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National Cancer Institute Thesaurus
Preferred Name | Cefepime Hydrochloride | |
Synonyms |
Cefepime Hydrochloride CEFEPIME HYDROCHLORIDE Pyrrolidinium, 1-((7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-1-methyl-, hydroxide, inner salt, (6R-(6alpha,7beta(Z)))- Maxipime |
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Definitions |
The hydrochloride salt of a semi-synthetic, beta-lactamase-resistant, fourth-generation cephalosporin antibiotic derived from an Acremonium fungal species with broad-spectrum bactericidal activity. Administered parenterally, cefepime inhibits bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity, resulting in a reduction of bacterial cell wall stability and cell lysis. This agent is more active against a variety of Gram-positive pathogens compared to third-generation cephalosporins. |
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ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C1041 |
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Accepted_Therapeutic_Use_For |
Upper respiratory tract and urinary tract infections; febrile neutropenic conditions
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CAS_Registry |
123171-59-5
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CHEBI_ID |
CHEBI:31368
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Chemical_Formula |
C19H24N6O5S2.2ClH.H2O
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code |
C1041
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Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C176424 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116978 |
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Contributing_Source |
CTRP FDA
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DEFINITION |
The hydrochloride salt of a semi-synthetic, beta-lactamase-resistant, fourth-generation cephalosporin antibiotic derived from an Acremonium fungal species with broad-spectrum bactericidal activity. Administered parenterally, cefepime inhibits bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity, resulting in a reduction of bacterial cell wall stability and cell lysis. This agent is more active against a variety of Gram-positive pathogens compared to third-generation cephalosporins.
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Display_Name |
Cefepime Hydrochloride
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FDA_UNII_Code |
I8X1O0607P
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FULL_SYN |
Cefepime Hydrochloride CEFEPIME HYDROCHLORIDE Pyrrolidinium, 1-((7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-2-carboxy-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methyl)-1-methyl-, hydroxide, inner salt, (6R-(6alpha,7beta(Z)))- Maxipime
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Has_Free_Acid_Or_Base_Form | ||
label |
Cefepime Hydrochloride
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Legacy Concept Name |
Cefepime
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NCI_Drug_Dictionary_ID |
38350
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PDQ_Closed_Trial_Search_ID |
38350
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PDQ_Open_Trial_Search_ID |
38350
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Preferred_Name |
Cefepime Hydrochloride
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prefixIRI |
Thesaurus:C1041
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Semantic_Type |
Organic Chemical Pharmacologic Substance Antibiotic
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UMLS_CUI |
C0771284
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subClassOf |
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