glyoxalase i inhibitor

Glyoxalase I inhibitor, a candidate for anticancer agents, is a potent Glyoxalase I (GLO1) inhibitor.

Glyoxalase I inhibitor (free base), a candidate for anticancer agents, is a potent Glyoxalase I (GLO1) inhibitor.

Glyoxalase I inhibitor 5 (Compound 9h) is a potent inhibitor of glyoxalase I (Glo-I), with an IC50 value of 1.28 μM. This compound holds promise as an anticancer agent [1].

Glyoxalase I inhibitor 7 (Compound 6) is a potent inhibitor of glyoxalase I (Glo-I) with an IC50 of 3.65 μM. It exhibits potential as an anticancer agent [1].

Glyoxalase I inhibitor 3 (compound 22g) 是一种有效的乙二醛酶 I (GLO1)抑制剂，IC50为 0.011 μM。Glyoxalase I inhibitor 3具有研究抑郁和焦虑的潜力。

Glyoxalase I inhibitor 6 (Compound 9j) is an inhibitor of glyoxalase I (Glo-I) with an IC50 value of 1.13 μM. This compound shows potential as an anticancer agent, demonstrating low toxicity [1].

Glyoxalase I inhibitor 2 (compound 26) 是一种 glyoxalase I (GLO1) 的有效抑制剂 (IC50: 0.5 μM)。Glyoxalase I inhibitor 2 具有潜力进行抑郁和焦虑的研究。

Glyoxalase I inhibitor 4 是乙二醛酶 I (GLO1) 的有效抑制剂 (Ki: 10 nM)。

Glyoxalase I inhibitor 1 是 glyoxalase I (GLO1) 的有效抑制剂 (IC50: 26 nM)。

4BAB (compound 29) 是一种乙二醛酶 I (GLO1) 的不可逆抑制剂，表现出抗癌活性。

TLSC702 is a novel Inhibitor of Human Glyoxalase I, Inducing Apoptosis in Tumor Cells.

N,S-Bis-Fmoc-Glutathione为一有效glyoxalase II抑制剂，其Ki值达0.32 mM。