Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TP2161 | Z-WEHD-FMK
化合物 TP2161
|
210345-00-9 | 98% |
|
Z-WEHD-FMK is a cell-permeable and irreversible inhibitor of caspase-1/5. It also shows a robust inhibitory effect on cathepsin B activity (IC50: 6 μM). | ||||
TN4160 | Goniothalamin
化合物Goniothalamin
|
17303-67-2 | 98% |
|
Goniothalamin 在各种癌细胞系中诱导细胞凋亡并具有胃保护活性。 | ||||
TN2034 | Paeoniflorigenone
芍药甙元酮
|
80454-42-8 | 98% |
|
Paeoniflorigenone is a depolarizing neuromuscular blocking agent, being similar to succinylcholine. | ||||
TN2691 | 2',3'-Dehydrosalannol
化合物 TN2691
|
97411-50-2 | 98% |
|
2',3'-Dehydrosalannol possesses antifeedant activity against Spodptera litura. It shows anticancer effects on triple-negative breast cancer(TNBC), it inhibits ca... | ||||
TN1532 | Crenulatin
大花红天素
|
63026-02-8 | 98% |
|
Crenulatin has dual- direction effects on apoptosis of cerebral microvascular endothelial cells, inhibitive effect in 25 mg/L and stimulative effect in 100 mg/L ... | ||||
TN4604 | Myricanone
化合物 TN4604
|
32492-74-3 | 98% |
|
Myricanone has antioxidant, and anticancer activities, it has apoptosis-promoting ability by triggering caspase activation, and suppression of cell proliferation... | ||||
T16998 | Tauroursodeoxycholate dihydrate
牛磺熊去氧胆酸二水合物
|
117609-50-4 | 98% |
|
Tauroursodeoxycholate dihydrate is an endoplasmic reticulum stress inhibitor. Tauroursodeoxycholate also inhibits ERK. Tauroursodeoxycholate significantly decrea... | ||||
TN3922 | Effusanin E
化合物 TN3922
|
76470-15-0 | 98% |
|
Effusanin E shows antibacterial and anti-cancer activities, it significantly inhibits cell proliferation and induces apoptosis in NPC cells by suppressing p50/p6... | ||||
TN4944 | Santamarine
化合物 TN4944
|
4290-13-5 | 98% |
|
Santamarine has significant anticancer activity, can inhibit L1210 cells because of its cytotoxic,cytostatic and blocking mitosis and reducing uptake of thymidin... | ||||
TN3931 | Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid
化合物 TN3931
|
57719-81-0 | 98% |
|
Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular ... | ||||
TN1837 | Kuguaglycoside C
化合物 TN1837
|
1041631-93-9 | 98% |
|
Kuguaglycoside C induces caspase-independent cell death, and is involved, at least in part, in the mechanism underlying cell necroptosis. | ||||
TN1086 | Dehydrotrametenolic acid
松苓新酸
|
6879-05-6 | 98% |
|
Dehydrotrametenolic acid (Dehydroeburicoic acid) 是从茯苓的菌核中分离的一种甾醇,具有抗肿瘤活性、抗炎和抗糖尿病作用。它通过 caspase-3途径诱导细胞凋亡。 | ||||
TN2040 | Panaxynol
人参炔醇
|
81203-57-8 | 98% |
|
Panaxynol is the most potent antiplatelet agent in ginseng and its mechanism of action is chiefly due to the inhibition of thromboxane formation. | ||||
TN4046 | Excisanin A
化合物 TN4046
|
78536-37-5 | 98% |
|
ExcisaninA may be a potent inhibitor of AKT signaling pathway in tumor cells, it can inhibit invasion by suppressing MMP-2 and MMP-9 expression, it may be a pote... | ||||
TMA0918 | Neochamaejasmine A
化合物 TMA0918
|
90411-13-5 | 98% |
|
Neochamaejasmin A can inhibit cellular (3)H-thymidine incorporation (IC 50 12.5 microg/mL) and subsequent proliferation of human prostate cancer LNCaP cells, it ... | ||||
TN4307 | Isolimonexic acid
化合物 TN4307
|
73904-93-5 | 98% |
|
Isolimonexic acid exhibits cytotoxicity on MCF-7 cell lines, it also inhibits Panc-28 cancer cell growth. | ||||
T5526 | Glycoborinine
化合物 T5526
|
233279-39-5 | 98% |
|
Glycoborinine is a potential molecule against cancer cells, it can induce HepG2 apoptosis through the mitochondrial-dependent pathway. Glycoborinine has photo-ac... | ||||
TN1538 | Curzerenone
莪术酮
|
20493-56-5 | 98% |
|
Curzerenone holds great promise for use in chemopreventive and chemotherapeutic strategies, it has slightly effective against E. coli (IZ = 10.8 ± 0.52). | ||||
T11210 | EP1013
化合物 T11210
|
223568-55-6 | 98% |
|
EP1013 is a broad-spectrum selective inhibitor of Caspase used in the study of type 1 diabetes. | ||||
TN4271 | Isochamaejasmine
异狼毒素
|
93859-63-3 | 98% |
|
Isochamaejasmine 分离自 S. chamaejasme L. 中分离出来,可抑制 NF-κB 活化。 Isochamaejasmine 通过抑制 Bcl-2 家族蛋白的活性诱导白血病细胞凋亡,可用于抗癌研究。 |