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. Author manuscript; available in PMC: 2015 Oct 14.
Published in final edited form as: Chem Commun (Camb). 2014 Oct 14;50(80):11788–11805. doi: 10.1039/c4cc00968a

Table 1.

Summary of H2S donors.

H2S donors Structures H2S release
mechanism
Representative
bioactivities
Key
ref.
H2S (gas) H2S Authentic H2S resource Hibernation induction Type II diabetes amelioration 6770
Sulfide salts NaHS & Na2S Hydrolysis Heart failure reduction Anti-inflammation 7583
Garlic-derived sulfur compounds R-S-Sn-S-R Thiol activation Vasodilation 86
Lawesson’s reagent graphic file with name nihms613528t1.jpg Hydrolysis Anti-inflammation Ion channel regulation 97, 98
GYY4137 graphic file with name nihms613528t2.jpg Hydrolysis Vasodilation Anti-inflammation Anti-cancer 99, 105, 106
Phosphorodithioates graphic file with name nihms613528t3.jpg Hydrolysis Prevention against oxidative damages 107
DTTs graphic file with name nihms613528t4.jpg Hydrolysis Anti-inflammation Anti-cancer 114, 124126, 129
N-(acylthio)-benzamides graphic file with name nihms613528t5.jpg Thiol activation No biological effects were reported to date. 132
S-SH compounds graphic file with name nihms613528t6.jpg Thiol activation MI/R protection 133
Dithioperoxyanhydrides graphic file with name nihms613528t7.jpg Thiol activation Vasodilation 137
Arylthioamides graphic file with name nihms613528t8.jpg Thiol activation Vasodilation 140
Gem-dithiol compounds graphic file with name nihms613528t9.jpg Light activation No biological effects were reported to date. 141
Ketoprofenate-caged compound graphic file with name nihms613528t10.jpg Light activation No biological effects were reported to date. 149
Thioamino acids graphic file with name nihms613528t11.jpg Bicarbonate activation Vasodilation 150