FB2026_02 , released June 18, 2026
Chemical: amoxicillin
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General Information
Name
amoxicillin
FlyBase ID
FBch0000671
ChEBI Name
amoxicillin
ChEBI ID
PubChem Name
Amoxicillin
PubChem ID
Chemical Structure
Chemical structure of amoxicillin
amoxicillin
InChIKey

LSQZJLSUYDQPKJ-NJBDSQKTSA-N

Definition (ChEBI)

ChEBI: Amoxicillin is a penicillin in which the substituent at position 6 of the penam ring is a 2-amino-2-(4-hydroxyphenyl)acetamido group. It has a role as an antibacterial drug. It is a penicillin and a penicillin allergen. It is a conjugate acid of an amoxicillin(1-).NCI Thesaurus (NCIt): Amoxicillin Anhydrous is the anhydrous form of a broad-spectrum, semisynthetic aminopenicillin antibiotic with bactericidal activity. Amoxicillin binds to and inactivates penicillin-binding proteins (PBPs) 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. This interrupts bacterial cell wall synthesis and results in the weakening of the bacterial cell wall and causes cell lysis.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (31)
Synonyms
(2S,5R,6R)-6-{[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
26787-78-0
6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid
6beta-[(2R)-2-amino-2-(4-hydroxyphenyl)acetamido]-2,2-dimethylpenam-3alpha-carboxylic acid
Amoxicillin
Amoxicillin anhydrous
Amoxicilline
Amoxycillin
Clamoxyl
D-Amoxicillin
PubChem:33613
alpha-amino-p-hydroxybenzylpenicillin
amopenixin
amoxicilina
amoxicillin anhydrous
amoxicillinum
amoxycilin
d-amoxicillin
p-Hydroxyampicillin
p-hydroxyampicillin
pubchem:33613
Secondary FlyBase IDs
    References (4)