Xenobiotica

Papers
(The median citation count of Xenobiotica is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-03-01 to 2025-03-01.)
ArticleCitations
Mechanism-based inactivation of cytochrome P450 3A by evodol25
Intracellular activation of 4-hydroxycyclophosphamide into a DNA-alkylating agent in human leucocytes16
Optimising pirfenidone dosage regimens in idiopathic pulmonary fibrosis: towards a guide for personalised treatment15
Oxidative metabolism of razuprotafib (AKB-9778), a sulfamic acid phosphatase inhibitor, in human microsomes and recombinant human CYP2C8 enzyme15
Inorganic mercury pharmacokinetics in man: a hybrid model15
Dolutegravir metabolism: impact of genetic variations on uridine diphosphate glucuronosyltransferase subfamilies13
In vitro and in vivo metabolic profiling of PD105, a PI3Kδ inhibitor, using UHPLC-Q-Exactive plus-MS12
Identification of in vivo metabolites of a potential anti-rheumatoid arthritis compound, the quinazolinone derivative PD110, using ultra-high performance liquid chromatography coupled with Q-Exactive 11
Meeting report of the second European biotransformation workshop11
Effects of multi-kinase inhibitors on the activity of cytochrome P450 2J29
A general perspective for the conduct of radiolabelled distribution, metabolism, and excretion studies for antibody-drug conjugates9
Emerging conjugation strategies and protein engineering technologies aim to improve ADCs in the fight against cancer9
Hypothesis of using albumin to improve drug efficacy in cancers accompanied by hypoalbuminemia9
Evaluation of species differences in the metabolism of the selective NaV1.7 inhibitor DS-1971a, a mixed substrate of cytochrome P450 and aldehyde oxidase8
Investigation of the pharmacokinetics and metabolic fate of Fasiglifam (TAK-875) in male and female rats following oral and intravenous administration8
Prevalence of SLCO1B1 single nucleotide variations and their association with hypercholesterolaemia in hypercholesterolemic patients in Gauteng, South Africa8
Association between pharmacokinetics of lenvatinib in healthy subjects and genetic polymorphisms of ABCB1 3435C>T and ABCB1 2677G>T/A8
Development of a physiologically based pharmacokinetic model for levetiracetam in patients with renal impairment to guide dose adjustment based on steady-state peak/trough concentrations8
Human keratinocyte response to 4,4’-methylene diphenyl diisocyanate-glutathione conjugate exposure7
Meeting report: oligonucleotide ADME workshop7
How predictive are isolated perfused liver data of in vivo hepatic clearance? A meta-analysis of isolated perfused rat liver data7
In vivo-in vitrocorrelation of antitumor activity of heat shock protein 90 (HSP90) inhibitors with a pharmacokinetics/pharmacodynamics analysis using NCI-N87 xenograft mice7
Meeting report: DMPK optimisation strategies and quantitative translational PKPD frameworks to predict human PK and efficacious dose of targeted protein degraders7
Toxicokinetic and mass balance of morpholine in rats7
A systematic review of allometric scaling exponents for IgG mAbs6
Pharmacokinetics, distribution and efficacy of triptolide PLGA microspheres after intra-articular injection in a rat rheumatoid arthritis model6
Metabolism, pharmacokinetics and excretion of [14C]dimethyl fumarate in healthy volunteers: an example of xenobiotic biotransformation following endogenous metabolic pathways6
Roles of cytochrome P450 2A6 in the oxidation of flavone, 4′-hydroxyflavone, and 4′-, 3′-, and 2′-methoxyflavones by human liver microsomes6
In vitro and in vivo preclinical pharmacokinetic characterization of aficamten, a small molecule cardiac myosin inhibitor6
Changes in the expression of drug-metabolising enzymes and drug transporters in mice with collagen antibody-induced arthritis6
Absorption, metabolism, and excretion of [14C]-sebetralstat (KVD900) following a single oral dose in healthy male participants6
One small step in time, one giant leap for DMPK kind – a CRO perspective of the evolving core discipline of drug development6
