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ChemicalBook--->CAS DataBase List--->176504-36-2

176504-36-2

176504-36-2 Structure

176504-36-2 Structure
IdentificationBack Directory
[Name]

BISINDOLYLMALEIMIDE I HYDROCHLORIDE
[CAS]

176504-36-2
[Synonyms]

BIS-I HCl
GO-6860 HCl
BIM 1 hydrochloride
GF 109203X hydrochloride >=95%
BisindolylMaleiMide I( Hydrochloride Salt)
BisindolylMaleiMide I . hydrochloride [GF-109203K
Bisindolylmaleimide I, Hydrochloride - CAS 176504-36-2 - Calbiochem
3-[1-(dimethylaminopropyl)indol-3-yl]-4-(indol-3-yl)maleimide hydrochloride
3-[1-[3-(dimethylamino)propyl]indol-3-yl]-4-(1H-indol-3-yl)pyrrole-2,5-dione
3-[1-[3-(Dimethylamino)propyl]-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione monohydrochloride
[Molecular Formula]

C25H24N4O2.HCl
[MDL Number]

MFCD00236429
[MOL File]

176504-36-2.mol
[Molecular Weight]

448.95
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMF: 10 mg/mL; DMSO: 16 mg/mL; DMSO:PBS(pH 7.2) (1:4): 0.2 mg/mL
[form ]

Orange-red solid
[color ]

Orange to red
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P301+P310
[WGK Germany ]

3
[HS Code ]

2933998090
Hazard InformationBack Directory
[Description]

Bisindolylmaleimide I (BIM I) is a highly selective, cell-permeable, and reversible PKC inhibitor (Ki = 14 nM) that is structurally similar to the poorly selective PKC inhibitor staurosporine . It acts as a competitive inhibitor for the ATP binding site of PKC and shows high selectivity for PKCα, β1, β2, γ, δ, and ε isozymes. BIM I directly inhibits glycogen synthase kinase 3 (GSK3) in primary adipocyte lysates (IC50 = 360 nM) and in GSK3β immunoprecipitates derived from rat epididymal adipocytes (IC50 = 170 nM). It also competitively antagonizes the serotonin (5-HT) receptor subtype 5-HT3 with a Ki value of 61 nM.
[Uses]

GF 109203X hydrochloride has been used to inhibit protein kinase C in human neuroblastoma-derived kelly cells.
[General Description]

GF 109203X prevents collagen-triggered adenosine and three phosphate (ATP) secretion. It also inhibits collagen and α-thrombin-induced platelet aggregation. It functions as an inhibitor of glycogen synthase kinase-3 (GSK-3). GF 109203X also functions as an anti-inflammatory agent.
[Biochem/physiol Actions]

Inhibitor of protein kinase C; potent inhibitor of GSK-3.
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