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  • T10578BO-264BO-264

    BO-264 is a highly potent and orally active inhibitor of transforming acidic coiled-coil 3 (TACC3; IC50: 188 nM; Kd: 1.5 nM) with broad-spectrum antitumor activity.

    价 格:¥电议型 号:T10578产 地:美洲

  • T1058CarboplatinCarboplatin,NSC 241240,JM-8

    Carboplatin is an organoplatinum compound that possesses antineoplastic activity.

    价 格:¥电议型 号:T1058产 地:美洲

  • T10580BOC-D-FMKBOC-D-FMK

    Boc-D-FMK is an irreversible, cell-permeable, and broad-spectrum caspase inhibitor and inhibits apoptosis stimulated by TNF-α (IC50: 39 ?M).

    价 格:¥电议型 号:T10580产 地:美洲

  • T10582BorrelidinBorrelidin,Treponemycin,

    Borrelidin (Treponemycin) is a bacterial and eukaryal threonyl-tRNA synthetase inhibitor. It is a macrolide antibiotic isolated from Streptomyces rochei.

    价 格:¥电议型 号:T10582产 地:美洲

  • T10584Bovinic acidBovinic acid

    Bovinic acid is a conjugated linoleic acid with anti-atherogenic and anticarcinogenic activities.

    价 格:¥电议型 号:T10584产 地:美洲

  • T10585BozitinibBozitinib,PLB-1001,CBT-101

    Bozitinib (PLB-1001) is a highly selective inhibitor of the c-MET kinase with blood-brain barrier permeability. Bozitinib binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily.

    价 格:¥电议型 号:T10585产 地:美洲

  • T10716CCR7 Ligand 1CCR7 Ligand 1,CCR7-Cmp2105,

    CCR7 Ligand 1 (CCR7-Cmp2105) is an allosteric Ligand and antagonist for human CC chemokine receptor 7 (CCR7) with a Kd of 3 nM. CCR7 Ligand 1, thiadiazole-dioxide ligan, suppresses arrestin binding in response to activation by CCL19 with an IC50 of 7.3 μM

    价 格:¥电议型 号:T10716产 地:美洲

  • T1105PenfluridolPenfluridol,R-16341,TLP-607

    Penfluridol is a highly potent antipsychotic.

    价 格:¥电议型 号:T1105产 地:美洲

  • T11050DipyrocetylDipyrocetyl

    Dipyrrolidinyl is extracted from patent WO 2011132171 A1 and has anti-inflammatory and analgesic effects.

    价 格:¥电议型 号:T11050产 地:美洲

  • T11052DisitertideDisitertide,P144,

    Disitertide (P144) is an inhibitor of TGF-β1.

    价 格:¥电议型 号:T11052产 地:美洲

  • T11053DJ001DJ001

    DJ001 is a highly specific, selective and non-competitive protein tyrosine phosphatase σ (PTPσ) inhibitor with IC50 of 1.43 μM. DJ001 promotes the regeneration of hematopoietic stem cells.

    价 格:¥电议型 号:T11053产 地:美洲

  • T11054DL-NorvalineDL-Norvaline,2-Aminopentanoic acid,

    DL-Norvaline is a non-competitive inhibitor of arginase. Derivatives of L-norvaline.

    价 格:¥电议型 号:T11054产 地:美洲

  • T11055DL-TBOADL-TBOA

    DL-TBOA inhibited [14C] glutamate uptake in COS-1 cells expressing human EAAT1 and EAAT2, with Ki values of 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner, with Ki values of 4.4 μM and 3.2 μM, respectively. DL-TBOA

    价 格:¥电议型 号:T11055产 地:美洲

  • T11056DLK-IN-1DLK-IN-1

    DLK-IN-1 is a selective oral active inhibitor of bisleucine zipper kinase (DLK, MAP3K12) with Ki of 3 nM. DLK-IN-1 is active in the Alzheimer´s disease model, retains excellent CNS permeability, and after multiple days of administration, its concentration

    价 格:¥电议型 号:T11056产 地:美洲

  • T11057DM3-SMeDM3-SMe

    DM3-SMe is a maytansine derivative and tubulin inhibitor. It is a cytotoxic part of antibody-drug conjugates (ADCs) and can bind to antibodies via disulfide bonds or stable thioether bonds. DM3-SMe has high cytotoxic activity in vitro with IC50 of 0.0011

    价 格:¥电议型 号:T11057产 地:美洲

  • T11059DM4-SMeDM4-SMe

    DM4-SMe is a cytotoxic part of antibody-drug conjugates (ADCs) and a metabolite of antibody-maytansin conjugates (AMCs) and tubulin inhibitors, which can also be stabilized by disulfide bonds or thioether The bond binds to the antibody. The IC50 of DM4-SM

    价 格:¥电议型 号:T11059产 地:美洲

  • T11065DMU2105DMU2105

    DMU2105 is a potent and specific CYP1B1 inhibitor, with IC50s of 10 nM and 742 nM for CYP1B1 and CYP1A1, respectively.

    价 格:¥电议型 号:T11065产 地:美洲

  • T11477GSK1059865GSK1059865

    GSK1059865 is a potent orexin 1 receptor antagonist.

    价 格:¥电议型 号:T11477产 地:美洲

  • T13383ZamicastatZamicastat,BIA 5-1058,

    Zamicastat is an inhibitor of dopamine β-hydroxylase (DBH), and is also a concentration-dependent dual inhibitor of P-gp and BCRP(IC50 values of 73.8?μM and 17.0?μM, respectively).

    价 格:¥电议型 号:T13383产 地:美洲

  • T14116ACP-105ACP-105

    ACP-105 is a selective amd potent androgen receptor modulator (SARM). For AR wild type and T877A mutant, the pEC50s values are 9.0 and 9.3 , respectively.

    价 格:¥电议型 号:T14116产 地:美洲

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