A PROTAC that drives aptamer-defined protein degradation
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Dth

Item No. 38925

Technical Information
Formal Name
(Z)-4-((6-(4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-5-oxo-4,5-dihydro-1H-imidazol-1-yl)hexyl)amino)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione
Molecular Formula
C30H29F2N5O6
Formula Weight
Purity
≥95%
A 1 mg/ml solution in ethanol
Ethanol: 1 mg/ml
SMILES
FC1=C(O)C(F)=CC(/C=C2N=C(C)N(CCCCCCNC3=CC=CC(C(N4C5CCC(NC5=O)=O)=O)=C3C4=O)C\2=O)=C1
InChi Code
InChI=1S/C30H29F2N5O6/c1-16-34-22(15-17-13-19(31)26(39)20(32)14-17)29(42)36(16)12-5-3-2-4-11-33-21-8-6-7-18-25(21)30(43)37(28(18)41)23-9-10-24(38)35-27(23)40/h6-8,13-15,23,33,39H,2-5,9-12H2,1H3,(H,35,38,40)/b22-15-
InChi Key
PSAVYAATVZHVSR-JCMHNJIXSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Dth is a proteolysis-targeting chimera (PROTAC) composed of the fluorescent probe for RNA DFHBI (Item No. 34555) and the immunomodulatory compound thalidomide (Item No. 14610).1 It binds to a genetically expressed RNA aptamer comprising Broccoli and a modifiable and selective protein targeting sequence and induces degradation of mCherry in HEK293T cells when used at a concentration of 20 µM. Dth (20 µM) induces degradation of the NF-κB subunit p50, as well as p50 and the E2F transcription factor subtype E2F1, in MCF-7 cells.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Xu, Y., Fu, D., Yuan, Y., et alA heterobifunctional molecule recruits cereblon to an RNA scaffold and activates its PROTAC function. Cell Rep. Phys. Sci. 3(10), 101064 (2022).