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  • T39280Nitrofen

    Nitrofen is a selective contact herbicide. Nitrofen is a retinal dehydrogenase and protoporphyrinogen oxidase inhibitor [1] [2] .

    价 格:¥电议型 号:T39280产 地:中国大陆

  • T3928Neoliquiritin

    Neoliquiritin may possess ytotoxiciy and Tumor-specificity.

    价 格:¥电议型 号:T3928产 地:中国大陆

  • T39275BefotertinibD-0316;Befotertinib

    Befotertinib (D-0316) is the third-generation EGFR tyrosine kinase inhibitor. Befotertinib can be used for the research of EGFR T790M-positive non-small cell lung cancer (NSCLC).

    价 格:¥电议型 号:T39275产 地:中国大陆

  • T3927Phellopterin

    Phellopterin is a partial agonist of the central benzodiazepine receptors in vitro. Phellopterin shows a cytotoxic effect on RAW264.7 cell at the concentration from 40 to 400 μM. Phellopterin reduce TNF-alpha-induced VCAM-1 expression through regulation o

    价 格:¥电议型 号:T3927产 地:中国大陆

  • T39268Azido-PEG4-azideAzido-PEG4-azide

    Azido-PEG4-azide is a PEG-based PROTAC linker that can be used to synthesize PROTACs.

    价 格:¥电议型 号:T39268产 地:中国大陆

  • T39262LBIM-23190 aceate

    BIM-23190 aceate, a somatostatin analog, a selective agonist of SSTR2 and SSTR5. BIM-23190 can be used in cancer and acromegaly studies.

    价 格:¥电议型 号:T39262L产 地:中国大陆

  • T3926EchinatinRetrochalcone;刺甘草查尔酮

    Echinatin disturb the mitochondrial energy transfer reactions and membrane permeability, at a low concentration cause deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria, inhibits DNP-ATPase activity while

    价 格:¥电议型 号:T3926产 地:中国大陆

  • T39250Bevurogant

    Bevurogant is a retinoid-related orphan receptor-gamma t (RORγt) antagonist. Bevurogant can be used for the research of chronic inflammatory diseases.

    价 格:¥电议型 号:T39250产 地:中国大陆

  • T3925Astragaloside I黄芪皂苷I;Cyclosieversioside B;Astrasieversianin IV

    Astragaloside I is a natural product isolated from Astragalus.

    价 格:¥电议型 号:T3925产 地:中国大陆

  • T3924Astragaloside IIAstrasieversianin VIII;黄芪皂苷 II

    Astragaloside II is an effective MDR reversal agent and may be a potential adjunctive agent for hepatic cancer chemotherapy. Astragaloside II also induces osteogenic activities, differentiation, proliferation, and mineralization, through the bone morphoge

    价 格:¥电议型 号:T3924产 地:中国大陆

  • T39233SIRT7 inhibitor 97491

    SIRT7 inhibitor 97491 is an HDAC inhibitor with high specificity for SIRT7 (IC50 = 325 nM). SIRT7 inhibitor 97491 promotes apoptosis through caspase pathway.

    价 格:¥电议型 号:T39233产 地:中国大陆

  • T3921Punicalagin安石榴甙;安石榴苷

    Punicalagin is a major ellagitannin found in pomegranates that is reported to produce antioxidant, anti-inflammatory, and anticancer effects. It has been shown to prevent high-fat diet-induced obesity-associated accumulation of cardiac triglyceride and ch

    价 格:¥电议型 号:T3921产 地:中国大陆

  • T39202CZC-54252 hydrochloride

    CZC-54252 hydrochloride is a potent and selective LRRK2 inhibitor with IC 50 s of 1.28 nM and 1.85 nM for wild-type and G2019S LRRK2 , respectively. G2019S LRRK2 -induced human neuronal injury is attenuated by CZC-54252 hydrochloride with an EC 50 of ~1 n

    价 格:¥电议型 号:T39202产 地:中国大陆

  • T3920Pseudoginsenoside F11Ginsenoside A1;拟人参皂苷 F11;拟人参皂苷F11

    Pseudoginsenoside-F11 is a component of Panax quinquefolium (American ginseng), can antagonize the learning and memory deficits induced by scopolamine, morphine, and methamphetamine in mice.

    价 格:¥电议型 号:T3920产 地:中国大陆

  • T3892IsoacteosideIsoverbascoside;异麦角甾苷

    Isoacteoside has the anti-inflammatory effect, mediated by action on caspase-1, mitogen-activated protein kinases (c-Jun N-terminal kinase, p38, extracellular signal-regulated protein kinase) and nuclear factor-kappa B pathways.

    价 格:¥电议型 号:T3892产 地:中国大陆

  • T38192Unifiram

    Unifiram is a cognition-enhancer. Unifiram induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the rat hippocampal CA1 region (EC50= 27 nM) and increases acetylcholine (ACh) release in the rat cerebral

    价 格:¥电议型 号:T38192产 地:中国大陆

  • T3792Ajugol益母草苷;益母草苷A;Leonuride

    Ajugol shows some trypanocidal potential against Trypanosoma brucei rhodesiense (IC50 values 29.3–73.0 ug/ml).

    价 格:¥电议型 号:T3792产 地:中国大陆

  • T37792A2A receptor antagonist 1A2A receptor antagonist 1

    A2A receptor antagonist 1 is an antagonist of both adenosine A2A receptor and A1 receptor with Kis of 4 and 264 nM, respectively.

    价 格:¥电议型 号:T37792产 地:中国大陆

  • T37292M62812M62812

    TLR4 inhibitor. Inhibits LPS-induced NF-κB activation in HEK293 cells (IC50 = 2.4 μg/mL). Also inhibits LPS-induced cytokine production and procoagulant effects in PBMCs and HUVECs. Prolongs survival in a mouse septic shock model.

    价 格:¥电议型 号:T37292产 地:中国大陆

  • T3692GNE-477GNE 477

    GNE-477 is a potent and efficacious dual PI3K/mTOR inhibitor.

    价 格:¥电议型 号:T3692产 地:中国大陆

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