Pharmacokinetics, mass balance, tissue distribution, metabolism, and excretion of [ 14 C]aficamten following single oral dose administration to rats6
A comprehensive analysis of six forms of cytochrome P450 2C (CYP2C) in pigs6
Sex differences in the pharmacokinetics and tissue residues of Macleaya cordata extracts in rats6
Absorption, metabolism and excretion of pictilisib, a potent pan-class I phosphatidylinositol-3-Kinase (PI3K) inhibitor, in rats, dogs, and humans6
Utility of human cytochrome P450 inhibition data in the assessment of drug-induced liver injury5
Population pharmacokinetics of sirolimus in Chinese adult liver transplant recipients: a retrospective study5
Evaluation of urinary acetaminophen metabolites and its association with the genetic polymorphisms of the metabolising enzymes, and serum acetaminophen concentrations in preterm neonates with patent d5
Pharmacokinetics, tissue distribution, plasma protein binding rate and excretion of sinoacutine following intravenous administration in female and male Sprague-Dawley rats5
Evaluation of the effect of Bovis Calculus Artifactus on eight rat liver cytochrome P450 isozymes using LC-MS/MS and cocktail approach5
Curcumin-loaded hydroxypropyl-β-cyclodextrin inclusion complex with enhanced dissolution and oral bioavailability for epilepsy treatment5
Utility of preclinical species for uncertainty assessment and correction of prediction of human volume of distribution using the Rodgers-Lukacova model5
Pomegranate peel polyphenols interaction with intestinal flora and its metabolic transformation5
Use of stable isotope labeled (SIL) antibodies in cassette dosing to improve pharmacokinetics screening efficiency of ADCs with novel cytotoxic payloads5
Assessment of P-glycoprotein function using canine intestinal organoid-derived epithelial interfaces5
The common indoor air pollutant α-pinene is metabolised to a genotoxic metabolite α-pinene oxide5
Vaginal administration of 17-alpha hydroxyprogesterone caproate appears to be safe in non-pregnant female rats and rabbits5
Effects of CYP3A5 polymorphism and renal impairment on the drug interaction between venetoclax and fluconazole in acute myeloid leukaemia patients5
Anastrozole and related glucuronic acid conjugate are electrophilic species5
In vitro metabolism, pharmacokinetics and drug interaction potentials of emvododstat, a DHODH inhibitor5
Developmental stage and infection status may affect drug distribution in the prostate of rats5
A physiologically-based pharmacokinetic/pharmacodynamic (PBPK/PD) model for the insecticide dimethoate5
Oral bioavailability and pharmacokinetics of esculetin following intravenous and oral administration in rats4
A population pharmacokinetic-pharmacodynamic model of navtemadlin, its glucuronide metabolite (M1) and serum macrophage inhibitory cykokine-1 (MIC-1)4
A translational strategy employing physiologically based modelling to predict the pharmacological active dose of RO7119929, an oral prodrug of a targeted cancer immunotherapy TLR7 agonist4
Absorption, distribution, metabolism and excretion of 14C-Emvododstat following a single oral dose in rats and dogs4
Curcumin and quercetin modify warfarin-induced regulation of porcine CYP1A2 and CYP3A expression and activity in vitro4
Pirfenidone 5-hydroxylation is mainly catalysed by CYP1A2 and partly catalysed by CYP2C19 and CYP2D6 in the human liver4
Metabolism of the antipsychotic drug olanzapine by CYP3A434
Prospective prediction of plasma pharmacokinetics of a novel immune-modulating agent in cancer patients after intra-tumoral administration: translation from non-clinical species to humans4
Effects of paeoniflorin on the activities and mRNA expression of rat CYP1A2, CYP2C11 and CYP3A1 enzymes in vivo4
Clinical pharmacokinetics of cefixime: a systematic review4
In vitro inhibition and induction of human liver cytochrome P450 enzymes by a novel anti-fibrotic drug fluorofenidone4
