94-24-6CCCCNc1ccc(C(=O)OCCN(C)C)cc1GKCBAIGFKIBETG-UHFFFAOYSA-NTetracaine is a benzoate ester in which 4-N-butylbenzoic acid and 2-(dimethylamino)ethanol have combined to form the ester bond; a local ester anaesthetic (ester caine) used for surface and spinal anaesthesia. It has a role as a local anaesthetic. It is a benzoate ester and a tertiary amino compound.
Pharmaceuticals
Pharmaceuticals -> Listed in ZINC15
Breast Feeding; Lactation; Milk, Human; Anesthetics, Local
FDA approved drugs -> Active ingredient
FDA approved drugs -> Active ingredient
Pharmaceuticals
Ophthalmological preparations > Local anaesthetics
8.49
8.5
8.6
164.78 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
173.1 Ų [M+H]+ [CCS Type: TW; Method: Major Mix IMS/Tof Calibration Kit (Waters)]
173.5 Ų [M+H]+ [CCS Type: DT; Method: single field calibrated]
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H301 (97.7%): Toxic if swallowed [Danger Acute toxicity, oral]
P203, P261, P264, P270, P272, P280, P301+P316, P302+P352, P318, P321, P330, P333+P317, P362+P364, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 43 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Skin Sensitizer - An agent that can induce an allergic reaction in the skin.
When dosing based on weight, clinicians should not exceed 1.5 to 3 mg/kg of the patient's actual weight. The toxicity of the drug is affected by the site of administration. Tetracaine undergoes absorption (from fastest to slowest) in the following order: IV > intercostal > caudal > epidural > brachial plexus > subcutaneous. Absorption speed may be mitigated by avoiding areas near a large vascular supply and adding local vasoconstrictors to the solution (epinephrine or phenylephrine).
S01HA03
N - Nervous system
S - Sensory organs
D - Dermatologicals
C - Cardiovascular system
QD - Dermatologicals
0619F35CGV
TETRACAINE
Established Pharmacologic Class [EPC] - Ester Local Anesthetic
Chemical Structure [CS] - Esters
Physiologic Effects [PE] - Local Anesthesia
Tetracaine is an Ester Local Anesthetic. The physiologic effect of tetracaine is by means of Local Anesthesia.
Drugs that block nerve conduction when applied locally to nerve tissue in appropriate concentrations. They act on any part of the nervous system and on every type of nerve fiber. In contact with a nerve trunk, these anesthetics can cause both sensory and motor paralysis in the innervated area. Their action is completely reversible. (From Gilman AG, et. al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed) Nearly all local anesthetics act by reducing the tendency of voltage-dependent sodium channels to activate.
読み込み中…
94-24-6DTXSID1043883CHEMBL698CHEBI:9468化学的特性White or light-yellow, waxy solid. Very slightly soluble in water; soluble in alcohol, ether, benzene, chloroform.
Drug-Induced Liver Injury Severity and Toxicity (DILIst)
tetracaine
DILI Negative
Topical
DOI:10.1016/j.drudis.2019.09.022
Systemic absorption of anaesthetic from the combination cream is directly related to the duration and surface area of application. Although peak plasma concentrations for lidocaine were measured, plasma levels for tetracaine could not be determined due to low levels (<0.9 ng/mL)
Tetracaine is rapidly hydrolyzed in the plasma; therefore, volume of distribution could not be determined.
Tetracaine is hydrolyzed rapidly in the plasma; therefore, clearance has not been determined.
Used as a local anesthetic by dentists and other surgeons; [Kanerva, p. 1748]
Use (kg; approx.) in Germany (2009): >50
使用Tetracaine has been used as an anesthetic and to lower the glucose synthesis in upper small intestinal infusions. It has also been used to inhibit ryanodine receptors (RyRs) in rats.
一般的な説明Tetracaine was developed to address the low potency andshort duration of action of procaine and chloroprocaine. The addition of the butyl side chain on the para nitrogen increasesthe lipid solubility of the drug and enhances the topical potencyof tetracaine. The plasma half-life is 120 to 150 seconds.Topically applied tetracaine to unbroken skin requires 30 to 45minutes to confer topical anesthesia. Tetracaine 4% gel is superiorthan eutectic mixture with lidocaine (EMLA) (an emulsionof lidocaine and prilocaine) in preventing pain associatedwith needle procedures in children. Tetracaine metabolism issimilar to procaine ester metabolism yielding parabutylaminobenzoicacid and dimethylaminoethanol and conjugatesexcreted in the urine. The pKa of the dimethylated nitrogen is8.4 and tetracaine is formulated as a hydrochloride salt with apH of 3.5 to 6.0. The increased absorption from topical siteshas resulted in reported toxicity. Overdoses of tetracaine mayproduce central nervous system (CNS) toxicity and seizure activitywith fatalities from circulatory depression reported.No selective cardiac toxicity is seen with tetracaine althoughhypotension has been reported. Tetracaine is employed for infiltrationanesthesia, spinal anesthesia, or topical use.
定義ChEBI: A benzoate ester in which 4-N-butylbenzoic acid and 2-(dimethylamino)ethanol have combined to form the ester bond; a local ester anaesthetic (ester caine) used for surface and spinal anaesthesia.