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Áߵ ¹× ½ÉÇÑ ÅëÁõ
[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Pentazocine]
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| Related FDA Approved Drug |
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| Mechanism of Action |
Pentazocine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The preponderance of evidence suggests that pentazocine antagonizes the opioid effects by competing for the same receptor sites, especially the opioid mu receptor.
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| Pharmacology |
Pentazocine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pentazocine is a potent analgesic which when administered orally in a 50 mg dose appears equivalent in analgesic effect to 60 mg (1 grain) of codeine. Onset of significant analgesia usually occurs between 15 and 30 minutes after oral administration, and duration of action is usually three hours or longer. Onset and duration of action and the degree of pain relief are related both to dose and the severity of pretreatment pain. Pentazocine weakly antagonizes the analgesic effects of morphine and meperidine; in addition, it produces incomplete reversal of cardiovascular, respiratory, and behavioral depression induced by morphine and meperidine. Pentazocine has about 1/50 the antagonistic activity of nalorphine. It also has sedative activity.
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| Protein Binding |
Pentazocine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Pentazocine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2 to 3 hours
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| Absorption |
Pentazocine¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed from the gastro-intestinal tract.
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| Pharmacokinetics |
Pentazocine HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ :
- °æ±¸, I,M, SC : 15-30ºÐ À̳»
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- ´ë»ç : ÃÊȸÅë°úÈ¿°ú Å. °£¿¡¼ »êÈ, glucuronide Æ÷ÇÕÀ¸·Î ´ë»çµÊ.
- »ýü³»ÀÌ¿ëÀ² : °æ±¸ : ¾à 20%. °£°æÈ ȯÀÚ¿¡¼´Â 60-70%
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- ¼Ò½Ç : ¼Ò·®Àº ¹Ìº¯Èü·Î ½Å¹è¼³µÊ
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| Toxicity |
Pentazocine¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available
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| Drug Interactions |
Pentazocine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Cimetidine Cimetidine increases the effect of the narcoticNaltrexone Naltrexone may precipitate a withdrawal syndrome in opioid dependent individuals
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Pentazocine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals. Avoid alcohol.
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| Drug Target |
[Drug Target]
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| Description |
Pentazocine¿¡ ´ëÇÑ Description Á¤º¸ The first mixed agonist-antagonist analgesic to be marketed. It is an agonist at the kappa and sigma opioid receptors and has a weak antagonist action at the mu receptor. (From AMA Drug Evaluations Annual, 1991, p97)
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| Dosage Form |
Pentazocine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution IntravenousTablet Oral
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| Drug Category |
Pentazocine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adjuvants, AnesthesiaAnalgesics, OpioidNarcotic AntagonistsNarcotics
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| Smiles String Canonical |
Pentazocine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1C2CC3=C(C=C(O)C=C3)C1(C)CCN2CC=C(C)C
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| Smiles String Isomeric |
Pentazocine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1[C@H]2CC3=C(C=C(O)C=C3)[C@]1(C)CCN2C\C=C(\C)C
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| InChI Identifier |
Pentazocine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C19H27NO/c1-13(2)7-9-20-10-8-19(4)14(3)18(20)11-15-5-6-16(21)12-17(15)19/h5-7,12,14,18,21H,8-11H2,1-4H3/t14-,18+,19+/m0/s1
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| Chemical IUPAC Name |
Pentazocine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (1S,9S,13S)-1,13-dimethyl-10-(3-methylbut-2-en-1-yl)-10-azatricyclo[7.3.1.02,7]trideca-2,4,6-trien-4-ol
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