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331001-62-8

331001-62-8 Structure

331001-62-8 Structure
IdentificationBack Directory
[Name]

2-[(4-Acetylphenyl)azo]-2-(3,4-dihydro-3,3-diMethyl-1(2H)- isoquinolinylidene)acetaMide
[CAS]

331001-62-8
[Synonyms]

IQ 1; IQ1
IQ-1 - CAS 331001-62-8 - Calbiochem
2-[(4-Acetylphenyl)hydrazinylidene]-2-(3,3-dimethyl-4H-isoquinolin-1-yl)acetamide
2-[(4-Acetylphenyl)azo]-2-(3,4-dihydro-3,3-diMethyl-1(2H)- isoquinolinylidene)acetaMide
2-[2-(4-Acetylphenyl)diazenyl]-2-(3,4-dihydro-3,3-diMethyl-1(2H)-isoquinolinylidene)-acetaMide
AcetaMide, 2-[2-(4-acetylphenyl)diazenyl]-2-(3,4-dihydro-3,3-diMethyl-1(2H)-isoquinolinylidene)-
[Molecular Formula]

C21H22N4O2
[MDL Number]

MFCD00354369
[MOL File]

331001-62-8.mol
[Molecular Weight]

362.42
Chemical PropertiesBack Directory
[Boiling point ]

591.2±50.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

DMF: 30 mg/ml; DMSO: 25 mg/ml; Ethanol: 10 mg/ml
[form ]

powder
[pka]

15.71±0.50(Predicted)
[color ]

yellow to orange
[InChI]

1S/C21H22N4O2/c1-13(26)14-8-10-16(11-9-14)24-25-19(20(22)27)18-17-7-5-4-6-15(17)12-21(2,3)23-18/h4-11,23H,12H2,1-3H3,(H2,22,27)/b19-18+,25-24?
[InChIKey]

ZXSRRUROLCGTBS-ASEVQSCHSA-N
[SMILES]

CC(C1=CC=C(N=N/C(C(N)=O)=C2NC(C)(C)CC3=C/2C=CC=C3)C=C1)=O
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H315-H319-H332-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

IQ 1 disrupts Wnt signaling. IQ-1 in conjunction with Wnt3a has been shown to be sufficient to maintain murine embryonic stem cell proliferation in the absence of serum. Binds to the PR72/PR130 subunit of protein phosphatase PP2A preventing β-catenin from switching co-activator usage from CBP to p300 leading to an increase in β-catenin/CBP-driven transcription at the expense of β-catenin/p300-driven transcription.
[Definition]

ChEBI: 2-[(4-acetylphenyl)hydrazinylidene]-2-(3,3-dimethyl-4H-isoquinolin-1-yl)acetamide is an aromatic ketone.
[Biological Activity]

IQ-1 enhances β-catenin/CBP interactions and blocks β-catenin/p300 driven transcriptionwhich enables mouse embryonic stem cells (ESCs) to be maintained in an undifferentiated pluripotent stateallowing expansion and self-renewal of mouse ESC populations.
[storage]

-20°C
Spectrum DetailBack Directory
[Spectrum Detail]

2-[(4-Acetylphenyl)azo]-2-(3,4-dihydro-3,3-diMethyl-1(2H)- isoquinolinylidene)acetaMide(331001-62-8)1HNMR
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