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Ketanserin

酮色林
Catalog No.
B2248
特异性5-HT2A受体拮抗剂
组合的产品项目
规格价格库存 数量
50mg
¥ 363.00
现货
100mg
¥ 454.00
现货
500mg
¥ 1,727.00
现货

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A

背景

Selective 5-HT2A serotonin receptor antagonist; can also be used to discriminate between 5-HT1D and 5-HT1B receptor subtypes.

化学属性

Physical AppearanceA solid
StorageStore at -20°C
M.Wt395.43
Cas No.74050-98-9
FormulaC22H22FN3O3
Solubility≥39.5 mg/mL in DMSO with gentle warming; insoluble in H2O; insoluble in EtOH
Chemical Name3-[2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl]-1H-quinazoline-2,4-dione
SDFDownload SDF
Canonical SMILESC1CN(CCC1C(=O)C2=CC=C(C=C2)F)CCN3C(=O)C4=CC=CC=C4NC3=O
运输条件 蓝冰运输或根据您的需求运输。
一般建议不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

试验操作

Cell experiment:[1]

Cell lines

Isolated rat caudal artery, canine basilar, carotid, coronary and gastrosplenic arteries, and canine gastrosplenic and saphenous veins

Reaction Conditions

30 min incubation

Applications

Ketanserin dose-dependently inhibited contractile responses to 5-hydroxytryptamine (5-HT) in isolated rat caudal artery, canine basilar, carotid, coronary and gastrosplenic arteries, and canine gastrosplenic (threshold 10-10 ~ 10-9 M) and saphenous veins (threshold 10-8 M).

Animal experiment:[2]

Animal models

Spontaneously hypertensive rats, 180 ~ 240 g

Dosage form

10 mg/kg/d

Administered orally for 5 months

Applications

Ketanserin significantly decreased blood pressure and blood pressure variability, ameliorated impaired arterial baroreflex function, and significantly prevented the target organs of spontaneously hypertensive rats from being damaged.

Note

The technical data provided above is for reference only.

References:

1. Van Nueten JM, Janssen PA, Van Beek J, et al. Vascular effects of ketanserin (R 41 468), a novel antagonist of 5-HT2 serotonergic receptors. Journal of Pharmacology and Experimental Therapeutics, 1981, 218(1): 217-230.

2. Du WM, Miao CY, Liu JG, et al. Effects of long-term treatment with ketanserin on blood pressure variability and end-organ damage in spontaneously hypertensive rats. Journal of Cardiovascular Pharmacology, 2003, 41(2): 233-239.

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