Table 5 Pro Tox II toxicity prediction of toxicity points and receptors for Chamanetin.

From: The natural breakthrough: phytochemicals as potent therapeutic agents against spinocerebellar ataxia type 3

Classification

Target

Prediction

Probability

Organ toxicity

Hepatotoxicity

Inactive

0.72

Toxicity endpoints

Carcinogenicity

Inactive

0.71

Toxicity endpoints

Immunotoxicity

Inactive

0.72

Toxicity endpoints

Mutagenicity

Inactive

0.68

Toxicity endpoints

Cytotoxicity

Inactive

0.68

Tox21-nuclear receptor signaling pathways

Aryl hydrocarbon receptor (AhR)

Inactive

0.64

Tox21-nuclear receptor signaling pathways

Androgen receptor (AR)

Inactive

0.76

Tox21-nuclear receptor signaling pathways

Androgen receptor ligand binding domain (AR-LBD)

Inactive

0.99

Tox21-nuclear receptor signalling pathways

Aromatase

Inactive

0.75

Tox21-Nuclear receptor signalling pathways

Estrogen receptor alpha (ER)

Active

0.69

Tox21-nuclear receptor signalling pathways

Estrogen receptor ligand binding domain (ER-LBD)

Active

0.5

Tox21-nuclear receptor signalling pathways

Peroxisome proliferator activated receptor gamma (PPAR-Gamma)

Inactive

0.69

Tox21-stress response pathways

Nuclear factor (erythroid-derived 2)-like 2/antioxidant responsive element (nrf2/ARE)

Inactive

0.93

Tox21-stress response pathways

Heat shock factor response element (HSE)

Inactive

0.93

Tox21-stress response pathways

Mitochondrial membrane potential (MMP)

Active

0.72

Tox21-stress response pathways

Phosphoprotein (tumor supressor) p53

Inactive

0.54

Tox21-stress response pathways

ATPase family AAA domain-containing protein 5 (ATAD5)

Inactive

0.78