1. Stem Cell/Wnt Apoptosis
  2. YAP Apoptosis
  3. IAG933

IAG933  (Synonyms: YAP-TEAD-IN-3)

製品番号: HY-153811 純度: 99.47%
COA 取扱説明書 Technical Support

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.

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IAG933

IAG933 構造式

CAS 番号 : 2714434-21-4

容量 価格(税別) 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 1108 在庫あり
Solution
10 mM * 1 mL in DMSO USD 1108 在庫あり
Solid
1 mg $420 在庫あり
5 mg $950 在庫あり
10 mg $1350 在庫あり
50 mg $1820 在庫あり
100 mg $2450 在庫あり
200 mg   お問い合わせ  
500 mg   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

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Based on 3 publication(s) in Google Scholar

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製品説明

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].

IC50 & Target

YAP/TAZ-TEAD

 

体外実験

IAG933 also has an inhibitory effect on NCI-H2052, with GI50 (inhibition of cell proliferation) and IC50 (inhibition of YAP reporter gene expression) values of 0.041 μM and 0.048 μM, respectively[1].
IAG933 (0-1 μM, 4 h) directly inhibits the interaction between YAP/TAZ and all four TEAD isoforms, selectively suppressing TEAD-driven transcriptional activity[2].
IAG933 (0.0001-10 μM, 24 h) shows a dose-dependent inhibition of TEAD target gene expression in MSTO211H and NCI-H226 cells, with IC50 values ranging from 11-26 nM[2].
IAG933 (0.001-10 μM, 72 h) demonstrates effective anti-proliferative activity in Hippo-dependent cell lines, with a GI50 of 13-91 nM in mesothelioma cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[2]

Cell Line: NCI-H2052, MSTO-211H
Concentration: 0, 0.3, 1 μM
Incubation Time: 4 h
Result: Inhibited the binding of YAP and TAZ with TEAD subtypes.

Real Time qPCR[2]

Cell Line: NCI-H2052, MSTO-211H
Concentration: 0.0001, 0.001, 0.01, 0.1, 1, 10 μM
Incubation Time: 24 h
Result: Decreased the expression of CYR61, ANKRD1, and CTGF.

Cell Viability Assay[2]

Cell Line: MSTO-211H,NCI-H2052,NCI-H226,IST-MES2,NCI-H28,SF-268,NUGC-3,LMSU,NCI-H292,NCI-H522, Ludlu1, MKN-45, NCI-H460, CCK81, LU-99, NCI-H1792, NCI-H1944, HCC-44, SW837, HCC-1171, MDST8, NCI-H1755, CAL-12T, Hs746T, KATO-Ⅲ, CALU-3, RERF-GC-1B
Concentration: 0.001, 0.01, 0.1, 1, 10 μM
Incubation Time: 72 h
Result: Suppressed the proliferation of mesothelioma and Hippo mutation cell lines showed moderate sensitivity against non-mesothelioma cell lines with Hippo mutations (SF-268, LMSU, and NUGC-3).
体内実験

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].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

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.
臨床実験
分子量

529.96

分子式

C27H26ClF2N3O4

CAS 番号
Appearance

Solid

Color

White to off-white

SMILES

ClC(C(F)=CC1=C2C[C@](C3=CC=CC=C3)([C@@H]4CCCN4)O1)=[C@]2[C@@]5=C(C(NC)=O)C=NC(OCCO)=C5F

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

DMSO : 116.67 mg/mL (220.15 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.8869 mL 9.4347 mL 18.8693 mL
5 mM 0.3774 mL 1.8869 mL 3.7739 mL
10 mM 0.1887 mL 0.9435 mL 1.8869 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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純度とドキュメンテーション

純度: 99.47%

参考文献

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.8869 mL 9.4347 mL 18.8693 mL 47.1734 mL
5 mM 0.3774 mL 1.8869 mL 3.7739 mL 9.4347 mL
10 mM 0.1887 mL 0.9435 mL 1.8869 mL 4.7173 mL
15 mM 0.1258 mL 0.6290 mL 1.2580 mL 3.1449 mL
20 mM 0.0943 mL 0.4717 mL 0.9435 mL 2.3587 mL
25 mM 0.0755 mL 0.3774 mL 0.7548 mL 1.8869 mL
30 mM 0.0629 mL 0.3145 mL 0.6290 mL 1.5724 mL
40 mM 0.0472 mL 0.2359 mL 0.4717 mL 1.1793 mL
50 mM 0.0377 mL 0.1887 mL 0.3774 mL 0.9435 mL
60 mM 0.0314 mL 0.1572 mL 0.3145 mL 0.7862 mL
80 mM 0.0236 mL 0.1179 mL 0.2359 mL 0.5897 mL
100 mM 0.0189 mL 0.0943 mL 0.1887 mL 0.4717 mL
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製品名:
IAG933
製品番号:
HY-153811
数量:
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