Prucalopride succinate
CAS No. 179474-85-2
Prucalopride succinate ( R-108512;R108512 )
产品货号. M12709 CAS No. 179474-85-2
Prucalopride succinate (R-108512) is a potent, selective 5-HT4 receptor agonist.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
10MG | ¥324 | 有现货 |
|
25MG | ¥405 | 有现货 |
|
50MG | ¥551 | 有现货 |
|
100MG | ¥932 | 有现货 |
|
200MG | ¥1466 | 有现货 |
|
500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Prucalopride succinate
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Prucalopride succinate (R-108512) is a potent, selective 5-HT4 receptor agonist.
-
产品描述Prucalopride succinate (R-108512) is a potent, selective 5-HT4 receptor agonist with pKi of 8.6 and 8.1 for 5-HT4a and 5-HT4b, >290-fold higher affinity for 5-HT4 receptors than for other receptors; targets the impaired motility associated with chronic constipation, thus normalizing bowel movements; induces contractions (pEC50=7.48) in the guinea-pig colon, demonstrates anti-cholinergic, anticholinesterase or nonspecific inhibitory activity and does not antagonise 5-HT2A, 5-HT2B and 5-HT3 receptors or motilin, CCK1 receptors.
-
同义词R-108512;R108512
-
通路Endocrinology/Hormones
-
靶点5-HT Receptor
-
受体5-HT4A ;5-HT4B
-
研究领域Other Indications
-
适应症——
化学信息
-
CAS Number179474-85-2
-
分子量485.96
-
分子式C22H32ClN3O7
-
纯度>98% (HPLC)
-
溶解度DMSO: ≥ 36 mg/mL
-
SMILESCOCCCN1CCC(CC1)NC(=O)C2=CC(=C(C3=C2OCC3)N)Cl.C(CC(=O)O)C(=O)O
-
化学全称Butanedioic acid, compd. with 4-amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (1:1)
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Prins NH, et al. Br J Pharmacol. 1999 Jul;127(6):1431-7.
2. Poen AC, et al. Aliment Pharmacol Ther. 1999 Nov;13(11):1493-7.
3. Bouras EP, et al. Gut. 1999 May;44(5):682-6.
4. Briejer MR, et al. Eur J Pharmacol. 2001 Jun 29;423(1):71-83.
2. Poen AC, et al. Aliment Pharmacol Ther. 1999 Nov;13(11):1493-7.
3. Bouras EP, et al. Gut. 1999 May;44(5):682-6.
4. Briejer MR, et al. Eur J Pharmacol. 2001 Jun 29;423(1):71-83.
产品手册
关联产品
-
XEN-445
XEN445, a potent and selective endothelial lipase(EL) inhibitor (IC50=0.237 uM), exhibitis good ADME and PK properties.
-
SB 242084 hydrochlor...
SB 242084 is a potent, selective, brain penetrant 5-HT2C receptor antagonist.
-
Peptide 401
Peptide 401 is an antimicrobial peptide (AMP) derived from the venom of bees and wasps. Peptide 401 induces mast cell degranulation, activating histamine release from peritoneal mast cells. Additionally, peptide 401 exhibits some anti-inflammatory activity, decreasing paw edema in animal models.