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       Carteolol¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The primary mechanism of the ocular hypotensive action of carteolol in reducing intraocular pressure is most likely a decrease in aqueous humor production. 
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       Carteolol¿¡ ´ëÇÑ Pharmacology Á¤º¸ Carteolol is a beta1 and beta2 (non-selective) adrenergic receptor-blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anesthetic (membrane-stabilizing) activity. Carteolol, when applied topically to the eye, has the action of reducing elevated, as well as normal, intraocular pressure, whether or not accompanied by glaucoma. Elevated intraocular pressure is a major risk factor in the pathogenesis of glaucomatous visual field loss and optic nerve damage. Carteolol reduces intraocular pressure with little or no effect on pupil size or accommodation in contrast to the miosis which cholinergic agents are known to produce. 
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    | Metabolism | 
    
       Carteolol¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6) 
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       Carteolol¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available 
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    | Half-life | 
    
       Carteolol¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available 
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    | Absorption | 
    
       Carteolol¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available 
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       Carteolol HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
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    | Biotransformation | 
    
       Carteolol¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. 
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    | Toxicity | 
    
       Carteolol¿¡ ´ëÇÑ Toxicity Á¤º¸ The most common effects expected with overdosage of a beta-adrenergic blocking agent are bradycardia, bronchospasm, congestive heart failure and hypotension. 
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    | Drug Interactions | 
    
       Carteolol¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Carteolol¿¡ ´ëÇÑ Description Á¤º¸ A beta-adrenergic antagonist used as an anti-arrhythmia agent, an anti-angina agent, an antihypertensive agent, and an antiglaucoma agent. [PubChem] 
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    | Dosage Form | 
    
       Carteolol¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution	Ophthalmic 
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    | Drug Category | 
    
       Carteolol¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AntagonistsAnti-Arrhythmia AgentsAntihypertensive AgentsSympatholytics 
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    | Smiles String Canonical | 
    
       Carteolol¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)NCC(O)COC1=CC=CC2=C1CCC(=O)N2 
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    | Smiles String Isomeric | 
    
       Carteolol¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)NC[C@@H](O)COC1=CC=CC2=C1CCC(=O)N2 
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    | InChI Identifier | 
    
       Carteolol¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C16H24N2O3/c1-16(2,3)17-9-11(19)10-21-14-6-4-5-13-12(14)7-8-15(20)18-13/h4-6,11,17,19H,7-10H2,1-3H3,(H,18,20)/f/h18H 
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    | Chemical IUPAC Name | 
    
       Carteolol¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 5-[3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-1H-quinolin-2-one 
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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. CARTEOLOL[GGT Increase][Composite Activity](Score)  I(Marginal)  0(Active)  0[Alkaline Phosphatase Increase](Activity Score)  I(Number of Rpts)  <4(Index value)  0[SGOT Increase](Activity Score)  I(Number of Rpts)  <4(Index value)  0.5[SGPT Increase](Activity Score)  I(Number of Rpts)  <4(Index value)  0.5[LDH Increase](Activity Score)  I(Number of Rpts)  <4(Index value)  0.5[GGT Increase](Activity Score)  I(Number of Rpts)  <4(Index value)  0
 
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