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    Results for Chemicals ( 21749 )

      • Ref: T74602
        Sizes: 1 mg, 5 mg, 10 mg
        From: €245.00

        PROTAC EZH2 Degrader-1 (Legacy Tebubio ref. 282T74602). PROTAC EZH2 Degrader-1 (Compound 150d) is a potent inhibitor that effectively suppresses EZH2 methyltransferase activity, with an IC50 of 2.7 nM. EZH2 plays a critical role in various tumorigenesis and development processes [1].

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      • Ref: T74896
        Sizes: 1 mg
        From: €384.00

        PROTAC STING Degrader-1 (Legacy Tebubio ref. 282T74896). PROTAC STING Degrader-1 (Compound SP23) is a STING-targeted PROTAC degrader with a DC50 of 3.2 μM, demonstrating anti-inflammatory activity [1].

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      • Ref: T75099
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg

        PROTAC STAT3 degrader-2 (Legacy Tebubio ref. 282T75099). PROTAC STAT3 degrader-2 is a selective and effective PROTAC degrader of the STAT3 protein, exhibiting a DC50 of 3.54 μM in Molm-16 cells. It holds potential for cancer research [1].

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      • Ref: T79250
        Sizes: 5 mg
        From: €1,121.00

        PROTAC α-synuclein degrader 5 (Legacy Tebubio ref. 282T79250). PROTAC α-synuclein degrader 5 is a highly selective (PROTAC) compound targeting and degrading α-synuclein aggregates, with a DC50 value of 7.51 μM and a maximum degradation rate (Dmax) of 89%. It incorporates the probe molecule sery308 and E3 ligase ligands, suitable for neurological disease research [1].

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      • Ref: T83857
        Sizes: 1 mg, 5 mg
        From: €653.00

        Soluble Epoxide Hydrolase PROTAC 1a (Legacy Tebubio ref. 282T83857). Soluble epoxide hydrolase (sEH) PROTAC 1a is a proteolysis-targeting chimera (PROTAC) comprising a cereblon ligand linked to the sEH inhibitor t-TUCB via a linker, promoting selective sEH degradation and inhibiting its hydrolase activity (IC50 = 0.8 nM) significantly more than its phosphatase activity (IC50 = >10,000 nM). This compound preferentially targets cytosolic sEH for lysosomal rather than proteasomal degradation. Furthermore, it mitigates thapsigargin-induced upregulation of phosphorylated inositol-requiring enzyme 1α (IRE1α) and X-box binding protein 1 (XBP1) splicing in HepG2 and 293T cells, thereby reducing endoplasmic reticulum stress.

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      • Ref: T8744
        Sizes: 5 mg
        From: €1,121.00

        PROTAC BRAF-V600E degrader-2 (Legacy Tebubio ref. 282T8744). PROTAC BRAF-V600E degrader-2 is a useful organic compound for research related to life sciences. The catalog number is T8744 and the CAS number is 2417296-82-1.

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      • Ref: T8745
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 200 mg
        From: €131.00

        PROTAC BRAF-V600E degrader-1 (Legacy Tebubio ref. 282T8745). PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF.

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      • Ref: T9417L
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 200 mg
        From: €122.00

        gamma-preprotachykinin amide (72-92) acetate (Legacy Tebubio ref. 282T9417L). gamma-preprotachykinin amide (72-92) acetate is a 21 amino acid peptide belonging to the tachykinin (TK) family and including neurokinin A (NKA) in its C-terminal sequence. gamma-preprotachykinin amide (72-92) acetate possesses higher affinity than NKA for central NK-2 receptors; it shows lower affinity for NK-1 receptors, however, it potently stimulates salivary secretion, which is mediated by NK-1 receptor activation.

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      • Ref: T13694
        Sizes: 1 mg
        From: €245.00

        FKBP12 PROTAC RC32 (Legacy Tebubio ref. 282T13694). FKBP12 PROTAC RC32 is a PROTAC-like degrader targeting FKBP12. It can degrade FKBP12 in organs after intraperitoneal administration.

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