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  • T70708U 92032;化合物 U 92032U 92032

    U 92032 is a T-channel antagonist and antioxidant that inhibits lipid peroxidation.

    价 格:¥电议型 号:T70708产 地:中国大陆

  • T70329SH-11037;化合物 SH-11037SH-11037

    SH-11037 is a novel potent seh inhibitor, effectively blocking key angiogenic properties of human retinal endothelial cells (hrecs), inhibiting choroidal sprouting and significantly suppressing cnv lesion volume

    价 格:¥电议型 号:T70329产 地:中国大陆

  • T70328HDM-201 succinate;化合物 HDM-201 succinateHDM-201 succinate

    HDM-201 succinate is an orally bioavailable human double minute 2 homolog (HDM2) inhibitor with potential antineoplastic activity.

    价 格:¥电议型 号:T70328产 地:中国大陆

  • T70327OD38;化合物 OD38OD38

    OD38 is a novel potent and selective receptor-interacting protein kinase 2 (ripk2) inhibitor

    价 格:¥电议型 号:T70327产 地:中国大陆

  • T70326Mevidalen HBA;化合物 Mevidalen HBAMevidalen HBA

    Mevidalen, also known as LY3154207, is a novel, potent, and subtype selective human D1 positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50 = 3 nM). In contrast to orthosteric agonists, LY3154207 showed a distinct pharmacological profile without a bell-shaped dose-response relationship or tachyphylaxis in preclinical models. Identification of a crystalline form of free LY3154207 from the discovery lots was not successful. Instead, a novel cocrystal form with superi

    价 格:¥电议型 号:T70326产 地:中国大陆

  • T70325Mifanertinib;化合物 MifanertinibMifanertinib

    Mifanertinib is a potent tyrosine kinase inhibitor with antineoplastic activity [1] .

    价 格:¥电议型 号:T70325产 地:中国大陆

  • T70324EGFR-IN-557;化合物 EGFR-IN-557EGFR-IN-557

    EGFR-IN-557 is an EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis.

    价 格:¥电议型 号:T70324产 地:中国大陆

  • T70323Diethanolamine Fusidate;化合物 Diethanolamine FusidateDiethanolamine Fusidate

    Diethanolamine Fusidate is a bacteriostatic antibiotic with similar activity and better absorption after oral administration (in animals) than the sodium salt of Fusidic Acid. This product inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA.

    价 格:¥电议型 号:T70323产 地:中国大陆

  • T70322Valbenazine dihydrochloride;化合物 Valbenazine dihydrochlorideValbenazine dihydrochloride

    Valbenazine dihydrochloride inhibits vesicular monoamine transporter 2 (VMAT2); used to treat tardive dyskinesia.

    价 格:¥电议型 号:T70322产 地:中国大陆

  • T70321CBB3001;化合物 CBB3001CBB3001

    CBB3001 is a selective lysine-specific histone demethylase LSD1 inhibitor.

    价 格:¥电议型 号:T70321产 地:中国大陆

  • T70320GNLPT-IN-1;化合物 GNLPT-IN-1GNLPT-IN-1

    GNLPT-IN-1 is an inhibitor of gram-negative lipoprotein trafficking.

    价 格:¥电议型 号:T70320产 地:中国大陆

  • T7032Eupatorin;半齿泽兰素Eupatorin

    Eupatorin has antiproliferative and antiangiogenic effects. Eupatorin has antiproliferative and cytostatic effects on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism. Eupatorin-induced cell death is mediated by both the extrinsic and the intrinsic apoptotic pathways and through a mechanism dependent on reactive oxygen species generation. Eupatorin also has meaningful anti-inflammatory property.

    价 格:¥电议型 号:T7032产 地:中国大陆

  • T70093JTP 103237;化合物 JTP 103237JTP 103237

    JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.

    价 格:¥电议型 号:T70093产 地:中国大陆

  • T70087EPZ032597;化合物EPZ032597EPZ032597

    EPZ032597 is a novel selective inhibitor of SMYD2 with an IC50 of 16 nM. EPZ032597 has anticancer activity and can be used to prevent and treat pancreatic cancer.

    价 格:¥电议型 号:T70087产 地:中国大陆

  • T70032NCI-006;化合物 NCI-006NCI-006

    NCI-006 is a potent new inhibitor of lactate dehydrogenase (LDH) that disrupts tumor growth in mice. LDH inhibition slows tumor growth but rapidly redirects pyruvate to support mitochondrial metabolism. Inhibiting both mitochondrial complex 1 and LDH suppresses metabolic plasticity of glycolytic tumors in vivo, significantly prolonging tumor growth inhibition.

    价 格:¥电议型 号:T70032产 地:中国大陆

  • T7000Tiagabine hydrochloride盐酸噻加宾NO328 hydrochloride|||盐酸噻加宾|||NO050328 hydrochloride|||TGB hydrochloride

    Tiagabine hydrochloride (NO050328 hydrochloride) is the hydrochloride salt form of tiagabine, a nipecotic acid derivative with anticonvulsant property. A selective gamma-aminobutyric acid (GABA) reuptake inhibitor.

    价 格:¥电议型 号:T7000产 地:中国大陆

  • T6S0325Glycitein;黄豆黄素Glycetein;黄豆黄素|||Glycetein

    1. Gycitein has weak estrogenic activity. 2. Glycitein (Glycetein) inhibits glioma cell invasion through down-regulation of MMP-3 and MMP-9 gene expression.

    价 格:¥电议型 号:T6S0325产 地:中国大陆

  • T69645BRD20322;化合物 BRD20322BRD20322

    BRD20322 is a novel potent inhibitor of spCas9, disrupting spCas9-DNA binding and exerting dose and temporal control of spCas9 in human cell lines.

    价 格:¥电议型 号:T69645产 地:中国大陆

  • T69368GKK1032B;化合物 GKK1032BGKK1032B

    GKK1032B is a fungal metabolite that has antiproliferative and antibacterial activities. GKK1032B inhibits the growth of HeLa S3 cervical and MCF-7 breast cancer cells and Vero cells. It also inhibits the growth of B. subtilis and M. tuberculosis.

    价 格:¥电议型 号:T69368产 地:中国大陆

  • T69032Org 6582;化合物 Org 6582Org 6582

    Org 6582 inhibits 3-hydroxytryptamine reuptake.

    价 格:¥电议型 号:T69032产 地:中国大陆

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