physalin a

Physalin A 是一种从 P. alkekengi 中分离的抗炎化合物，具有抗纤维化作用，通过 ERK 和 p38 调节 Nrf2 通路以诱导解毒酶。 Physalin A 阻断 NF-kappaB 信号通路的激活。Physalin A 通过降低 GLI1 基因和 YAP1 基因的表达来减少乳腺球的形成。

Physalin C, a natural product derived from Physalis alkekengi, is classified as a secosteriod [seco-16,17]. It displays a yellow powder form and has a molecular formula of C28H36O10. This compound is notable for its multiple bioactivities, including anticancer, antifungal, and antiviral effects.

Physalin D shows antimalarial activity; it also exhibits a minimum inhibitory concentration value (MIC) against Mycobacterium tuberculosis H(37)Rv strain of 32 microg mL. Physalin D displays considerable cytotoxicity against several cancer cell lines. It

Physalin H is an Hh signaling inhibitor blocks GLI1-DNA-complex formation, it also strong quinone reductase induction activity with IR (Induction ratio, QR induction activity) value of 3.74±0.02. Physalin H shows immunosuppressive effects on T cells both

Physalin G has antinociceptive property.

Physalin O possesses anti-inflammatory activity, it exhibited conjugating abilities with GSH and also showed significant nitric oxide (NO) production inhibiting activities.

Physalin X demonstrated the capability to inhibit NO production, exhibiting an IC50 value of 68.50μM.

Isophysalin A exhibits anti-inflammatory activitiy, it exhibits conjugating abilities with glutathione and also shows significant nitric oxide (NO) production inhibiting activities.

Withaphysalin 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 TN5321，CAS号为 57423-72-0。

Physalin F 是一种分泌型甾体，诱导人外周血单个核细胞凋亡，降低人 T 淋巴细胞 1 型病毒感染后的自发增殖和细胞因子的产生，具有强烈抗炎和免疫调节作用。

Physalin L 抑制巨噬细胞中 LPS 诱导的 NO 生成，平均抑制率是 70.97%。它具有抗炎作用。

Physalin B 是茄科植物的主要活性化合物之一，具有广泛的生物活性，可用于治疗炎症湿疹和疱疹等疾病。Physalin B 通过激活 PI3K Akt 通路抑制 NF-κB 和 NLRP3，从而改善脂多糖诱导的急性肺损伤造成的炎症反应。Physalin B 通过激活 Nrf2 通路抑制 PDGF-BB 诱导的 VSMC 增殖、迁移和表型转化。Physalin B 通过抑制 LAP2α-HDAC1 介导的胶质瘤相关癌基因 1 的去乙酰化和肝星状细胞活化来发挥抗肿瘤活性。