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    Results for Chemicals ( 21749 )

      • Ref: T39837
        Sizes: 5 mg, 25 mg, 50 mg, 10 mg

        PROTAC ERRα Degrader-3 (Legacy Tebubio ref. 282T39837). PROTAC ERRα Degrader-3 is a highly effective and selective von Hippel-Lindau-based ligand that efficiently degrades the ERRα protein, reducing its levels by >80% at a concentration of 30 nM. Notably, this compound shows no activity against the ERRβ and ERRγ proteins.

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      • Ref: T39996
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg
        From: €366.00

        PROTAC CDK9 degrader 4 (Legacy Tebubio ref. 282T39996). PROTAC CDK9 degrader 4 is a highly potent CDK9 degrader that targets transcriptional regulation and has potential anticancer activity for the study of acute myelogenous leukemia (AML).

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      • Ref: T40112
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 200 mg
        From: €288.00

        PROTAC PD-1/PD-L1 degrader-1 (Legacy Tebubio ref. 282T40112). PROTAC PD-1/PD-L1 degrader-1, a Cereblon E3 ligand-based compound, is a PD-1/PD-L1 PROTAC that effectively inhibits the PD-1/PD-L1 interaction with an IC50 of 39.2 nM. It restores the suppressed immune response in a co-culture model of Hep3B/OS-8/hPD-L1 cells and CD3 T cells and moderately decreases PD-L1 protein levels through a lysosome-dependent mechanism.

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      • Ref: T40143
        Sizes: 5 mg, 10 mg

        PROTAC CBP/P300 Degrader-1 (Legacy Tebubio ref. 282T40143). PROTAC CBP/P300 Degrader-1 is an effective compound that potently degrades CBP/P300, significantly reducing cell viability in various cancer cell lines.

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      • Ref: T40334
        Sizes: 5 mg
        From: €3,176.00

        PROTAC IRAK3 degrade-1 (Legacy Tebubio ref. 282T40334). PROTAC IRAK3 degrade-1 is a potent and selective degrader of IRAK3 ( IC 50 = 5 nM).

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      • Ref: T11291
        Sizes: 5 mg
        From: €1,533.00

        FKBP12 PROTAC dTAG-13 (Legacy Tebubio ref. 282T11291). FKBP12 PROTAC dTAG-13 (dTAG-13) is a heterobifunctional degrader that targets FKBP12F36V with FKBP12F36V expressed in-frame with a protein of interest, and selectively degrades the BET bromodomain transcriptional co-activator BRD4 by bridging BET bromodomains to the E3 ubiquitin ligase CRBN.

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      • Ref: T11292
        Sizes: 5 mg
        From: €1,453.00

        FKBP12 PROTAC dTAG-7 (Legacy Tebubio ref. 282T11292). FKBP12 PROTAC dTAG-7 (dTAG-7) is a heterobifunctional compound that selectively degrades the BET bromodomain transcriptional co-activator BRD4 by linking BET bromodomains to the E3 ubiquitin ligase CRBN. It also functions as a degrader of FKBP12F36V when FKBP12F36V is expressed in-frame with a targeted protein.

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      • Ref: T11975
        Sizes: 1 mg, 5 mg, 25 mg, 50 mg, 10 mg
        From: €517.00

        PROTAC Mcl1 degrader-1 (Legacy Tebubio ref. 282T11975). PROTAC Mcl1 degrader-1 is a Cereblon ligand-based targeted chimeric protein degrader (PROTAC), a selective Mcl-1 inhibitor. By hijacking the CRBN ubiquitin ligase to form a ternary complex with the target protein, it induces Mcl-1 ubiquitination. It can be used for cancer research.

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      • Ref: T41267
        Sizes: 1 mg, 500 μg
        From: €560.00

        PROTAC(H-PGDS)-7 (Legacy Tebubio ref. 282T41267). PROTAC(H-PGDS)-7 is a selective and potent small molecule hematopoietic prostaglandin D synthase (H-PGDS) PROTAC degradation agent that exhibits degradation activity in KU812 cells with a DC50 of 17.3 pM. It effectively inhibits prostaglandin D2 (PGD2) and is a candidate compound for the treatment of DMD and other H-PGDS-related diseases.

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