Dicyclomine hydrochloride structure
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Common Name | Dicyclomine hydrochloride | ||
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CAS Number | 67-92-5 | Molecular Weight | 345.94800 | |
Density | N/A | Boiling Point | 399.8ºC at 760 mmHg | |
Molecular Formula | C19H36ClNO2 | Melting Point | 164-166ºC | |
MSDS | Chinese USA | Flash Point | 116.5ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Dicyclomine hydrochlorideDicyclomine hydrochloride is a potent and orally active muscarinic cholinergic receptors antagonist. Dicyclomine hydrochloride shows high affinity for muscarinic M1 receptor subtype (Ki=5.1 nM) and M2 receptor subtype (Ki=54.6 nM) in brush-border membrane and basal plasma membranes, respectively[1]. Dicyclomine is an antispasmodic agent and relieves smooth muscle spasm of the gastrointestinal tract in vivo[2]. |
Name | dicyclomine hydrochloride |
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Synonym | More Synonyms |
Description | Dicyclomine hydrochloride is a potent and orally active muscarinic cholinergic receptors antagonist. Dicyclomine hydrochloride shows high affinity for muscarinic M1 receptor subtype (Ki=5.1 nM) and M2 receptor subtype (Ki=54.6 nM) in brush-border membrane and basal plasma membranes, respectively[1]. Dicyclomine is an antispasmodic agent and relieves smooth muscle spasm of the gastrointestinal tract in vivo[2]. |
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Related Catalog | |
Target |
Ki: 5.1 nM (muscarinic M1 receptor subtype in brush-border membrane) Ki: 54.6 nM (muscarinic M2 receptor subtype in basal plasma membrane[1] |
In Vivo | Dicyclomine hydrochloride (intraperitoneal injection; 8 mg/kg; daily) exacerbates the cognitive impairments in all the measurements. In addition, the memory impairments are worse in dicyclomine-treated 3xTg-AD mice compared to dicyclomine-treated NonTg mice[2]. Dicyclomine hydrochloride (intraperitoneal injection; 2.0, 4.0, and 8.0 mg/kg; 7 days) produces a highly significant effect on performance in the paired-associates learning (PAL) task in mice.And systemic treatment at lower doses show behavioral impairments in mice in spatial tasks[3]. Animal Model: C57Bl/6 mice[1] Dosage: 2.0, 4.0, and 8.0 mg/kg Administration: Intraperitoneal injection; daily; 7 days Result: Produced impairments due to actions of the agent outside of the hippocampus. |
References |
Boiling Point | 399.8ºC at 760 mmHg |
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Melting Point | 164-166ºC |
Molecular Formula | C19H36ClNO2 |
Molecular Weight | 345.94800 |
Flash Point | 116.5ºC |
Exact Mass | 345.24300 |
PSA | 29.54000 |
LogP | 5.20420 |
Appearance of Characters | powder | off-white |
Water Solubility | H2O: 50 mg/mL |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335 |
Precautionary Statements | P301 + P312 + P330-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | 22-36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | DT7350000 |
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2-(diethylamino)ethyl 1-cyclohexylcyclohexane-1-carboxylate,hydrochloride |
Dicyclomine, Hydrochloride |