iDeg-3
iDeg-3 is a potent IDO1 molecular glue degrader. iDeg-3 binds to apo-IDO1 and alters its C-terminal conformation, promoting CRL2-KLHDC3 E3 ligase-mediated ubiquitination and degradation of IDO1. iDeg-3 is suitable for cancer-related research.
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- 화학식: C31H38N2O4S
- 분자량:534.71
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
IC50 & Target
[1]|
IDO1 |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| BXPC-3 | IC50 |
46 nM
|
Inhibition of IDO1-mediated kynurenine formation in IFN-γ-stimulated human BxPC3 cells incubated for 48 h by Kyn assay.
Inhibition of IDO1-mediated kynurenine formation in IFN-γ-stimulated human BxPC3 cells incubated for 48 h by Kyn assay.
|
41501556 |
In Vitro
iDeg-3 (48 h) potently inhibits Kyn production in IFN-γ (HY-P7025)-stimulated BxPC3 cells, with an IC50 of 46 nM[1].
iDeg-3 (1-3.33 μM; 24 h) reduces IDO1 protein levels by 62% in IFN-γ-stimulated BxPC3 cells and decreases IDO1 reporter protein levels in KBM7 cells[1].
iDeg-3 (50 μM; 3 h) stabilizes recombinant rhIDO1 protein in in vitro biochemical assays (nanoDSF)[1].
iDeg-3 (5 μM; 2.5 h) enhances the interaction between IDO1 and KLHDC3 in HEK293T cells (expressing TurboID-IDO1)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:IFN-γ-stimulated BxPC3 cells
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Concentration:3.33 μM
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Incubation Time:24 h
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Result:Reduced IDO1 protein levels by 62% compared to vehicle control.
Chemical Information
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분자량 534.71
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화학식 C31H38N2O4S
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SMILES
C#CC1=CC=C(C=C1)NC(OC[C@@]23[C@H](C[C@@H]4C[C@]2([H])CN(C3)S(C5=CC=C(C(C)(C)C)C=C5)(=O)=O)C4(C)C)=O
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)