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N-(4-BUTYLPHENYL)-4-FLUOROBENZENESULFONAMIDE
化合物 DC260126
化合物 DC260126|T7127|TargetMol
价格
¥
415
¥
581
¥
1255
包装
5mg
10mg
25mg
最小起订量
1mg
发货地
上海
更新日期
2025-11-17
QQ交谈
微信洽谈
产品详情
中文名称:
化合物 DC260126
英文名称:
DC260126
CAS:
346692-04-4
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
产品类别:
抑制剂
货号:
T7127
2025-11-17
化合物 DC260126
DC260126
5mg/415RMB;10mg/581RMB;25mg/1255RMB
415
TargetMol
美国
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
抑制剂
Product Introduction
Bioactivity
名称
DC260126
描述
DC260126 is a small-molecule antagonist of FFA1 (GPR40)
动物实验
To investigate the dose-dependent effect of DC260126, nine-week-old db/db male mice were divided into four groups (n = 6/group). Mice were give vehicle (5% DMSO in PBS) or DC260126 (3, 10, 30 mg/kg) once daily by tail vein injection for 5 days. At day 5, each group of mice were fasted for 6 h and blood samples were collected from orbital venous plexus and centrifuged for serum separation. Then the concentration of serum insulin level was measured by ELISA kit following its protocol. For long term experiments, six-week-old obese db/db male mice were divided into two groups (n = 8/group) and given vehicle (5% DMSO in PBS) or DC260126 (10 mg/kg) once daily by tail vein injection for 24 days, respectively. Meanwhile, their lean littermates were treated with vehicle in an identical manner as normal control. Body weight and food intake were recorded regularly. After 6 h fasting, blood glucose concentrations were monitored by tail vein blood using a glucometer every week. At the end of the experiment, mice were fasted for 12 h to perform oral glucose tolerance test (OGTT, day 21) and for 6 h to generate insulin tolerance test (ITT, day 23) as described with slight modification indicated . Meanwhile, the insulin release during OGTT was also measured, blood sample was obtained from tail veins and serum insulin concentration was determined by ELISA kit (Alpco, USA). At the end of experiment (day 24), mice were fasted for 6 h, and blood samples were collected from orbital venous plexus and centrifuged for serum separation. Then the animals were killed by CO2 inhalation, the pancreas tissue were removed and kept in 4% paraformaldehyde[1].
体内活性
DC260126, a small molecule antagonist of GPR40, on β-cell function following administration of 10 mg/kg dose of DC260126 to obese diabetic db/db mice. Oral glucose tolerance test, glucose stimulated insulin secretion and insulin tolerance test were used to investigate the pharmacological effects of DC260126 on db/db mice after 21-days treatment. Immunohistochemistry and serum biochemical analysis were also performed. Although no significant change of blood glucose levels was found in DC260126-treated mice, DC260126 significantly inhibited glucose stimulated insulin secretion, reduced blood insulin level and improved insulin sensitivity after 3 weeks administration in db/db mice. Moreover, DC260126 reduced the proinsulin/insulin ratio and the apoptotic rate of pancreatic β-cells remarkably in DC260126-treated db/db mice compared to vehicle-treated mice (p<0.05, n = 8). Suggest that although DC260126 could not provide benefit for improving hyperglycemia, it could protect against pancreatic β-cells dysfunction through reducing overload of β-cells, and it increases insulin sensitivity possibly via alleviation of hyperinsulinemia in db/db mice[1].
存储条件
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度
DMSO : 100 mg/mL (325.33 mM), Sonication is recommended.
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 4 mg/mL (13.01 mM), Sonication is recommended.
关键字
stress | secretion | phosphorylation | insulin | Inhibitor | inhibit | GPR40 | Free Fatty Acid Receptor | FFAR | elevation | DC-260126 | DC260126 | DC 260126 | Ca2+ | Apoptosis
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L-Glutamic acid | Cysteamine hydrochloride | Alginic acid | Flubendazole | Dextran sulfate sodium salt (MW 5000) | 5-Fluorouracil | Stavudine | Tributyrin | Myricetin | L-Ascorbic acid sodium salt | L-Ascorbic acid | Sodium 4-phenylbutyrate
相关库
抑制剂库 | 经典已知活性库 | 抗癌化合物库 | 已知活性化合物库 | 含氟化合物库 | 细胞凋亡化合物库 | 内分泌激素分子库 | NO PAINS 化合物库 | GPCR靶点分子库 | 膜蛋白靶向化合物库 | 内质网应激化合物库
关键字:
DC260126|TargetMol
公司简介
TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。
成立日期
2013-04-18
(13年)
注册资本
566.265100万人民币
员工人数
100-500人
年营业额
¥ 1亿以上
主营行业
天然产物,生化试剂,分子生物学,分子砌块,生物技术服务
经营模式
贸易,工厂,试剂,定制,服务
TargetMol中国(陶术生物)
VIP
4年
公司成立:
13年
注册资本:
566.265100万人民币
企业类型:
有限责任公司(自然人投资或控股)
主营产品:
小分子抑制剂、药物筛选化合物库、药物筛选等
公司地址:
静安区江场三路238号8楼
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