ganoderic acid ε

Ganoderic acid ε, a naturally occurring terpenoid, is extracted from the Fungus Ganoderma lucidum. This compound possesses an ED 50 value of 12.2 μg mL, as demonstrated in its impact on Meth-A tumor cells.

The binding affinities of ganoderic acid DM andGanoderic acid ζ (ΔGbind, -16.83 and-10.99 kcal mol-1) are comparable to that of current commercial drug oseltamivir (-23.62 kcal mol-1);Ganoderic acid DM is a potential source of anti-influenza ingredient, with novel binding pattern and advantage over oseltamivir, it has steric hindrance on the 150 cavity of N1 protein, and exerts activities across the H274Y and N294S mutations, is the attractive candidates of novel neuraminidase (NA) inhibitors.Ganoderic acid zeta has cytotoxicity in vitro against Meth-A and LLC cell lines.

Ganoderic acid M 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T126539。

Ganoderic acid beta is a constituent from the fruiting body of Ganoderma lucidum (Fr.) Karst].

Ganoderic acid R为一种高效的抗癌化合物，通过促进肿瘤细胞系的凋亡(apoptosis)机制来抑制其生长。它对多药耐药(MDR)肿瘤细胞系(KB-A-1 Dox)及敏感肿瘤细胞系(KB-A-1)展现出显著的细胞毒性效应。

Ganoderic acid GS-1 是一种高度氧化的羊毛甾烷型三萜类化合物，具有抗 HIV-1蛋白酶活性，IC50为 58 μM。

Ganoderic acid Df 是一种羊毛甾烷型三萜类化合物，可从灵芝的子实体中分离得到。Ganoderic acid Df 有效抑制醛糖还原酶 (aldose reductase)，其 IC50为 22.8 ± 0.6 μM。

Ganoderic acid Mk (GA-Mk)为来源于灵芝菌丝的三萜酸类化合物，能有效抑制细胞增殖，并通过线粒体途径诱导HeLa细胞的细胞凋亡(apoptosis)，在宫颈癌研究中具有应用价值。

Ganoderic acid Mf为具有抗肿瘤活性的三萜类化合物，能导致细胞周期在G1期停滞，并在正常细胞与癌细胞中显示高度选择性，通过线粒体介导途径促进细胞凋亡(apoptosis)。

Ganoderic acid T1是Ganoderic acid T的去乙酰化衍生物，具有促进癌细胞凋亡(apoptosis)的功能。它通过降低线粒体膜电位以及激活caspase-9和caspase-3来引发细胞凋亡，并增加细胞内ROS的产生，从而表现出促氧化活性和细胞性毒作用，同时减弱抗氧化防御系统。

Methyl Ganoderic acid B, 一种从灵芝中分离得到的三萜类化合物，具有类似神经生长因子的神经元存活促进作用。

Ganoderic acid T为ganoderma lucidum中的一种天然化合物。

Ganoderic acid Me是来源于ganoderma lucidum的三萜类化合物。

A novel combination of triterpenoids includes at least ganoderic acid S (GAS), ganoderic acid T (GAT), ganoderic acid Me (GAMe), ganoderic acid R (GAR), and ganodermic acid S (GMAS), the composition is suitable for the treatment or prophylaxis of colon ca

Ganoderic acid Y significantly inhibits the replication of the viral RNA (vRNA) of EV71 replication through blocking EV71 uncoating.

Ganoderic acid AM1 treatment for 48 h inhibited the proliferation of HeLa human cervical carcinoma cells with IC(50) values of 19.8+ -0.7 microM.

Ganoderic acid K is an angiotensin-converting enzyme inhibitor. It has anti-tumor, and anti-inflammatory activities.

Ganoderic acid SZ是一种天然产物，其产品编号为 TN4104，CAS号为 865543-37-9。Ganoderic acid SZ可用作对照参考。

Ganoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs.

Ganoderic acid TN是一种天然产物，其产品编号为 TN4106，CAS号为 112430-64-5。Ganoderic acid TN可用作对照参考。

Ganoderic acid X is a potential Mdm2 inhibitor(K(i) = 16nM). It is a potential anticancer drug, inhibits topoisomerases and induces apoptosis of cancer cells.

Ganoderic acid L is a natural product from the fruiting body of the fungus Ganoderma lucidum (Reishi).

Ganoderic acid GS-2 inhibits the activity of the human immunodeficiency virus-1 (HIV-1) protease.

12-Acetoxy ganoderic acid D 是一种天然化合物，可作为天然产物对照品。