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AZD 3965

  • 產(chǎn)品貨號:CS-01Y74736
  • 產(chǎn)品價格:電議
  • 產(chǎn)品產(chǎn)地:進口、國產(chǎn)
  • 包裝類型:2mg 5mg 10mg 50mg 100mg
  • 采購熱度:225
  • 庫存:100
  • CAS號:1448671-31-5
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C21H24F3N5O5S
  • 分子量:515.5

簡介內(nèi)容:質(zhì)量保證、價格優(yōu)惠

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標簽:AZD 3965 

產(chǎn)品目錄

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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(zhì):                                                                                                             

規(guī)格

2mg 5mg 10mg 50mg 100mg

CAS

1448671-31-5

別名

N/A

化學名

5-[[(4S)-4-hydroxy-4-methyl-2-isoxazolidinyl]carbonyl]-3-methyl-1-(1-methylethyl)-6-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]methyl]-thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

分子式

C21H24F3N5O5S

分子量

515.5

溶解度

51.6mg/mL in EtOH, 51.5mg/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(chǎn)品描述:                                                                                                            

Ki = 1.6 nM for MCT1

AZD 3965 is a potent inhibitor of monocarboxylate transporter 1 (MCT1).

Inhibition of monocarboxylate transporter 1 (MCT1) is currently considered as a promosing therapeutic way to block lactate shuttling in tumor cells lacking monocarboxylate transporter 4.

In vitro: Previous study found that the in-vitro AZD3965 sensitivity varied and was highest in hypoxia. To further support that AZD3965 targeted MCT1, NCIH1048 cells were engineered to inducibly overexpress MCT1. It was found that when MCT1 was overexpressed, the EC50 of AZD 3965 against NCI-H1048 was increased from 0.14 to 10.5 nM, which was consistent with AZD3965 acting through MCT1 inhibition [1].

In vivo: COR-L103 xenograft studies were conducted to test whether the in-vitro effect of AZD3965 could be recapitulated in vivo. COR-L103 tumor-bearing mice were treated with AZD3965 at 100 mg/kg BID for 21 days. The pharmacokinetic analyses showed that AZD3965 at 100 mg/kg BID led to free concentrations of AZD3965 predicted to inhibit lactate transport. Moreover, AZD3965 treatment was able to reduce the growth of CORL103 tumors significantly, though tumor regression was not observed, which was consistent with AZD3965 only targeting the hypoxic fraction of the tumor [1].

Clinical trial: A phase I trial of AZD3965 in patients with advanced cancer is currently recruiting participants [2].

特別提醒:                                                                                                              

1. 本產(chǎn)品僅供科研使用。請勿用于醫(yī)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(qū)。

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(chuàng)作者:上海莼試生物技術(shù)有限公司

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