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  • T76111Hexokinase (ScHEX1);化合物 Hexokinase (ScHEX1)Hexokinase (ScHEX1)

    Hexokinase (ScHEX1), a glycolytic enzyme, is inhibited by n-acetylglucosamine, which causes it to detach from the mitochondrial outer membrane. This detachment activates the NLRP3 inflammasome [1].

    价 格:¥电议型 号:T76111产 地:中国大陆

  • T76110β-Glucosidase;化合物 β-Glucosidaseβ-Glucosidase

    β-Glucosidase, a pivotal enzyme in cellulose degradation, belongs to the extensive family of glycoside hydrolases. It plays a crucial role in breaking down cellulose in soils and holds promise for assessing biological soil quality [1] [2] [3].

    价 格:¥电议型 号:T76110产 地:中国大陆

  • T7611ODM-203;化合物ODM-203ODM-203

    ODM-203, a Selective Inhibitor of FGFR and VEGFR, Shows Strong Antitumor Activity, and Induces Antitumor Immunity

    价 格:¥电议型 号:T7611产 地:中国大陆

  • T75611Tibesaikosaponin V;化合物 Tibesaikosaponin VTibesaikosaponin V

    Tibesaikosaponin V (TKV), a triterpene diglycoside isolated from the methanol extract of Bupleurum chinense DC roots, effectively inhibits lipid accumulation and triacylglycerol content in adipocytes without inducing cytotoxicity. It suppresses mRNA expression of nuclear transcription factors, including peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT/enhancer binding protein α (C/EBPα), and impedes 3T3-L1 preadipocyte differentiation. Considering these properties, Tibesaikosaponin

    价 格:¥电议型 号:T75611产 地:中国大陆

  • T74611EphA2 agonist 1;化合物 EphA2 agonist 1EphA2 agonist 1

    EphA2 Agonist 1 (Compound 7bg) is a potent and selective EphA2 receptor agonist, demonstrating significant efficacy in targeting overexpressed EphA2 glioblastoma cells and inducing EphA2 phosphorylation [1].

    价 格:¥电议型 号:T74611产 地:中国大陆

  • T74513RPR103611;化合物 RPR103611RPR103611

    RPR103611, a derivative of betulinic acid, serves as an effective inhibitor of HIV-1 entry, exhibiting IC50 values of 80, 0.27, and 0.17 for CCR5-tropic virus YU2, CXCR4-tropic virus NL4-3, and dual-tropic virus 89.6, respectively [1].

    价 格:¥电议型 号:T74513产 地:中国大陆

  • T73611Kallikrein;化合物 KallikreinKallikrein

    Kallikrein is capable of forming the kallikrenase kalinin system (KKS) in plasma and tissues, producing bradykinin and kalin peptides , respectively [1] .

    价 格:¥电议型 号:T73611产 地:中国大陆

  • T73220RO5461111;化合物 RO5461111RO5461111

    RO5461111, a highly specific and orally active Cathepsin S antagonist, exhibits potent inhibitory effects with IC50 values of 0.4 nM (human Cathepsin S) and 0.5 nM (murine Cathepsin S), respectively. It effectively suppresses the activation of antigen-specific T cells and B cells, and can ameliorate pulmonary inflammation and lupus nephritis.

    价 格:¥电议型 号:T73220产 地:中国大陆

  • T72611GLP-1R agonist 17;化合物 GLP-1R agonist 17GLP-1R agonist 17

    GLP-1R agonist 17 is a potent GLP-1 receptor agonist that demonstrates excellent efficacy in activating a GLP-1 receptor. It is primarily utilized in the research of cardiovascular metabolic diseases.

    价 格:¥电议型 号:T72611产 地:中国大陆

  • T72241Teslexivir hydrochloride;化合物 Teslexivir hydrochlorideBTA074 hydrochloride ; AP 611074 hydrochloride

    Teslexivir hydrochloride (BTA074) is a potent antiviral agent that serves as a selective inhibitor of the E1 and E2 viral proteins´ interaction, a crucial step for DNA replication and viral production in Human Papilloma Virus (HPV) types 6 and 11. This compound is utilized in research on condyloma.

    价 格:¥电议型 号:T72241产 地:中国大陆

  • T71611αSyn-IN-576755;化合物 αSyn-IN-576755αSyn-IN-576755

    αSyn-IN-576755 is a novel inhibitor of αSyn fibrillization, blocking fibril growth and suppressing A53T αSyn neurotoxicity.

    价 格:¥电议型 号:T71611产 地:中国大陆

  • T71603MV061194;化合物 MV061194MV061194

    MV061194 is a potent and selective cathepsin K (Cat K) inhibitor.

    价 格:¥电议型 号:T71603产 地:中国大陆

  • T71521NK-611 free acid;化合物 NK-611 free acidNK-611 free acid

    NK-611 free acid is a new semisynthetic analogue of etoposide, which presumably also acts through inhibition of topoisomerase II, and has been found to be more potent against several cancer cell lines in vitro than etoposide.

    价 格:¥电议型 号:T71521产 地:中国大陆

  • T70611ATSP-7041;化合物 ATSP-7041ATSP-7041

    ATSP-7041 is a novel potent and selective dual inhibitor of mdm2 (ki = 0.9 nm) and mdmx (ki = 7 nm)

    价 格:¥电议型 号:T70611产 地:中国大陆

  • T69800T-3861174;化合物 T-3861174T-3861174

    T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in vitro anti-tumor activity with GCN2-ATF4 pathway activation.

    价 格:¥电议型 号:T69800产 地:中国大陆

  • T69611R-(+)-EU-1180-453;化合物 R-(+)-EU-1180-453R-(+)-EU-1180-453

    R-(+)-EU-1180-453 is a useful organic compound for research related to life sciences. The catalog number is T69611 and the CAS number is 2488764-06-1.

    价 格:¥电议型 号:T69611产 地:中国大陆

  • T69390T-0902611 benzenesulfonate;化合物 T-0902611 benzenesulfonateT-0902611 benzenesulfonate

    T-0902611 benzenesulfonate is a cytomegalovirus replication inhibitor that may be useful in the treatment of cytomegalovirus infections.

    价 格:¥电议型 号:T69390产 地:中国大陆

  • T69349HPR-611;化合物 HPR-611HPR-611

    HPR-611 is a potent inhibitor of anaphylactic chemical mediator release.

    价 格:¥电议型 号:T69349产 地:中国大陆

  • T68611GW837016X;化合物 GW837016XGW837016X

    GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation. GW837016X extended life of treated mice by 50%, compared to untreated controls. At the cellular level, GW837016X inhibited mitosis and cytokinesis in T. brucei.

    价 格:¥电议型 号:T68611产 地:中国大陆

  • T676114-Morpholinopicolinic acid;化合物 4-Morpholinopicolinic acid4-Morpholinopicolinic acid

    4-Morpholinopicolinic acid is a useful organic compound for research related to life sciences. The catalog number is T67611 and the CAS number is 66933-68-4.

    价 格:¥电议型 号:T67611产 地:中国大陆

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