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  • T16350NSC-87877

    NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50=0.318 μM, 0.355 μM of shp2 and shp1, respectively).It also inhibits dual-specificity phosphatase 26 (DUSP26).

    价 格:¥电议型 号:T16350产 地:中国大陆

  • T1635FenchlorphosDermafos;Ronnel;皮蝇磷

    Fenchlorphos is a cholinesterase inhibitor, used as an insecticide.

    价 格:¥电议型 号:T1635产 地:中国大陆

  • T15635JZP-430

    JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).

    价 格:¥电议型 号:T15635产 地:中国大陆

  • T14635Bis-PEG3-NHS ester

    Bis-PEG3-NHS ester is a nonclaevable 3-unit PEG linker for antibody-drug-conjugation (ADC).

    价 格:¥电议型 号:T14635产 地:中国大陆

  • T11339Furegrelate sodiumU-63557A

    Furegelate sodium is a selective thromboxane synthase inhibitor with oral activity. Furegrelate sodium inhibits thromboxane A2 (TXA2) synthase in human platelet microsomes with an IC50 of 15 nM.

    价 格:¥电议型 号:T11339产 地:中国大陆

  • T0932CefiximeFK-027;Cefspan;FR-17027;Cephoral;Cefiximum;CL-284635;头孢克肟

    Cefixime is a broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell

    价 格:¥电议型 号:T0932产 地:中国大陆

  • T0635p-(2-Methoxyethyl) phenol

    p-(2-Methoxyethyl) phenol, an important kind of pharmaceutical intermediates, is primarily used in the synthesis of metoprolol which is effective drugs in the therapy of cardiovascular disease.

    价 格:¥电议型 号:T0635产 地:中国大陆

  • T0466CelecoxibSC 58635;塞来西布;塞来昔布

    Celecoxib is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of celecoxib is as a Cyclooxygenase Inhibitor.

    价 格:¥电议型 号:T0466产 地:中国大陆

  • T0466CelecoxibCelecoxib,SC 58635,

    Celecoxib is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of celecoxib is as a Cyclooxygenase Inhibitor.

    价 格:¥电议型 号:T0466产 地:美洲

  • T0635p-(2-Methoxyethyl) phenolp-(2-Methoxyethyl) phenol

    p-(2-Methoxyethyl) phenol, an important kind of pharmaceutical intermediates, is primarily used in the synthesis of metoprolol which is effective drugs in the therapy of cardiovascular disease.

    价 格:¥电议型 号:T0635产 地:美洲

  • T0932CefiximeCefixime,CL-284635,FK-027

    Cefixime is a broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell

    价 格:¥电议型 号:T0932产 地:美洲

  • T11339Furegrelate sodiumFuregrelate sodium,U-63557A,

    Furegrelate Sodium inhibits human platelet microsomal thromboxane A2 (TxA2) synthase with an IC50 of 15 nM. Furegrelate Sodium is being developed as an antiplatelet agent.Furegrelate Sodium is a potent, orally available, and selective thromboxane synthas

    价 格:¥电议型 号:T11339产 地:美洲

  • T13635D-(+)-MelezitoseD-(+)-Melezitose,(+)-Melezitose,D-Melezitose

    D-(+)-Melezitose can be used to identify indole-positive and indole-negative Klebsiella clinical isolates.

    价 格:¥电议型 号:T13635产 地:美洲

  • T15635JZP-430JZP-430

    JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).

    价 格:¥电议型 号:T15635产 地:美洲

  • T16350NSC-87877NSC-87877

    NSC-87877 also inhibits dual-specificity phosphatase 26 (DUSP26). NSC-87877 is an effective inhibitor of Shp2 and Shp1 protein tyrosine phosphatases (IC50: 0.318 μM, 0.355 μM shp2 and shp1, respectively).

    价 格:¥电议型 号:T16350产 地:美洲

  • T16351NSC16168NSC16168

    NSC16168 inhibits DNA repair and potentiates CDDP efficacy in cancer. NSC16168 is a specific ERCC1-XPF inhibitor (IC50: 0.42 μM).

    价 格:¥电议型 号:T16351产 地:美洲

  • T16352NSC23925NSC23925

    NSC23925 is a selective and effective inhibitor of P-glycoprotein (Pgp).

    价 格:¥电议型 号:T16352产 地:美洲

  • T16355NSC781406NSC781406

    NSC781406 is a highly effective inhibitor of PI3K and mTOR (IC50: 2 nM for PI3Kα).

    价 格:¥电议型 号:T16355产 地:美洲

  • T16356Glyoxalic acidGlyoxalic acid,NSC 27785,Formylformic acid

    Glyoxalic acid is an organic compound. It is both an aldehyde and a carboxylic acid.

    价 格:¥电议型 号:T16356产 地:美洲

  • T16357NSC 663284NSC 663284,DA-3003-1,

    NSC 663284 is a cell-permeable and irreversible Cdc25 dual specificity phosphatase inhibitor (IC50 for Cdc25B2: 0.21 μM). NSC 663284 inhibits NSD2 (IC50 of 170 nM) through direct interaction with the catalytic SET domain (Kd of 370 nM). NSC 663284 display

    价 格:¥电议型 号:T16357产 地:美洲

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