Drug intelligence / Profile preview

alismatis rhizoma

Development stage
Preclinical
Modality
Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

Alismatis Rhizoma is a traditional Chinese medicine (TCM) derived from the dried rhizomes of *Alisma orientale* (Sam.) Juzep. or *Alisma plantago-aquatica* Linn. It is widely utilized for its diuretic, lipid-lowering, and anti-inflammatory properties. The therapeutic efficacy of Alismatis Rhizoma is attributed to its diverse chemical constituents, primarily triterpenoids (such as alisol A, alisol B 23-acetate, and alisol C 23-acetate) and polysaccharides (arabinogalactans). Research indicates that these components exert protective effects against metabolic dysfunction-associated steatohepatitis (MASH), hyperlipidemia, and obesity by modulating targets such as SIRT1, pancreatic lipase, and bile acid-CoA: amino acid N-acyltransferase (BAAT). Additionally, Alismatis Rhizoma has shown potential in treating acute liver injury, diabetic nephropathy, and hypertension through multi-target regulatory paradigms involving the activation of JNK/p38 MAPK signaling and the modulation of gut microbiota.

Other names
ZexieAlisma orientaleAlisma plantago-aquaticaAlismatis Rhizoma polysaccharideARPAlisma starch
02

Targets

EGFR (Epidermal growth factor receptor)FXR (Farnesoid x-activated receptor)MAPK3 (Mitogen-activated protein kinase 1)PNLIP (Pancreatic triacylglycerol lipase)SRC (Proto-oncogene tyrosine-protein kinase Src)SIRT1 (NAD-dependent protein deacetylase sirtuin-1)JNK (Mitogen-activated protein kinase kinase kinase family)RK (Ribokinase)BAAT (Bile acid-CoA:amino acid N-acyltransferase)GehA (Triacylglycerol lipase GehA)MAPK14 (p38 mitogen-activated protein kinase alpha)

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