Drug intelligence / Profile preview

15,16-dihydrotanshinone I

Development stage
Preclinical
Modality
Small Molecules
Administration
Oral (in Herbal/nutritional Preparations), Topical (in Cosmetic Formulations), Experimental (in Vitro/in Vivo Research Applications)
01

Overview

15,16-dihydrotanshinone I is a **bioactive abietane diterpenoid compound** primarily isolated from the roots of *Salvia miltiorrhiza* (Danshen)[1][2][3][4][5]. It has been employed historically in traditional Chinese medicine and is now under investigation for its pharmacological effects: - **Mechanisms of action** include anti-proliferative and anti-inflammatory activities through cell cycle arrest (G0/G1 phase), inhibition of cyclins and cyclin-dependent kinases, upregulation of p21, and modulation of key signaling pathways, notably **AMP-activated protein kinase (AMPK)** activation, and suppression of **Akt/mTOR** and **MAPK** signaling in cancer cells[3][5]. - Demonstrates **antioxidant**, **anti-inflammatory**, **antimicrobial**, and pronounced **anticancer** effects (particularly against various tumor cell lines)[1][2][3][5]. - Also studied for cardiovascular protection, neuroprotection, and skin applications[1][5]. Most data come from preclinical models; definitive human efficacy remains unproven.

Brand names
none
Other names
dihydrotanshinone I(-)-dihydrotanshinone Idihydrotanshinone-Itanshinone I, dihydro-15,16-dihydrotanshinone-I (alternative spelling)(1R)-1,6-dimethyl-1,2-dihydronaphtho[1,2-g][1]benzofuran-10,11-dione(1R)-1,6-dimethyl-1,2-dihydrophenanthro[1,2-b]furan-10,11-dionecannabisin A standard
02

Targets

AMPK (Adenosine monophosphate–activated protein kinase)CTNNB1 (Beta-catenin)EGFR T790M (Epidermal growth factor receptor T790M mutant)ELAVL1 (Human Antigen R)

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