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Cat. No.	Product Name	Target	Signaling Pathways
T72403	Ferroptosis inducer-1
	Ferroptosisinducer-1 是一种铁凋亡 (Ferroptosis) 诱导剂，具有抗肿瘤的潜力。
T74069	Fluorescein-diisobutyrate-6-amide
	Fluorescein-diisobutyrate-6-amide，作为一种有效的铁死亡(ferroptosis)诱导剂，展示了其在癌症研究中的潜力。
T79777	GPX4-IN-7	Ferroptosis	Apoptosis
	GPX4-IN-7 (Compound 31)，一种靛玉红衍生物，作为结肠癌铁死亡的诱导剂，对HCT-116细胞显示出卓越的抗肿瘤效果，IC50为0.49 μM。该化合物通过促进GPX4降解和脂质ROS积累，有效触发铁死亡。
T79639	Lepadin H	Ferroptosis	Apoptosis
	Lepadin H 是一种具有显著细胞毒性的海洋生物碱，能够诱导铁死亡。它通过增加 p53 表达、提升 ROS 生成和脂质过氧化来展开作用，同时抑制 SLC7A11 和 GPX4，上调 ACSL4。Lepadin H 主要通过 p53-SLC7A11-GPX4 路径实现其诱导铁死亡的功能。
T37851	Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III)
	Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) is an inducer of ferroptosis.1 It induces ferroptosis, but not apoptosis or necroptosis, in NB1 cancer cells when used at a concentration of 3 μM.1 Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) inhibits proliferation of BJAB, NALM-6, Jurkat, MelHO, and MCF-7 cancer cells (IC50s = 0.07, 2.5, 1.5, 3, and 5 μM, respectively), as well as NALM-6 cells resistant to daunorubicin and vincristine when used at concentrations ranging...
T35994	Erastin2 Erastin2
	Erastin2 is a ferroptosis inducer and an inhibitor of the system xc- cystine/glutamate transporter.[1] [2] It inhibits glutamate release in CCF-STTG1 cells (IC50 = 0.0035 &#181M).[2] It induces cell death in HAP1 cells when used at a concentration of 5 &#181M, an effect that can be blocked by the ferroptosis inhibitor ferrostatin-1 or deferoxamine . [1] Erastin2 also induces ferroptotic cell death in HT-1080 cells (EC50 = 0.15 &#181M), an effect that can be blocked by the reducing agent β-merc...
T79359	Anticancer agent 147	Ferroptosis	Apoptosis
	Anticanceragent 147（化合物6j），作为槐定碱的衍生物，功能为铁死亡（Ferroptosis）诱导剂。该化合物能促进Fe2+、活性氧（ROS）及丙二醛（MDA）在细胞内的积累，并通过增加内质网（ER）应激和上调转录因子ATF3的表达发挥作用。在体外及体内实验中，Anticanceragent 147展现了出色的抗肝癌活性。
T36882	CAY10773
	CAY10773 is a derivative of the ferroptosis inducer sorafenib .1It selectively inhibits proliferation of BEL-7402, MGC803, and T24 bladder cancer cells (IC50s = 5.77, 5.21 and 3.97 μM, respectively) over non-cancerous HCV-29 cells (IC50= 23.19 μM). CAY10773 induces apoptosis in T24 cells when used at concentrations ranging from 2 to 6 μM but induces ferroptosis at concentrations greater than or equal to 6 μM with 10 hour or longer incubation times. It increases the production of reactive oxygen ...