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SD-208

SIGMA/S7071 - ≥98% (HPLC), powder

Synonym: 2-(5-Chloro-2-fluorophenyl)pteridin-4-yl]pyridin-4-yl-amine

CAS Number: 627536-09-8
Empirical Formula (Hill Notation): C17H10ClFN6
Molecular Weight: 352.75
MDL Number: MFCD11519969
Linear Formula: C17H10ClFN6
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-S7071-5MG 5 mg
$244.00
1/EA
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45-S7071-25MG 25 mg
$845.00
1/EA
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assay ≥98% (HPLC)
color off-white to tan
form powder
InChI 1S/C17H10ClFN6/c18-10-1-2-13(19)12(9-10)15-24-16-14(21-7-8-22-16)17(25-15)23-11-3-5-20-6-4-11/h1-9H,(H,20,22,23,24,25)
InChI key BERLXWPRSBJFHO-UHFFFAOYSA-N
Quality Level 100 
SMILES string Fc1ccc(Cl)cc1-c2nc(Nc3ccncc3)c4nccnc4n2
solubility DMSO: >5 mg/mL
storage temp. 2-8°C
Application: SD-208 was used to inhibit the activity of ALK5 kinase in bovine retinal vascular cells.2
Biochem/physiol Actions: SD-208 is a novel transforming growth factor beta receptor I (TGF-βR I) kinase inhibitor. SD-208 inhibits growth and invasiveness and enhances immunogenicity of murine and human glioma cells in vitro and in vivo.
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
Biochem/physiol Actions: SD-208 is TGF-βR I kinase inhibitor with IC50 =49 nM based on direct enzymatic assay of TGFRI kinase (ALK5) activity with a specificity of >100-fold against TGFRII and at least 17-fold over members of a panel of related protein kinases including p38a, p38b, p38d, JNK1, EGFR, MAPKAPK2, MKK6, ERK2, PKC, PKA, PKD, CDC2, and CaMKII.
Packaging: 5, 25 mg in glass bottle
Symbol GHS07  GHS07
Signal word Warning
Hazard statements H302
Hazard Codes Xn
Risk Statements 22
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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