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[ketorolac tromethamine]
[ketorolac tromethamine]
[methotrexate]
[methotrexate]
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Ibuprofen ¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do
Mechanism of Action
Ibuprofen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The exact mechanisms of action of Ibuprofen is unknown. Its antiinflammatory effects are believed to be due to inhibition of both cylooxygenase-1 (COX-1) and cylooxygenase-2 (COX-2) which leads to the inhibition of prostaglandin synthesis, and results in the inhibition of prostaglandin synthesis. Antipyretic effects may be due to action on the hypothalamus, resulting in an increased peripheral blood flow, vasodilation, and subsequent heat dissipation.
Pharmacology
Ibuprofen¿¡ ´ëÇÑ Pharmacology Á¤º¸ Ibuprofen is a nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. Ibuprofen has pharmacologic actions similar to those of other prototypical NSAIAs, that is thought to be associated with the inhibition of prostaglandin synthesis. Ibuprofen is used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and to alleviate moderate pain.
Metabolism
Ibuprofen¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C9 (CYP2C9)Monoamine oxidase type B (MAO-B)
Protein Binding
Ibuprofen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 99%
Half-life
Ibuprofen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1.8-2.0 hours
Absorption
Ibuprofen¿¡ ´ëÇÑ Absorption Á¤º¸ rapidly absorbed
Pharmacokinetics
IbuprofenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
ÁøÅëÈ¿°ú ¹ßÇö½Ã°£ : 30-60ºÐ
ÀÛ¿ëÁö¼Ó½Ã°£ : 4-6 ½Ã°£
Ç׿°È¿°ú ¹ßÇö½Ã°£ : 7ÀϱîÁö
ÃÖ´ë Ç׿°È¿°ú ¹ßÇö½Ã°£ : 1-2ÁÖ
Èí¼ö : °æ±¸ : ½Å¼ÓÇÏ°Ô Èí¼öµÊ (85%)
´Ü¹é°áÇÕ : 90-99%
´ë»ç : °£¿¡¼ »êÈ´ë»ç
¹Ý°¨±â : 2-4 ½Ã°£ (¸»±â ½ÅÁúȯ¿¡¼µµ ¹Ý°¨±â´Â º¯ÈÇÏÁö ¾ÊÀ½)
Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 1-2 ½Ã°£ À̳»
¼Ò½Ç : ½Å¹è¼³(¹Ìº¯Èü·Î´Â 1% ¹Ì¸¸), ÀϺΠ´ãÁó¹è¼³µµ ÀϾ
Biotransformation
Ibuprofen¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
Toxicity
Ibuprofen¿¡ ´ëÇÑ Toxicity Á¤º¸ Abdominal pain, breathing difficulties, coma, drowsiness, headache, irregular heartbeat, kidney failure, low blood pressure, nausea, ringing in the ears, seizures, sluggishness, vomiting; LD50 =1255mg/kg(orally in mice)
Drug Interactions
Ibuprofen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acebutolol Risk of inhibition of renal prostaglandinsAtenolol Risk of inhibition of renal prostaglandinsBetaxolol Risk of inhibition of renal prostaglandinsBevantolol Risk of inhibition of renal prostaglandinsBisoprolol Risk of inhibition of renal prostaglandinsCarteolol Risk of inhibition of renal prostaglandinsCarvedilol Risk of inhibition of renal prostaglandinsEsmolol Risk of inhibition of renal prostaglandinsLabetalol Risk of inhibition of renal prostaglandinsNadolol Risk of inhibition of renal prostaglandinsMetoprolol Risk of inhibition of renal prostaglandinsOxprenolol Risk of inhibition of renal prostaglandinsPenbutolol Risk of inhibition of renal prostaglandinsPindolol Risk of inhibition of renal prostaglandinsPractolol Risk of inhibition of renal prostaglandinsPropranolol Risk of inhibition of renal prostaglandinsSotalol Risk of inhibition of renal prostaglandinsTimolol Risk of inhibition of renal prostaglandinsWarfarin The NSAID increases the anticoagulant effectAcenocoumarol The NSAID increases the anticoagulant effectDicumarol The NSAID increases the anticoagulant effectAnisindione The NSAID increases the anticoagulant effectEthacrynic acid The NSAID decreases the diuretic and antihypertensive effect of the loop diureticFurosemide The NSAID decreases the diuretic and antihypertensive effect of the loop diureticTorasemide The NSAID decreases the diuretic and antihypertensive effect of the loop diureticBumetanide The NSAID decreases the diuretic and antihypertensive effect of the loop diureticAspirin Ibuprofen reduces ASA cardioprotective effectsMethotrexate The NSAID increases the effect and toxicity of methotrexateAlendronate Increased risk of gastric toxicityCyclosporine Monitor for nephrotoxicityLithium The NSAID increases serum levels of lithium
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸] Ibuprofen¿¡ ´ëÇÑ P450 table SUBSTRATES
CYP 2C9
NSAIDs:
diclofenac
**ibuprofen**
piroxicam
Oral Hypoglycemic Agents:
tolbutamide
glipizide
Angiotensin II Blockers:
NOT candesartan
irbesartan
losartan
NOT valsartan
celecoxib
fluvastatin naproxen
phenytoin
sulfamethoxazole
tamoxifen
tolbutamide
torsemide
warfarin
INHIBITORS
CYP 2C9
amiodarone
fluconazole
isoniazid
INDUCERS
CYP 2C9
rifampin
secobarbital
Food Interaction
Ibuprofen¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food to reduce irritation.
Drug Target
[Drug Target]
Description
Ibuprofen¿¡ ´ëÇÑ Description Á¤º¸ A nonsteroidal anti-inflammatory agent with analgesic properties used in the therapy of rheumatism and arthritis. [PubChem]
Dosage Form
Ibuprofen¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralSuspension OralTablet OralTablet, chewable Oral
Drug Category
Ibuprofen¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnalgesicsAnalgesics, Non-NarcoticAnti-Inflammatory Agents, Non-SteroidalAnti-inflammatory AgentsCyclooxygenase InhibitorsNonsteroidal Antiinflammatory Agents (NSAIDs)
Smiles String Canonical
Ibuprofen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)CC1=CC=C(C=C1)C(C)C(O)=O
Smiles String Isomeric
Ibuprofen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)CC1=CC=C(C=C1)[C@@H](C)C(O)=O
InChI Identifier
Ibuprofen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C13H18O2/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15/h4-7,9-10H,8H2,1-3H3,(H,14,15)/f/h14H
Chemical IUPAC Name
Ibuprofen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-[4-(2-methylpropyl)phenyl]propanoic acid
Drug-Induced Toxicity Related Proteins
IBUPROFEN ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Myeloperoxidase Drug :ibuprofen Toxicity :increase the incidence of ventricular fibrillation. [¹Ù·Î°¡±â] Replated Protein :Myeloperoxidase Drug :ibuprofen Toxicity :increase the incidence of haemorrhagic infarction. [¹Ù·Î°¡±â] Replated Protein :Arylamine N-acetyltransferase 2Drug :ibuprofen Toxicity :ibuprofen inhibition. [¹Ù·Î°¡±â]
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