Results 181 to 190 of about 116,988 (242)

Tanshinone IIA delays liver aging by modulating oxidative stress. [PDF]

Front Pharmacol
Liu Q, Li X, Luo Y.
europepmc   +1 more source

Tanshinone IIA suppresses the proliferation and fibrosis of mesangial cell in diabetic nephropathy though WTAP-mediated m⁶A methylation. [PDF]

Sci Rep
Peng H, Zhang X.
europepmc   +1 more source

Tanshinone IIA suppresses fibro-adipogenic progenitor differentiation and attenuates fat infiltration in rotator cuff injury via Wnt/β-catenin pathway. [PDF]

Regen Ther
Zhang Y, Li X, Zhang R, Wang M, Wang T, Liu G, Kuati A, Mao W.   +7 more
europepmc   +1 more source

Preparation of pH-Responsive Tanshinone IIA-Loaded Calcium Alginate Nanoparticles and Their Anticancer Mechanisms. [PDF]

Pharmaceutics
Ren T, Wang J, Ma Y, Huang Y, Yoon S, Mu L, Li R, Wang X, Zhang L, Li P, Ji L.   +10 more
europepmc   +1 more source

Tanshinone IIA inhibits heat-induced growth of p53-mutant Huh-7 hepatocellular carcinoma by modulating osmotic homeostasis and glycolysis through targeting ALDH7A1. [PDF]

Cell Death Discov
Li H, Ju S, Wang J, Kuang D, Chen P, Zhang M, Qian R, Liang C, Han D, Duan X.   +9 more
europepmc   +1 more source

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Total synthesis of tanshinone IIA

Tetrahedron Letters, 2020
Abstract A novel synthetic route toward tanshinone IIA has been developed. Key steps involve a base mediated furan ring formation, and an acyloin condensation reaction to construct the ortho-quinone ring.
Junbiao Chang, Chuanjun Song
exaly   +2 more sources

Studies on the spectroscopic behavior of cryptotanshinone, tanshinone IIA, and tanshinone I

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2004
A comparative study on the spectroscopic behavior of cryptotanshinone (CTan), tanshinone IIA (Tan IIA), and tanshinone I (Tan I) has been investigated, including UV-Vis absorption, low temperature phosphorescence (LTP), low temperature fluorescence (LTF), paper substrate-room temperature phosphorescence (PS-RTP), paper substrate-room temperature ...
Chuan Dong, Zhi-Cheng Xu
exaly   +3 more sources

Tanshinone-IIA mediated neuroprotection by modulating neuronal pathways

Naunyn-Schmiedeberg's Archives of Pharmacology, 2023
The progression of neurological diseases is mainly attributed to oxidative stress, apoptosis, inflammation, and trauma, making them a primary public concern. Since no drugs can stop these neurological disorders from happening, active phytochemical intervention has been suggested as a possible treatment.
Kajal Sherawat, Sidharth Mehan
semanticscholar   +3 more sources

Anti-Adipogenic Effects on 3T3-L1 Cells and Zebrafish by Tanshinone IIA

International Journal of Molecular Sciences, 2017
Tanshinone IIA is a diterpene quinone isolated from the roots of Salvia miltiorrhiza bunge that has traditionally been used in China for the treatment of cardiovascular and cerebrovascular disorders.
Jinho Lee, Byeong-Churl Jang, Jong-Soon Choi   +2 more
exaly   +2 more sources

Evaluation of Tanshinone IIA Developmental Toxicity in Zebrafish Embryos [PDF]

Molecules, 2017
Tanshinone IIA (Tan-IIA) is derived from the dried roots of Salvia miltiorrhiza Bunge, a traditional Chinese medicine. Although Salvia miltiorrhiza has been applied for many years, the toxicity of the mono-constituent of Salvia miltiorrhiza, tanshinone IIA, is still understudied.
Tao Wang, Baoguo Wang, Qiong Wu
exaly   +4 more sources