Nhận Dạng Quốc Tế & Đặc Tính Hóa Học
Monoisotopic mass
232.08479226
InChI
InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)
InChI Key
InChIKey=DDBREPKUVSBGFI-UHFFFAOYSA-N
IUPAC Name
5-ethyl-5-phenyl-1,3-diazinane-2,4,6-trione
Traditional IUPAC Name
phenobarbital
SMILES
CCC1(C(=O)NC(=O)NC1=O)C1=CC=CC=C1
Độ hòa tan
1110 mg/L (at 25 °C)
pKa (strongest acidic)
8.14
Refractivity
59.75 m3·mol-1
Dược Lực Học :
Phenobarbital, the longest-acting barbiturate, is used for its anticonvulsant and sedative-hypnotic properties in the management of all seizure disorders except absence (petit mal).
Cơ Chế Tác Dụng :
A barbituric acid derivative that acts as a nonselective central nervous system depressant. It promotes binding to inhibitory gamma-aminobutyric acid subtype receptors, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. [PubChem]
Phenobarbital acts on GABAA receptors, increasing synaptic inhibition. This has the effect of elevating seizure threshold and reducing the spread of seizure activity from a seizure focus. Phenobarbital may also inhibit calcium channels, resulting in a decrease in excitatory transmitter release. The sedative-hypnotic effects of phenobarbital are likely the result of its effect on the polysynaptic midbrain reticular formation, which controls CNS arousal.
Dược Động Học :
▧ Absorption :
Absorbed in varying degrees following oral, rectal or parenteral administration. The salts are more rapidly absorbed than are the acids. The rate of absorption is increased if the sodium salt is ingested as a dilute solution or taken on an empty stomach.
▧ Protein binding :
20 to 45%
▧ Metabolism :
Hepatic (mostly via CYP2C19).
▧ Half Life :
53 to 118 hours (mean 79 hours)
Độc Tính :
CNS and respiratory depression which may progress to Cheyne-Stokes respiration, areflexia, constriction of the pupils to a slight degree (though in severe poisoning they may wshow paralytic dilation), oliguria, tachycardia, hypotension, lowered body temperature, and coma. Typical shock syndrome (apnea, circulatory collapse, respiratory arrest, and death) may occur.
Chỉ Định :
For the treatment of all types of seizures except absence seizures.
Tương Tác Thuốc :
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Abiraterone
Strong CYP3A4 inducers may decrease levels of abiraterone. Monitor concomitant therapy closely.
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Acenocoumarol
The barbiturate, phenobarbital, decreases the anticoagulant effect of acenocoumarol.
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Aminophylline
The barbiturate, phenobarbital, decreases the effect of aminophylline.
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Anisindione
The barbiturate, phenobarbital, decreases the anticoagulant effect of anisindione.
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Asenapine
Phenobarbital is a CYP1A2 inducer and may increase metabolism of asenapine.
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Bendamustine
Increases levels of bendamustine by decreasing metabolism. Ethinyl Estradiol is a CYP1A2 inhibitor and concurrent administration may result in elevated plasma concentrations of bendamustine.
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Betamethasone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, betamethasone.
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Boceprevir
Strong CYP3A4 inducers will decrease levels of boceprevir. Concomitant therapy is contraindicated.
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Cabazitaxel
Concomitant therapy with a strong CYP3A inducer may decrease concentrations of cabazitaxel. Avoid concomitant therapy.
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Canagliflozin
Nonselective inducers of UGT enzymes may decrease levels of canagliflozin, thus decreasing efficacy. Consider increase the dose to 300 mg once daily.
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Chlorotrianisene
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, chlorotrianisene.
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Clomifene
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, clomifene.
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Conjugated Estrogens
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, conjugated estrogens.
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Cortisone acetate
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, cortisone acetate.
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Cyclosporine
The barbiturate, phenobarbital, may decrease the therapeutic effect of cyclosporine by increasing its metabolism.
