Amoxicillin
Synonyms: amoxicillin, "Amoxycillin", "Amoxicillin anhydrous", "Amoxicilline", "p-Hydroxyampicillin", "Amoxicillinum", "Amoxicilina", "Amopenixin", "Amolin", "Moxal", "D-Amoxicillin", "Clamoxyl", "Histocillin", "Delacillin", "Moxacin", "Flemoxin", "Efpenix", "Cemoxin", "Bristamox", "Anemolin", "Amoxiden", "Amoclen", "Piramox", "Ibiamox", "Hiconcil", "Aspenil", "Vetramox", "Unicillin", "Imacillin", "Amoxivet", "Amoxi", "Sumox", "DisperMox", "Amoxil", "Wymox", "Amoxi-Mast", "Sawamox PM", "Metifarma capsules", "Metafarma capsules", "Robamox", "Ospamox", "Amopen", "Utimox".
Source: Amoxicillin is an antibiotic.
Identifiers:
IUPAC Name: (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
CAS Number: 26787-78-0
PubChem ID: 33613
InChiKey: LSQZJLSUYDQPKJ-NJBDSQKTSA-N
Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C
Structural Properties:
Molecular Formula: C16H19N3O5S
Molecular Weight: 365.4
Pharmacophore Features:
Number of bond donors: 4
Number of bond acceptors: 7
Number of atoms different from hydrogen: 25
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Evidence Supporting This Chemical as an Emerging Contaminant
Brito, L. B., Garcia, L. F., Caetano, M. P., Lob?n, G. S., de Oliveira, M. T., de Oliveira, R., ... & Grisolia, C. K. (2018). Electrochemical remediation of amoxicillin: detoxification and reduction of antimicrobial activity.?Chemico-biological interactions,?291, 162-170.Omidvar, M., Hejri, Z., & Moarefian, A. (2019). The effect of Merpol surfactant on the morphology and performance of PES/PVP membranes: antibiotic separation. International Journal of Industrial Chemistry, 1-9.
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