fa16

FA16 是一种选择性、代谢稳定的铁死亡 (ferroptosis) 诱导剂 ，IC50 值为1.26 μM。FA16 是 2-(三氟甲基) 苯并咪唑的衍生物。FA16 对胱氨酸/谷氨酸反转运蛋白 (system Xc-) 介导了细胞内谷氨酸和细胞外胱氨酸的交换有抑制作用。FA16 在 HepG2 异种移植瘤模型中显著抑制肿瘤生长。

BODIPY-Palmitate, a fluorescent derivative of palmitic acid, exhibits excitation and emission maxima at 488 nm and 508 nm, respectively. It is employed in the monitoring of fatty acid uptake and metabolism within cultured cells.

Bevacizumab 是一种人源化靶向 VEGF 的单克隆抗体，特异性与 VEGF 结合，阻断 VEGR 与 VEGFR 结合，抑制血管生成信号通路。Bevacizumab 具有抗肿瘤活性，可以抑制肿瘤细胞生长。

PD-1-IN-17 TFA is a inhibitor of programmed cell death-1 (PD-1) .

Targaprimir-96 TFA is a potent microRNA-96 (miR-96) processing inhibitor.

αvβ1 integrin-IN-1 TFA 是一种有效的αvβ1整合素抑制剂(IC50: 0.63 nM)。

Palmitoleic acid alkyne, an ω-terminal alkyne derivative of palmitoleic acid, facilitates click chemistry applications. This compound has played a crucial role in examining protein palmitoylation processes. Specifically, the cis form of palmitoleic acid alkyne selectively tags wild-type Wnt3a protein within mouse fibroblast L-cells expressing Wnt3a and its secretion in conditioned media, distinguishing itself from the trans form and proving ineffective against the S209A mutant Wnt3a.

AMARA peptide (TFA) is a substrate for salt-induced kinase (SIK) and adenosine activated protein kinase (AMPK).

PD-1/PD-L1-IN 3 TFA inhibits the binding of human PD-1 to PD-Ll with an IC50 of 9 nM.

HPV16 E7 (86-93) TFA is a human leukocyte antigen (HLA)-A2.1 restricted HPV16 E7-derived peptide.