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Dabrafenib
Strong CYP3A4 inducers may decrease levels of dabrafenib. Consider alternate therapy.
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Dasatinib
Phenobarbital may decrease the serum level and efficacy of dasatinib.
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Delavirdine
The anticonvulsant, phenobarbital, decreases the effect of delavirdine.
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Dexamethasone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, dexamethasone.
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Dicoumarol
The barbiturate, phenobarbital, decreases the anticoagulant effect, dicumarol.
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Diethylstilbestrol
The enzyme inducer, phenobarbital, may decrease the therapeutic effect of diethylstilbestrol.
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Disopyramide
Phenobarbital decreases levels of disopyramide
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Doxycycline
The anticonvulsant, phenobarbital, may decrease the therapeutic effect of doxycycline.
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Dyphylline
The barbiturate, phenobarbital, decreases the effect of dyphylline.
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Estradiol
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, estradiol.
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Estradiol valerate/Dienogest
Affects CYP3A4 metabolism, decreases or effects levels of Estradiol valerate/Dienogest.
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Estriol
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, estriol.
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Estrone
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, estrone.
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Estropipate
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, estropipate.
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Ethinyl Estradiol
This product may cause a slight decrease of contraceptive effect
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Etravirine
Etravirine, when used concomitantly with phenobarbital, may experience a decrease in serum concentration. It is recommended to avoid concurrent therapy.
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Felbamate
Felbamate increases the effect and toxicity of phenobarbital/primidone
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Felodipine
The barbiturate, phenobarbital, decreases the effect of felodipine.
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Fludrocortisone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, fludrocortisone.
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Folic Acid
Folic acid decreases the effect of anticonvulsant, phenobarbital.
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Gefitinib
The CYP3A4 inducer, phenobarbital, may decrease the serum concentration and therapeutic effects of gefitinib.
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Griseofulvin
The barbiturate, phenobarbital, decreases the effect of griseofulvin.
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Hydrocortisone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, hydrocortisone.
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Imatinib
Phenobarbital decreases levels of imatinib
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Itraconazole
The barbiturate, phenobarbital, decreases the effect of itraconazole.
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Ivacaftor
Strong CYP3A4 inducers may decrease levels of ivacaftor. Monitor concomitant therapy closely.
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Levonorgestrel
Phenobarbital decreases the effect of levonorgestrel
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Medroxyprogesterone Acetate
The enzyme inducer, phenobarbital, may decrease the effect of the hormone, medroxyprogesterone.
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Megestrol acetate
The enzyme inducer, phenobarbital, may decrease the effect of the hormone, megestrol.
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Mestranol
This product may cause a slight decrease of contraceptive effect
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Methadone
The barbiturate, phenobarbital, decreases the effect of methadone.
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Methoxyflurane
The barbiturate, phenobarbital, increases the renal toxicity of methoxyflurane.
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Methylprednisolone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, methylprednisolone.
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Metoprolol
The barbiturate decreases the effect of the metabolized beta-blocker
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Metronidazole
The barbiturate, phenobarbital, decreases the effect of metronidazole.
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Nifedipine
The barbiturate, phenobarbital, may decrease the effect of the calcium channel blocker, nifedipine.
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Norethindrone
This product may cause a slight decrease of contraceptive effect
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Oxtriphylline
The barbiturate, phenobarbital, decreases the effect of oxtriphylline.
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Paramethasone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, paramethasone.
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Prednisolone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, prednisolone.
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Prednisone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, prednisone.
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Propranolol
The barbiturate decreases the effect of the metabolized beta-blocker
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Quinestrol
The enzyme inducer, phenobarbital, decreases the effect of the hormone agent, quinestrol.
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Quinidine
The anticonvulsant, phenobarbital, decreases the effect of quinidine.
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Regorafenib
Strong CYP3A4 inducers may decrease levels of regorafenib.
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Rilpivirine
Strong inducers of CYP3A4 decrease the exposure of rilpivirine thus decreasing efficacy.
