Other Apoptosis
- Cat.No. Product Name Information
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GC45213
α-NETA
Choline acetyltransferase (ChAT) mediates the synthesis of the neurotransmitter acetylcholine from acetyl-CoA and choline.
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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。