Aconitine: A review of its pharmacokinetics, pharmacology, toxicology and detoxification
Y Gao, H Fan, A Nie, K Yang, H Xing, Z Gao… - Journal of …, 2022 - Elsevier
Ethnopharmacological relevance Aconitine, a C 19-norditerpenoid alkaloid, derives from
many medicinal plants such as Aconitum carmichaelii Debx.(Chinese: 乌头), Aconitum …
many medicinal plants such as Aconitum carmichaelii Debx.(Chinese: 乌头), Aconitum …
[HTML][HTML] An insight into current advances on pharmacology, pharmacokinetics, toxicity and detoxification of aconitine
S Li, L Yu, Q Shi, Y Liu, Y Zhang, S Wang… - Biomedicine & …, 2022 - Elsevier
Aconitine is a diterpenoid alkaloid, which mainly exists in the plants of Aconitum. In the last
decade, a plethora of studies on the pharmacological activities of aconitine has been …
decade, a plethora of studies on the pharmacological activities of aconitine has been …
The expanding utility of iron-sulfur clusters: Their functional roles in biology, synthetic small molecules, maquettes and artificial proteins, biomimetic materials, and …
AE Boncella, ET Sabo, RM Santore, J Carter… - Coordination Chemistry …, 2022 - Elsevier
The ubiquity, structural variation, and functional diversity of iron-sulfur (Fe-S) clusters in
biological environments has long fascinated scientists. In nature, Fe-S clusters form a variety …
biological environments has long fascinated scientists. In nature, Fe-S clusters form a variety …
Fe‐S Clusters Emerging as Targets of Therapeutic Drugs
L Vernis, N El Banna, D Baïlle, E Hatem… - Oxidative Medicine …, 2017 - Wiley Online Library
Fe‐S centers exhibit strong electronic plasticity, which is of importance for insuring fine
redox tuning of protein biological properties. In accordance, Fe‐S clusters are also highly …
redox tuning of protein biological properties. In accordance, Fe‐S clusters are also highly …
A comprehensive in silico method to study the QSTR of the aconitine alkaloids for designing novel drugs
MY Wang, JW Liang, K Mohamed Olounfeh, Q Sun… - Molecules, 2018 - mdpi.com
A combined in silico method was developed to predict potential protein targets that are
involved in cardiotoxicity induced by aconitine alkaloids and to study the quantitative …
involved in cardiotoxicity induced by aconitine alkaloids and to study the quantitative …
Aconitine induces cell apoptosis via mitochondria and death receptor signaling pathways in hippocampus cell line
H Wang, Y Liu, Z Guo, K Wu, Y Zhang, Y Tian… - Research in Veterinary …, 2022 - Elsevier
Aconitine is a plant toxin derived from aconitum genus and well known for its neurological
and vascular toxicity. However, the mechanism of toxicity on the growth and apoptosis of the …
and vascular toxicity. However, the mechanism of toxicity on the growth and apoptosis of the …
[HTML][HTML] Aconitine inhibits the proliferation of hepatocellular carcinoma by inducing apoptosis
X Qi, L Wang, H Wang, L Yang, X Li… - International Journal of …, 2018 - ncbi.nlm.nih.gov
Hepatocellular carcinoma (HCC) is the primary liver cancer that occurs with a high incidence
in Asia. Owing to the poor prognosis of the disease, the mortality rate remains high, making …
in Asia. Owing to the poor prognosis of the disease, the mortality rate remains high, making …
Influence of metformin, sodium dichloroacetate and their combination on the hematological and biochemical blood parameters of rats with gliomas C6
IV Prokhorova, ON Pyaskovskaya… - Experimental …, 2018 - dspace.nbuv.gov.ua
Background: The efficacy of antimetabolic therapy of malignant neoplasms could not be
explained solely by the direct mechanisms of action of such energy metabolism inhibitors as …
explained solely by the direct mechanisms of action of such energy metabolism inhibitors as …
Comparison of antitumor effects of combined and separate treatment with NO synthase inhibitor T1023 and PDK1 inhibitor dichloroacetate
MV Filimonova, TS Podosinnikova… - Bulletin of Experimental …, 2019 - Springer
Combined chronic treatment of Ehrlich solid carcinoma (EC) with an NOS inhibitor 1-
isobutanoyl-2-isopropylisothiourea hydrobromide (T1023) and a PDK1 inhibitor …
isobutanoyl-2-isopropylisothiourea hydrobromide (T1023) and a PDK1 inhibitor …
[PDF][PDF] 乌头碱抑制食管癌EC-1 细胞增殖与侵袭并诱导其凋亡作用研究
周小剑, 李玉华, 唐湘, 吕钰冰, 周嘉彬 - 中国医药生物技术, 2019 - cmbp.net.cn
目的研究乌头碱对食管癌EC-1 细胞增殖, 侵袭和凋亡的影响. 方法CCK8 法及克隆形成抑制实验
检测乌头碱对食管癌EC-1 细胞的生长抑制作用; 采用Hoechst 33258 染色检测乌头碱对EC-1 …
检测乌头碱对食管癌EC-1 细胞的生长抑制作用; 采用Hoechst 33258 染色检测乌头碱对EC-1 …