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GSK180

  • 產品貨號:CS-01Y68835
  • 產品價格:電議
  • 產品產地:進口、國產
  • 包裝類型:5mg 25mg
  • 采購熱度:212
  • 庫存:100
  • CAS號:N/A
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C10H7Cl2NO4
  • 分子量:276.07

簡介內容:質量保證、價格優惠

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標簽:GSK180 

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商品詳情購物流程代測服務付款方式常見問題

化學性質:                                                                                                             

規格

5mg 25mg

CAS

N/A

別名

 

化學名

3-(5,6-dichloro-2-oxobenzo[d]oxazol-3(2H)-yl)propanoic acid

分子式

C10H7Cl2NO4

分子量

276.07

溶解度

27.6mg/mL in DMSO

儲存條件

Store at -20°C

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

產品描述:                                                                                                            

GSK180 is a potent, selective and competitive inhibitor of kynurenine-3-monooxygenase (KMO) with an IC50 of ~6 nM. [1]

GSK180 inhibited endogenous KMO action in primary human hepatocytes with similar potency (IC50 = 2.6 μM). GSK180 is proper for i.v. administration. GSK180 inhibited rat KMO mildly less potently than it did the human enzyme with an IC50 of 7 μM. GSK180 exhibited a concentration-dependent displacement of tryptophan from plasma proteins. [1]

GSK180 was dosed to Kmowt and Kmonull mice as a bolus injection at 30 mg/kg, which delivered plasma levels 1 h after dosage of 263 ± 98 μM and 351 ± 87 μM, respectively. GSK180 resulted in a promotion in kynurenine in Kmowt mice, but no change was detected in the Kmonull mice, which confirms that this increase results from the inhibition of KMO. GSK180 caused an evident reduction in circulating tryptophan levels in both Kmowt and Kmonull mice, suggesting that the chemical had an additional effect unrelated to KMO inhibition. GSK180 is excepted from rat erythrocytes (blood:plasma ratio of 0.46), and it is modestly bound to rat plasma proteins (free fraction 7.7% at 1 mM, n = 2), meaning that the top free drug levels in plasma (92 μM) are >12-fold above the IC50 in cells. Treatment with GSK180 resulted in a rapid promotion in the circulating levels of both kynurenine and kynurenic acid, which restablished to baseline as the drug levels dropped. The fierce inflammatory cell infiltrate in AP consisted of MPO-positive neutrophils and monocytes positive for the ED1 antigen, the rat ortholog of CD68, which were present to the same extent in the pancreas tissue of rats with induced AP and rats with induced AP treated with GSK180. [1]

特別提醒:                                                                                                              

1. 本產品僅供科研使用。請勿用于醫藥、臨床診斷或治療,食品及化妝品等用途。請勿存放于普通住宅區。

2. 為了您的安全和健康,請穿好實驗服并佩戴一次性手套和口罩操作。

原創作者:上海莼試生物技術有限公司

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