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| Brandname Á¤º¸ |
Benztropine
Brand Names/Synonyms
- Akitan
- Apo-Benztropine
- Benzatropina [Inn-Spanish]
- Benzatropine
- Benzatropinum [Inn-Latin]
- Benztropine Mesylate
- Benztropinum
- Cobrentin
- Cogentin
- Cogentine
- Cogentinol
- Pms Benztropine
- Tropine Benzohydryl Ether
Brand Name MixturesNot Available
Chemical IUPAC Name3-benzhydryloxy-8-methyl-8-azabicyclo[3.2.1]octane
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| Mechanism of Action |
Benztropine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Benztropine is a selective M1 muscarinic acetylcholine receptor antagonist. It is able to discriminate between the M1 (cortical or neuronal) and the peripheral muscarinic subtypes (cardiac and glandular). Benztropine partially blocks cholinergic activity in the CNS, which is responsible for the symptoms of Parkinson's disease. It is also thought to increase the availability of dopamine, a brain chemical that is critical in the initiation and smooth control of voluntary muscle movement.
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| Pharmacology |
Benztropine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Benztropine is an anticholinergic used in the symptomatic treatment of all etiologic groups of parkinsonism and drug induced extrapyramidal reactions (except tardive dyskinesia). Benztropine possesses both anticholinergic and antihistaminic effects, although only the former has been established as therapeutically significant in the management of parkinsonism. Benztropine's anticholinergic activity is about equal to that of atropine.
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| Protein Binding |
Benztropine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Benztropine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Benztropine¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Pharmacokinetics |
Benztropine MesylateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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| Biotransformation |
Benztropine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Benztropine¿¡ ´ëÇÑ Toxicity Á¤º¸ Signs of overdose include confusion, nervousness, listlessness, hallucinations, dizziness; muscle weakness, ataxia, dry mouth, mydriasis, blurred vision, palpitations, tachycardia, elevated blood pressure, nausea, vomiting, dysuria, numbness of fingers, headache, delirium, coma, shock, convulsions, respiratory arrest, anhidrosis, hyperthermia, glaucoma, and constipation.
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| Drug Interactions |
Benztropine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Donepezil Possible antagonism of actionGalantamine Possible antagonism of actionHaloperidol The anticholinergic increases the risk of psychosis and tardive dyskinesiaRivastigmine Possible antagonism of action
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Benztropine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.Avoid alcohol.
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| Drug Target |
[Drug Target]
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| Description |
Benztropine¿¡ ´ëÇÑ Description Á¤º¸ A centrally active muscarinic antagonist that has been used in the symptomatic treatment of parkinson disease. Benztropine also inhibits the uptake of dopamine. [PubChem]
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| Dosage Form |
Benztropine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid IntravenousSolution OralTablet Oral
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| Drug Category |
Benztropine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntidyskineticsAntiparkinson AgentsDopamine Uptake InhibitorsMuscarinic AntagonistsParasympatholytics
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| Smiles String Canonical |
Benztropine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1C2CCC1CC(C2)OC(C1=CC=CC=C1)C1=CC=CC=C1
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| Smiles String Isomeric |
Benztropine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1[C@@H]2CC[C@@H]1CC(C2)OC(C1=CC=CC=C1)C1=CC=CC=C1
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| InChI Identifier |
Benztropine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H25NO/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-11,18-21H,12-15H2,1H3/t18-,19-/m1/s1
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| Chemical IUPAC Name |
Benztropine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (1R,5R)-3-[di(phenyl)methoxy]-8-methyl-8-azabicyclo[3.2.1]octane
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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The database contains the following fields: The generic name of each chemical For module A10 (liver enzyme composite module): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method) Number of endpoints at which each compound is marginally active (M) Number of endpoints at which each compound is active (A) For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method) Number of ADR reports for each compound, given as <4 or ¡Ã4 Reporting Index value for each compound, except where no shipping units were available (NSU) Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period. BENZTROPINE[GGT Increase][Composite Activity](Score) NA(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[SGOT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[SGPT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[LDH Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA[GGT Increase](Activity Score) NA(Number of Rpts) NA(Index value) NA
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