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Mechanism of Action
Cefpodoxime¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Cefpodoxime is active against a wide spectrum of Gram-positive and Gram-negative bacteria. Cefpodoxime is stable in the presence of beta-lactamase enzymes. As a result, many organisms resistant to penicillins and cephalosporins, due to their production of beta-lactamase, may be susceptible to cefpodoxime. Cefpodoxime is inactivated by certain extended spectrum beta-lactamases. The bactericidal activity of cefpodoxime results from its inhibition of cell wall synthesis.
Pharmacology
Cefpodoxime¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. Notable exceptions include Pseudomonas aeruginosa , Enterococcus , and Bacteroides fragilis .
Protein Binding
Cefpodoxime¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 22 to 33% in serum and from 21 to 29% in plasma.
Half-life
Cefpodoxime¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.09 to 2.84 hours
Absorption
Cefpodoxime¿¡ ´ëÇÑ Absorption Á¤º¸ Cefpodoxime proxetil is a prodrug that is absorbed from the gastrointestinal tract and de-esterified to its active metabolite, cefpodoxime. Following oral administration of 100 mg of cefpodoxime proxetil to fasting subjects, approximately 50% of the administered cefpodoxime dose was absorbed systemically.
Biotransformation
Cefpodoxime¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
Toxicity
Cefpodoxime¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available
Drug Interactions
Cefpodoxime¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Cefpodoxime¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take on empty stomach: 1 hour before or 2 hours after meals.
Drug Target
[Drug Target]
Description
Cefpodoxime¿¡ ´ëÇÑ Description Á¤º¸ Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. It is commonly used to treat acute otitis media, pharyngitis, and sinusitis.
Drug Category
Cefpodoxime¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAntibacterial AgentsCephalosporins
Smiles String Canonical
Cefpodoxime¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COCC1=C(N2C(SC1)C(NC(=O)C(=NOC)C1=CSC(N)=N1)C2=O)C(O)=O
Smiles String Isomeric
Cefpodoxime¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COCC1=C(N2[C@H](SC1)[C@H](NC(=O)C(=N/OC)\C1=CSC(N)=N1)C2=O)C(O)=O
InChI Identifier
Cefpodoxime¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H17N5O6S2/c1-25-3-6-4-27-13-9(12(22)20(13)10(6)14(23)24)18-11(21)8(19-26-2)7-5-28-15(16)17-7/h5,9,13H,3-4H2,1-2H3,(H2,16,17)(H,18,21)(H,23,24)/b19-8-/t9-,13-/m1/s1/f/h18,23H,16H2
Chemical IUPAC Name
Cefpodoxime¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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The database contains the following fields:
The generic name of each chemical
For module A10 (liver enzyme composite module):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method)
Number of endpoints at which each compound is marginally active (M)
Number of endpoints at which each compound is active (A)
For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method)
Number of ADR reports for each compound, given as <4 or ¡Ã4
Reporting Index value for each compound, except where no shipping units were available (NSU)
Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period.
CEFPODOXIME [GGT Increase] [Composite Activity] (Score) I (Marginal) 0 (Active) 0 [Alkaline Phosphatase Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 1 [SGOT Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 1 [SGPT Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 0.8 [LDH Increase] (Activity Score) I (Number of Rpts) <4 (Index value) 0.2 [GGT Increase] (Activity Score) I (Number of Rpts) <4 (Index value) 0.5 CEFPODOXIME PROXETIL [GGT Increase] [Composite Activity] (Score) I (Marginal) 0 (Active) 0 [Alkaline Phosphatase Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 1 [SGOT Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 1 [SGPT Increase] (Activity Score) I (Number of Rpts) ¡Ã4 (Index value) 0.8 [LDH Increase] (Activity Score) I (Number of Rpts) <4 (Index value) 0.2 [GGT Increase] (Activity Score) I (Number of Rpts) <4 (Index value) 0.5
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