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目錄:MedChemExpress LLC>>天然產物>> Tacrolimus | MedChemExpress

Tacrolimus | MedChemExpress
  • Tacrolimus | MedChemExpress
參考價 312
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參考價 312
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更新時間:2023-09-28 14:45:39瀏覽次數:230評價

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CAS 104987-11-3 純度 99.93%
分子量 804.02 分子式 C??H??NO??
供貨周期 現貨 規格 5 mg
貨號 HY-13756 應用領域 醫療衛生,化工,生物產業,制藥/生物制藥
Tacrolimus (FK506),大環內酯類,與 FK506 結合蛋白 (<b>FKBP</b>) 結合形成復合物并抑制鈣調神經磷酸酶 (<b>calcineurin phosphatase</b>),從而抑制 T 淋巴細胞信號轉導和 IL-2 轉錄。具有強免疫抑制特性。

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Tacrolimus

CAS No. : 104987-11-3

MCE 國際站:Tacrolimus

產品活性:Tacrolimus (FK506),大環內酯類,與 FK506 結合蛋白 (FKBP) 結合形成復合物并抑制鈣調神經磷酸酶 (calcineurin phosphatase),從而抑制 T 淋巴細胞信號轉導和 IL-2 轉錄。具有強免疫抑制特性。

研究領域:Metabolic Enzyme/Protease  |  Autophagy  |  Apoptosis  |  Immunology/Inflammation  |  Anti-infection

作用靶點:Phosphatase  |  FKBP  |  Bacterial  |  Autophagy  |  Antibiotic

結構分類:抗生素  |  疾病研究  |  抗炎/免疫調劑  |  抗生素  |  大環內脂類  |  結構分類

In Vitro: Tacrolimus (FK506) inhibits calcium-dependent events, such as IL-2 gene transcription, NO synthase activation, cell degranulation, and apoptosis. Tacrolimus also potentiates the actions of glucocorticoids and progesterone by binding to FKBPs contained within the hormone receptor complex, preventing degradation. The agent may enhance expression of the TGFβ-1 gene in a fashion analogous to that demonstrated for CsA. T cell proliferation in response to ligation of the T cell receptor is inhibited by Tacrolimus. Treatment with a low concentration of Tacrolimus (FK506,10 μg/L) does not significantly affect the proliferation of MH3924A cells (P=0.135). Upon treatment with higher concentrations of Tacrolimus (100-1,000 μg/L), the proliferation of MH3924A cells is significantly enhanced (P<0.01). Treatment with AMD3100 at any concentration (10, 50 or 100 μg/L), has no obvious effect on MH3924A cell proliferation (P>0.05). However, when different concentrations of AMD3100 are combined with 100 μg/L Tacrolimus, the in vitro proliferation of MH3924A cells is increased (P<0.01).

In Vivo: The therapeutic effect of Tacrolimus is investigated on progression and perpetuation of colitis by administering Tacrolimus to Dextran sulfate sodium (DSS)-treated mice from Days 10 to 16 or to 23. At Days 17 and 24, colon length is significantly shortened, and colon weight is significantly higher in DSS-treated control animals than in normal animals. In addition, colon weight per unit length in the control group is more than twice that in the normal group. While both 7 and 14 d treatment with Tacrolimus significantly suppresses increases in colon weight per unit length in DSS-treated animals compared with the control group, this treatment does not actually restore the colon shortening. In addition, this inhibitory effect of Tacrolimus on increases in colon weight per unit length is more pronounced with 14-d than 7-d treatment, as shown by the inhibitory percentages (59% vs. 28%).

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