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Roflumilast
Affects CYP3A4 metabolism, decreases level or effect of roflumilast. Also decreases the level or effect of roflumilast by affecting CYP1A2 metabolism.
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Rufinamide
Increases clearance of rufinamide thus decreasing plasma concentration of rufinamide.
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Sunitinib
Possible decrease in sunitinib levels
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Tacrolimus
Phenobarbital may decrease the blood concentration of Tacrolimus. Monitor for changes in the therapeutic/toxic effects of Tacrolimus if Phenobarbital therapy is initiated, discontinued or altered.
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Telithromycin
Phenobarbital may decrease the plasma concentration of Telithromycin. Consider alternate therapy.
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Temsirolimus
Phenobarbital may increase the metabolism of Temsirolimus decreasing its efficacy. Concomitant therapy should be avoided.
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Theophylline
The barbiturate, phenobarbital, decreases the effect of theophylline.
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Ticlopidine
Ticlopidine may decrease the metabolism and clearance of Phenobarbital. Consider alternate therapy or monitor for adverse/toxic effects of Phenobarbital if Ticlopidine is initiated, discontinued or dose changed.
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Tipranavir
Phenobarbial decreases the concentration of Tipranavir. Monitor for decreased Tipranavir efficacy.
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Tramadol
Phenobarbital may decrease the effect of Tramadol by increasing Tramadol metabolism and clearance.
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Trazodone
The CYP3A4 inducer, Phenobarbital, may decrease Trazodone efficacy by increasing Trazodone metabolism and clearance. Monitor for changes in Trazodone efficacy/toxicity if Phenobarbital is initiated, discontinued or dose changed.
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Tretinoin
The strong CYP2C8 inducer, Phenobarbital, may increase the metabolism and clearance of oral Tretinoin. Consider alternate therapy to avoid failure of Tretinoin therapy or monitor for changes in Tretinoin effectiveness and adverse/toxic effects if Phenobarbital is initiated, discontinued or dose changed.
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Triamcinolone
The barbiturate, phenobarbital, may decrease the effect of the corticosteroid, triamcinolone.
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Trimipramine
The barbiturate, Phenobarbital, may increase the metabolism and clearance of Trimipramine. Monitor for changes in the therapeutics and adverse effects of Trimipramine if Phenobarbital is initiated, discontinued or dose changed. Dose adjustments of Trimipramine may be required.
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Triprolidine
The CNS depressants, Triprolidine and Phenobarbital, may increase adverse/toxic effects due to additivity. Monitor for increased CNS depressant effects during concomitant therapy.
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Ulipristal
Concomitant therapy with strong CYP3A4 inducers may decrease plasma concentrations of ulipristal and ultimately its effectiveness. Avoid combination therapy.
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Vandetanib
Decreases levels of vandetanib by affecting CYP3A4 metabolism. Contraindicated.
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Vemurafenib
Strong CYP3A4 inducers may decrease levels of vemurafenib. Monitor concomitant therapy closely.
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Verapamil
Phenobarbital, a CYP3A4 inducer, may increase the serum concentration of Verapamil, a CYP3A4 substrate. Monitor for changes in the therapeutic/adverse effects of Verapamil if Phenobarbital is initiated, discontinued or dose changed.
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Vigabatrin
Vigabatrin reduces serum concentrations of phenobarbital by 8-16%.
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Voriconazole
Phenobarbital may reduce serum concentrations and efficacy of voriconazole. Concomitant voriconazole and long-acting barbiturates therapy is contraindicated.
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Warfarin
Phenobarbital may decrease the serum concentration of warfarin by increasing its metabolism. Monitor for changes in the therapeutic and adverse effects of warfarin if phenobarbital is initiated, discontinued or dose changed.
Liều Lượng & Cách Dùng :
Elixir - Oral
Solution - Intramuscular
Tablet - Oral
Dữ Kiện Thương Mại
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