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Mechanism of Action
Etoposide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Etoposide inhibits DNA topoisomerase II, thereby inhibiting DNA synthesis at the premitotic stage of cell division. Etoposide is cell cycle dependent and phase specific, affecting mainly the S and G2 phases of cell division.
Pharmacology
Etoposide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Etoposide is an antineoplastic agent and an epipodophyllotoxin (a semisynthetic derivative of the podophyllotoxins). It inhibits DNA topoisomerase II, thereby inhibiting DNA synthesis. Etoposide is cell cycle dependent and phase specific, affecting mainly the S and G2 phases. Two different dose-dependent responses are seen. At high concentrations (10 µg/mL or more), lysis of cells entering mitosis is observed. At low concentrations (0.3 to 10 µg/mL), cells are inhibited from entering prophase. It does not interfere with microtubular assembly. The predominant macromolecular effect of etoposide appears to be the induction of DNA strand breaks by an interaction with DNA-topoisomerase II or the formation of free radicals.
Metabolism
Etoposide¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)
Protein Binding
Etoposide¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 97%
Half-life
Etoposide¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 4-12 hours
Absorption
Etoposide¿¡ ´ëÇÑ Absorption Á¤º¸ Absorbed well, time to peak plasma concentration is 1-1.5 hrs. Mean bioavailability is 50%.
Pharmacokinetics
EtoposideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Èí¼ö : etoposide capsule : 50% (25-75 %) ; 200 mg ÀÌ»óÀÇ °í¿ë·®¿¡¼ ÇöÀúÈ÷ °¨¼Ò
etoposide phosphate : 68% (36-112 %)
À½½Ä¹° : ¿µÇâ¾øÀ½
ºÐÆ÷ : IV : ³úô¼ö¾× : 10% ¹Ì¸¸
Vd : 7-17 L/m2
ºÐÆ÷ ¹Ý°¨±â : 1-1.5 ½Ã°£
´Ü¹é°áÇÕ : 97%
¹Ý°¨±â : 4-11 ½Ã°£ (¼Ò¾Æ : 3.37-5.8 ½Ã°£)
´ë»ç : °£´ë»ç
¼Ò½Ç : ½Å¹è¼³ (42-67 %), ´ãÁó¹è¼³ (6% ÀÌÇÏ), ´ëº¯¹è¼³ (0-16%)
ÃÑ Å¬¸®¾î·±½º : 16-36 mL/min/m2
Æò±Õ ½ÅŬ¸®¾î·±½º : 7-10 mL/min/m2
ÃÖ°í Ç÷Áß³óµµ µµ´Þ : °æ±¸ : 1-1.5 ½Ã°£
Biotransformation
Etoposide¿¡ ´ëÇÑ Biotransformation Á¤º¸ Primarily hepatic (through O-demethylation via the CYP450 3A4 isoenzyme pathway) with 40% excreted unchanged in the urine.
Toxicity
Etoposide¿¡ ´ëÇÑ Toxicity Á¤º¸ Side effects include alopecia, constipation, diarrhea, nausea and vomiting and secondary malignancies (leukemia).
Drug Interactions
Etoposide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aprepitant Aprepitant may change levels of chemotherapy agentCyclosporine Cyclosporine increases the effect of etoposideQuinupristin This combination presents an increased risk of toxicity
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Etoposide¿¡ ´ëÇÑ Food Interaction Á¤º¸ Grapefruit and grapefruit juice should be avoided throughout treatment as grapefruit can decrease serum levels of this product.
Drug Target
[Drug Target]
Description
Etoposide¿¡ ´ëÇÑ Description Á¤º¸ A semisynthetic derivative of podophyllotoxin that exhibits antitumor activity. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent entry into the mitotic phase of cell division, and lead to cell death. Etoposide acts primarily in the G2 and S phases of the cell cycle. [PubChem]
Drug Category
Etoposide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antineoplastic Agents, PhytogenicNucleic Acid Synthesis Inhibitors
Smiles String Canonical
Etoposide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=CC(=CC(OC)=C1O)C1C2C(COC2=O)C(OC2OC3COC(C)OC3C(O)C2O)C2=CC3=C(OCO3)C=C12
Smiles String Isomeric
Etoposide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=CC(=CC(OC)=C1O)[C@H]1[C@@H]2[C@H](COC2=O)[C@H](O[C@@H]2O[C@@H]3CO[C@@H](C)O[C@H]3[C@H](O)[C@H]2O)C2=CC3=C(OCO3)C=C12
InChI Identifier
Etoposide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3/t11-,15+,20-,21-,22+,24-,25-,26-,27-,29+/m1/s1
Chemical IUPAC Name
Etoposide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4'-demethyl-epipodophyllotoxin 9-[4,6-O-(R)-ethylidene-beta-D-glucopyranoside], 4'-(dihydrogen phosphate)
Drug-Induced Toxicity Related Proteins
ETOPOSIDE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :p44-extracellular signal receptor-activated kinase 2Drug :etoposide Toxicity :apoptotic cell death and DNA damage. [¹Ù·Î°¡±â] Replated Protein :Mitogen-activated protein kinase p42Drug :etoposide Toxicity :apoptotic cell death and DNA damage. [¹Ù·Î°¡±â] Replated Protein :SAPK enzymes p46Drug :etoposide Toxicity :apoptotic cell death and DNA damage. [¹Ù·Î°¡±â] Replated Protein :DNA topoisomerase 2-alphaDrug :etoposide Toxicity :DNA damage and cell death. [¹Ù·Î°¡±â] Replated Protein :DNA topoisomerase 2Drug :etoposide Toxicity :apoptosis. [¹Ù·Î°¡±â] ETOPOSIDE (VP16) ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Caspase-8 Drug :etoposide (VP16) Toxicity :cell death. [¹Ù·Î°¡±â] Replated Protein :B-cell receptor-associated protein 31(BAP31)Drug :etoposide (VP16) Toxicity :cell death. [¹Ù·Î°¡±â] Replated Protein :Caspase-8 Drug :etoposide (VP16) Toxicity :cell death. [¹Ù·Î°¡±â] Replated Protein :Caspase-3 Drug :etoposide (VP16) Toxicity :cell death. [¹Ù·Î°¡±â] ETOPOSIDE (VP-16) ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein :Apoptosis regulator Bcl-2Drug :etoposide (VP-16) Toxicity :cytotoxicity. [¹Ù·Î°¡±â] Replated Protein :Hypoxanthine-guanine phosphoribosyltransferaseDrug :etoposide (VP-16) Toxicity :etoposide (VP-16)-induced DNA recombination . [¹Ù·Î°¡±â] Replated Protein :Apoptosis regulator Bcl-2Drug :etoposide (VP-16) Toxicity :VP-16-induced genetic recombination, mutation, and cytotoxicity. [¹Ù·Î°¡±â]
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