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  • T81175SETD7-IN-1;化合物 SETD7-IN-1SETD7-IN-1

    SETD7-IN-1 (compound 7), a PFI-2 analogue, acts as both a substrate and inhibitor of histone lysine methyltransferase SETD7, exhibiting an inhibitory concentration (IC50) of 0.96 ± 0.10 ?M [1].

    价 格:¥电议型 号:T81175产 地:中国大陆

  • T81174Setoxaximab;化合物 SetoxaximabSetoxaximab

    Setoxaximab is a chimeric humanized antibody of the IgG1-κ isotype that specifically targets Shiga toxin type 1 (Stx1).

    价 格:¥电议型 号:T81174产 地:中国大陆

  • T81173Setrusumab;化合物 SetrusumabBPS 804;BPS 804

    Setrusumab (BPS 804) is a fully humanized monoclonal antibody targeting sclerostin, effectively enhancing bone strength. It is utilized in research on Osteogenesis Imperfecta (OI) and cancer [1].

    价 格:¥电议型 号:T81173产 地:中国大陆

  • T81172Sex Pheromone Inhibitor iPD1;化合物 Sex Pheromone Inhibitor iPD1Sex Pheromone Inhibitor iPD1

    Sex Pheromone Inhibitor iPD1 is a compound that functions as an inhibitor of the sex pheromone cPD1 [1].

    价 格:¥电议型 号:T81172产 地:中国大陆

  • T81171SH491;化合物 SH491SH491

    SH491 (Compound 33) serves as an antiosteoporosis agent, effectively inhibiting RANKL-induced osteoclast differentiation in bone-marrow-derived monocytes (BMMs) with an IC50 of 11.8 nM. Additionally, SH491 suppresses the expression of genes and proteins related to osteoclastogenesis, specifically TRAP, CTSK, MMP-9, and ATPase v0d2 [1].

    价 格:¥电议型 号:T81171产 地:中国大陆

  • T81170Shishijimicin A;化合物 Shishijimicin AShishijimicin A

    Shishijimicin A, a novel antitumor agent isolated from the ascidian Didemnum proliferum, exhibits highly potent cytotoxicities and demonstrates considerable anti-tumor activity [1] [2]. This compound also serves as a click chemistry reagent due to its alkyne group, enabling it to partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules.

    价 格:¥电议型 号:T81170产 地:中国大陆

  • T81169Shishijimicin B;化合物 Shishijimicin BShishijimicin B

    Shishijimicin B, an enediyne class compound, exhibits extremely potent cytotoxicity, with IC50 values ranging from 2.0-3.3 nM. This compound has been noted for its antitumor activity, making it valuable for cancer research [1]. Additionally, Shishijimicin B serves as a click chemistry reagent due to its Alkyne group, allowing for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Azide-containing molecules.

    价 格:¥电议型 号:T81169产 地:中国大陆

  • T81168Shishijimicin C;化合物 Shishijimicin CShishijimicin C

    Shishijimicin C, a novel antitumor agent isolated from the ascidian Didemnum proliferum, exhibits highly potent cytotoxicities and anti-tumor activities. This compound also serves as a click chemistry reagent, featuring an alkyne group that can partake in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules.

    价 格:¥电议型 号:T81168产 地:中国大陆

  • T81167Shizukanolide;化合物 ShizukanolideShizukanolide

    Shizukanolide, a sesquiterpene lactone extracted from Chloranthus japonicus (Chloranthaceae), has a dehydro derivative that exhibits moderate antifungal activity [1].

    价 格:¥电议型 号:T81167产 地:中国大陆

  • T81166Shizukaol G;化合物 Shizukaol GShizukaol G

    Shizukaol G, a dimeric sesquiterpene, can be isolated from the roots of Chloranthus japonicus [1].

    价 格:¥电议型 号:T81166产 地:中国大陆

  • T81165SHP2-IN-17;化合物 SHP2-IN-17SHP2-IN-17

    SHP2-IN-17 (compound 192) is a potent inhibitor of SHP2, exhibiting an IC50 of 2 nM and holds potential for use in glioblastoma research [1].

    价 格:¥电议型 号:T81165产 地:中国大陆

  • T81164SHP2-IN-18;化合物 SHP2-IN-18SHP2-IN-18

    SHP2-IN-18 (compound 183) is a potent SHP2 inhibitor, exhibiting an IC50 of 3 nM and applicable to glioblastoma research [1].

    价 格:¥电议型 号:T81164产 地:中国大陆

  • T81163SHP2-IN-19;化合物 SHP2-IN-19SHP2-IN-19

    SHP2-IN-19 (compound 183) is a SHP2 inhibitor exhibiting potent activity with an IC50 of 3 nM, and is utilized in glioblastoma research [1].

    价 格:¥电议型 号:T81163产 地:中国大陆

  • T81162SHP2-IN-20;化合物 SHP2-IN-20SHP2-IN-20

    SHP2-IN-20 (compound 193), a potent SHP2 inhibitor, exhibits an IC50 of 3 nM, making it suitable for glioblastoma research [1].

    价 格:¥电议型 号:T81162产 地:中国大陆

  • T81161SHP2-IN-21;化合物 SHP2-IN-21SHP2-IN-21

    SHP2-IN-21 (compound 208) is an inhibitor of SHP2, exhibiting an IC50 of 3 nM, and is utilized in glioblastoma research [1].

    价 格:¥电议型 号:T81161产 地:中国大陆

  • T81160Sialyllacto-N-tetraose b;化合物 Sialyllacto-N-tetraose bSialyllacto-N-tetraose b

    Sialyllacto-N-tetraose b, a sialylated oligosaccharide, naturally occurs in mammalian milk [1].

    价 格:¥电议型 号:T81160产 地:中国大陆

  • T8116Azulene;甘菊蓝Bicyclo[5.3.0]Decapentaene;甘菊蓝|||奥苷菊环|||Bicyclo[5.3.0]Decapentaene

    Azulene (Bicyclo[5.3.0]Decapentaene) is a natural product.

    价 格:¥电议型 号:T8116产 地:中国大陆

  • T81159Sibiricine;化合物 SibiricineSibiricine

    Sibiricine (Compound 8), an isoquinoline alkaloid extracted from the medicinal plant Corydalis crispa, exhibits substantial anti-inflammatory effects by inhibiting TNF-α production in LPS-activated THP-1 cells [1].

    价 格:¥电议型 号:T81159产 地:中国大陆

  • T81158Siderin;化合物 SiderinSiderin

    Siderin, a Photosystem II inhibitor, effectively impedes ATP synthesis and chloroplast electron transport in photosynthesis within isolated spinach chloroplasts and is utilized in research on plant photosynthesis [1].

    价 格:¥电议型 号:T81158产 地:中国大陆

  • T81157SIGSLAK;化合物 SIGSLAKSIGSLAK

    SIGSLAK comprises the active site analogous to that of Escherichia coli (E. coli) penicillin-binding protein 1b (PBP 1b) [1].

    价 格:¥电议型 号:T81157产 地:中国大陆

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