PeptideDB

SLC7A11-IN-1

CAS: F: C13H15Cl2F3N4O5PtS W: 662.33

SLC7A11-IN-1 is a potent solute carrier family 7 member 11 (SLC7A11, xCT) inhibitor. SLC7A11-IN-1 shows antiproliferativ
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Bioactivity SLC7A11-IN-1 is a potent solute carrier family 7 member 11 (SLC7A11, xCT) inhibitor. SLC7A11-IN-1 shows antiproliferative activity. SLC7A11-IN-1 inhibits cell invasion and metastasis. SLC7A11-IN-1 induces Apoptosis and cell cycle arrest at S-phase. SLC7A11-IN-1 shows anti-tumor activity[1].
Target SLC7A11
Invitro SLC7A11-IN-1 (compound 2; 0-100 µM; 72 h) 显示出抗增殖活性,对于 HCT-116, MDA-MB-231, MCF-7, HepG2, LO2 细胞的 IC50 值分别为 0.03、0.11、0.18、0.17、0.27 µM[1]。SLC7A11-IN-1 (0.5 µM; 24 h) 抑制 HCT-116 细胞的侵袭和转移[1]。SLC7A11-IN-1 (0.5 µM; 24 h) 诱导细胞凋亡和细胞周期停滞在 S 期[1]。SLC7A11-IN-1明显降低细胞内 GSH 含量,显着增强活性氧 (ROS) 的表达[1]。SLC7A11-IN-1 (1 µM; 15 h) 显著诱导 HCT-116 细胞的 DNA 损伤和相关蛋白表达[1]。 Cell Cycle Analysis[1] Cell Line:
In Vivo SLC7A11-IN-1 (2 mg/kg; i.v.; 每三天连续3次) 抑制小鼠肿瘤的生长[1] Animal Model:
Name SLC7A11-IN-1
Formula C13H15Cl2F3N4O5PtS
Molar Mass 662.33
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Li Z, et al. Blocking xCT and PI3K/Akt pathway synergized with DNA damage of Riluzole-Pt(IV) prodrugs for cancer treatment. Eur J Med Chem. 2023 Mar 15;250:115233.