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  • T22317DRB18DRB-18,DRB18

    DRB18 is a potent pan-class GLUT inhibitor. DRB18 alters energy-related metabolism in A549 cells by changing the abundance of metabolites in glucose-related pathways. DRB18 can eventually lead to G1/S phase arrest and increase oxidative stress and necrotic cell death and has anti-tumor activity [1].

    价 格:¥电议型 号:T22317产 地:中国大陆

  • T23426TC-A 2317 hydrochloride

    TC-A 2317 hydrochloride is an inhibitor of Aurora kinase A with a Ki of 1.2 nM compared to Aurora kinase B with a Ki of 101 nM. TC-A 2317 hydrochloride shows antitumor activity.

    价 格:¥电议型 号:T23426产 地:中国大陆

  • T23176PP 3

    PP 3 is a Negative control for the Src kinase inhibitor PP 2

    价 格:¥电议型 号:T23176产 地:中国大陆

  • T23175Potassium phosphate monobasic

    Potassium dihydrogen phosphate is a potassium salt in which dihydrogen phosphate(1-) is the counterion. It has a role as a fertilizer. It is a potassium salt and an inorganic phosphate.

    价 格:¥电议型 号:T23175产 地:中国大陆

  • T23172Polygodial水蓼二醛;Tadeonal

    Polygodial is an antifungal potentiator and an antibiotic, particularly against Saccharomyces cerevisiae, Candida utilis, and Sclerotinia libertiana.

    价 格:¥电议型 号:T23172产 地:中国大陆

  • T23171Polyinosinic-polycytidylic acidPoly(I:C);聚胞苷酸

    Poly (I:C) is a synthetic double-stranded RNA (dsRNA) analog and is an immunostimulant that acts as the most potent interferon (IFN) inducer. It also is a Toll-like receptor- 3 (TLR3) agonist.

    价 格:¥电议型 号:T23171产 地:中国大陆

  • T2317Almotriptan MalateLAS 31416;PNU180638;马来酸阿莫曲坦

    Almotriptan Malate, a selective 5-HT1B/1D receptor agonist, is used in the therapy of Migraine attacks in adults.

    价 格:¥电议型 号:T2317产 地:中国大陆

  • T12317OrelabrutinibICP-022

    Orelabrutinib is an orally active and irreversible inhibitor of Bruton´s tyrosine kinase (BTK).

    价 格:¥电议型 号:T12317产 地:中国大陆

  • T2317Almotriptan MalateAlmotriptan Malate,LAS 31416,PNU180638

    Almotriptan Malate, a selective 5-HT1B/1D receptor agonist, is used in the therapy of Migraine attacks in adults.

    价 格:¥电议型 号:T2317产 地:美洲

  • T82317GIP, rat;化合物 GIP, ratGIP, rat

    GIP (rat) (Glucose-dependent Insulinotropic Polypeptide), also known as Gastric Inhibitory Polypeptide, is a biologically active 42-amino acid peptide secreted by the K cells of the duodenum and jejunum following food consumption. It belongs to the incretin hormone peptide family, which includes GLP (Gastric-like Peptide), and it not only stimulates insulin release from pancreatic islet β-cells but also may encourage β-cell proliferation and survival. Additionally, recent research indicates GIP

    价 格:¥电议型 号:T82317产 地:中国大陆

  • T72317CEP-28122 mesylate salt;化合物 CEP-28122 mesylate saltCEP-28122 mesylate salt

    CEP-28122 mesylate salt, a diaminopyrimidine derivative, serves as a potent, selective, and orally bioavailable ALK (anaplastic lymphoma kinase) inhibitor, exhibiting an IC 50 value of 1.9 nM against recombinant ALK kinase activity. It demonstrates antitumor efficacy in ALK-positive human cancer experimental models and possesses favorable pharmacodynamic and pharmacokinetic profiles.

    价 格:¥电议型 号:T72317产 地:中国大陆

  • T62317α7 nAchR-JAK2-STAT3 agonist 1;化合物 α7 nAchR-JAK2-STAT3 agonist 1α7 nAchR-JAK2-STAT3 agonist 1

    α7 nAchR-JAK2-STAT3 agonist 1 is a potent inhibitor of the α7 nAchR-JAK2-STAT3 pathway that acts on nitric oxide (NO) (IC50: 0.32 μM). α7 nAchR-JAK2-STAT3 agonist 1 has been shown to have a positive effect on iNOS, IL-1β and IL-1β in murine macrophages RAW264.7. α7 nAchR-JAK2-STAT3 agonist 1 was effective in inhibiting the expression of iNOS, IL-1β and IL-6 in mouse macrophages. α7 nAchR-JAK2-STAT3 agonist 1 inhibited LPS-induced NO release, NF-κB activation and cytokine production. α7 nAchR-JAK

    价 格:¥电议型 号:T62317产 地:中国大陆

  • T32317Jtp 2942;化合物 T32317Jtp2942|||Jtp-2942;Jtp2942|||Jtp-2942

    Jtp 2942 is a new thyrotropin-releasing hormone analog.

    价 格:¥电议型 号:T32317产 地:中国大陆

  • T28322PD 123177;化合物 T28322PD-123177|||PD123177|||Exp-655|||Exp655|||Exp 655;PD-123177|||PD123177|||Exp-655

    PD 123177 is an inhibitor of Nonpeptide angiotensin AII-2.

    价 格:¥电议型 号:T28322产 地:中国大陆

  • T23426TC-A 2317 hydrochloride;化合物TC-A 2317 hydrochlorideTC-A 2317 hydrochloride

    TC-A 2317 hydrochloride is an inhibitor of Aurora kinase A with a Ki of 1.2 nM compared to Aurora kinase B with a Ki of 101 nM. TC-A 2317 hydrochloride shows antitumor activity.

    价 格:¥电议型 号:T23426产 地:中国大陆

  • T23179PPDA;化合物 T23179PPDA

    Subtype-selective NMDA receptor antagonist

    价 格:¥电议型 号:T23179产 地:中国大陆

  • T23177PPACK Dihydrochloride (71142-71-7 free base);化合物 T23177PPACK Dihydrochloride;PPACK Dihydrochloride

    PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective, and irreversible inhibitor of thrombin that inhibits human α-thrombin with inhibition constant (Ki: 0.24 nM).

    价 格:¥电议型 号:T23177产 地:中国大陆

  • T23176PP 3;4-氨基-1-苯基吡唑[3,4-D]嘧啶PP 3

    PP 3 is a Negative control for the Src kinase inhibitor PP 2

    价 格:¥电议型 号:T23176产 地:中国大陆

  • T23175Potassium phosphate monobasic;磷酸二氢钾Potassium phosphate monobasic

    Potassium dihydrogen phosphate is a potassium salt in which dihydrogen phosphate(1-) is the counterion. It has a role as a fertilizer. It is a potassium salt and an inorganic phosphate.

    价 格:¥电议型 号:T23175产 地:中国大陆

  • T23174Posaconazole hydrate;泊沙康唑水合物Posaconazole hydrate

    Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity. Posaconazole is a sterol C14ɑ demethylase inhibitor (IC50: 0.25 nM). Posaconazole strongly inhibits 14-alpha demethylase, a cytochrome P450-dependent enzyme.

    价 格:¥电议型 号:T23174产 地:中国大陆

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