Tacrolimus
Also called fujimycin.
An immunosuppressant from a Japanese soil bacterium, used to stop organ rejection after transplant and as an eczema ointment.
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
Where you encounter it
Dispensed on prescription, not sold on a shelf. Tacrolimus 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.
An ester closed into a ring: the C=O carbon and the oxygen beside it are both ring atoms. Like any ester, it can be split by water, which opens the ring.
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 C=O with a carbon on each side. Its oxygen accepts hydrogen bonds but has no hydrogen to give, and it resists oxidation better than an aldehyde.
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.
Properties and sources
Calculated by PubChem
- Molecular formula
- C44H69NO12
- Molecular weight
- 804 g/mol
- XLogP3octanol/water, log units
- 2.7
- Polar surface areatopological
- 178 Ų
- H-bond donors
- 3
- H-bond acceptors
- 12
- Rotatable bonds
- 7
- Complexity
- 1480
Measured LD50, HSDB via PubChem
134 mg/kg pure tacrolimus, rat, oral
An LD50 is an animal study measurement, not a dose for a person.
Reported Hazard label (GHS), ECHA, HSDB via PubChem
Danger Toxic pictogram (GHS06) and Health hazard pictogram (GHS08); hazard statements H301, H361, H372
Reported Licence
The US Food and Drug Administration licenses Tacrolimus for human use (NDA 050708, authorized April 8, 1994), as Prograf. Drugs@FDA
Groups it belongs to
- Category
- Prescription medicine
- Family
- Immunosuppressants
- Elements
- Nitrogen
- Hazard classes
- Acutely toxic, Health hazard, GHS Danger
C[C@@H]1C[C@@H]([C@@H]2[C@H](C[C@H]([C@@](O2)(C(…176 charactersPubChem CID 445643 · Wikidata Q411648 · InChIKey QJJXYPPXXYFBGM-LFZNUXCKSA-N · Data refreshed
Questions
- What is Tacrolimus?
- An immunosuppressant from a Japanese soil bacterium, used to stop organ rejection after transplant and as an eczema ointment.
- How toxic is Tacrolimus?
- The reported LD50 of Tacrolimus is 134 mg/kg (rat, oral). An LD50 is an animal study measurement, not a dose for a person. Its GHS hazard label carries the signal word Danger and the hazard pictograms Toxic and Health hazard. from sourcefrom source
- What kind of molecule is Tacrolimus?
- Tacrolimus has the formula C44H69NO12 and a molecular weight of 804 g/mol. MoleculeFinder files it under immunosuppressants, in the prescription medicine group. from sourcefrom sourcefrom sourcefrom source
- What else is Tacrolimus called?
- Tacrolimus is also called fujimycin. from source
- Who licenses Tacrolimus as a medicine?
- The US Food and Drug Administration licenses Tacrolimus for human use (NDA 050708, authorized April 8, 1994), as Prograf. from source
Sources and notes
- Calculated valuescomputedPubChemComputed from the structure, so no laboratory conditions apply; complexity is PubChem's own structural score.
- LD50from sourceHSDB via PubChemOther values the sources report: rat, intravenous, 23.6 mg/kg. The page shows the one LD50 the site uses everywhere.
- 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
- 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