SB 203186 hydrochloride structure
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Common Name | SB 203186 hydrochloride | ||
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CAS Number | 207572-69-8 | Molecular Weight | 308.803 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C16H21ClN2O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of SB 203186 hydrochlorideSB-203186 hydrochloride is a potent and competitive 5-HT4 antagonist. SB-203186 hydrochloride antagonizes the 5-HT4 receptor-mediated relaxations of the carbachol-contracted rat isolated oesophagus against 5-HT with pKB values of 10.9 (rat oesophagus), 9.5 (guinea-pig ileum), and 9.0 (human colon) respectively[1][2][3]. |
Name | 2-(1-Piperidinyl)ethyl 1H-indole-3-carboxylate hydrochloride (1:1) |
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Synonym | More Synonyms |
Description | SB-203186 hydrochloride is a potent and competitive 5-HT4 antagonist. SB-203186 hydrochloride antagonizes the 5-HT4 receptor-mediated relaxations of the carbachol-contracted rat isolated oesophagus against 5-HT with pKB values of 10.9 (rat oesophagus), 9.5 (guinea-pig ileum), and 9.0 (human colon) respectively[1][2][3]. |
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Related Catalog | |
Target |
pKB: 10.9 (5-HT4 in rat oesophagus), 9.5 (5-HT4 in guinea-pig ileum), and 9.0 (5-HT4 in human colon)[3]. |
In Vitro | SB-203186 (0.1-3mg/kg, i.v.) surmountably antagonised 5-HT-evoked tachycardia in anaesthetized Yucatan minipigs or new-born Camborough piglets with similar potency[1]. Pretreatment with SB-203186 (10 μM) enhances the 5-HT-induced contractions of the antral strips[2]. |
In Vivo | Intraduodenally administered SB-203186 (0.3-3 mg/kg) to new-born Camborough piglets produced blockade of 5-HT-evoked tachycardia which was maximal after 20 min and lasted for more than 3 h with 0.3 mg/kg[1]. |
References |
Molecular Formula | C16H21ClN2O2 |
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Molecular Weight | 308.803 |
Exact Mass | 308.129150 |
2-(Piperidin-1-yl)ethyl 1H-indole-3-carboxylate hydrochloride (1:1) |
2-(1-Piperidinyl)ethyl 1H-indole-3-carboxylate hydrochloride (1:1) |
1H-Indole-3-carboxylic acid, 2-(1-piperidinyl)ethyl ester, hydrochloride (1:1) |
SB-203186 hydrochloride |