Chemoprotective isothiocyanates
AssigneeThe Johns Hopkins University
InventorsCheon-Gyu Cho, Gary H. Posner, Paul Talalay, Yuesheng Zhang
Life of this patent
Estimating the term…
Loading patent…
AssigneeThe Johns Hopkins University
InventorsCheon-Gyu Cho, Gary H. Posner, Paul Talalay, Yuesheng Zhang
Estimating the term…
Sulforaphane has been isolated and identified as a major and very potent phase II enzyme inducer in broccoli (Brassica oleracea italica). Sulforaphane is a monofunctional inducer, inducing phase II enzymes selectively without the induction of aryl hydrocarbon receptor-dependent cytochromes P-450 (phase I enzymes). Analogues differing in the oxidation state of sulfur and the number of methylene groups were synthesized, and their inducer potencies were measured. Sulforaphane is the most potent of these analogues. Other analogues having different substituent groups in place of the methylsulfinyl group of sulforaphane were also synthesized and assessed. Of these, the most potent are 6-isothiocyanato-2-hexanone and exo-2-acetyl-6-isothiocyanatonorbornane.
A pharmaceutical composition comprising an active ingredient which is sulforaphane ((-)1-isothiocyanato-(4R)-(methylsulfinyl)butane) (CAS 4478-93-7) or an analogue thereof, said analogue being selected from the group consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A compound consisting of:
A method for suppressing the formation of chemically-induced mammary tumors or hepatomas, comprising:
Dependencies are inferred from the claim text.