Ambeed.cn

首页 / / / ATP柠檬酸裂解酶 / NDI-091143

NDI-091143 {[allProObj[0].p_purity_real_show]}

货号:A1194991

NDI-091143 is a small-molecule inhibitor of human ACLY. It is located in an allosteric, mostly hydrophobic cavity next to the citrate-binding site, and requires extensive conformational changes in the enzyme that indirectly disrupt citrate binding.

NDI-091143 化学结构 CAS号:2375840-87-0
NDI-091143 化学结构
CAS号:2375840-87-0
NDI-091143 3D分子结构
CAS号:2375840-87-0
NDI-091143 化学结构 CAS号:2375840-87-0
NDI-091143 3D分子结构 CAS号:2375840-87-0
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]}

{[ getRatePrice(item.pr_rmb, 1,1) ]}

{[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]}
{[ getRatePrice(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_am, item.pr_size) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} 现货 咨询 - +
购物车0 收藏 询单

NDI-091143 纯度/质量文件 产品仅供科研

货号:A1194991 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

全球学术期刊中引用的产品

Nat. Biomed. Eng., 2024, 8, 1412-1424. Ambeed. [ A538667 , A631746 ]
JMC, 2024. Ambeed. [ A833302 , A475501 , A341986 , A356070 ]
BMC Cancer, 2024, 24(1): 1415. Ambeed. [ A809692 , A209020 ]
J. Am. Soc. Mass Spectrom., 2024, 35(12): 3192-3202. Ambeed. [ A166127 , A902473 , A753371 , A961334 , A292945 , A230770 , A300620 , A1114580 , A1159765 , A206238 ]
PloS One, 2024, 19(11): e0308060. Ambeed. [ A302917 ]
更多 >

NDI-091143 生物活性

描述 ATP-citrate lyase (ACLY) connects glucose and lipid metabolism, converting a metabolite derived from glycolysis (citrate) to a substrate (acetyl-CoA) for the biosynthesis of fatty acids and cholesterol. Cancer cells that have high aerobic glycolysis are especially susceptible to ACLY inhibition, and ACLY is overexpressed and correlated with poor prognosis in several types of cancer. NDI-091143 is a potent human ACLY inhibitor[1]. It showed excellent nanomolar potency in the inhibition of human ACLY (IC50 values ranging from 2.1 to 4.8 nM depending on the enzymatic assay employed) and proved to be competitive with the substrate citrate (Ki value of 7.0 nM)[2].
作用机制 NDI-091143 is located in an allosteric, mostly hydrophobic cavity next to the citrate-binding site, and requires extensive conformational changes in the enzyme that indirectly disrupt citrate binding[1].

NDI-091143 参考文献

[1]An allosteric mechanism for potent inhibition of human ATP-citrate lyase

[2]Granchi C. Discovery of Allosteric Inhibition of Human ATP-Citrate Lyase. Trends Pharmacol Sci. 2019;40(6):364-366.

NDI-091143 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.20mL

0.44mL

0.22mL

11.02mL

2.20mL

1.10mL

22.03mL

4.41mL

2.20mL

NDI-091143 技术信息

CAS号2375840-87-0
分子式C20H14ClF2NO5S
分子量 453.844
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Room temperature

溶解度

DMSO: 105 mg/mL(231.36 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
Ambeed 相关网站 Ambeed.cn Ambeed.com
Ambeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    Ambeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。