Progoitrin

Progoitrin
Identifiers
CAS Number
  • 585-95-5 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:79352
ChemSpider
  • 58145377
KEGG
  • C08425
PubChem CID
  • 5281139
UNII
  • S27T66W417 checkY
CompTox Dashboard (EPA)
  • DTXSID20974057 Edit this at Wikidata
InChI
  • InChI=1S/C11H19NO10S2/c1-2-5(14)3-7(12-22-24(18,19)20)23-11-10(17)9(16)8(15)6(4-13)21-11/h2,5-6,8-11,13-17H,1,3-4H2,(H,18,19,20)/t5-,6+,8+,9-,10+,11-/m0/s1
    Key: MYHSVHWQEVDFQT-ILPXZUKPSA-N
  • OC[C@H]1O[C@@H](SC(C[C@@H](O)C=C)=NOS(O)(=O)=O)[C@H](O)[C@@H](O)[C@@H]1O
Properties
Chemical formula
C11H19NO10S2
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Progoitrin is a biochemical from the glucosinolate family that is found in some food, which is inactive but after ingestion is converted to goitrin. Goitrin decreases the thyroid hormone production.

Progoitrin has been isolated in cabbage, brussels sprouts, kale, peanuts, mustard, rutabaga, kohlrabi, spinach, cauliflower, horseradish, and rapeseed oil.[1]

References

  1. ^ Comprehensive Pharmacy Review, Leon Shargel, 6th edition, p1191.

Bibliography

  • Greer, Monte A. (20 March 1956). "Isolation from Rutabaga Seed of Progoitrin, the Precursor of the Naturally Occurring Antithyroid Compound, Goitrin (L-5-Vinyl-2-Thioöxazolidine)1". Journal of the American Chemical Society. 78 (6): 1260–1261. doi:10.1021/ja01587a052.