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Ginkgo biloba Extracts: A Review of the Pharmacokinetics of the Active Ingredients

Clinical pharmacokinetics, 2013-09, Vol.52 (9), p.727-749

2013

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An exploratory study on the effect of mechanical stress on particle formation in monoclonal antibody infusions

Archiv der Pharmazie (Weinheim), 2023-08, Vol.356 (8), p.e2300101-n/a

2023

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Differential antiviral and anti-inflammatory mechanisms of the flavonoids biochanin A and baicalein in H5N1 influenza A virus-infected cells

Antiviral research, 2013-01, Vol.97 (1), p.41-48

2013

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Molecular tuning of farnesoid X receptor partial agonism

Nature communications, 2019-07, Vol.10 (1), p.2915-14, Article 2915

2019

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Influence of bleaching and coloring on ethyl glucuronide content in human hair

Drug testing and analysis, 2018-01, Vol.10 (1), p.177-183

2018

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Carnosic acid and carnosol potently inhibit human 5-lipoxygenase and suppress pro-inflammatory responses of stimulated human polymorphonuclear leukocytes

Biochemical pharmacology, 2008-07, Vol.76 (1), p.91-97

2008

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PTCA (1H‐pyrrole‐2,3,5‐tricarboxylic acid) as a marker for oxidative hair treatment

Drug testing and analysis, 2018-04, Vol.10 (4), p.768-773

2018

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MH84 improves mitochondrial dysfunction in a mouse model of early Alzheimer's disease

Alzheimer's research & therapy, 2018-02, Vol.10 (1), p.18-12, Article 18

2018

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Letter to the Editor regarding “Comparison of phytochemical composition of Ginkgo biloba extracts using a combination of non-targeted and targeted analytical approaches”

Analytical and bioanalytical chemistry, 2021-12, Vol.413 (30), p.7625-7626

2021

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Revealing the macromolecular targets of complex natural products

Nature chemistry, 2014-12, Vol.6 (12), p.1072-1078

2014

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Quantification of active ingredients in semi-solid pharmaceutical formulations by near infrared spectroscopy

Journal of pharmaceutical and biomedical analysis, 2017-08, Vol.142, p.178-189

2017

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Analysis of 4‐fluoroamphetamine in cerumen after controlled oral application

Drug testing and analysis, 2020-07, Vol.12 (7), p.968-974

2020

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Extending the Structure–Activity Relationship of Anthranilic Acid Derivatives As Farnesoid X Receptor Modulators: Development of a Highly Potent Partial Farnesoid X Receptor Agonist

Journal of medicinal chemistry, 2014-10, Vol.57 (19), p.8035-8055

2014

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First Structure–Activity Relationship Study of Potent BLT2 Agonists as Potential Wound-Healing Promoters

Journal of medicinal chemistry, 2020-10, Vol.63 (20), p.11548-11572

2020

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Medicinal chemistry and pharmacological effects of Farnesoid X Receptor (FXR) antagonists

Current topics in medicinal chemistry, 2014-01, Vol.14 (19), p.2188-2205

2014

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Urate transporter inhibitor lesinurad is a selective peroxisome proliferator-activated receptor gamma modulator (sPPARγM) in vitro

Scientific reports, 2018-09, Vol.8 (1), p.13554-11, Article 13554

2018

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Degradation of ginsenosides in humans after oral administration

Drug metabolism and disposition, 2003-08, Vol.31 (8), p.1065-1071

2003

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Discovery of 3-Amino-1H-pyrazole-Based Kinase Inhibitors to Illuminate the Understudied PCTAIRE Family

International journal of molecular sciences, 2022-12, Vol.23 (23), p.14834

2022

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Pirinixic Acid Derivatives as Novel Dual Inhibitors of Microsomal Prostaglandin E2 Synthase-1 and 5-Lipoxygenase

Journal of medicinal chemistry, 2008-12, Vol.51 (24), p.8068-8076

2008

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Sportsponsoring: Grundlagen, Konzeption und Wirkungen

2018

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Allosteric modulation of the farnesoid X receptor by a small molecule

