moleculefinder

Amoxicillin

C16H19N3O5S365.4 g/mol Calculated

Also called amoxil, Amoxi-Tabs, Larotid and Robamox.

A penicillin antibiotic used for ear, chest, throat and dental infections. One extra hydroxyl group over ampicillin lets far more of it reach the blood when swallowed.

Sources and notes
  • The introductionfrom sourceMoleculeFinder curated
  • Other namesfrom sourceWikidataIts English label and aliases on Wikidata.
  • Formula and weightcomputedPubChem
  • 2D drawingcomputedPubChem structure, drawn by RDKit
  • 3D modelfrom sourcePubChem 3D conformerLoaded after the page has painted, and on a phone only when you ask for it; the 2D drawing shows until it arrives.

Where you encounter it

Dispensed on prescription, not sold on a shelf. Amoxicillin on the product labels we hold.

Medicines

AugmentinAdded by the makerActive ingredient

Every product and list we hold

Sources and notes
  • The product labels and their strengthsfrom sourceDailyMed (FDA label)Each label lists the molecule as an ingredient, and an active ingredient at the strength shown.
  • How it gets therefrom sourceMoleculeFinder curatedEach mark is set by hand on our lists, never inferred; a label's ingredient is added by the maker. A row with no mark data says Not marked.
  • The line abovefrom sourceMoleculeFinder curatedFrom the group the molecule belongs to.

Explore its structure

Choose a part to light it up.

A carbon carrying both a C=O and an O-H, written COOH. In water it gives up that hydrogen, which is what makes the molecule an acid.

From: standard chemistry.

Sources and notes
  • The drawingcomputedPubChem structure, drawn by RDKitThe page's one shipped drawing, with the chosen part lit in amber under it.
  • The partscomputedFound by ruleEach part is found by a chemical pattern, never picked by hand atom by atom; its words say where they come from.

Compare a related molecule

Amoxicillin

Azithromycin

Amoxicillin is a penicillin that blocks bacterial cell wall building, while azithromycin is a macrolide that stops protein synthesis and lingers for days.

Amoxicillin vs Azithromycin, side by side
Sources and notes
  • The sentencefrom sourceMoleculeFinder comparison notesThe pair's answer line.
  • The two drawingscomputedPubChem structures, drawn by RDKitThe two drawings side by side.

Properties and sources

Calculated by PubChem

Molecular formula
C16H19N3O5S
Molecular weight
365.4 g/mol
XLogP3octanol/water, log units
−2
Polar surface areatopological
158 Ų
H-bond donors
4
H-bond acceptors
7
Rotatable bonds
4
Complexity
590

Reported Hazard label (GHS), ECHA, HSDB via PubChem

Danger Irritant pictogram (GHS07) and Health hazard pictogram (GHS08); hazard statements H317, H334

Reported Licence

The US Food and Drug Administration licenses Amoxicillin for human use (NDA 050760, authorized April 15, 1999). Drugs@FDA

Groups it belongs to

Category
Prescription medicine
Family
Antibiotics
Chemical groups
Carboxylic Acids, Amines, Aromatics, Amides, Phenols
Elements
Nitrogen, Sulfur
Hazard classes
Irritant, Health hazard, GHS Danger
SMILESCC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)C(=O)O)C

PubChem CID 33613 · Wikidata Q201928 · InChIKey LSQZJLSUYDQPKJ-NJBDSQKTSA-N · Data refreshed

How MoleculeFinder sources and labels its data

Questions
What is Amoxicillin?
A penicillin antibiotic used for ear, chest, throat and dental infections. One extra hydroxyl group over ampicillin lets far more of it reach the blood when swallowed.
How toxic is Amoxicillin?
Its GHS hazard label carries the signal word Danger and the hazard pictograms Irritant and Health hazard. from source
What kind of molecule is Amoxicillin?
Amoxicillin has the formula C16H19N3O5S and a molecular weight of 365.4 g/mol. MoleculeFinder files it under antibiotics, in the prescription medicine group. from sourcefrom sourcefrom sourcefrom source
What else is Amoxicillin called?
Amoxicillin is also called amoxil, Amoxi-Tabs, Larotid and Robamox. from source
Who licenses Amoxicillin as a medicine?
The US Food and Drug Administration licenses Amoxicillin for human use (NDA 050760, authorized April 15, 1999). from source
Sources and notes
  • Calculated valuescomputedPubChemComputed from the structure, so no laboratory conditions apply; complexity is PubChem's own structural score.
  • Hazard labelfrom sourceECHA, HSDB via PubChemThe label combines these classifications.
  • ECHAfrom sourceAttributionSource: European Chemicals Agency, echa.europa.eu.
  • Licencefrom sourceDrugs@FDARead 2026-10-21.
  • Data refreshedfrom sourceMoleculeFinder2026-11-09

Keep exploring

Sources and notes
  • Compared side by sidefrom sourceMoleculeFinder comparison notesA molecule we compare it with on its own page.
  • The same kind of moleculefrom sourceMoleculeFinder curated groupsA structural neighbour in the same family or type group; the line names the group in its own words.
  • The drawingscomputedPubChem structures, drawn by RDKit