Finasteride
Also called Propecia, Chibro-Proscar, Finastid and Finpecia.
A hormone medicine sold as Proscar and Propecia, used for enlarged prostate and for male pattern hair loss.
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. Finasteride 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 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.
Rings joined where they share atoms, or a single ring standing alone. Atoms in a ring are held in place, so this part keeps its shape while chains around it can bend.
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
Finasteride
Minoxidil
Finasteride blocks the enzyme that makes DHT, the hormone behind male pattern hair loss, while minoxidil leaves hormones alone and widens scalp vessels.
Finasteride vs Minoxidil, 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
- C23H36N2O2
- Molecular weight
- 372.5 g/mol
- XLogP3octanol/water, log units
- 3
- Polar surface areatopological
- 58.2 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Rotatable bonds
- 2
- Complexity
- 678
Reported Hazard label (GHS), ECHA via PubChem
Danger Irritant pictogram (GHS07), Health hazard pictogram (GHS08) and Environmental pictogram (GHS09); hazard statements H302, H360, H372, H410
Reported Licence
The US Food and Drug Administration licenses Finasteride for human use (NDA 020180, authorized June 19, 1992), as Proscar. Drugs@FDA
Groups it belongs to
- Category
- Prescription medicine
- Family
- Hormone medicines
- Chemical groups
- Amides
- Elements
- Nitrogen
- Hazard classes
- Irritant, Health hazard, Environmental hazard, GHS Danger
C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2C(=O)NC(C)(C)C)CC[C@@H]4[C@@]3(C=CC(=O)N4)CPubChem CID 57363 · Wikidata Q424167 · InChIKey DBEPLOCGEIEOCV-WSBQPABSSA-N · Data refreshed
Questions
- What is Finasteride?
- A hormone medicine sold as Proscar and Propecia, used for enlarged prostate and for male pattern hair loss.
- How toxic is Finasteride?
- Its GHS hazard label carries the signal word Danger and the hazard pictograms Irritant, Health hazard and Environmental. from source
- What kind of molecule is Finasteride?
- Finasteride has the formula C23H36N2O2 and a molecular weight of 372.5 g/mol. MoleculeFinder files it under hormone medicines, in the prescription medicine group. from sourcefrom sourcefrom sourcefrom source
- Who licenses Finasteride as a medicine?
- The US Food and Drug Administration licenses Finasteride for human use (NDA 020180, authorized June 19, 1992), as Proscar. 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