Predicting routes of phase I and II metabolism based on quantum mechanics and machine learning4
A cysteine trapping assay for risk assessment of reactive acyl CoA metabolites4
In vitro hepatic metabolism of the natural product quebecol4
In silico models to predict tubular secretion or reabsorption clearance pathway using physicochemical properties and structural characteristics4
Evaluation of MTBH, a novel hesperetin derivative, on the activity of hepatic cytochrome P450 isoform in vitro and in vivo using a cocktail method by HPLC-MS/MS4
Nrf2 signaling pathway studies in Drosophila melanogaster : parallel roles in human health and insect environmental responses4
Role of amino acids at positions 34, 296, and 486 of cytochrome P450 2D6 in the stimulatory and inhibitory effects of psychotropic agents on dopamine formation from p-tyramine4
Preclinical metabolism and disposition of an orally bioavailable macrocyclic FXIa inhibitor4
Hepatotoxic effect of tramadol and O-desmethyltramadol in HepG2 cells and potential role of PI3K/AKT/mTOR4
Through a computer monitor darkly: artificial intelligence in absorption, distribution, metabolism and excretion science4
Academic foreign compound metabolism – ‘ quo vadis ’?4
Comparison between lab variability andin silicoprediction errors for the unbound fraction of drugs in human plasma4
Metabolic profiling in liver microsomes and mice of E28, a potent FLT3 inhibitor4
Rutaecarpine enhances the anti-diabetic activity and hepatic distribution of metformin via up-regulation of Oct1 in diabetic rats4
Estimation of contribution of CYP2D6 to tipepidine metabolism in humans and prolongation of the half-life of tipepidine by combination use with a CYP2D6 inhibitor in chimeric mice with humanised liver4
Effect of formulation and route of administration on the distribution of 17-hydroxyprogesterone caproate in rats4
Influence of vitamin D treatment on functional expression of drug disposition pathways in human kidney proximal tubule cells during simulated uremia4
Thank you to reviewers4
Influence of UGT2B7 and UGT1A6 polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children4
Species differences in oxidative metabolism of regorafenib4
Phenolic benzotriazoles: a class comparison of toxicokinetics of ultraviolet-light absorbers in male rats3
Preparation, characterisation, pharmacokinetics and distribution of esculin microspheres administered via intravitreal injection into rabbit brain3
Validation of population pharmacokinetic models: a comparison of internal and external validation approaches for hydrochlorothiazide3
Population pharmacokinetics and dosage optimisation of tacrolimus coadministration with Wuzhi capsule in adult liver transplant patients3
Metabolite characterisation of the peptide–drug conjugate LN005 in liver S9s by UHPLC-Orbitrap-HRMS3
Relevance of gene polymorphisms of NAT2 and NR1I2 to anti-tuberculosis drug-induced hepatotoxicity3
Power of integrating PBPK with PBBM (PBPK-BM): a single model predicting food effect, gender impact, drug-drug interactions and bioequivalence in fasting & fed conditions3
Time matters – in vitro cellular disposition kinetics help rationalizing cellular potency disconnects3
Metabolic exhaustion and casein kinase 1α drive deguelin-induced premature red blood cell death3
Quantitative prediction of OATP1B-mediated drug–drug interactions using endogenous biomarker coproporphyrin I3
Herb–drug interaction: pharmacokinetics and pharmacodynamics of anti-hypertensive drug amlodipine besylate in presence of Lepidium sativum and Curcuma longa3
Comparative metabolism of THCA and THCV using UHPLC-Q-Exactive Orbitrap-MS3
Diurnal hepatic CYP3A11 contributes to chronotoxicity of the pyrrolizidine alkaloid retrorsine in mice3
Improved preclinical drug metabolism and pharmacokinetics of pibothiadine (HEC121210), a novel hepatitis B virus capsid assembly modulator3
Pharmacokinetics and metabolism of mirogabalin, a novel α2δ ligand, in rats and monkeys3
