Default: Drug Metabolism and Disposition

ISSN: 0090-9556

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Drug Metabolism and Disposition Q1 Unclaimed

American Society for Pharmacology and Experimental Therapeutics United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Drug Metabolism and Disposition is a journal indexed in SJR in Pharmacology and Pharmaceutical Science with an H index of 175. It has an SJR impact factor of 1,025 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,025.

Drug Metabolism and Disposition focuses its scope in these topics and keywords: p, cytochrome, human, hepatic, clearance, drug, characterization, prediction, parathion, vitro, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

Drug Metabolism and Disposition

1,025

SJR Impact factor

175

H Index

144

Total Docs (Last Year)

513

Total Docs (3 years)

6847

Total Refs

1751

Total Cites (3 years)

507

Citable Docs (3 years)

3,39

Cites/Doc (2 years)

47,55

Ref/Doc

Aims and Scope


p, cytochrome, human, hepatic, clearance, drug, characterization, prediction, parathion, vitro, liver, targeted, mice, cype, x, cells, diazepam, digoxin, catalyzed, association, bacterial, bcrp, bin, binding, bm, cancer, carboxydichlorofluorescein,



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AN ASSESSMENT OF UDP-GLUCURONOSYLTRANSFERASE INDUCTION USING PRIMARY HUMAN HEPATOCYTES

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CHARACTERIZATION OF N-GLUCURONIDATION OF THE LUNG CARCINOGEN 4-(METHYLNITROSAMINO)-1-(3-PYRIDYL)-1-BUTANOL (NNAL) IN HUMAN LIVER: IMPORTANCE OF UDP-GLUCURONOSYLTRANSFERASE 1A4

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Evaluation of the Potential for Drug-Induced Liver Injury Based on in Vitro Covalent Binding to Human Liver Proteins

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AN ANALYSIS OF THE REGIOSELECTIVITY OF AROMATIC HYDROXYLATION AND N-OXYGENATION BY CYTOCHROME P450 ENZYMES

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Effect of Solvents on the Time-Dependent Inhibition of CYP3A4 and the Biotransformation of AZD3839 in Human Liver Microsomes and Hepatocytes

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DISPOSITION OF TACROLIMUS IN ISOLATED PERFUSED RAT LIVER: INFLUENCE OF TROLEANDOMYCIN, CYCLOSPORINE, AND GG918

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KEY STRUCTURAL FEATURES OF LIGANDS FOR ACTIVATION OF HUMAN PREGNANE X RECEPTOR

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CONJUGATION OF CATECHOLS BY RECOMBINANT HUMAN SULFOTRANSFERASES,

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THE 2002 BERNARD B. BRODIE AWARD LECTURE

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Inhibitory Effects of Commonly Used Herbal Extracts on UDP-Glucuronosyltransferase 1A4, 1A6, and 1A9 Enzyme Activities

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Effects of Pregnancy on the Pharmacokinetics of Metformin

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COMPARISON OF PREDICTION METHODS FOR IN VIVO CLEARANCE OF (S,S)-3-[3-(METHYLSULFONYL)PHENYL]-1-PROPYLPIPERIDINE HYDROCHLORIDE, A DOPAMINE D2 RECEPTOR ANTAGONIST, IN HUMANS

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Quantitative Investigation of the Impact of P-Glycoprotein Inhibition on Drug Transport across Blood-Brain Barrier in Rats

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ASSESSMENT OF ARGININE 97 AND LYSINE 72 AS DETERMINANTS OF SUBSTRATE SPECIFICITY IN CYTOCHROME P450 2C9 (CYP2C9)

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GYKI-47261, A NEW AMPA [2-AMINO-3-(3-HYDROXYMETHYLISOXAZOLE-4-YL)PROPIONIC ACID] ANTAGONIST, IS A CYP2E1 INDUCER

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INDUCTION OF MULTIDRUG RESISTANCE PROTEIN 3 (MRP3) IN VIVO IS INDEPENDENT OF CONSTITUTIVE ANDROSTANE RECEPTOR

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STEREO- AND REGIOSELECTIVITY ACCOUNT FOR THE DIVERSITY OF DEHYDROEPIANDROSTERONE (DHEA) METABOLITES PRODUCED BY LIVER MICROSOMAL CYTOCHROMES P450

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MECHANISM-BASED INHIBITION OF HUMAN LIVER MICROSOMAL CYTOCHROME P450 1A2 BY ZILEUTON, A 5-LIPOXYGENASE INHIBITOR

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Oxidation of the Flavonoids Galangin and Kaempferide by Human Liver Microsomes and CYP1A1, CYP1A2, and CYP2C9

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Evaluation of Cytochrome P450 Probe Substrates Commonly Used by the Pharmaceutical Industry to Study in Vitro Drug Interactions

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Multidrug Resistance-Associated Protein 2 Is Primarily Responsible for the Biliary Excretion of Fexofenadine in Mice

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