Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN4038 | Eupatolide
泽兰内酯
|
6750-25-0 | 98% |
|
Eupatolide 是从 Inula japonica 的花中分离出来的,具有抗炎活性。 Eupatolide 可用于研究乳腺癌细胞对 TRAIL 的耐药性。 | ||||
T10274 | AKT-IN-2
化合物 T10274
|
1295514-91-8 | 98% |
|
AKT-IN-2 is a selective, and orally bioavailable AKT inhibitor (IC50: 5 nM for AKT1). | ||||
T11743 | Kanosamine hydrochloride
化合物 T11743
|
57649-10-2 | 98% |
|
Kanosamine hydrochloride is an antibiotic which inhibits the growth of plant-pathogenic oomycetes, certain fungi and a few bacterial species. Kanosamine inhibits... | ||||
TN4263 | Isoangustone A
化合物 TN4263
|
129280-34-8 | 98% |
|
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation ... | ||||
TN4390 | Kihadanin B
化合物 TN4390
|
73793-68-7 | 98% |
|
Kihadanin B can repress the adipogenesis by decreasing lipid accumulation through the suppression of the Akt-FOXO1-PPARγ axis in 3T3-L1 adipocytes. | ||||
TN1376 | α-Solanine
α-茄碱
|
20562-02-1 | 98% |
|
Alpha-Solanine alters antioxidative enzyme activities and MDA and PCO concentrations and GST activity in fat body and midgut. | ||||
TN1235 | 3,4,5-Tricaffeoylquinic acid
3,4,5-三咖啡酰奎宁酸
|
86632-03-3 | 98% |
|
3,4,5-Tricaffeoylquinic acid may attenuate the TNF-α±- and LPS-stimulated production of inflammatory mediators in keratinocytes by suppressing the Toll-like rece... | ||||
TN3691 | Communic acid
化合物 TN3691
|
2761-77-5 | 98% |
|
Communic acid has antibacterial activity, including against mycobacterial. trans-Communic acid has potential to be utilized as anti-wrinkling agents and cosmetic... | ||||
TN3525 | Boehmenan
化合物 TN3525
|
57296-22-7 | 98% |
|
(±)-Boehmenan shows potent protein-tyrosine phosphatase 1B (PTP1B) inhibitory activity in vitro with the IC(50) values of 43.5 uM, it inhibits PTP1B activity in ... | ||||
TN3219 | 7,8-Didehydrocimigenol
化合物 TN3219
|
150972-72-8 | 98% |
|
7,8-Didehydrocimigenol can be used for the treatment of cardiovascular disorders such as atherosclerosis. It upregulates PPAR-γ in EC inhibits NF-kB activity of ... | ||||
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... | ||||
TN4244 | Icariside B1
淫羊藿次甙B1
|
109062-00-2 | 98% |
|
Icariside B1 shows inhibitory effects on LPS-induced NO production in RAW264.7 cells. | ||||
TN1889 | Lupalbigenin
化合物Lupalbigenin
|
76754-24-0 | 98% |
|
Lupalbigenin sensitizes detachment-induced cell death in human lung cancer cell through down-regulation of pro-survival proteins. | ||||
TN4506 | (+)-Matairesinol
化合物 TN4506
|
148409-36-3 | 98% |
|
(+)-Matairesinol exhibits immunomodulatory activity; it also shows inhibition of the discoloration of yellowtail dark muscle. | ||||
TN3139 | 5α-Hydroxycostic acid
化合物 TN3139
|
132185-83-2 | 98% |
|
5alpha-Hydroxycostic acid possesses anti-angiogenic ability by interfering the VEGF- and Ang2-related pathways, and it may be a good drug candidate. | ||||
T15056 | DB07107
化合物 T15056
|
552332-71-5 | 98% |
|
DB07107 is a potent inhibitor of drug resistant T315I mutant Bcr-Abl tyrosine kinase and a potent Akt1 inhibitor (IC50: 360 nM). | ||||
T2S0606 | Bakkenolide A
蜂斗菜内酯A
|
19906-72-0 | 98% |
|
Bakkenolide A has antifeedant and growth inhibitory effects on neonate variegated cutworms, it inhibits leukemia by regulation of HDAC3 and PI3K/Akt-related sign... | ||||
TMA1743 | Ergosterol peroxide
过氧麦角甾醇
|
2061-64-5 | 98% |
|
Ergosterol peroxide is an inhibitor of osteoclast differentiation, which has antiviral, trypanocidal, antitumor, and antiangiogenic actions, it can stimulate Fox... | ||||
TN2328 | Zeylenone
山椒子烯酮
|
193410-84-3 | 98% |
|
Zeylenone 是一种来自 Uvaria grandiflora的环己烯氧化物,具有抗肿瘤和抗癌细胞增殖活性,通过 PI3K/AKT/mTOR 和 MAPK/ERK 信号通路抑制宫颈癌细胞增殖,诱导细胞凋亡 (apoptosis)。 | ||||
T75078 | Antitumor agent-86
化合物 Antitumor agent-86
|
2907704-65-6 | 98% |
|
Antitumor agent-86 (compound 5a) 对MCF-7乳腺癌细胞线具有IC50值2.62 µM的抑制活性。该化合物通过促进细胞凋亡和引发细胞周期阻滞来表现其抗癌效能,并对RAS/PI3K/Akt/JNK信号传导途径具有靶向作用。 |