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Merck
CN

M7319

ML 10302

≥98%, solid

别名:

2-Piperidinoethyl 4-amino-5-chloro-2-methoxybenzoate

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关于此项目

经验公式(希尔记法):
C15H21ClN2O3
化学文摘社编号:
分子量:
312.79
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
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产品名称

ML 10302, ≥98%, solid

InChI

1S/C15H21ClN2O3/c1-20-14-10-13(17)12(16)9-11(14)15(19)21-8-7-18-5-3-2-4-6-18/h9-10H,2-8,17H2,1H3

SMILES string

COc1cc(N)c(Cl)cc1C(=O)OCCN2CCCCC2

InChI key

RVFIAQAAZUEPPE-UHFFFAOYSA-N

assay

≥98%

form

solid

color

white to off-white

solubility

DMSO: >20 mg/mL
H2O: insoluble

storage temp.

2-8°C

Quality Level

Gene Information

Biochem/physiol Actions

Potent, selective 5-HT4 serotonin receptor agonist

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D Yang et al.
Journal of medicinal chemistry, 40(4), 608-621 (1997-02-14)
A number of benzoates derived from 4-amino-5-chloro-2-methoxybenzoic acid and substituted 1-piperidineethanol were synthesized and found to be potent 5-HT4 receptor agonists in the electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum and the rat esophagus muscle. Monosubstitution
Jean-Louis Soulier et al.
Journal of medicinal chemistry, 48(20), 6220-6228 (2005-09-30)
Recently, human 5-HT4 receptors have been demonstrated to form constitutive dimers in living cells. To evaluate the role of dimerization on the 5-HT4 receptor function, we investigated the conception and the synthesis of bivalent molecules able to influence the dimerization
F De Ponti et al.
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society, 13(6), 543-553 (2002-03-21)
5-Hydroxytryptamine (5-HT)4 receptor agonists stimulate gut motility through cholinergic pathways, although there are data suggesting that noncholinergic (tachykininergic) excitatory pathways may also be involved. Differences may exist between the small bowel and colon. Our aims were: (i) to compare the

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