HispidolCAS号5786-54-9
HispidolCAS号5786-54-9

Hispidol

¥1,056.00 ~¥5,853.00
1mg / 5mg / 10mg / 25mg
1mg
北京
索莱宝
2025-12-11
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产品详情
中文名称:Hispidol中文别名:Hispidol
英文名称:HispidolCAS:5786-54-9
产品分类:小分子化合物纯度:≥98%
产品编号品牌纯度规格库存价格
IH4110索莱宝≥98%1mg有现货1,056.00 元
IH4110索莱宝≥98%5mg有现货2,465.00 元
IH4110索莱宝≥98%10mg有现货3,490.00 元
IH4110索莱宝≥98%25mg有现货5,853.00 元
标准名称:毛地尔英文名称:Hispidol
CAS:5786-54-9分子式:C15H10O4
分子量:254.2375颜色与性状:
密度:沸点:
熔点:288°C水溶性:
CAS5786-54-9
英文名称Hispidol
分子式C15H10O4
分子量254.24
规格1mg ; 5mg ; 10mg ; 25mg
溶解性Soluble in DMSO ≥10mg/mL
纯度≥98%
外观(性状)Light yellow to yellow Solid
储存条件Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
运输条件冷藏运输
靶点Others
通路Others
背景说明是一种化合物,具有多种生物学或化学活性。
生物活性Hispidol ((Z)-Hispidol) is a potential therapeutic for inflammatory bowel disease; inhibits TNF-α induced adhesion of monocytes to colon epithelial cells with an IC50 of 0.50 μM.[1]
In VitroHispidol shows potent inhibitory effect (>70%) on the TNF-α-induced adhesion of monocytes to colon epithelial cells, which is one of the hallmark events leading to inflammatory bowel disease (IBD). Hispidol shows strong inhibitory activities against TNF-α-induced monocytic-colonic epithelial cell adhesion as well as LPS-induced TNF-α expression, is as an excellent candidate for IBD drug development. This inhibition of TNF-α expression by hispidol corresponds to the additional inhibitory activity against AP-1 transcriptional activity, which is another transcription factor required for high level TNF-α expression[1].
In VivoThe oral administration of hispidol suppresses significantly and dose-dependently TNBS-induced rat colitis. Oral administration of hispidol suppresses TNBS-induced colitis in a dose-dependent manner. There is a significant recovery in body weight decrease and colon tissue edematous inflammation. A higher dose (30 mg/kg) of hispidol shows a similar recovery effect to that of 300 mg/kg sulfasalazine. In the colon tissues, TNBS induces a dramatic increase in the level of MPO, a biochemical marker of inflammation, which is suppressed significantly by hispidol in a dose-dependent manner[1].
动物实验Rats: To study the effect of the drugs, hispidol (10 or 30 mg/Kg/day in corn oil) is administered orally once in a day, until 5 days after TNBS administration. The doses of 10 or 30 mg/kg are selected based on previous studies. The concentration of the compound inhibiting 70% and 90% (μM) cell-to-cell adhesion is selected and regarded as the in vivo test dose (mg/kg). Sulfasalazine (300 mg/Kg/day) is administered in corn oil as a positive control. On the 6th day, the rats are sacrificed and the severity of colitis and macroscopic ulceration are evaluated by two independent investigators who are blinded to the experiments. The colon tissues (5-7 cm proximal to rectum) are cut and used to measure the amount of myeloperoxidase and for the histological examinations[1].
数据来源文献[1]. Kadayat TM, et al. Discovery and structure-activity relationship studies of 2-benzylidene-2,3-dihydro-1H-inden-1-one and benzofuran-3(2H)-one derivatives as a novel class of potential therapeutics for inflammatory bowel disease. Eur J Med Chem. 2017 Sep 8
单位
1mM-5mg19.6665mL
1mM-1mg3.9333mL
1mM-10mg39.3329mL
5mM-1mg0.7867mL
5mM-5mg3.9333mL
5mM-10mg7.8666mL
10mM-1mg0.3933mL
10mM-5mg1.9666mL
10mM-10mg3.9333mL
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