Lisinopril
Also called Carace, Novatec, Prinivil and Qbrelis.
An ACE inhibitor used for high blood pressure and heart failure. Its lineage traces to a peptide in Brazilian pit viper venom.
Sources and notes
- The introductionfrom sourceMoleculeFinder curated
- Other namesfrom sourcePubChem / 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. Lisinopril on the product labels we hold.
Medicines
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.
A C=O bonded to a nitrogen, the same link that joins amino acids in a protein. It is sturdy, and its nitrogen is not a base the way an amine's is.
From: standard chemistry.
A nitrogen carrying one or two hydrogens. Its spare pair of electrons can pick up a hydrogen ion, so an amine is a base.
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
Lisinopril
Losartan
Lisinopril blocks the enzyme that makes angiotensin II and losartan blocks its receptor, which is why lisinopril can cause a dry cough and losartan does not.
Lisinopril vs Losartan, side by sideAlso compared
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
- C21H31N3O5
- Molecular weight
- 405.5 g/mol
- XLogP3octanol/water, log units
- −2.9
- Polar surface areatopological
- 133 Ų
- H-bond donors
- 4
- H-bond acceptors
- 7
- Rotatable bonds
- 12
- Complexity
- 550
Reported Hazard label (GHS), ECHA via PubChem
Danger Irritant pictogram (GHS07) and Health hazard pictogram (GHS08); hazard statements H315, H319, H360, H361, H362, H373
Reported Licence
The US Food and Drug Administration licenses Lisinopril for human use (NDA 019777, authorized May 19, 1988). Drugs@FDA
Groups it belongs to
- Category
- Prescription medicine
- Family
- Blood-pressure medicines
- Chemical groups
- Carboxylic Acids, Amines, Aromatics, Amides
- Elements
- Nitrogen
- Hazard classes
- Irritant, Health hazard, GHS Danger
C1C[C@H](N(C1)C(=O)[C@H](CCCCN)N[C@@H](CCC2=CC=CC=C2)C(=O)O)C(=O)OPubChem CID 5362119 · Wikidata Q412208 · InChIKey RLAWWYSOJDYHDC-BZSNNMDCSA-N · Data refreshed
Questions
- What is Lisinopril?
- An ACE inhibitor used for high blood pressure and heart failure. Its lineage traces to a peptide in Brazilian pit viper venom.
- How toxic is Lisinopril?
- Its GHS hazard label carries the signal word Danger and the hazard pictograms Irritant and Health hazard. from source
- What kind of molecule is Lisinopril?
- Lisinopril has the formula C21H31N3O5 and a molecular weight of 405.5 g/mol. MoleculeFinder files it under blood-pressure medicines, in the prescription medicine group. from sourcefrom sourcefrom sourcefrom source
- Who licenses Lisinopril as a medicine?
- The US Food and Drug Administration licenses Lisinopril for human use (NDA 019777, authorized May 19, 1988). 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 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.
- Similar in shapecomputedRDKit Morgan/TanimotoNeighbours by structural fingerprint; the sentence names the chemical groups the two share.
- The drawingscomputedPubChem structures, drawn by RDKit