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  • T1085L-Glutathione reduced谷胱甘肽;还原型谷胱甘肽;γ-L-Glutamyl-L-cysteinyl-glycine;Tathion;Glutathione;GSH;Isethion;

    Glutathione is a tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.

    价 格:¥电议型 号:T1085产 地:中国大陆

  • T10098PGS-IN-1KME-4

    PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS, IC50: 0.28 μM) and 5-lipoxygenase (IC50: 1.05 μM).

    价 格:¥电议型 号:T10098产 地:中国大陆

  • T0180Benazepril hydrochloride盐酸贝那普利;CGS14824A;Benazepril HCl;CGS 14824A HCl

    Benazepril is an angiotensin-converting enzyme (ACE) inhibitor widely used in the therapy of hypertension. Benazepril is associated with a low rate of transient serum aminotransferase elevations and has been linked to rare instances of acute liver injury.

    价 格:¥电议型 号:T0180产 地:中国大陆

  • T0078Lapatinib拉帕替尼;GSK572016;GW572016

    Lapatinib is a dual inhibitor of Lapatinib is a dual ErbB2/EGFR (IC50: 9.2/10.8 nM) inhibitor

    价 格:¥电议型 号:T0078产 地:中国大陆

  • T0078LapatinibLapatinib,GW572016,GSK572016

    Lapatinib is a dual ErbB2/EGFR (IC50: 9.2/10.8 nM) inhibitor.

    价 格:¥电议型 号:T0078产 地:美洲

  • T0180Benazepril hydrochlorideBenazepril hydrochloride,CGS14824A,Benazepril HCl

    Benazepril is an angiotensin-converting enzyme (ACE) inhibitor widely used in the therapy of hypertension. Benazepril is associated with a low rate of transient serum aminotransferase elevations and has been linked to rare instances of acute liver injury.

    价 格:¥电议型 号:T0180产 地:美洲

  • T10098PGS-IN-1PGS-IN-1,KME-4,

    PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS; IC50: 0.28 μM) and also inhibits 5-lipoxygenase (IC50: 1.05 μM).

    价 格:¥电议型 号:T10098产 地:美洲

  • T1085GlutathioneGlutathione,γ-L-Glutamyl-L-cysteinyl-glycine,GSH

    Glutathione is a tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.

    价 格:¥电议型 号:T1085产 地:美洲

  • T1085LL(-)-GlutathioneL(-)-Glutathione,GSSG,L-Glutathione oxidized

    A GLUTATHIONE dimer formed by a disulfide bond between the cysteine sulfhydryl side chains during the course of being oxidized.

    价 格:¥电议型 号:T1085L产 地:美洲

  • T11391LGepotidacinGepotidacin,GSK2140944,

    Gepotidacin is a novel triazaacenaphthylene inhibitor of bacterial type II topoisomerase.

    价 格:¥电议型 号:T11391L产 地:美洲

  • T11465GS-6207GS-6207

    GS-6207 displays a mean EC50 of 50 pM (20-160 pM) against 23 HIV-1 clinical isolates from different subtypes in peripheral blood mononuclear cells (PBMCs). GS-6207 is a HIV-1 capsid inhibitor. GS-6207 shows anti-HIV activity with an EC50 of 100 pM in MT-4

    价 格:¥电议型 号:T11465产 地:美洲

  • T11468GSK-3 inhibitor 1GSK-3 inhibitor 1

    GSK-3 inhibitor 1 is an inhibitor of GSK-3.

    价 格:¥电议型 号:T11468产 地:美洲

  • T11469GSK-3484862GSK-3484862

    GSK-3484862 induces DNA hypomethylation to against cancer.?GSK-3484862 is a non-covalent inhibitor for Dnmt1.?

    价 格:¥电议型 号:T11469产 地:美洲

  • T11470GSK 366GSK 366

    GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor with IC50s of 0.7 nM and 2.3 nM for P. fluorescens-KMO (Pf-KMO)?and human KMO, respectively.

    价 格:¥电议型 号:T11470产 地:美洲

  • T11472GSK 525768AGSK 525768A

    GSK 525768A has no activity towards BET. GSK 525768A is the inactive enantiomer of GSK525762A.

    价 格:¥电议型 号:T11472产 地:美洲

  • T11472LMolibresib besylateMolibresib besylate,GSK 525762C,I-BET 762 besylate

    Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM).

    价 格:¥电议型 号:T11472L产 地:美洲

  • T11476GSK-J2GSK-J2

    GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A.?GSK-J2 is an isomer of GSK-J1 that does not have any specific activity.?

    价 格:¥电议型 号:T11476产 地:美洲

  • T11477GSK1059865GSK1059865

    GSK1059865 is a potent orexin 1 receptor antagonist.

    价 格:¥电议型 号:T11477产 地:美洲

  • T11480GSK205GSK205

    GSK205 is a potent, selective TRPV4 antagonist with an IC50 of 4.19? μM for inhibiting TRPV4-mediated Ca2+ influx.?

    价 格:¥电议型 号:T11480产 地:美洲

  • T11481GSK2239633AGSK2239633A

    GSK2239633A inhibits the binding of [125I]-TARC to human CCR4 with a pIC50 of 7.96?±?0.11.?GSK2239633A is a CC-chemokine receptor 4 (CCR4) antagonist.

    价 格:¥电议型 号:T11481产 地:美洲

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