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ChemicalBook--->CAS DataBase List--->168649-23-8

168649-23-8

168649-23-8 Structure

168649-23-8 Structure
IdentificationBack Directory
[Name]

1H-Indole-3-acetic acid, 5-phenyl-
[CAS]

168649-23-8
[Synonyms]

5-Ph-IAA
1H-Indole-3-acetic acid, 5-phenyl-
[Molecular Formula]

C16H13NO2
[MDL Number]

MFCD21897325
[MOL File]

168649-23-8.mol
[Molecular Weight]

251.28
Chemical PropertiesBack Directory
[Boiling point ]

521.3±35.0 °C(Predicted)
[density ]

1.291±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 125 mg/mL (497.45 mM)
[form ]

A solid
[pka]

4.47±0.30(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Biological Activity]

5-Ph-IAA is a derivative of IAA. 5-Ph-IAA is a ligand that together with the OsTIR1 (F74G) mutant establishes the auxin-inducible degron 2 system (AID2). AID2 induces rapid and efficient depletion of mAID fusion proteins to study protein function in living cells. AID2 can suppress tumors.
[in vitro]

HCT116 cells constitutively expressing OsTIR1(F74G) are exposed to 5-Ph-IAA (1 μM; 6 hours), leading to DHC1-mAC degradation, which means the AID2 system better than the original AID system in generating conditional mutant cell lines.

Western Blot Analysis

Cell Line: HCT116 cells
Concentration: 1 μM
Incubation Time: 6 hours
Result: Depleted DHC1-mAC efficiently in HCT116 cells constitutively expressing OsTIR1(F74G).
[in vivo]

5-Ph-IAA (0-10 mg/kg; intraperitoneally injection; every day; 7 days), used for the AID2 system , is sufficient to deplete mAID-BRD4 and TOP2A-mAC, leading to tumor suppression.

Animal Model: Balb/c-nu female mice (7 weeks old; 16–20 g ) bearing mAID-BRD4 and TOP2A-mAC xenograft tumours cells
Dosage: 0 mg/kg, 1 mg/kg , 3 mg/kg and 10 mg/kg
Administration: Intraperitoneally injection; every day; 7 days
Result: Displayed significant tumor suppression of mAID-BRD4 xenografts and TOP2A-mAC xenografts .
[storage]

Store at -20°C
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