Prucalopride
CAS No. 179474-81-8
Prucalopride ( Prucalopride; Prucalopride free base )
Catalog No. M12708 CAS No. 179474-81-8
Prucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively.
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 29 | Get Quote |
|
10MG | 47 | Get Quote |
|
25MG | 61 | Get Quote |
|
50MG | 73 | Get Quote |
|
100MG | 126 | Get Quote |
|
200MG | 178 | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NamePrucalopride
-
NoteResearch use only, not for human use.
-
Brief DescriptionPrucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively.
-
DescriptionPrucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively, exhibits >290-fold selectivity against other 5-HT receptor subtypes.
-
SynonymsPrucalopride; Prucalopride free base
-
PathwayEndocrinology/Hormones
-
Target5-HT Receptor
-
Recptor5-HT1A; 5-HT1B; 5-HT3; 5-HT4A; 5-HT4B
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number179474-81-8
-
Formula Weight367.87
-
Molecular FormulaC18H26ClN3O3
-
Purity>98%(HPLC)
-
SolubilityEthanol: 38 mg/mL (103.29 mM); DMSO: 60 mg/mL (163.1 mM)
-
SMILESClC1=CC(C(NC2CCN(CCCOC)CC2)=O)=C3C(CCO3)=C1N
-
Chemical Name4-amino-5-chloro-N-(1-(3-methoxypropyl)piperidin-4-yl)-2,3-dihydrobenzofuran-7-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Briejer MR, et al. Eur J Pharmacol, 2001, 423(1), 71-83.
molnova catalog
related products
-
Tryptamine
Tryptamine is a monoamine alkaloid found in plants, fungi, and animals. It contains an indole ring structure, and is structurally similar to the amino acid tryptophan, from which it derives its name.
-
PF-03246799
A potent and selective 5-HT2C receptor agonist with EC50 of 190 nM, with excellent selectivity for 5-HT2C over 5-HT2A.
-
Nelotanserin
A potent, selective 5-HT2A inverse agonist with pKi of 9.2; displays >30- and 5000-fold selectivity compared with 5-HT2C and 5-HT2B receptors.