITOR V
2-(5-chloro-2-fluorophenyl)-N-4-pyridinyl-
2-(5-Chloro-2-fluorophenyl)-N-4-pyridinyl-4-pteridinamine
2-(5-Chloro-2-fluorophenyl)-4-[(4-pyridyl)amino]pteridine
4-PteridinaMine, 2-(5-chloro-2-fluorophenyl)-N-4-pyridinyl-
2-(5-chloro-2-fluorophenyl)-N-(pyridin-4-yl)pteridin-4-amine
2-[(5-CHLORO-2-FLUOROPHENYL)PTERIDIN-4-YL]PYRIDIN-4-YL-AMINE
[Molecular Formula]

C17H10ClFN6
[MDL Number]

MFCD09038685
[MOL File]

627536-09-8.mol
[Molecular Weight]

352.753
Chemical PropertiesBack Directory
[Boiling point ]

460.4±45.0 °C(Predicted)
[density ]

1.487
[storage temp. ]

2-8°C
[solubility ]

DMSO: >5mg/mL
[form ]

powder
[pka]

4.56±0.26(Predicted)
[color ]

off-white to tan
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

SD-208 was used to inhibit the activity of ALK5 kinase in bovine retinal vascular cells.2
[Biological Activity]

Potent, orally active ATP-competitive transforming growth factor- β receptor 1 (TGF- β RI) inhibitor (IC 50 = 49nM). Displays > 100-fold and > 17-fold selectivity over TGF- β RII and other common kinases respectively. Exhibits anti-inflammatory and antitumor activity.
[Biochem/physiol Actions]

SD-208 is an inhibitor of TGF β receptor 1 kinase that is reportedly effective against human malignant gliomas. It increases the lytic activity and tumor infiltration by polyclonal natural killer cells, CD8 T cells and macrophages.1
[in vivo]

SD-208 (1 mg/mL, p.o.) significantly prolongs the median survival of SMA-560 glioma-bearing mice[1]. In syngeneic 129S1 mice, SD-208 (60 mg/kg/d, p.o.) inhibits primary R3T tumor growth, and reduces the number and the size of lung metastases[2]. In the murine aortic allograft model, SD-208 effectively reduces the formation of intimal hyperplasia of transplant arteriosclerosis (TA)[3].

[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

SD-208(627536-09-8)1HNMR
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