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DUR (ÀǾàǰ»ç¿ëÆò°¡)
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[amiloride hydrochloride]
[potassium chloride]
[tacrolimus hydrate (as tacrolimus)]
[tacrolimus hydrate (as tacrolimus)]
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Mechanism of Action
Spironolactone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Spironolactone is a specific pharmacologic antagonist of aldosterone, acting primarily through competitive binding of receptors at the aldosterone-dependent sodium-potassium exchange site in the distal convoluted renal tubule. Spironolactone causes increased amounts of sodium and water to be excreted, while potassium is retained. Spironolactone acts both as a diuretic and as an antihypertensive drug by this mechanism. It may be given alone or with other diuretic agents which act more proximally in the renal tubule.
Pharmacology
Spironolactone¿¡ ´ëÇÑ Pharmacology Á¤º¸ Spironolactone is a synthetic 17-lactone steroid which is a renal competitive aldosterone antagonist in a class of pharmaceuticals called potassium-sparing diuretics. On its own, spironolactone is only a weak diuretic, but it can be combined with other diuretics. Due to its anti-androgen effect, it can also be used to treat hirsutism, and is a common component in hormone therapy for male-to-female transgendered people. Spironolactone inhibits the effect of aldosterone by competing for intracellular aldosterone receptor in the distal tubule cells. This increases the secretion of water and sodium, while decreasing the excretion of potassium. Spironolactone has a fairly slow onset of action, taking several days to develop and similarly the effect diminishes slowly.
Metabolism
Spironolactone¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
Protein Binding
Spironolactone¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Spironolactone and its metabolites are more than 90% bound to plasma proteins.
Half-life
Spironolactone¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 10 minutes
Absorption
Spironolactone¿¡ ´ëÇÑ Absorption Á¤º¸ Fairly rapidly absorbed from the gastrointestinal tract. Food increases the bioavailability of unmetabolized spironolactone by almost 100%.
Pharmacokinetics
SpironolactoneÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
´Ü¹é°áÇÕ : 91-98%
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Biotransformation
Spironolactone¿¡ ´ëÇÑ Biotransformation Á¤º¸ Rapidly and extensively metabolized. The metabolic pathway of spironolactone is complex and can be divided into two main routes: those in which the sulfur moiety is retained and those in which the sulfur moiety is removed by dethioacetylation. Spironolactone is transformed to a reactive metabolite that can inactivate adrenal and testicular cytochrome P450 enzymes. It also has anti-androgenic activity.
Toxicity
Spironolactone¿¡ ´ëÇÑ Toxicity Á¤º¸ The oral LD50 of spironolactone is greater than 1,000 mg/kg in mice, rats, and rabbits. Acute overdosage of spironolactone may be manifested by drowsiness, mental confusion, maculopapular or erythematous rash, nausea, vomiting, dizziness, or diarrhea. Spironolactone has been shown to be a tumorigen in chronic toxicity studies in rats.
Drug Interactions
Spironolactone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Spironolactone¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Avoid salt substitutes containing potassium.Take with food.
Drug Target
[Drug Target]
Description
Spironolactone¿¡ ´ëÇÑ Description Á¤º¸ A potassium sparing diuretic that acts by antagonism of aldosterone in the distal renal tubules. It is used mainly in the treatment of refractory edema in patients with congestive heart failure, nephrotic syndrome, or hepatic cirrhosis. Its effects on the endocrine system are utilized in the treatments of hirsutism and acne but they can lead to adverse effects. (From Martindale, The Extra Pharmacopoeia, 30th ed, p827)
Drug Category
Spironolactone¿¡ ´ëÇÑ Drug_Category Á¤º¸ Aldosterone AntagonistsDiuretics
Smiles String Canonical
Spironolactone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(=O)SC1CC2=CC(=O)CCC2(C)C2CCC3(C)C(CCC33CCC(=O)O3)C12
Smiles String Isomeric
Spironolactone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(=O)S[C@@H]1CC2=CC(=O)CC[C@]2(C)[C@H]2CC[C@@]3(C)[C@@H](CC[C@@]33CCC(=O)O3)[C@H]12
InChI Identifier
Spironolactone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C24H32O4S/c1-14(25)29-19-13-15-12-16(26)4-8-22(15,2)17-5-9-23(3)18(21(17)19)6-10-24(23)11-7-20(27)28-24/h12,17-19,21H,4-11,13H2,1-3H3/t17-,18-,19+,21+,22-,23-,24+/m0/s1
Chemical IUPAC Name
Spironolactone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ S-[(7R,8R,9S,10R,13S,14S,17R)-10,13-dimethyl-3,5'-dioxospiro[2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-7-yl] ethanethioate
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