PROTAC IDO1 Degrader-1

 CAS No.: 2488851-89-2  Cat No.: BP-400184 4.5  

PROTAC IDO1 Degrader-1 is a novel chemical tool designed for the targeted degradation of indoleamine 2,3-dioxygenase 1 (IDO1), a key enzyme involved in tryptophan metabolism and immune regulation. This degrader operates by binding specifically to the IDO1 active site, facilitating its recruitment to the E3 ubiquitin ligase complex via a linker that connects to a ligand for the ligase. By leveraging the ubiquitin-proteasome system, PROTAC IDO1 Degrader-1 induces ubiquitination and subsequent proteasomal degradation of IDO1, effectively reducing its cellular levels. This targeted degradation mechanism not only offers a strategic approach to modulate IDO1 activity but also serves as a valuable tool in elucidating the biological roles of IDO1 in various cellular contexts. Researchers can employ PROTAC IDO1 Degrader-1 to explore IDO1's involvement in immune escape mechanisms and its potential as a therapeutic target in cancer and other diseases. Its precise action and specificity make it an essential component in the development of next-generation therapeutics within the realm of PROTAC technology.

PROTAC IDO1 Degrader-1

Structure of 2488851-89-2

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PROTAC
Molecular Formula
C40H53BrFN9O13
Molecular Weight
966.8
Appearance
Solid

* For research and manufacturing use only. Not for human or clinical use.

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Appearance
Solid
Storage
Store at -20°C
Mechanism

Target: Targets indoleamine 2,3-dioxygenase 1 (IDO1) for experimental targeted protein degradation studies.

Binding Site: Binds the IDO1 heme-containing catalytic pocket and recruited E3 ligase ligand site to support productive ternary complex formation.

Mechanism of Action: PROTAC IDO1 Degrader-1 is designed for use in PROTAC or targeted protein degradation experiments directed toward indoleamine 2,3-dioxygenase 1 (IDO1). The bifunctional molecule links a target-recognition element to cereblon, promoting proximity between the protein of interest and ubiquitination machinery. Productive ternary-complex formation can drive polyubiquitination and proteasome-dependent target depletion, allowing researchers to compare pharmacological inhibition with protein removal. It is suitable for evaluating degradation potency, kinetics, pathway selectivity, and downstream signaling consequences in engineered or disease-relevant cellular models.

Applications

• PROTAC-Mediated IDO1 Degradation: This application focuses on utilizing PROTAC IDO1 Degrader-1 for the selective degradation of indoleamine 2,3-dioxygenase 1 (IDO1) in cellular models. It enables researchers to investigate the role of IDO1 in immune modulation and its potential as a therapeutic target in cancer and autoimmune diseases.

• Targeted Degradation in Cancer Research: By employing PROTAC IDO1 Degrader-1, scientists can explore the effects of IDO1 protein depletion on tumor microenvironment dynamics. This approach aids in elucidating the mechanisms by which IDO1 contributes to tumor immune evasion and could inform the development of novel cancer immunotherapies.

• PROTAC-Driven Protein Knockdown Studies: PROTAC IDO1 Degrader-1 serves as a valuable tool for conducting protein knockdown experiments, providing insights into IDO1's regulatory pathways. Researchers can utilize this compound to dissect the downstream signaling events following IDO1 degradation, advancing our understanding of its biological functions.

• Exploring Immune Pathway Modulation: With PROTAC IDO1 Degrader-1, researchers can delve into the modulation of immune pathways mediated by IDO1. This application supports the study of how targeted protein degradation affects immune cell behavior and cytokine production, offering a deeper understanding of immune regulation.

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* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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