Pharmacokinetics, tissue distribution and excretion of five rhubarb anthraquinones in rats after oral administration of effective fraction of anthraquinones from rheum officinale3
Elucidating the structure and cytochrome P450-mediated mechanism for novel metabolites of GDC-0575 in rats3
Response to the comments raised by Fernando Tricta3
Metabolic activation of zolmitriptan mediated by CYP2D63
Chronic Toxoplasma infection affects gene expression of drug-metabolizing enzymes in mouse liver3
Comparisons between human and rodent hepatic glutathione S-Transferase activities reveal sex and species differences3
Comparison of mouse and human cytochrome P450 mediated-drug metabolising activities in hepatic and extrahepatic microsomes3
Metabolic map of the antiviral drug podophyllotoxin provides insights into hepatotoxicity3
Pharmacokinetics, metabolism and excretion of radiolabeled fostemsavir administered with or without ritonavir in healthy male subjects3
Predictive marker for exposure-driven haematological toxicity of tegafur-uracil and proposed modified-dosage regimen by pharmacometric approach in rats3
ADME and DMPK considerations for the discovery and development of antibody drug conjugates (ADCs)3
Mechanism-based inactivation of cytochromes P450: implications in drug interactions and pharmacotherapy3
Exploring the pharmacokinetics of second-generation cephalosporin, cefaclor: a systematic review in healthy and diseased populations2
Pharmacokinetics and pharmacodynamic interaction of bergamottin with atorvastatin in rats2
A commentary on the use of pharmacoenhancers in the pharmaceutical industry and the implication for DMPK drug discovery strategies2
Population pharmacokinetics of methotrexate in paediatric patients with acute lymphoblastic leukaemia and malignant lymphoma2
The effect of ARVs on the MEKKK1 gene promoter, inflammatory cytokine expression and signalling in acute treated Jurkat T cells2
Effect of genetic polymorphisms on the pharmacokinetics of gefitinib in healthy Chinese volunteers2
In vitro ADME, mouse pharmacokinetics of LD14b, and bioanalysis of a novel aβ 17β-HSD10 modulator for the treatment of Alzheimer’s disease2
In vivo evaluation of intestinal human CYP3A inhibition by macrolide antibiotics in CYP3A-humanised mice2
Absorption, distribution, metabolism and excretion of 14 C-vatiquinone in rats, dogs, and human subjects2
In vivo evaluation of pharmacokinetic drug–drug interactions between fluorinated pyrimidine anticancer drugs, 5-fluorouracil and capecitabin, and an anticoagulant, warfarin2
Two curcumin analogs inhibited the function and protein expression of breast cancer resistance protein: in vitro and in vivo studies2
Effects of benzophenone-3 on the liver and thyroid of adult zebrafish2
Interactions between cadmium and zinc on gene expression pattern of differentiation markers in MC3T3-E1 cell line2
Prediction of the liver safety profile of a first-in-class myeloperoxidase inhibitor using quantitative systems toxicology modeling2
Selection of the candidate compound at an early stage of new drug development: retrospective pharmacokinetic and metabolic evaluations of valsartan using common marmosets2
Metabolite profiling and identification of enzymes responsible for the metabolism of hirsutine, a major alkaloid from Uncaria rhynchophylla2
Drug-drug interaction between danshensu and irbesartan and its potential mechanism2
Bioanalytical approaches to support the development of antibody-oligonucleotide conjugate (AOC) therapeutic proteins2
Adenine-related compounds modulate UDP-glucuronosyltransferase (UGT) activity in mouse liver microsomes2
Effects of the total flavonoid extracts and the monomers of Daphne genkwa on CYP2C8 activity2
Development and validation of a highly sensitive and selective LC-MS/MS method for the determination of 15-hydroxylubiprostone in human plasma: application to a pharmacokinetic study in healthy Chines2
In vitro assessment of the inhibitory effect of goreisan extract and its ingredients on the P-glycoprotein drug transporter and cytochrome P-450 metabolic enzymes2
