Progoitrin

Progoitrin
	File:Progoitrin.svg
Identifiers
CAS Number	585-95-5 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:79352;
ChemSpider	58145377;
ECHA InfoCard	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
E number	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
KEGG	C08425;
PubChem CID	5281139;
UNII	S27T66W417 ;
CompTox Dashboard (EPA)	{{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).;
	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;
	SMILES 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

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

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

Bibliography

Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

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

[1]

v t e Cruciferous biochemistry
Types of compounds	Phenylthiocarbamide (PTC/PTU) Thiocyanates Nitriles Indoles Gibberellin
Glucosinolates	Glucobrassicin Glucocapparin Glucoraphanin Gluconasturtiin Glucotropaeolin Progoitrin Sinigrin Sinalbin
Isothiocyanates (ITC, mustard oils)	Sulforaphane (SFN) Raphanin Allyl isothiocyanate (AITC) Methyl isothiocyanate (MITC) Benzyl isothiocyanate (BITC) Fluorescein isothiocyanate (FITC) Phenyl isothiocyanate (PITC) Phenethyl isothiocyanate (PEITC) 6-MITC Erucin
Bioactive metabolites	Goitrin Indole-3-carbinol
Brassicaceae (Cruciferous vegetables): Brassica Cruciferous Biochemistry genera (list)

Identifiers
File:Progoitrin.svg
CAS Number	585-95-5^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:79352
ChemSpider	58145377
ECHA InfoCard	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
E number	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
KEGG	C08425
PubChem CID	5281139
UNII	S27T66W417^Y
CompTox Dashboard (EPA)	{{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
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
SMILES 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

Progoitrin

References

Bibliography

Navigation menu

Search