National Cancer Institute Thesaurus

Last uploaded: February 23, 2024
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

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.

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C1041

Accepted_Therapeutic_Use_For

Upper respiratory tract and urinary tract infections; febrile neutropenic conditions

CAS_Registry

123171-59-5

CHEBI_ID

CHEBI:31368

Chemical_Formula

C19H24N6O5S2.2ClH.H2O

code

C1041

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

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C63923

Contributing_Source

CTRP

FDA

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.

Display_Name

Cefepime Hydrochloride

FDA_UNII_Code

I8X1O0607P

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

Has_Free_Acid_Or_Base_Form

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C65294

label

Cefepime Hydrochloride

Legacy Concept Name

Cefepime

NCI_Drug_Dictionary_ID

38350

PDQ_Closed_Trial_Search_ID

38350

PDQ_Open_Trial_Search_ID

38350

Preferred_Name

Cefepime Hydrochloride

prefixIRI

Thesaurus:C1041

Semantic_Type

Organic Chemical

Pharmacologic Substance

Antibiotic

UMLS_CUI

C0771284

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C357

Delete Subject Author Type Created
No notes to display