Pharmacokinetics of levonorgestrel and etonogestrel in rat or minipig following intravenous, subcutaneous, or intradermal administration2
In silico ADME/tox comes of age: twenty years later2
Teratogenicity is more likely a function of primary and secondary pharmacology than caused by chemically reactive metabolites: a critical evaluation of 40 years of scientific research2
Determination of enzymatic kinetics of metabolism of dimethoate and omethoate in rats and humans2
Evaluation system for cell-permeable CYP3A4 inhibitory activity using 1α,25-dihydroxy-vitamin D3-induced intestinal cell lines2
Cadmium-induced preeclampsia-like phenotype in the rat is related to decreased progesterone synthesis in the placenta2
Perspectives on the use of machine learning for ADME prediction at AstraZeneca2
Empirical and theoretical approaches for the prediction of human hepatic clearance using chimeric mice with humanised liver: the use of physiologically based scaling, a novel solution for potential ov2
Population pharmacokinetics of mycophenolic acid and dose optimisation in adult Chinese kidney transplant recipients2
Epifriedelanol enhances adriamycin-induced cytotoxicity towards K562/ADM cells by down regulating of P-gp and MRP22
In vitro safety evaluation of (6-methoxy-9-oxo-9 H -xanthen-2-yl)methyl ( E )-3-(2,4-dimethoxyphenyl)acrylate (K-116) –2
S-Carboxymethyl-l-cysteine: a multiple dosing study using pharmacokinetic modelling2
Subcutaneous catabolism of peptide therapeutics: bioanalytical approaches and ADME considerations2
Predictive role of polymorphic variants of phase II drug metabolising enzyme in modulating toxicity in North Indian lung cancer patients undergoing chemotherapy2
In vitro study of the drug–drug interaction potential of cetagliptin and clinical study of pharmacokinetic interaction of cetagliptin and metformin in healthy volunteers2
Untargeted metabolomics-assisted comparative cytochrome P450-dependent metabolism of fenbendazole in human and dog liver microsomes2
Effect of drug combination on tacrolimus target dose in renal transplant patients with different CYP3A5 genotypes2
Effect of capsaicin on breast cancer resistance protein (BCRP/Abcg2) and pharmacokinetics of probe substrates in rats2
Do differences in cell lines and methods used for calculation of IC50 values influence categorisation of drugs as P-glycoprotein substrates and inhibitors?2
Prediction of human serum concentration–time profiles of therapeutic monoclonal antibodies using common marmosets ( Callithrix jacchus ): initial assessment with canakin2
Exploring precision-cut liver slices for comparative xenobiotic metabolism profiling in swine and cattle2
Mirogabalin, a novel α2δ ligand, is not a substrate of LAT1, but of PEPT1, PEPT2, OAT1, OAT3, OCT2, MATE1 and MATE2-K2
Metabolites identification and species comparison of Oroxylin A, an anti-cancer flavonoid, in vitro and in vivo by HPLC-Q-TOF-MS/MS2
Notable drug-drug interaction between omeprazole and voriconazole in CYP2C19 *1 and *2 (rs4244285, 681G>A) alleles in vitro2
In vitro modulatory effects of ginsenoside compound K, 20(S)-protopanaxadiol and 20(S)-protopanaxatriol on uridine 5′-diphospho-glucuronosyltransferase activity and expression2
Evaluation of the non-linearity of NA808 in liver not reflected in plasma using a rat pharmacokinetic study and PBPK modelling2
Novel omeprazole delayed release orally disintegrating tablets for enhanced patient compliance: a case of model informed formulation development1
Absorption, distribution, metabolism, and excretion of [14C]TPN729 after oral administration to rats1
Assessment of cytochrome P450 induction in canine intestinal organoid models1
UGT1A1 and UGT1A3 activity and inhibition in human liver and intestinal microsomes and a recombinant UGT system under similar assay conditions using selective substrates and inhibitors1
Effect of tubeimoside I on the activity of cytochrome P450 enzymes in human liver microsomes1
