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    Results for Activators & Inhibitors ( 70838 )

      • Ref: T38338
        Sizes: 1 mg, 5 mg, 500 μg
        From: €242.00

        Quinolactacin A (Legacy Tebubio ref. 282T38338). Quinolactactin A is a quinolone fungal metabolite originally isolated from Penicillium. It inhibits TNF production induced by LPS in murine peritoneal macrophages (IC50 = 12.2 μg/ml). It is not active against a variety of bacteria, fungi, and yeasts. Quinolactacin A is a mixture of quinolactacin A1 and A2.

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      • Ref: T38339
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg
        From: €106.00

        R-8507 (Legacy Tebubio ref. 282T38339). R-8507 is a small molecule antagonist of the TNF-α type 1 receptor (TNF-αRI). It inhibits the expression of intercellular adhesion molecule-1 (ICAM-1) induced by TNF-α and IL-1β with EC50 values of 2.45 and 3.79 μM, respectively, in an ELISA using A549 lung epithelial cells. It also disrupts the interaction of the TNF-αRI with receptor interacting protein 1 (RIP1) and TNF-αR-associated death domain protein (TRADD), preventing internalization of the receptor complex.

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      • Ref: T3834
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 500 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: €95.00

        8-Epideoxyloganic acid (Legacy Tebubio ref. 282T3834). 8-Epideoxyloganic acid possesses bioactivities of analgesia, homeostasis and anti-inflammatory. It has the potential to serve as anti-inflammatory agents during oxidative stress, the inhibition of ROS production, possibly through modulation of NOX activity and/or the radical scavenging effect, and beta2 integrin expression in leucocytes. 8-Epideoxyloganic acid (oral) shows weak antinociceptive activity.

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      • Ref: T38340
        Sizes: 1 mg
        From: €551.00

        10-Norparvulenone (Legacy Tebubio ref. 282T38340). 10-Norparvulenone is a fungal metabolite originally isolated fromMicrosphaeropsis.1It decreases viral sialidase activity in, and increases survival of, MDCK cells infected with the mouse-adapted influenza virus A/PR/8/34 when used at a concentration of 1 μg/ml.

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      • Ref: T38341
        Sizes: 100 mg, 50 mg
        From: €267.00

        11(Z),14(Z)-Eicosadienoic Acid methyl ester (Legacy Tebubio ref. 282T38341). 11(Z),14(Z)-Eicosadienoic acid methyl ester is a more lipid soluble form of the ω-6 C20-2 fatty acid 11(Z),14(Z)-eicosadienoic acid , a naturally occurring PUFA. 11(Z),14(Z)-Eicosadienoic acid competitively inhibits inosine 5'-monophosphate dehydrogenase (Ki = 3.1 μM) and inhibits the binding of LTB4 to its receptor on neutrophils (Ki = 3.0 μM). Also, serum levels of eicosadienoic acids negatively correlate with degree of sleep disturbance. Eicosadienoic acids are converted by desaturases, in vivo, to eicosatrienoic acids, which are potent vasodilators.

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      • Ref: T38342
        Sizes: 1 mg, 5 mg, 10 mg
        From: €182.00

        11-deoxy Prostaglandin E2 (Legacy Tebubio ref. 282T38342). 11-deoxy Prostaglandin E2 (11-deoxy PGE2) is a stable, synthetic analog of PGE2 . In contrast to PGE2 which has bronchodilation effects, 11-deoxy PGE2 is a powerful bronchoconstrictor and contracts human respiratory tract smooth muscle with potencies ranging from 5 to 30 times higher than PGF2α .

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      • Ref: T38343
        Sizes: 5 mg, 2 mg, 1 mL * 10 mM (in DMSO)
        From: €41.00

        Quercetin pentaacetate (Legacy Tebubio ref. 282T38343). Quercetin pentaacetate (Pentaacetylquercetin) has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties. Quercetin pentaacetate interacts with RSV and inhibit the viral adhesion on cell surface.

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      • Ref: T38344
        Sizes: 5 mg, 25 mg, 100 mg, 50 mg, 10 mg
        From: €53.00

        Lalistat 1 (Legacy Tebubio ref. 282T38344). Lalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae. Lalistat 1 can be used in studies about niemann-pick type C diseases.

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      • Ref: T38345
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg
        From: €35.00

        SQ609 (Legacy Tebubio ref. 282T38345). SQ609 is a potential anti-tuberculosis drug selected from a library of dipiperidine derivatives. SQ609 showed significant anti-tuberculous activity in mouse macrophages in vitro[1].

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