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  • T15805LY2510924LY2510924

    LY2510924 is an effective and selective CXCR4 antagonist. It blocks SDF-1 binding to CXCR4 (IC50: 0.079 nM).

    价 格:¥电议型 号:T15805产 地:美洲

  • T15806LY2562175LY2562175

    LY2562175 is an effective and selective FXR agonist (EC50: 193 nM).

    价 格:¥电议型 号:T15806产 地:美洲

  • T15807LY2794193LY2794193

    LY2794193 is a highly effective and selective agonist of the mGlu3 receptor (hmGlu3 Ki=0.927 nM,EC50=0.47 nM; hmGlu2 Ki=412 nM,EC50=47.5 nM).

    价 格:¥电议型 号:T15807产 地:美洲

  • T15808Merestinib dihydrochlorideMerestinib dihydrochloride,LY2801653 dihydrochloride,

    Merestinib dihydrochloride is an effective and orally bioavailable c-Met inhibitor (Ki=2 nM). It has anti-tumor activities and also has potent activity against MST1R (IC50=11 nM), FLT3 (IC50=7 nM), AXL (IC50=2 nM), MERTK (IC50=10 nM), TEK (IC50=63 nM), RO

    价 格:¥电议型 号:T15808产 地:美洲

  • T15809LY2812223LY2812223

    LY2812223 is a highly effective and functionally selective mGlu2 receptor agonist. It has a mGlu2 binding affinity for mGlu2 and mGlu3 (Ki=144 nM and 156 nM, respectively).

    价 格:¥电议型 号:T15809产 地:美洲

  • T1581PicolaminePicolamine

    Picolamine acts as a potential inhibitor of DPP-4.

    价 格:¥电议型 号:T1581产 地:美洲

  • T15810LY2922470LY2922470

    LY2922470 reduces glucose levels along with significant enhancements in insulin and GLP-1, which is the potential for the treatment of type 2 diabetes mellitus (T2DM). LY2922470 is an effective, selective, and orally available agonist of the G protein-cou

    价 格:¥电议型 号:T15810产 地:美洲

  • T15811LY2955303LY2955303

    LY2955303 is an effective and selective retinoic acid receptor gamma (RARγ) antagonist (Ki: 1.09 nM).

    价 格:¥电议型 号:T15811产 地:美洲

  • T15812LY2979165LY2979165

    LY2979165 is a mGlu2 agonist and is a novel potent agent. It is used as anti-depressants.

    价 格:¥电议型 号:T15812产 地:美洲

  • T15815LY3295668LY3295668,AK-01,

    LY3295668 is an effective and orally active and highly specific inhibitor of Aurora-A kinase (Ki: 0.8 nM and 1038 nM for AurA and AurB, respectively).

    价 格:¥电议型 号:T15815产 地:美洲

  • T15816LY341495LY341495

    LY341495 is an antagonist of metabotropic glutamate receptor (IC50s: 2.9 nM, 10 nM, 170 nM for mGluR-2, mGluR-3, mGluR-8, respectively).

    价 格:¥电议型 号:T15816产 地:美洲

  • T15817EglumegadEglumegad,LY354740,Eglumetad

    Eglumegad is a highly effective and selective agonist of group II (mGlu2/3) receptor (IC50s: 5 and 24 nM on transfected human mGlu2 and mGlu3 receptors, respectively).

    价 格:¥电议型 号:T15817产 地:美洲

  • T15818LY367385LY367385

    LY367385 is a highly effective and selective mGluR1a antagonist. LY367385 has neuroprotective, anticonvulsant, and antiepileptic effects. Compared with > 100 μM for mGlu5a, LY367385 has an IC50 of 8.8 μM for inhibits of quisqualate-induced phosphoinositid

    价 格:¥电议型 号:T15818产 地:美洲

  • T1582NaproxenNaproxen,(S)-Naproxen,

    Naproxen is a propionic acid derivative and a non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory, antipyretic and analgesic activities.

    价 格:¥电议型 号:T1582产 地:美洲

  • T15820MibampatorMibampator,LY451395,

    Mibampator is an effective and highly selective AMPA receptor potentiator.

    价 格:¥电议型 号:T15820产 地:美洲

  • T15821LY518674LY518674,LY-674,

    LY518674 decreases triglycerides in and increased HDL-C and is used for the treatment of atherosclerosis. LY518674 is an effective and selective PPARα antagonist (EC50: 42 nM for human PPARα).

    价 格:¥电议型 号:T15821产 地:美洲

  • T15824LysergolLysergol

    Lysergol has been used as a hypotensive, psychotropic analgesic, and uterus- and intestine-stimulating drug. Lysergol is a clavinet alkaloid isolated from seeds of Ipomoea muricata and is a bioenhancer for the drugs and nutrients and has antibacterial act

    价 格:¥电议型 号:T15824产 地:美洲

  • T15826LometrexolLometrexol,DDATHF,

    Lometrexol has anticancer activity. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and apoptosis, even cell cycle arrest. Lometrexol is an antipurine antifolate, can inhibit the activity of glycinamide ribonuc

    价 格:¥电议型 号:T15826产 地:美洲

  • T15827LY 345899LY 345899

    LY 345899 is a Folate analog and is a methylenetetrahydrofolate dehydrogenase and MTHFD2 inhibitor (IC50: 96 nM and 663 nM, respectively and a Ki: 18 nM for MTHFD1).

    价 格:¥电议型 号:T15827产 地:美洲

  • T15828L 888607L 888607

    L 888607 is an effective and selective CRTH2 agonist (Ki: 0.8 nM).

    价 格:¥电议型 号:T15828产 地:美洲

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