Fig. 1 · Structure

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PROTAC mHTT Degrader-1

mHTT PROTAC Degrader

PROTAC mHTT Degrader-1 targets mutant huntingtin (mHTT) through a PROTAC mechanism, effectively penetrating the blood-brain barrier. This compound selectively binds to pathogenic mHTT aggregates and recruits Cereblon (CRBN), leading to the ubiquitination and subsequent proteasomal degradation of mHTT. Research indicates that PROTAC mHTT Degrader-1 mitigates mHTT-induced cytotoxicity and neuroinflammation. In preclinical studies involving the R6/2 Huntington's disease mouse model, it has demonstrated the ability to decrease cerebral protein aggregation, enhance body weight, improve motor coordination, and increase survival rates. This reagent is pivotal for investigating PROTAC therapies in Huntington's disease and other neurodegenerative conditions.

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Specifications

Manufacturer Adooq Bioscience
Actions Degrader
CAS Number 2919475-43-5
Applications mHTT PROTAC Degrader
Formula C33H35N5O7
Molecular Weight 613.66
SMILES
CNC1=CC=C(C=C1)/C=C/C2=CC=C(N=C2)OCCOCCOCCNC3=C4C(N(C(C4=CC=C3)=O)C5CCC(NC5=O)=O)=O

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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