构树属

Broussochalcone A 是一种从桑科植物中提取的天然化合物，具有抗氧化和黄嘌呤氧化酶抑制活性（IC50 = 2.21 μM），能够清除自由基，抑制铁诱导的脂质过氧化，并减少脂多糖激活的巨噬细胞中一氧化氮的合成，也能够通过增加活性氧（ROS）水平和激活 FOXO3 信号通路，诱导人肾癌细胞凋亡。Broussochalcone A还是一种新型的 NR4A1 核受体抑制剂，能够通过 NR4A1 依赖的途径诱导胰腺癌细胞凋亡。

Isolicoflavonol 以可逆和混合的方式抑制人羧酸酯酶2介导的荧光素二乙酸酯水解， Ki 小于1.0 μM。

5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone 具有抗癌活性，体外对 ER 阳性乳腺癌MCF-7细胞表现出较强的抗增殖作用，对MCF-7细胞的IC50值为4.41 uM。5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone 能显著下调雌激素受体-α (ER-α)的表达浓度，并能抑制人乳腺癌细胞系BCAP-37异种移植模型体内的肿瘤生长。

Kazinol U may have therapeutic value in delaying pancreatic β-cell destruction in type 1 diabetes by blocking the NF-κB pathway in pancreatic β-cells reduces cell damage. Kazinol U shows estrogenic activity with ligand-activity of estrogen receptor, transcriptional activity of estrogen -responsive element-reporter genes, it may have beneficial effects in the treatment of menopausal symptoms.

2'-O-Methylbroussonin C 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN2499，CAS号为 376362-03-7。

Broussoflavonol F has antiplatelet effect, is partially due to an inhibitory effect on cyclooxygenase, can inhibit arachidonic acid (AA)-induced platelet aggregation. Broussoflavonol F shows inhibitory activities on mushroom tyrosinase. Broussoflavonol F

7,3'-Dihydroxy-4'-methoxyflavan是一种天然产物，属于桑科构树属，其产品编号为 TN3211，CAS号为 162290-05-3。7,3'-Dihydroxy-4'-methoxyflavan可用作对照参考。

Dodonaflavonol 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN3880，CAS号为 1392213-93-2。

Kazinol A shows strong inhibition of arachidonic acid (AA)-induced platelet aggregation. It also exhibits potent inhibition with IC50 values ranging 0.6-164 M against XOD. Kazinol A may be a candidate for the development of effective anti-cancer drug on h

7,4'-Dihydroxy-3'-prenylflavan has antibacterial activity.

Broussonins A and B, new phytoalexins from diseased paper mulberry. Broussonin B can induce neurite outgrowth in PC-12 cells at concentration of 50 microg/ml, and show moderate inhibitory activities against a chymotrypsin-like activity of the proteasome.B

Broussonins A and B, new phytoalexins from diseased paper mulberry. Broussonin A shows estrogenic activity with ligand-binding activity of estrogen receptor, transcriptional activity of estrogen-responsive element-luciferase reporter genes. Broussonin A c

Broussonin E could suppress inflammation by modulating macrophages activation state via inhibiting the ERK and p38 MAPK and enhancing JAK2-STAT3 signaling pathway, and can be further developed as a promising drug for the treatment of inflammation-related

5,7,3',4'-Tetrahydroxy-3-methoxy-8-geranylflavone is a natural compound isolated from Broussonetia papyrifera.

Broussonin C and broussin are antifungal compounds. Broussonin C exerts simple reversible slow-binding inhibition against diphenolase.

Broussonetines A-H are glycosidase inhibitors.

4'-O-Demethylbroussonin A 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN3053，CAS号为 376361-97-6。

2'-O-Methylbroussonin A 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN2788，CAS号为 127757-13-5。