Valepotriate (Valtrate) 是从蜘蛛香分离而来的一种天然产物，是一类新的细胞毒剂和抗肿瘤剂，对 HTC 肝癌细胞是非常有效的细胞毒剂。 它可能对焦虑的精神症状具有潜在的抗焦虑作用。

Valeranone shows antileishmanial and cytotoxic activity.

Homobaldrinal has low toxic activity. It has genotoxic activity in the Salmonella/microsome test and the SOS-chromotest.

Valeriotetrate C is a natural product from Valeriana jatamansi.

Hydroxyvalerenic acid is a natural product

Heishuixiecaoline A protects against neurotoxicity in PC12 cells.

Volvalerenic acid A is a natural product

Valeriotriate B 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 TN5553，CAS号为 862255-64-9。

Jatamanvaltrate B shows cytotoxicity against lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8),and hepatoma (Bel7402) cell lines.

VHD-valtrate has anticancer effects against human ovarian cancer cells in vitro and in vivo, it is a potential therapeutic agent for ovarian cancer, providing a basis for development of the compound as a novel chemotherapeutic agent.

1-O-Methyljatamanin D 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 TN5552，CAS号为 54656-47-2。

Volvaltrate B shows cytotoxic activity against the lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8), and hepatoma (Bel7402) cell lines, with IC50 values of 8.5, 2.0, 3.2, and 6.1 uM, respectively.

Valerosidate is a natural product from Valeriana jatamansi.

(-)-Olivil displays a higher antioxidative effect against the free radical DPPH.

Valerenic acid is a natural product

Chlorovaltrate K shows moderate cytotoxicity against lung adenocarcinoma (A 549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8) and hepatoma (Bel 7402) cell lines with IC50 values of 0.89-9.76 uM.

Prostephanaberrine is a natural product from Valeriana officinalis.

Baldrinal, valtrate, and acevaltrate are the quality control compounds of Valeriana jatamansi Jones.

Valeriandoid B 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 TN5216，CAS号为 1380399-57-4。

Didrovaltrate shows cytotoxic against human cancer cell lines. Didrovaltrate blocks I(Ca-L) in a concentration-dependent manner and probably inhibits I(Ca-L) in its inactive state, which may contribute to its cardiovascular effect.