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  • T27161,3-Diphenylurea

    1, 3-Diphenylurea is involved with Epoxide hydrolase activity.

    价 格:¥电议型 号:T2716产 地:中国大陆

  • T2695TBB4,5,6,7-tetrabromobenzotriazole;NSC 231634;Casein Kinase II Inhibitor I

    TBB(NSC 231634) is a highly selective, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2).

    价 格:¥电议型 号:T2695产 地:中国大陆

  • T2684JNJ-1661010JNJ 1661010;Takeda-25;JNJ1661010

    JNJ-1661010 is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.

    价 格:¥电议型 号:T2684产 地:中国大陆

  • T26712AZD-1656AZD 1656;AZD1656

    AZD-1656 is a glucokinase activator (GKA) that can cause dose-limiting hypoglycemia in normal animals used in embryofetal development studies and type 2 diabetes.

    价 格:¥电议型 号:T26712产 地:中国大陆

  • T2670ML167NCGC00188654;CID44968231

    ML167 is a highly selective Cdc2-like kinase 4 (Clk4) inhibitor.

    价 格:¥电议型 号:T2670产 地:中国大陆

  • T26193SKLB-163SKLB163;SKLB 163

    SKLB-163 acts by downregulating RhoGDI, activating JNK-1 signaling pathway and caspase-3, and reducing phosphorylated Akt and p44/42 MAPK.

    价 格:¥电议型 号:T26193产 地:中国大陆

  • T2616PIK-93PIK 93;PIK93

    PIK-93 is the first potent, synthetic PI4K inhibitor with IC50 of 19 nM; inhibits PI3Kα with IC50 of 39 nM.

    价 格:¥电议型 号:T2616产 地:中国大陆

  • T2607MSDC 0160MSDC0160;CAY10415;Mitoglitazone;MSDC-0160

    MSDC-0160 is a prototype mTOT-modulating insulin sensitizer being used in trials studying the treatment of Type 2 Diabetes and Alzheimer´s Disease.

    价 格:¥电议型 号:T2607产 地:中国大陆

  • T25487Haloperidol decanoateKD 136;KD-136;Neoperidole;Haldol;KD 16

    Haloperidol decanoate is a typical antipsychotic agent utilized as maintenance treatment for schizophrenia and mood disorders formulated as an ester for intramuscular injection.

    价 格:¥电议型 号:T25487产 地:中国大陆

  • T2543Cabazitaxel卡巴他塞;TXD 258;taxoid XRP6258;RPR-116258A;XRP6258

    Cabazitaxel is a taxane and antineoplastic agent which is currently used in the therapy of castration-resistant metastatic prostate cancer after failure of docetaxel.

    价 格:¥电议型 号:T2543产 地:中国大陆

  • T2535Ivabradine hydrochloride盐酸伊伐布雷定;S 16257-2;Ivabradine HCl

    Ivabradine hydrochloride is a new If inhibitor (IC50: 2.9 μM). Ivabradine Hydrochloride is the hydrochloride salt form of ivabradine, an orally bioavailable, hyperpolarization-activated, cyclic nucleotide-gated (HCN) channel blocker, with negative chronot

    价 格:¥电议型 号:T2535产 地:中国大陆

  • T2529Zanamivir扎那米韦;GG167

    Zanamivir is a guanido-neuraminic acid that is used to inhibit NEURAMINIDASE.

    价 格:¥电议型 号:T2529产 地:中国大陆

  • T2516AmuvatinibHPK 56;MP470

    Amuvatinib is an orally bioavailable synthetic carbothioamide with potential antineoplastic activity.

    价 格:¥电议型 号:T2516产 地:中国大陆

  • T2508BinimetinibMEK162;ARRY-162;ARRY-438162

    Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.

    价 格:¥电议型 号:T2508产 地:中国大陆

  • T2504Pritelivir普瑞利韦;BAY 57-1293;AIC316

    Pritelivir (BAY 57-1293) is a potent helicase-primase inhibitor with active against HSV-1 and HSV-2 (IC50: 20 nM).

    价 格:¥电议型 号:T2504产 地:中国大陆

  • T2496(Z)-SemaxinibSU5416

    Semaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor (IC50: 1.23 μM), 20-fold more selective for VEGFR over PDGFRβ, no inhibition for FGFR, InsR, and EGFR. Semaxanib is a quinolone derivative with potential antineoplastic activity.

    价 格:¥电议型 号:T2496产 地:中国大陆

  • T24827SR 16832SR-16832;SR16832

    SR 16832 is a dual-site PPARγ inhibitor. It also inhibits the binding of endogenous ligands and transcriptional activity of PPARγ, more effectively than the orthosteric covalent antagonist GW 9662 and T 0070907.

    价 格:¥电议型 号:T24827产 地:中国大陆

  • T2477UNBS5162UNBS 5162;UNBS-5162

    UNBS-5162 is a novel naphthalimide that decreases CXCL chemokine expression in experimental prostate cancers.

    价 格:¥电议型 号:T2477产 地:中国大陆

  • T2445FG-2216FG 2216;YM-311;FG2216

    FG-2216 is a potent HIF-prolyl hydroxylase inhibitor for the PDH2 enzyme (IC50: 3.9 uM); orally bioavailable and induced reversible and significant Epo induction in vivo.

    价 格:¥电议型 号:T2445产 地:中国大陆

  • T2432PD 169316

    PD 169316 is a potent, cell-permeable and selective p38 MAP kinase inhibitor.

    价 格:¥电议型 号:T2432产 地:中国大陆

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