Metabolic activation of aegeline mediated by CYP2C191
Human pharmacokinetics prediction with an in vitroin vivo correction factor approach and in vitro drug-drug interaction profile of bictegravir, a potent integrase-strand transfer1
Coptisine modulates the pharmacokinetics of florfenicol by targeting CYP1A2, CYP2C11 and CYP3A1 in the liver and P-gp in the jejunum of rats: a pilot study1
Metal-metal interaction and metal toxicity: a comparison between mammalian and D. melanogaster1
In silico prediction of volume of distribution of drugs in man using conformal prediction performs on par with animal data-based models1
The metabolite profiling of YR-1702 injection in human plasma, urine and feces by HPLC-Q-TOF-MS/MS1
Potential influence of interleukin-6 -174G/C gene polymorphism on kidney graft function and tacrolimus dose requirements: five-year follow-up1
In vitro drug-drug interactions of decitabine and tetrahydrouridine involving drug transporters and drug metabolising enzymes1
Simultaneous determination of four phytoecdysteroids by LC-MS/MS: application to a comparative pharmacokinetic study in normal and adjuvant arthritis rats after oral administration of C1
Xenobiotica Special Edition Preface1
Pharmacokinetics and mass balance of vericiguat in rats and dogs and distribution in rats1
Three methods to optimise polymyxin B dosing using estimated AUC after first dose: validation with the data generated by Monte Carlo simulation1
Potential application of mass spectrometry imaging in pharmacokinetic studies1
Effect of naringenin on the pharmacokinetics of metoprolol succinate in rats1
The effects of genetic polymorphism on toxicity and pharmacokinetics of methotrexate in Egyptian adult patients with leukaemia or lymphoma1
2-Oxidation, 3-methyl hydroxylation, and 6-hydroxylation of skatole, a contributor to the odour of boar-tainted pork meat, mediated by porcine liver microsomal cytochromes P450 1A2, 2A19, 2E1, and 3A21
Agrimoniin inhibits the activity of CYP1A2, 2D6, and 3A4 in human liver microsomes1
Indirubin mediates adverse intestinal reactions in guinea pigs by downregulating the expression of AchE through AhR1
Molecular docking and oxidation kinetics of 3-phenyl coumarin derivatives by human CYP2A131
Spectroscopic observations of β-eudesmol binding to human cytochrome P450 isoforms 3A4 and 1A2, but not to isoforms 2C9, 2C19, and 2D61
Empirical scaling factor for predicting human pharmacokinetic profiles of disproportionate metabolites using the Css–MRTpo method and chimeric mice with humanised livers1
Genetic polymorphism of Arg213His variant in the SULT1A1 gene is associated with reduced susceptibility to lung cancer in North Indian population1
Tree shrew cytochrome P450 2E1 is a functional enzyme that metabolises chlorzoxazone and p -nitrophenol1
Metabolic activation of deferiprone mediated by CYP2A61
Preclinical characterization of the absorption and disposition of the brain penetrant PI3K/mTOR inhibitor paxalisib and prediction of its pharmacokinetics and efficacy in human1
In vitro evaluation of intestinal absorption of tiliroside from Edgeworthia gardneri (Wall.) Meisn.1
Metabolic conversion of β-pinene to β-ionone in rats1
Assessment of drug-drug interactions of CC-90001, a potent and selective inhibitor of c-Jun N-terminal kinase1
Preclinical pharmacokinetic investigation of the bioavailability and skin distribution of HY-072808 ointment, a novel drug candidate for the treatment of atopic dermatitis, in minipigs by a newly LC-M1
Synthesis and evaluation of indomethacin prodrugs with a diester structure that are metabolically activated by human carboxylesterases1
mRNA expression levels of cytochrome P450 CYP1A2 , CYP3A4 , and CYP3A5 in the epidermis: a focus on individ1
Metabolism and disposition of zamicastat in rats1
In vitro study on the effect of leonurine hydrochloride on the enzyme activity of cytochrome P450 enzymes in human liver microsomes1
Disposition study of the novel dipeptidyl peptidase 4 inhibitor cetagliptin in rats1
