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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16777 |
ROC-325
|
Apoptosis; Autophagy | Apoptosis; Autophagy |
ROC-325 是一种有效的口服活性自噬抑制剂,具有抗癌活性。 ROC-325 诱导肾细胞癌凋亡并表现出良好的特异性。 | |||
T60036 |
ML-SA5
|
Autophagy | Autophagy |
ML-SA5 是一种 MCOLN1 激动剂,通过扰乱自噬体和溶酶体之间的融合来阻止自噬通量。 | |||
T1908 |
MHY1485
|
mTOR; Autophagy | Autophagy; PI3K/Akt/mTOR signaling |
MHY1485 是一种 mTOR 激活剂。它通过抑制自噬体和溶酶体之间的融合来抑制自噬过程,导致 LC3II 蛋白的积累和自噬体增大。 | |||
T11142 |
EACC
|
Autophagy | Autophagy |
EACC 是自噬的可逆抑制剂,可阻断自噬通量。它对自噬体特异性的 SNARE Stx17 易位具有选择性抑制作用,从而阻止自噬体与溶酶体的融合。 | |||
T8081 |
LC3-mHTT-IN-AN1
|
Others; Autophagy; ATTECs | Autophagy; Others; PROTAC |
LC3-mHTT-IN-AN1 是一种 mHTT-LC3 接头化合物,可与突变亨廷顿蛋白 (mHTT) 和 LC3B 相互作用。 它将 mHTT 靶向自噬体以等位基因选择性方式降低培养的亨廷顿病小鼠神经元中的 mHTT 水平。 | |||
T27187 |
DK-1-49
|
||
DK-1-49 is an autophagonizer. It causes accumulation of autophagy-associated LC3-II and enhanced levels of autophagosomes and acidic vacuoles. | |||
T19188 |
ALLO-1
|
Autophagy | Autophagy |
ALLO-1 is a crucial autophagy receptor responsible for facilitating the formation of autophagosomes around paternal organelles. It directly interacts with the worm LC3 homologue, LGG-1, through its LC3-interacting region (LIR) motif. | |||
T28107 |
MRT-68601 HCl
|
||
MRT-68601 HCl, a potent TBK1 (TANK-binding kinase-1), inhibits the formation of autophagosomes in lung cancer cells. | |||
T36995 |
MRT 68601 hydrochloride
|
||
Potent TBK1 (TANK-binding kinase-1) inhibitor (IC50 = 6 nM). Inhibits the formation of autophagosomes in lung cancer cells. Newman et al (2012) TBK1 kinase addiction in lung cancer cells is mediated via autophagy of Tax1bp1/Ndp52 and non-canonical NF-κB signalling. PLoS ONE 7 e50672 PMID:23209807 |McIver et al (2012) Synthesis and structure-activity relationships of a novel series of pyrimidines as potent inhibitors of TBK1/IKKe kinases. Bioorg.Med.Chem.Lett. 22 7169 PMID:23099093 | |||
T73550 | CUR5g | ||
CUR5g 是一种有效的自噬 (autophagy) 抑制剂。CUR5g 通过阻断自噬体-溶酶体融合选择性地抑制癌细胞中的自噬体降解。CUR5g 通过依赖 UVRAG 的机制阻止 STX17 募集到自噬体,导致自噬体无法与溶酶体融合。CUR5g 可提高顺铂 (Cisplatin) 在体外和体内对 A549 细胞的抗癌作用。 | |||
T60858 | MOPIPP | ||
MOPIPP 是新型的吲哚基查尔酮,可以透过血脑屏障。MOPIPP 对胶质母瘤细胞的肿瘤进展有抑制作用。MOPIPP 诱导细胞空泡化并增加自噬体数量。MOPIPP 还会触发细胞巨泡式死亡,并且中断葡萄糖摄取和糖酵解代谢。 | |||
T35922 |
NAADP (sodium salt)
|
||
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a secondary messenger that induces calcium mobilization. It induces calcium release from endosomes and lysosomes via two-pore channel 2 (TPC2) and TPC1, which then stimulates large-scale calcium release from granules and the endoplasmic reticulum mediated by type 1 ryanodine receptors (RyR2s), RyR3s, and inositol-(1,4,5)-triphosphate receptors (IP3Rs). NAADP induces calcium mobilization in sea urchin and starfish eggs post fertilization to... | |||
T60453 |
TrxR-IN-3
|
||
TrxR-IN-3 (Compound 2c) 是TrxR 的有效抑制剂。TrxR-IN-3 对五种人类癌细胞系表现出强大的抗增殖活性,特别是对乳腺肿瘤细胞。TrxR-IN-3 增加 ROS 水平并通过调节乳腺癌细胞中细胞凋亡相关蛋白的表达导致明显的细胞凋亡。TrxR-IN-3 还通过促进 LC3-II 和 Beclin-1 的表达并减少 LC3-I 和 p62 蛋白的表达,来触发自噬体和自溶酶体的形成。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6740 |
Bafilomycin A1
巴佛洛霉素A1,巴佛洛霉素 A1 |
Apoptosis; Proton pump; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Membrane transporter/Ion channel; Microbiology/Virology |
Bafilomycin A1 属于大环内酯类抗生素,是一种 V-ATPase (IC50=0.44 nM),具有特异性和可逆性。Bafilomycin A1 是自噬晚期阶段抑制剂,阻断自噬体与溶酶体的融合。Bafilomycin A1 也诱导凋亡。 | |||
T83281 | 6-(1-Hydroxyethyl)-5,6-dihydrochelerythrine | ||
6-(1-Hydroxyethyl)-5,6-dihydrochelerythrine 显著影响细胞器特性,涉及早期内体、线粒体及自噬体(源自帕金森病患者的嗅觉细胞)。 |