Results 161 to 170 of about 1,066 (203)
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Determination of higenamine in dietary supplements by UHPLC/MS/MS method
Journal of Pharmaceutical and Biomedical Analysis, 2017From 1st January 2017 higenamine was added on the WADA (World Anti-doping Agency) Prohibited list under S3 group beta-2 agonists as at all times banned substance for the athletes. The main origine of higenamine (or norcoclaurine) are different plants including Nandina domestica, Aconitum carmichaelii, Asarum heterotropioides, Galium divaricatum, Annona
Nenad Dikić +1 more
exaly +5 more sources
Clinical safety assessment of oral higenamine supplementation in healthy, young men
Human and Experimental Toxicology, 2015Objective: Higenamine, an herbal agent also known as norcoclaurine, is thought to stimulate β-androgenic receptors and possess lipolytic activity. It is currently making its way into the dietary supplement market. To our knowledge, no studies have been conducted to determine the safety profile of oral higenamine when used alone and in conjunction with ...
R J, Bloomer +2 more
exaly +3 more sources
Bronchodilatory Effect of Higenamine as Antiallergic Asthma Treatment
Journal of Investigative Medicine, 2022Asthma is a complex airway disease that affects more than 350 million humans worldwide. Allergic asthma symptoms are induced by Th2 immune response with the release of cytokines and allegro-inflammatory mediators that amplify the inflammatory response, airway hyper-responsiveness (AHR) and hyperproduction of mucus.
Jing Du +3 more
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Anti-Thrombotic Effects of Higenamine
Planta Medica, 2001The anti-platelet and anti-thrombotic effects of higenamine, a benzyltetrahydroisoquinoline alkaloid of the roots of Aconitum japonicum (Ranunculaceae), were investigated. The degree of platelet aggregation was measured with platelet rich plasma (PRP).
H S, Yun-Choi +4 more
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PHARMACOKINETICS OF HIGENAMINE IN RABBITS
Biopharmaceutics & Drug Disposition, 1996The pharmacokinetics of higenamine were investigated in rabbits by IV bolus, PO route, and IV infusion. Plasma higenamine concentration declined rapidly in a biexponential pattern, with a terminal half-life of 22 min. The AUC increased proportionally with increasing dose, whereas the percentage of unchanged higenamine excreted from urine remained ...
C F, Lo, C M, Chen
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Journal of Radioanalytical and Nuclear Chemistry, 2003
The synthesis of [3H]-higenamine by a four steps reaction, namely condensation, cyclization, catalytic tritiation and demethoxylation is described. The acidulated product was purified by thin layer chromatography and the final component has a high specific activity and radiochemical purity.
Dezhu Wu +3 more
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The synthesis of [3H]-higenamine by a four steps reaction, namely condensation, cyclization, catalytic tritiation and demethoxylation is described. The acidulated product was purified by thin layer chromatography and the final component has a high specific activity and radiochemical purity.
Dezhu Wu +3 more
openaire +1 more source
Applications of Higenamine in pharmacology and medicine
Journal of Ethnopharmacology, 2017Aconitum has been used as local and traditional medicines in many asian regions for the treatment of various diseases such as collapse, syncope, painful joints, oedema, bronchial asthma et al. Higenamine, a plant-based alkaloid, was initially isolated from Aconitum and identified as the active cardiotonic component of Aconitum.
Nana, Zhang +4 more
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Blood‐to‐muscle distribution and urinary excretion of higenamine in rats
Drug Testing and Analysis, 2021AbstractHigenamine is a β2‐agonist that has been prohibited in sports by the World Anti‐Doping Agency. Higenamine could potentially promote anabolism and lipolysis; however, its crucial pharmacokinetics data, particularly muscle distribution, remain unavailable.
William Chih‐Wei Chang +5 more
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ELISA for the Detection of the Prohibited Doping Agent Higenamine
Planta Medica, 2020AbstractHigenamine is a natural benzyltetrahydroisoquinoline alkaloid produced by various plants. In the World Anti-Doping Agency report of 2020, higenamine is classified as a class S3 (selective and nonselective β2-agonist) prohibited substance. To minimize the problems resulting from the misuse of higenamine-containing products as well as from the ...
Poomraphie, Nuntawong +3 more
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A novel β2-AR agonist, Higenamine, induces β-arrestin-biased signaling
Science China Life Sciences, 2021The biased ligands in G protein-coupled receptors (GPCRs) have opened new avenues for developing safer and more effective drugs. However, the identification of such biased ligands as drug candidates is highly desirable. Here, we report that Higenamine, a compound isolated from a Chinese herb, functions as a novel β-arrestin-biased ligand of the β2 ...
Nana, Zhang +3 more
openaire +2 more sources

