GF 109203X
Catalog No. A13197
GF 109203X是一种有效且选择性的蛋白激酶C抑制剂,对α和β1亚型具有选择性(对于α,β1,δ,δ,ε和ζ亚型,IC50分别为0.0084、0.0180、0.210、0.132和5.8μM)。对MLCK,PKG和PKA具有选择性(IC50值分别为0.6、4.6和33μM)。5-HT3受体的强效拮抗剂(Ki = 29.5 nM)。= 29.5 nm)。
Catalog Num | A13197 |
---|---|
M. Wt | 412.49 |
Formula | C25H24N4O2 |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 133052-90-1 |
Synonyms | GF-109203X, GF109203X, GO6850, GO-6850, Bisindolylmaleimide I |
SMILES | CN(C)CCCN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CNC5=CC=CC=C54 |
GF 109203X是一种有效且选择性的蛋白激酶C抑制剂,对α和β1亚型具有选择性(对于α,β1,δ,δ,ε和ζ亚型,IC50分别为0.0084、0.0180、0.210、0.132和5.8μM)。对MLCK,PKG和PKA具有选择性(IC50值分别为0.6、4.6和33μM)。5-HT3受体的强效拮抗剂(Ki = 29.5 nM)。= 29.5 nm)。
Targets
Target | Value |
---|---|
PKCβ2 | IC50: 16nM |
PKCβ1 | IC50: 17nM |
PKCα | IC50: 20nM |
PKCγ | IC50: 20nM |
PDGFR | IC50: 65μM |
EGFR | IC50: >100μM |
Insulin Receptor | IC50: >100μM |
In vitro | DMSO | 70 mg/mL (169.7 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 24.24 mL | 121.22 mL | 242.43 mL |
0.5 mM | 4.85 mL | 24.24 mL | 48.49 mL |
1 mM | 2.42 mL | 12.12 mL | 24.24 mL |
5 mM | 0.48 mL | 2.42 mL | 4.85 mL |
*The above data is based on the productmolecular weight 412.49. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.