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Procaine

产品号 DB00721 公司名称 DrugBank
CAS号 59-46-1 公司网站 http://www.ualberta.ca/
分子式 C13H20N2O2 电 话 (780) 492-3111
分子量 236.3101 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 602

产品价格信息

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产品别名

标题
Procaine
IUPAC标准名
2-(diethylamino)ethyl 4-aminobenzoate
IUPAC传统名
procaine
商标名
Spinocaine
Nesacaine
Jenacain
Duracillin A.S.
Procaine Hcl
Scurocaine
Allocaine
Chloroprocaine Hcl
Diethylaminoethyl P-Aminobenzoate
Duracaine
Gerovital H-3
Neocaine
Norocaine
Novocaine
P-Aminobenzoyldiethylaminoethanol
Penicillin G Procaine
Procain
Procaine, Base
Gerovital
Jenacaine
Nissocaine
Novocain
Pfizerpen-As
Procaine Hydrochloride
Vitamin H3
Anticort
别名
procaine HCl

产品登记号

CAS号 59-46-1
PubChem CID 4914
PubChem SID 46507724

产品性质

疏水性(logP) 1.8
溶解度 9450 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved; investigational
Description A local anesthetic of the ester type that has a slow onset and a short duration of action. It is mainly used for infiltration anesthesia, peripheral nerve block, and spinal block. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1016). [PubChem]
Indication Used as a local anesthetic primarily in oral surgery
Pharmacology Procaine is an anesthetic agent indicated for production of local or regional anesthesia, particularly for oral surgery. Procaine (like cocaine) has the advantage of constricting blood vessels which reduces bleeding, unlike other local anesthetics like lidocaine. Procaine is an ester anesthetic. It is metabolized in the plasma by the enzyme pseudocholinesterase through hydrolysis into para-aminobenzoic acid (PABA), which is then excreted by the kidneys into the urine.
Affected Organisms
Humans and other mammals
Biotransformation Hydrolysis by plasma esterases to PABA
Half Life 7.7 minutes
Elimination With normal kidney function, the drug is excreted rapidly by tubular excretion.
References
Gentry CL, Lukas RJ: Local anesthetics noncompetitively inhibit function of four distinct nicotinic acetylcholine receptor subtypes. J Pharmacol Exp Ther. 2001 Dec;299(3):1038-48. [Pubmed]
External Links
Wikipedia
Drugs.com

参考文献

  • Gentry CL, Lukas RJ: Local anesthetics noncompetitively inhibit function of four distinct nicotinic acetylcholine receptor subtypes. J Pharmacol Exp Ther. 2001 Dec;299(3):1038-48. Pubmed