Other Apoptosis - Apoptosis - Signaling Pathways

Cat.No. Product Name Information

GC45213 α-NETA Choline acetyltransferase (ChAT) mediates the synthesis of the neurotransmitter acetylcholine from acetyl-CoA and choline.

GC46008 (±)-Thalidomide-d4

GC45256 (+)-ar-Turmerone (+)-ar-Turmerone is an aromatic compound from the rhizomes of C.

GC41345 (-)-α-Bisabolol (-)-α-Bisabolol is a sesquiterpene alcohol that has been found in the essential oils of several aromatic plants, including C.

GC11965 (-)-Huperzine A NMDA receptor antagonist/AChE inhibitor

GC40698 (-)-Perillyl Alcohol (-)-Perillyl alcohol is a monoterpene alcohol that has been found in lavender essential oil and has diverse biological activities.

GC34965 (20S)-Protopanaxatriol (20S)-Protopanaxatriol 是人参皂苷的代谢物，通过 glucocorticoid receptor 和 oestrogen receptor 起作用，同时为 LXRα 的抑制剂。

GC34981 (E)-Flavokawain A (E)-Flavokawain A 是从卡瓦胡椒中提取的查尔酮，具有抗癌作用。(E)-Flavokawain A 通过介入 bax 蛋白依赖和线粒体依赖的凋亡通路，诱导膀胱癌细胞凋亡，抑制小鼠肿瘤生长。

GC34125 (E)-[6]-Dehydroparadol (E)-[6]-Dehydroparadol来自专利US9272994化合物M15,能够抑制人体癌细胞生长并且诱导细胞凋亡。在HCT-116和H-1299细胞中的IC50值分别为43.02和41.59μM。

GN10783 (R) Ginsenoside Rh2 Extracted from Panax ginseng C. A. Mey. dried roots;Store the product in sealed, cool and dry condition

GC15104 (R)-(+)-Etomoxir sodium salt carnitine palmitoyltransferase I (CPT1) inhibitor

GC41716 (R)-CR8 Cyclin-dependent kinases (CDKs) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.

GC19541 (rac)-Antineoplaston A10

(rac)-Antineoplaston A10 is the racemate of Antineoplaston A10

GC10098 (S)-10-Hydroxycamptothecin inhibitor of topoisomerase I

GC11988 15-acetoxy Scirpenol mycotoxin that induce apoptotic cell death

GC11720 17-AAG (KOS953) Hsp90 inhibitor

GC13044 17-DMAG (Alvespimycin) HCl Hsp90 inhibitor

GN10065 2-Atractylenolide Extracted from Atractylodes macrocephala Koidz. rhizome;Store the product in sealed, cool and dry condition

GC17430 2-Deoxy-D-glucose Glycolysis inhibitor

GC38318 2-Methoxycinnamaldehyde 2-Methoxycinnamaldehyde (o-Methoxycinnamaldehyde) 是一种肉桂中的天然化合物，具有抗肿瘤活性。2-Methoxycinnamaldehyde 能通过使线粒体膜电位 (δψm) 损失、激活 caspase-3 和 caspase-9，来抑制细胞增殖和诱导细胞凋亡。2-Methoxycinnamaldehyde 能有效抑制血小板衍生生长因子诱导的 HASMC 迁移。