Niloticin is a mosquito insecticide from Limonia acidissima L.

24-Methylenecycloartanyl ferulate, a compound belonging to the γ-oryzanol family, demonstrates the ability to enhance parvin-beta expression within human breast cancer cells. Furthermore, it exhibits potential as an ATP-competitive Akt1 inhibitor, with an EC 50 value of 33.3 μM.

Neogrifolin is a potential candidate for osteosarcoma, it can induce concentration- and time-dependent suppression of proliferation and induce apoptosis in U2OS and MG63 osteosarcoma cell lines; it exhibits inhibitory activity against nitric oxide (NO) production stimulated by lipopolysaccharide (LPS) in RAW 264.7 cells with the IC50value of 23.3 microM. Neogrifolin possesses antimicrobial activities against Bacillus cereus and Enterococcus faecalis, the MIC values of 20 and 0.5 microg/mL, respectively.

Diosbulbin C has hepatotoxicity.

Dalbergioidin exhibits tyrosinase inhibitory activity with an IC50 of 20 mM. It shows a melanin biosynthesis inhibition zone in the culture plate of Streptomyces bikiniensis that has commonly been used as an indicator organism. Dalbergioidin protects MC3T3-E1 osteoblastic cells against H2O2-induced cell damage through activation of the PI3K/AKT/SMAD1 pathway, suggests that it may be useful in bone metabolism diseases, particularly osteoporosis. Dalbergioidin also ameliorates doxorubicin-induced renal fibrosis by suppressing the TGF-β signal pathway.

α-Linolenic acid-d14 是 α-Linolenic acid 的氘代物。α-Linolenic acid 是一种必需脂肪酸，无法由人体合成，通常从种子油中提取。它能够通过调节PI3K/Akt信号通路影响血栓形成过程，并且具有抗心律失常特性，与心血管疾病及癌症相关。

6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therapeutic Index) values of 1.77 microg/mL and 14.6, respectively. 6-Acetonyldihydrochelerythrine is

Ipfencarbazone herbicide agent, is a substance being developed for the control of weeds such as watergrass in rice.

SKI-349 is a dual-target inhibitor of sphingosine kinase 1/2 (SPHK1/2) and microtubule assembly (MDA), exhibiting anticancer activity by inhibiting the vitality, invasion, and AKT/mTOR signaling pathway of liver cells [1] [2].