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\270 ¿ø/1mL/¾ÚÇÃ(2017.02.01)(º¯°æÀü¾à°¡)
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| Mechanism of Action |
Methylergonovine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Methylergonovine acts directly on the smooth muscle of the uterus and increases the tone, rate, and amplitude of rhythmic contractions through binding and the resultant antagonism of the dopamine D1 receptor. Thus, it induces a rapid and sustained tetanic uterotonic effect which shortens the third stage of labor and reduces blood loss.
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| Pharmacology |
Methylergonovine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Methylergonovine is a semisynthetic ergot alkaloid and a derivative of ergonovine and is used for the prevention and control of postpartum and post-abortion hemorrhage. In general, the effects of all the ergot alkaloids appear to results from their actions as partial agonists or antagonists at adrenergic, dopaminergic, and tryptaminergic receptors. The spectrum of effects depends on the agent, dosage, species, tissue, and experimental or physiological conditions. All of the alkaloids of ergot significantly increase the motor activity of the uterus. After small doses contractions are increased in force or frequency, or both, but are followed by a normal degree of relaxation. As the dose is increased, contractions become more forceful and prolonged, resting tonus is markedly increased, and sustained contracture can result.
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| Half-life |
Methylergonovine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 3.39 hours
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| Absorption |
Methylergonovine¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption is rapid after oral (60% bioavailability) and intramuscular (78% bioavailability) administration.
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| Pharmacokinetics |
Methylergonovine MaleateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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- Á¤¸ÆÁÖ»ç : 45ºÐ
- Èí¼ö : ½Å¼ÓÈ÷ Èí¼öµÊ
- »ýü³»ÀÌ¿ëÀ² : °æ±¸ : 60%
- ºÐÆ÷ : Á¤¸ÆÁÖ»ç½Ã Ç÷Àå, ¼¼Æ÷¿Ü¾×¿¡ ½Å¼ÓÇÏ°Ô ºÐÆ÷Çϸç, Á¶Á÷À¸·ÎÀÇ ºÐÆ÷µµ ½Å¼ÓÇÏ°Ô ÀÌ·ç¾îÁü
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- ¼Ò½Ç : ´ëº¯ ¹× ´¢¸¦ ÅëÇØ ½Å¼ÓÇÏ°Ô ¹è¼³µÊ
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| Biotransformation |
Methylergonovine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic, with extensive first-pass metabolism.
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| Toxicity |
Methylergonovine¿¡ ´ëÇÑ Toxicity Á¤º¸ Signs and symptoms of overexposure: hypertension, seizures, headache, hypotension, nausea, and vomiting.
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| Drug Interactions |
Methylergonovine¿¡ ´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 |
Methylergonovine¿¡ ´ëÇÑ Description Á¤º¸ A homolog of ergonovine containing one more CH2 group. (Merck Index, 11th ed)
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| Drug Category |
Methylergonovine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Oxytocics
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| Smiles String Canonical |
Methylergonovine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCC(CO)NC(=O)C1CN(C)C2CC3=CNC4=CC=CC(C2=C1)=C34
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| Smiles String Isomeric |
Methylergonovine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC[C@@H](CO)NC(=O)[C@H]1CN(C)[C@@H]2CC3=CNC4=CC=CC(C2=C1)=C34
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| InChI Identifier |
Methylergonovine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C20H25N3O2/c1-3-14(11-24)22-20(25)13-7-16-15-5-4-6-17-19(15)12(9-21-17)8-18(16)23(2)10-13/h4-7,9,13-14,18,21,24H,3,8,10-11H2,1-2H3,(H,22,25)/t13-,14+,18-/m1/s1/f/h22H
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| Chemical IUPAC Name |
Methylergonovine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ Not Available
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| Drug-Induced Toxicity Related Proteins |
MALEATE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Intercellular adhesion molecule 1 Drug:maleate Toxicity:hepatic injury. [¹Ù·Î°¡±â]
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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