物质信息

ID:381

名称和标识
IUPAC传统名
phenindione
IUPAC标准名
2-phenyl-2,3-dihydro-1H-indene-1,3-dione
商标名
BindanDindevanDinevalFenhydrenHedulinIndionPIDPhenylindanedioneTromazalTrombolAthrombonDaniloneEridioneFenilinEmandioneHemolidioneIndemaPhenylindionePhenylineTheradioneDanilonDiadilanDiophindaneEmandionPhenillinPhenylenPhenylinPhenyllinPindioneThrombasalRectadioneCronodioneDanedionFenindionIndonPhenhydren
别名
Phenindione
数据登录号
PubChem CID
CAS号
PubChem SID
化合物性质
理化性质
疏水性(logP)
2.6
溶解度
27 mg/L (at 20 oC)
描述信息
Drug Groups
approved
Description
An indandione that has been used as an anticoagulant. Phenindione has actions similar to warfarin, but it is now rarely employed because of its higher incidence of severe adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p234)
Indication
For the treatment of pulmonary embolism, cardiomyopathy, atrial fibrillation and flutter, cerebral embolism, mural thrombosis, and thrombophili. Also used for anticoagulant prophylaxis.
Pharmacology
Phenindione thins the blood by antagonizing vitamin K which is required for the production of clotting factors in the liver. Anticoagulants such as Phenindione have no direct effect on an established thrombus, nor do they reverse ischemic tissue damage (damage caused by an inadequate blood supply to an organ or part of the body). However, once a thrombus has occurred, the goal of anticoagulant treatment is to prevent further extension of the formed clot and prevent secondary thromboembolic complications which may result in serious and possibly fatal sequelae. Phenindione has actions similar to warfarin, but it is now rarely employed because of its higer incidence of severe adverse effects.
Toxicity
Oral, mouse: LD50 = 175 mg/kg; Oral, rat: LD50 = 163 mg/kg.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic.
Absorption
Absorbed slowly from the gastrointestinal tract.
Half Life
5-10 hours
Protein Binding
88%
References
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