Uptake of antiepileptic drugs in forskolin-induced differentiated BeWo cells: alteration of gabapentin transport1
Evaluation of molecular markers GSTM1 and GSTT1 and clinical factors in breast cancer: case-control study and literature review1
In vitro and in vivo evaluation of organic anion-transporting polypeptide 2B1-mediated pharmacokinetic interactions by apple polyphenols1
Comparative study on ABCB1-dependent efflux of anthracyclines and their metabolites: consequences for cancer resistance1
Beyond cytotoxic potency: disposition features required to design ADC payload1
Newly identified tree shrew cytochrome P450 2B6 (CYP2B6) and pig CYP2B6b are functional drug-metabolising enzymes1
An HPLC-UV validated bioanalytical method for measurement of in vitro phase 1 kinetics of α-synuclein binding bifunctional compounds1
MicroRNA-mediated Krüppel-like factor 4 upregulation induces alternatively activated macrophage-associated marker and chemokine transcription in 4,4’-methylene diphenyl diisocyanate exposed macrophage1
Effect of berberine on pharmacokinetics and pharmacodynamics of atorvastatin in hyperlipidemia rats1
A discovery biotransformation strategy: combining in silico tools with high-resolution mass spectrometry and software-assisted data analysis for high-throughput metabolism1
Renal tubular transporter-mediated interactions between mirogabalin and cimetidine in rats1
Effects of pharmacogenetics on pharmacokinetics and toxicity of doxorubicin in Egyptian breast cancer patients1
Reversible oxidation/reduction steps in the metabolic degradation of the glycerol side chain of the S1P 1 modulator ponesimod1
The metabolism and excretion of the dipeptidyl peptidase 4 inhibitor [14C] cetagliptin in healthy volunteers1
Disposition and metabolism of ethylene glycol 2-ethylhexyl ether in Sprague Dawley rats, B6C3F1/N mice, and in vitro in rat hepatocytes1
Approaches to improve the translation of safety, pharmacokinetics and therapeutic index of ADCs1
Bioavailability, safety and tolerability of intravenous brivaracetam in healthy Japanese participants1
Thank you to reviewers1
N-Acetyltransferase 2, glutathione S-transferase gene polymorphisms and susceptibility to hepatocellular carcinoma in an Algerian population1
Prediction of combination effect of quinidine on the pharmacokinetics of tipepidine using a physiologically based pharmacokinetic model1
Thank you to reviewers1
Species and tissue differences in regorafenib glucuronidation1
Translational PK/PD framework for antibody-drug conjugates to inform drug discovery and development1
N, N -dimethyltryptamine forms oxygenated metabolites via CYP2D6 - an in vitro investigation1
Physiologically based pharmacokinetic modelling to predict drug–drug interactions for encorafenib. Part I. Model building, validation, and prospective predictions with enzyme inhibitors, inducers, and1
Non-specific binding of compounds in in vitro metabolism assays: a comparison of microsomal and hepatocyte binding in different species and an assessment of the accuracy of prediction models1
Experimental and computational models to investigate intestinal drug permeability and metabolism1
Optimal pH 8.5 to 9 for the hydrolysis of vixotrigine and other basic substrates of carboxylesterase-1 in human liver microsomes1
Oxidation of 3’-methoxyflavone, 4’-methoxyflavone, and 3’,4’-dimethoxyflavone and their derivatives having 5,7-dihydroxyl moieties by human cytochromes P450 1B1 and 2A131
The impact of CYP3A5 , NR1I2 , and POR polymorphisms on tacrolimus dose-adjusted concentration and clinical1
2-Naphthalenemethanol participates in metabolic activation of 2-methylnaphthalene1
Safflower yellow for injection enhances anti-coagulation of warfarin in rats: implications in pharmacodynamics and pharmacokinetics1
The metabolic activation of and platelet response to vicagrel vary with P-glycoprotein deficiency, rather than P-glycoprotein inhibition, in mice1
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