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
PKCβ2IC50: 16nM
PKCβ1IC50: 17nM
PKCαIC50: 20nM
PKCγIC50: 20nM
PDGFRIC50: 65μM
EGFRIC50: >100μM
Insulin ReceptorIC50: >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.