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Sitagliptin
Catalog Number: E1KS4002
Amount: 200mg1​ PHYSICAL AND CHEMICAL PROPERTIES
Applications: Reactivity:
产品类型: Unconjugated
发货周期: 现货
说明书:     PDF
总价格:    211.2元
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概述
  • Catalog Number:

    E1KS4002
  • Amount:

    200mg1​ PHYSICAL AND CHEMICAL PROPERTIES

2​ Biological Activity
Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP) are important incretin hormones contributing to 50-70% of the stimulation of insulin secretion after a meal.Dipeptidyl-peptidase IV(DPP-4) inhibitors inhibit the degradation of GLP-1 and GIP as well as that of other regulatory peptides. [1]
Sitagliptin phosphate monohydrate abolished sDPP-IV effects on splenic CD4+ T-cell migration whereas incretins decreased migration of lymph node, but not splenic, CD4+ T-cells. Sitagliptin phosphate monohydrate decreases migration of splenic CD4+ T-cells through a pathway involving Rac1/VASP, whereas its inhibitory effects on the migration of lymph node CD4+ T-cells involve incretin-activation of the NF-κB pathway. [2]
It is eliminated renally, with a terminal half-life of 11.8-14.4 hours. [3]
3​ References:
[1] Gallwitz B. Drugs Today (Barc). 2007 Nov; 43(11):801-14
[2] Su-Jin Kim et al. Diabetes, 2010 July; 59(7):1739-1750
[3] Shannon A Miller et al. The Annals of Pharmacotherapy. 40(7):1336-1343
The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

2​ Biological Activity Glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP) are important incretin hormones contributing to 50-70% of the stimulation of insulin secretion after a meal.Dipeptidyl-peptidase IV(DPP-4) inhibitors inhibit the degradation of GLP-1 and GIP as well as that of other regulatory peptides. [1] Sitagliptin phosphate monohydrate abolished sDPP-IV effects on splenic CD4+ T-cell migration whereas incretins decreased migration of lymph node, but not splenic, CD4+ T-cells. Sitagliptin phosphate monohydrate decreases migration of splenic CD4+ T-cells through a pathway involving Rac1/VASP, whereas its inhibitory effects on the migration of lymph node CD4+ T-cells involve incretin-activation of the NF-κB pathway. [2] It is eliminated renally, with a terminal half-life of 11.8-14.4 hours. [3] 3​ References: [1] Gallwitz B. Drugs Today (Barc). 2007 Nov; 43(11):801-14 [2] Su-Jin Kim et al. Diabetes, 2010 July; 59(7):1739-1750 [3] Shannon A Miller et al. The Annals of Pharmacotherapy. 40(7):1336-1343 The pharmacological and toxicological properties of this product have not been fully investigated. Exercise caution in use and handling. This product must not be used in humans.

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