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Chemicals & Small Molecules

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    Results for Chemicals & Small Molecules ( 97587 )

      • REV 5901

        Ref: T21821
        Sizes: 5 mg, 100 mg, 50 mg, 10 mg
        From: DKK668.00

        REV 5901 (Legacy Tebubio ref. 282T21821). REV 5901 is a competitive and orally effective leukotriene receptor antagonist (Ki of 0.7 μM) and a 5-lipoxygenase inhibitor, suitable for research on asthma involving leukotriene release [1] [2].

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      • REV 5901A

        Ref: T21821L
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg
        From: DKK1,665.00

        REV 5901A (Legacy Tebubio ref. 282T21821L). REV 5901A (REV 5901 HCl) is an orally active leukotriene receptor antagonist and 5-lipoxygenase inhibitor with antimicrobial activity that attenuates colon cancer growth in mice.REV 5901A has been used in studies of asthma and myocardial infarction. REV 5901A is used to study asthma and myocardial infarction.

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      • Se-Aspirin

        Ref: T21823
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg
        From: DKK1,163.00

        Se-Aspirin (Legacy Tebubio ref. 282T21823). Se-Aspirin (Se-NSAID-8) has anticancer activity and gastroprotective effects, inhibits activation of proinflammatory and pro-survival NF-ĸB pathways, and inhibits the expression of anti-apoptotic targets downstream of NF-ĸB (e.g., Bcl-xL, Mcl-1, and survivin).Se-Aspirin induces Cell cycle arrest and activation of apoptosis accelerates ulcer healing and can be used to study pancreatic and colorectal cancer.

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      • Sephin1

        Ref: T21824
        Sizes: 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: DKK300.00

        Sephin1 (Legacy Tebubio ref. 282T21824). Sephin1 (IFB-088) is reportedly a selective inhibitor of GADD34 (PPP1R15A), which is a stress-induced regulatory subunit of protein phosphatase 1 complex that dephosphorylates eIF2α

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      • TAE-1

        Ref: T21825
        Sizes: 25 mg, 100 mg, 50 mg
        From: DKK458.00

        TAE-1 (Legacy Tebubio ref. 282T21825). TAE-1 is an inhibitor of amyloid-β fibril formation and aggregation. It inhibits cholinesterases AChE and BuChE with IC50 of 0.3 μM and 3.9 μM, respectively.

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      • TC-E 5003

        Ref: T21826
        Sizes: 25 mg, 100 mg, 50 mg, 200 mg, 1 mL * 10 mM (in DMSO)
        From: DKK338.00

        TC-E 5003 (Legacy Tebubio ref. 282T21826). TC-E 5003 (NSC-30176) is a selective inhibitor of PRMT1 with IC50 of 1.5 μM.

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      • UCM05

        Ref: T21831
        Sizes: 1 mg, 5 mg, 25 mg, 100 mg, 50 mg, 10 mg, 1 mL * 10 mM (in DMSO)
        From: DKK293.00

        UCM05 (Legacy Tebubio ref. 282T21831). UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibitor of the Filamentous temperature-sensitive protein Z (FtsZ), selectively inhibiting the growth of the Gram-positive bacterium B. subtilis with minimum inhibitory concentration (MIC) values of 100 μM, while showing no activity against the Gram-negative bacterium E. coli [2].

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      • YM-155 hydrochloride

        Ref: T21834
        Sizes: 5 mg, 25 mg, 50 mg, 10 mg
        From: DKK1,065.00

        YM-155 hydrochloride (Legacy Tebubio ref. 282T21834). Sepantronium hydrochloride (YM-155 hydrochloride) is a novel survivin suppressant that inhibits the survivin promoter with an IC₅₀ of 0.54 nM[1].

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      • Z-LEHD-fmk

        Ref: T21835
        Sizes: 1 mg, 5 mg, 25 mg, 50 mg, 10 mg
        From: DKK1,688.00

        Z-LEHD-fmk (Legacy Tebubio ref. 282T21835). Z-LEHD-FMK is a selective and potent caspase-9 inhibitor that protects against reperfusion injury and slows apoptosis. Z-LEHD-FMK exhibits antitumor and neuroprotective activity, increases the yield of in vitro-produced preimplantation embryos of [Bubalus bubalis], and alters the cellular stress response.

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