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テトラカイン

Tetracaine

HCID 5411
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
94-24-6
標準SMILES
CCCCNc1ccc(C(=O)OCCN(C)C)cc1
InChIKey
GKCBAIGFKIBETG-UHFFFAOYSA-N
分子式
C15H24N2O2
平均分子量
264.36 g/mol
単同位体質量
264.18377801

概要

Tetracaine 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.

名称と識別子

優先名称
Tetracaine
IUPAC
2-(dimethylamino)ethyl 4-(butylamino)benzoate
現地名
テトラカイン
英語名
Tetracaine
分子式
C15H24N2O2
分子量
264.36

名称と別名

tetracaine94-24-6Amethocaine2-(Dimethylamino)ethyl 4-(butylamino)benzoateLaudocaineMetrasprayPontocaineAnetainDicaineUromucaesthinContralginFissucain
名称をさらに表示
ポントカインウロムカエスチンメジカインレキソカインパントカインコントラルギンニファノイドメトバルムテトラカインアメトカインフイッシュカインラウドカインムカエストヒムメトラスプライ4-(ブチルアミノ)安息香酸2-(ジメチルアミノ)エチルアネタインコーパロンインテルカインムカエスチン2-(ジメチルアミノ)エチル 4-(ブチルアミノ)ベンゾアートTETRACAINE BASETETRACAINTetracainumDlcalnetetracine
IntercainMedicaineMeethobalmMucaesthinNiphanoidMedihaler-TetracaineTetracainaTetrakain

データベース識別子

物性

構造計算による物性

XLogP
3.7
極性表面積
41.6 Ų
水素結合供与体数
1
水素結合受容体数
4
回転可能結合数
9
重原子数
19
形式電荷
0
複雑度
249

実験および物理化学的性質

Chemical ClassesOther Uses -> Pharmaceuticals
Drugs · 2 件

Pharmaceuticals

Pharmaceuticals -> Listed in ZINC15

SpringerMaterials PropertiesNuclear quadrupole resonance spectroscopy
LogP3.46
Human Drugs · 5 件

Breast Feeding; Lactation; Milk, Human; Anesthetics, Local

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Pharmaceuticals

Ophthalmological preparations > Local anaesthetics

Dissociation Constants · 3 件

8.49

8.5

8.6

Collision Cross Section · 3 件

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]

物理化学的性質

融点

安全と法規制

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。

GHS分類

GHS Classification · 4 件

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.

危険有害性情報

Other Safety InformationIMAP assessments - Benzoic acid, 4-(butylamino)-, 2-(dimethylamino)ethyl ester: Environment tier I assessment
Hazards SummaryProcaine allergy used to be a common skin sensitizer for dentists. There exists cross-reactivity between procaine, benzocaine, and tetracaine but not with lidocaine and other amide-type local anesthetics currently used. [Kanerva, p. 434]
Hazard Classes and CategoriesAcute Tox. 3 (97.7%)

毒性情報

Adverse Effects · 2 件

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).

Toxicity SummarySigns and Symptoms of Overdose

化学と産業

薬理情報

ATC Code · 6 件

S01HA03

N - Nervous system

S - Sensory organs

D - Dermatologicals

C - Cardiovascular system

QD - Dermatologicals

Protein BindingTetracaine is rapidly hydrolyzed in the plasma; therefore, protein binding could not be determined.
Mechanism of ActionTetracaine is an ester-type anesthetic and produces local anesthesia by blocking the sodium ion channels involved in the initiation and conduction of neuronal impulses.
Biological Half-LifeTetracaine is hydrolyzed rapidly in the plasma; therefore, half-life has not been determined.
Metabolism/MetabolitesTetracaine is rapidly hydrolyzed by plasma esterases to the following primary metabolites: para-aminobenzoic acid and diethylaminoethanol. The activity of both metabolites is unspecified.
FDA Pharmacological Classification · 6 件

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.

MeSH Pharmacological Classification · 1 件

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.

Absorption, Distribution and Excretion

関連反応

2 件
反応記録を作成
HRID 1378501 の反応式
HRID 1378501生成物としてuspto-grants-1997_09
HRID 2424241 の反応式
HRID 2424241反応物としてuspto-grants-2011_06

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
CAS
94-24-6
PubChem CID
5411
DTXSID
DTXSID1043883
ChEMBL
CHEMBL698
ChEBI
CHEBI:9468
UNII
0619F35CGV
EC Number
202-316-6
Nikkaji
J3.945D
41 to · 41.0 to 45.0 °C
沸点
407.59 °C · 407.59°C (rough estimate)
比重(密度)
1.02 · 1.0200 (rough estimate)
屈折率
1.58 · 1.5800 (estimate)
貯蔵温度
2 · 2-8°C
溶解性
soluble in Methanol
外見
powder to crystal
酸解離定数(Pka)
8.33 · pKa 8.33±0.03(H2O t = 20.0 I = 0.10 (KCl)) (Uncertain)
色
White to Almost white
水溶解度
156 mg/L · 156mg/L(温度表記なし)
主な用途
医薬品
InChI
InChI=1S/C15H24N2O2/c1-4-5-10-16-14-8-6-13(7-9-14)15(18)19-12-11-17(2)3/h6-9,16H,4-5,10-12H2,1-3H3
InChIKey
GKCBAIGFKIBETG-UHFFFAOYSA-N
SMILES
C(OCCN(C)C)(=O)C1=CC=C(NCCCC)C=C1
LogP
3.51 · 3.510
CAS データベース
94 · 94-24-6(CAS DataBase Reference)
NISTの化学物質情報
Tetracaine(94-24-6)

化学的性質

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 · 5 件

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

tetracaine

DILI Negative

Topical

DOI:10.1016/j.drudis.2019.09.022

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

安全データ

wgk
3
rtecs
DG4725000
ridadr
UN 2811
hs_code
29224999
risk_code
22-40-42/43-43
hazard_code
Xn,Xi
safety_code
22-36/37
hazard_class
6.1
packing_group
III
Hazard Classifications
Acute Tox. 3 OralCarc. 2Skin Sens. 1
ストレージクラス
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
· 3 件

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.

用途と製造

Uses · 2 件

Used as a local anesthetic by dentists and other surgeons; [Kanerva, p. 1748]

Use (kg; approx.) in Germany (2009): >50

Use ClassificationPharmaceuticals
応用分野 · 2 件

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.

上流・下流製品情報

上流原料

Dimethylprocaine炭酸カリウムN,N-ジメチルホルムアミド1-ブロモブタン

下流製品

テトラカイン 塩酸塩

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補足説明

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.