Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN2511 | Britannilactone diacetate
化合物 TN2511
|
1286694-67-4 | 98% |
|
1,6-O,O-Diacetylbritannilactone(OODBL) has anti-inflammatory activity, it has a potential therapeutic efficacy on inflammatory diseases especially allergic airwa... | ||||
TN1458 | Buddlejasaponin IV
醉鱼草皂苷 Ⅳ
|
139523-30-1 | 98% |
|
Buddlejasaponin IV has analgesic and anti-inflammatory effects, the inhibitions of the expressions of iNOS, COX-2, TNF-alpha, IL-1beta and IL-6 by blocking NF-ka... | ||||
T16979 | Talazoparib tosylate
化合物 T16979
|
1373431-65-2 | 98% |
|
Talazoparib tosylate is a novel and potent PARP1/2 (n IC50: 0.57 nM for PARP1). | ||||
TN4999 | Serratenediol
化合物 TN4999
|
2239-24-9 | 98% |
|
Serratenediol demonstrates strong inhibitory effects on the Epstein-Barr virus early antigen (EBV-EA) activation without showing any cytotoxicity, its effects be... | ||||
TN3619 | Cedrusin
化合物 TN3619
|
75775-36-9 | 98% |
|
Cedrusin shows a cytotoxic effect on A375 and HeLa cells. | ||||
TN4340 | Ivangustin
化合物 TN4340
|
14164-59-1 | 98% |
|
Ivangustin exhibits remarkable cytotoxicity against HEp2, SGC-7901 and HCT116 human cancer cell lines. | ||||
TN4637 | Neogrifolin
化合物 TN4637
|
23665-96-5 | 98% |
|
Neogrifolin is a potential candidate for osteosarcoma, it can induce concentration- and time-dependent suppression of proliferation and induce apoptosis in U2OS ... | ||||
T12366 | PARP14 inhibitor H10
化合物 T12366
|
2084811-68-5 | 98% |
|
PARP14 inhibitor H10 is a selective inhibitor against PARP14 with IC50 of 490 nM | ||||
TN2106 | Protodeltonin
化合物 TN2106
|
94992-08-2 | 98% |
|
Protodeltonin may have anti-thrombotic activity by both improving the anticoagulation activity and inhibiting platelet aggregation action. Protodeltonin can inhi... | ||||
TN4341 | IVHD-valtrate
化合物 TN4341
|
28325-56-6 | 98% |
|
VHD-valtrate has anticancer effects against human ovarian cancer cells in vitro and in vivo, it is a potential therapeutic agent for ovarian cancer, providing a ... | ||||
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... | ||||
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。 | ||||
TN3070 | 4beta-Hydroxywithanolide E
化合物 TN3070
|
54334-04-2 | 98% |
|
4beta-Hydroxywithanolide E(4bHWE) can inhibit the growth of colon cancer monolayer and spheroid cultures, it assert its anti-tumor activity in carcinogenic progr... | ||||
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. | ||||
TN4028 | Euchrestaflavanone B
化合物 TN4028
|
87402-91-3 | 98% |
|
Euchrestaflavanone B shows antibacterial activity against Gram positive bacteria, Staphylococcus aureus, Bacillus subtilis and Bacillus cereus. Euchrestaflavanon... | ||||
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... | ||||
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... | ||||
TN1728 | Hellebrigenin
蟾蜍它里定
|
465-90-7 | 98% |
|
Hellebrigenin has anti-hepatoma activities, it induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells through inhibition of Akt. H... | ||||
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... |