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Activators & Inhibitors

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    Results for Activators & Inhibitors ( 18112 )

      • ABT-702 dihydrochloride

        Ref: T4668
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 500 mg, 10 mg, 2 mg, 1 mL * 10 mM (in DMSO)
        From: €64.00

        ABT-702 dihydrochloride (Legacy Tebubio ref. 282T4668). ABT-702 dihydrochloride is a highly potent inhibitor of adenosine kinase (AK).

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      • Fantofarone

        Ref: T4669
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €36.00

        Fantofarone (Legacy Tebubio ref. 282T4669). Fantofarone (SR 33557) is a highly potent antagonist of Calcium Channel.

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      • SR0987

        Ref: T4670
        Sizes: 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €73.00

        SR0987 (Legacy Tebubio ref. 282T4670). SR0987 is a RORγt agonist,

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      • BN82002

        Ref: T4671
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €44.00

        BN82002 (Legacy Tebubio ref. 282T4671). BN82002 (CDC25 Phosphatase Inhibitor I) is a synthetic inhibitor of CDC25 phophatases

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      • Brevilin A

        Ref: T4672
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 500 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €111.00

        Brevilin A (Legacy Tebubio ref. 282T4672). Brevilin A is a sesquiterpene lactone isolated from Centipeda minima, inhibits janus kinase activity and blocks STAT3 signaling in cancer cells with anti-tumor activity. Brevilin A is a selective inhibitor of JAK-STAT signal pathway by attenuating the JAKs activity and blocking STAT3 signaling (IC50 = 10.6 μM) in Cancer Cells.Brevilin A induces apoptosis and autophagy via mitochondrial pathway and PI3K/AKT/mTOR inactivation in colon adenocarcinoma cell CT26.antitumour

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      • SB297006

        Ref: T4674
        Sizes: 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 2 mg, 1 mL * 10 mM (in DMSO)
        From: €35.00

        SB297006 (Legacy Tebubio ref. 282T4674). SB297006 is an antagonist of C-C chemokine receptor 3 (CCR3; IC50 = 39 nM), which normally is activated by eotaxin, eotaxin-3, MCP-3, MCP-4, RANTES, and MIP-1δ. It is at least 250-fold selective for CCR3 over a panel of other chemokine receptors. SB 297006 blocks CCR3-mediated calcium mobilization induced by eotaxin, eotaxin-2, and MCP-4 in transfected cells. It suppresses antigen-induced accumulation of Th2 lymphocytes and eosinophils in lungs of mice when delivered subcutaneously (100 mg/kg).

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      • 4-Carboxyisothiazole

        Ref: T4675
        Sizes: 50 mg
        From: €35.00

        4-Carboxyisothiazole (Legacy Tebubio ref. 282T4675). 4-Carboxyisothiazole is a useful organic compound for research related to life sciences. The catalog number is T4675 and the CAS number is 822-82-2.

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      • Sardomozide dihydrochloride

        Ref: T4676
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €35.00

        Sardomozide dihydrochloride (Legacy Tebubio ref. 282T4676). Sardomozide dihydrochloride (CGP 48664 dihydrochloride) is an inhibitor of S-adenosylmethionine decarboxylase (SAMDC, IC50 = 5 nM).

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      • MMAD

        Ref: T4677
        Sizes: 5 mg, 25 mg, 100 mg, 50 mg, 10 mg
        From: €46.00

        MMAD (Legacy Tebubio ref. 282T4677). MMAD (Demethyldolastatin 10) is a potent tubulin inhibitor. MMAD is a toxin payload in antibody drug conjugates (ADCs).

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