| S1692 |
Busulfan
|
Busulfan is a cell cycle non-specific alkylating antineoplastic agent. It causes DNA damage by cross-linking DNAs and DNA and proteins. Busulfan inhibits thioredoxin reductase activity. It also induces apoptosis. It is an immunosuppressive and myeloablative chemotherapeutic agent.Busulfan (NSC-750) can be used to induce animal models of Anemia.
|
-
Biomolecules, 2025, 15(2)297
-
J Immunother Cancer, 2024, 12(11)e009805
-
iScience, 2024, 27(10):110862
|
|
| S4307 |
Auranofin (SKF-39162)
|
Auranofin is an inhibitor of thioredoxin reductase (TrxR) with IC50 of 88 nM for purified H. pylori TrxR in cell-free assay. Auranofin has anti-cancer activity and can completely inhibit bacterial growth at 1.2 μM. Auranofin is an FDA-approved gold-containing compound used for the treatment of rheumatoid arthritis.
|
-
Cell, 2025, S0092-8674(25)00751-2
-
Antimicrob Agents Chemother, 2025, e0047125.
-
Cancers (Basel), 2024, 16(21)3606
|
|
| S0267 |
TRi-1
|
TRi-1 (HUN20688, TXNRD1 inhibitor 1) is a potent, specific and irreversible cytosolic thioredoxin reductase 1 (TXNRD1) inhibitor with IC50 of 12 nM. This compound exhibits anti-cancer activity while having little mitochondrial toxicity.
|
-
Antimicrobial Agents and Chemotherapy, 2025, e00471-25
-
Antimicrob Agents Chemother, 2025, e0047125.
-
Int J Mol Sci, 2023, 24(15)12460
|
|
| S8068 |
Chaetocin
|
Chaetocin, a natural product from Chaetomium species, is a histone methyltransferase inhibitor with IC50 of 0.8 μM, 2.5 μM and 3 μM for dSU(VAR)3-9, mouse G9a and Neurospora crassa DIM5, respectively. Chaetocin is an anticancer agent and inhibitor of thioredoxin reductase (TrxR).
|
-
Research (Wash D C), 2025, 8:0602
-
Cell Rep, 2025, 44(6):115742
-
Int J Mol Sci, 2024, 25(17)9215
|
|