ChemicalBook--->CAS DataBase List--->149719-06-2

149719-06-2

149719-06-2 Structure

149719-06-2 Structure
IdentificationBack Directory
[Name]

RS 23597-190 HYDROCHLORIDE
[CAS]

149719-06-2
[Synonyms]

RS23597-190HCl
RS 23597-190 hydroch
RS 23597-190 >=98% (HPLC)
RS 23597-190 HYDROCHLORIDE
RS 23597 190 hydrochloride,RS 23597190 hydrochloride
3-(PIPERIDIN-1-YL)PROPYL-4-AMINO-5-CHLORO-2-METHOXYBENZOATE HCL
3-(PIPERIDIN-1-YL)PROPYL 4-AMINO-5-CHLORO-2-METHOXYBENZOATE HYDROCHLORIDE
3-piperidin-1-ylpropyl 4-azanyl-5-chloro-2-methoxy-benzoate hydrochloride
3-(piperidine-1-yl)propyl 4-amino-5-chloro-2-methoxybenzoate hydrochloride
4-amino-5-chloro-2-methoxy-benzoic acid 3-piperidinopropyl ester hydrochloride
4-amino-5-chloro-2-methoxybenzoic acid 3-(1-piperidinyl)propyl ester hydrochloride
4-amino-5-chloro-2-methoxy-Benzoic acid 3-(1-piperidinyl)propyl ester hydrochloride (1:1)
Benzoic acid, 4-amino-5-chloro-2-methoxy-, 3-(1-piperidinyl)propyl ester, hydrochloride (1:1)
[Molecular Formula]

C16H24Cl2N2O3
[MDL Number]

MFCD00672672
[MOL File]

149719-06-2.mol
[Molecular Weight]

363.28
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Water:36.33(Max Conc. mg/mL);100.0(Max Conc. mM)
[form ]

Powder
[Water Solubility ]

Soluble to 100 mM in water
Hazard InformationBack Directory
[Uses]

RS 23597-190 Hydrochloride is a selective and competitive SR-4 and 5-HT4 receptor antagonist.
[Biological Activity]

A high affinity, selective competitive antagonist at 5-HT 4 receptors.
[Biochem/physiol Actions]

RS 23597-190 is a high affinity 5-HT4-selective antagonist with in vitro and in vivo efficacy. RS 23597-190 is a 4-amino-5-chloro-2-methoxybenzoate that antagonizes 5-HT-mediated relaxation of carbachol-contracted rat oesphageal muscularis mucosae ex vivo (pA2 = 7.5) and prevents 5-HT-induced tachycardia (tachyarrhythmia) of anaesthetized micropigs in vivo (6 mg/kg RS 23597-190 and 3-10 μ/kg 5-HT via i.v.) by targeting 5-HT4 with high affinity (pKB = 7.8) and selectivity, while exhibiting no efficacy against 5-methoxytryptamine-mediated 5-HT3 activation in guinea-pig ileum and displaying much reduced or little affinity toward 5-HT3 (pKi = 5.7/mouse NG108-15 cells and pKB <5/guinea-pig ileum), dopamine receptors (pKi <4/D1 & <3/D2), muscarinic receptors (pKi <4.5 toward M1/2/3/4), 5-HT1A & 5-HT2 (pKi <5.2).
[storage]

Store at RT
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