Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN3152 | 6-Acetonyldihydrochelerythrine
化合物 TN3152
|
22864-92-2 | 98% |
|
6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therape... | ||||
TN4490 | Manassantin B
化合物 TN4490
|
88497-88-5 | 98% |
|
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV ... | ||||
T14499 | Bax activator-1
化合物 T14499
|
1638526-94-9 | 98% |
|
Bax activator-1 (compound 106) is a Bax activator. It induces Bax-dependent tumor cell apoptosis[1]. | ||||
TN1139 | Dehydrocavidine
岩黄连碱
|
83218-34-2 | 98% |
|
Dehydrocavidine (Dehydrocorydaline) 具有抗肿瘤活性,它通过诱导调节 Bax/Bcl-2 介导的细胞凋亡、激活半胱天冬酶以及切割 PARP 来抑制 MCF-7 细胞增殖。 | ||||
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 ... | ||||
TN3653 | Cimidahurinine
化合物 TN3653
|
142542-89-0 | 98% |
|
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity... | ||||
T10485 | PROTAC Bcl2 degrader-1
化合物 T10485
|
2378801-85-3 | 98% |
|
PROTAC Bcl2 degrader-1 is a PROTAC, which potently and selectively induces the degradation of Mcl-1 (IC50: 11.81 μM) and Bcl-2 (IC50: 4.94 μM; DC50: 3.0 μM). | ||||
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. | ||||
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... | ||||
T13337 | WEHI-539 hydrochloride
化合物 T13337
|
2070018-33-4 | 98% |
|
WEHI-539 hydrochloride is a selective Bcl-XL inhibitor (IC50: 1.1 nM). | ||||
T13337L | WEHI-539
化合物WEHI-539
|
1431866-33-9 | 98% |
|
WEHI-539是一种选择性的 Bcl-XL 抑制剂(IC50:1.1 nM)。 | ||||
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。 | ||||
TN3614 | Cearoin
化合物 TN3614
|
52811-37-7 | 98% |
|
Cearoin has anti-inflammatory, and antiallergic activities, it can markedly inhibit inflammatory responses including LPS-induced NO production by suppressing the... | ||||
TN2308 | Wilfortrine
雷公藤春碱
|
37239-48-8 | 98% |
|
Wilfortrine can induce liver cancer cell HepG2 apoptosis, but with no effect on the cell cycle, mainly by promoting Bax expression and inhibiting anti-apoptotic ... | ||||
TMA0153 | Safflor Yellow A
化合物 TMA0153
|
85532-77-0 | 98% |
|
Safflor Yellow A protects cultured rat cardiomyocytes against A/R injury, maybe via inhibiting cellular oxidative stress and apoptosis. | ||||
T11973 | Mcl1-IN-11
化合物 T11973
|
2042211-13-0 | 98% |
|
Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively. | ||||
T10577 | BM 957
化合物 T10577
|
1391107-54-2 | 98% |
|
BM 957 is an effective Bcl-2 and Bcl-xL inhibitor (Kis: 1.2 and <1 nM; IC50s: 5.4 and 6.0 nM). | ||||
T16043 | Metaproterenol
化合物 T16043
|
586-06-1 | 98% |
|
Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM). | ||||
TN3486 | Bakkenolide IIIa
化合物 TN3486
|
915289-60-0 | 98% |
|
Bakkenolide IIIa has antioxidant, and neuroprotective effects, it protects against cerebral damage by inhibiting AKT and ERK1/2 activation and inactivated NF-κB... |