Scientific reports, 2018-05, Vol.8 (1), p.6846-11, Article 6846

2018

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Trafficking of the NMDAR2B receptor subunit distal cytoplasmic tail from endoplasmic reticulum to the synapse

PloS one, 2012-06, Vol.7 (6), p.e39585-e39585

2012

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Carnosic Acid and Carnosol, Phenolic Diterpene Compounds of the Labiate Herbs Rosemary and Sage, are Activators of the Human Peroxisome Proliferator-Activated Receptor Gamma

Planta medica, 2006-08, Vol.72 (10), p.881-887

2006

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Tertiary alkylamines as nucleophiles in substitution reactions at heteroaromatic halide during the synthesis of the highly potent pirinixic acid derivative 2-(4-chloro-6-(2,3-dimethylphenylamino)pyrimidin-2-ylthio)octanoic acid (YS-121)

Molecules (Basel, Switzerland), 2011-12, Vol.16 (12), p.10013-10028

2011

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Zafirlukast Is a Dual Modulator of Human Soluble Epoxide Hydrolase and Peroxisome Proliferator-Activated Receptor γ

Frontiers in pharmacology, 2019-03, Vol.10, p.263-263

2019

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Ginkgo biloba Extracts: A Review of the Pharmacokinetics of the Active Ingredients

An exploratory study on the effect of mechanical stress on particle formation in monoclonal antibody infusions

Differential antiviral and anti-inflammatory mechanisms of the flavonoids biochanin A and baicalein in H5N1 influenza A virus-infected cells

Molecular tuning of farnesoid X receptor partial agonism

Influence of bleaching and coloring on ethyl glucuronide content in human hair

Carnosic acid and carnosol potently inhibit human 5-lipoxygenase and suppress pro-inflammatory responses of stimulated human polymorphonuclear leukocytes

PTCA (1H‐pyrrole‐2,3,5‐tricarboxylic acid) as a marker for oxidative hair treatment

MH84 improves mitochondrial dysfunction in a mouse model of early Alzheimer's disease

Letter to the Editor regarding “Comparison of phytochemical composition of Ginkgo biloba extracts using a combination of non-targeted and targeted analytical approaches”

Revealing the macromolecular targets of complex natural products

Quantification of active ingredients in semi-solid pharmaceutical formulations by near infrared spectroscopy

Analysis of 4‐fluoroamphetamine in cerumen after controlled oral application

Extending the Structure–Activity Relationship of Anthranilic Acid Derivatives As Farnesoid X Receptor Modulators: Development of a Highly Potent Partial Farnesoid X Receptor Agonist

First Structure–Activity Relationship Study of Potent BLT2 Agonists as Potential Wound-Healing Promoters

Medicinal chemistry and pharmacological effects of Farnesoid X Receptor (FXR) antagonists

Urate transporter inhibitor lesinurad is a selective peroxisome proliferator-activated receptor gamma modulator (sPPARγM) in vitro

Degradation of ginsenosides in humans after oral administration

Discovery of 3-Amino-1H-pyrazole-Based Kinase Inhibitors to Illuminate the Understudied PCTAIRE Family

Pirinixic Acid Derivatives as Novel Dual Inhibitors of Microsomal Prostaglandin E2 Synthase-1 and 5-Lipoxygenase

Sportsponsoring: Grundlagen, Konzeption und Wirkungen

Allosteric modulation of the farnesoid X receptor by a small molecule

Trafficking of the NMDAR2B receptor subunit distal cytoplasmic tail from endoplasmic reticulum to the synapse

Carnosic Acid and Carnosol, Phenolic Diterpene Compounds of the Labiate Herbs Rosemary and Sage, are Activators of the Human Peroxisome Proliferator-Activated Receptor Gamma

Tertiary alkylamines as nucleophiles in substitution reactions at heteroaromatic halide during the synthesis of the highly potent pirinixic acid derivative 2-(4-chloro-6-(2,3-dimethylphenylamino)pyrimidin-2-ylthio)octanoic acid (YS-121)

Zafirlukast Is a Dual Modulator of Human Soluble Epoxide Hydrolase and Peroxisome Proliferator-Activated Receptor γ

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