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ChemicalBook--->CAS DataBase List--->2714434-21-4

2714434-21-4

2714434-21-4 Structure

2714434-21-4 Structure
IdentificationBack Directory
[Name]

IAG933
[CAS]

2714434-21-4
[Synonyms]

IAG933
[Molecular Formula]

C27H26ClF2N3O4
[MOL File]

2714434-21-4.mol
[Molecular Weight]

529.96
Chemical PropertiesBack Directory
[Boiling point ]

626.125±55.00 °C(Press: 760.00 Torr)(predicted)
[density ]

1.367±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[form ]

Solid
[pka]

13.275±0.46(predicted)
[color ]

White to off-white
[InChIKey]

HUVOYQMXUNTUAI-UHFFFAOYSA-N
[SMILES]

ClC1=C(C=C2C(=C1C1=C(C(=NC=C1C(=O)NC)OCCO)F)CC(C1C=CC=CC=1)(C1NCCC1)O2)F
Hazard InformationBack Directory
[Uses]

IAG933 (YAP-TEAD-IN-3) is an orally available YAP/TAZ-TEAD inhibitor that has anti-tumor effects and promotes apoptosis. IAG933 YAP-TEAD-IN-3 inhibits Avi-human TEAD4217-434, with an IC50 value of 9 nM[1][2].
[in vivo]

IAG933 (30-240 mg/kg, i.g., once a day, 28 days) shows a dose-dependent anti-tumor effect in mouse xenograft models, promoting cell apoptosis[2].
IAG933 (3-30 mg/kg, i.g., once a day, 2 weeks) causes tumor regression in the MSTO-211H rat xenograft model[2].

Animal Model:Mouse MSTO-211H cell-derived xenograft (CDX) model; mouse NCI-H226 cell-derived xenograft (CDX) model[2]
Dosage:30, 60, 120, 240 mg/kg, single dose; 70, 210 mg/kg, once daily, 28 days
Administration:i.g.
Result:Had a short half-life in mice, inhibiting the transcription of TEAD in the body, promoting apoptosis, and lowering the expression of BCL2L1 and MCL1.
Led to tumor regression and a decrease in Ki67 expression.
Animal Model:A rat MSTO-211H xenograft model[2]
Dosage:3, 10, 30 mg/kg, once daily, 2 weeks
Administration:i.g.
Result:Showed the tumor stagnant at 10 mg/kg, and shrank at 30 mg/kg.
[IC 50]

YAP/TAZ-TEAD
[References]

[1] Bordas V, et al. Preparation of biaryl derivatives as YAP/TAZ-TEAD protein-protein interaction inhibitors. World Intellectual Property Organization, WO2021186324 A1. 2021-09-23.
[2] Emilie A Chapeau, et al. Direct and selective pharmacological disruption of the YAP-TEAD interface by IAG933 inhibits Hippo-dependent and RAS-MAPK-altered cancers. Nat Cancer. 2024 Jul;5(7):1102-1120. DOI:10.1038/s43018-024-00754-9
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