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Structure‐based prediction of human intestinal membrane permeability for rapidin silicoBCS classification

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jps.21009openalex-snapshot

Pharmacokinetics in Drug Discovery

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Valacyclovir: A Substrate for the Intestinal and Renal Peptide Transporters PEPT1 and PEPT2

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Nonlinearity of amoxicillin absorption kinetics in human

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Cyclophosphamide metabolite inducing apoptosis in RLS mouse lymphosarcoma cells is a substrate for P-glycoprotein

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Caco-2 cell permeability modelling: a neural network coupled genetic algorithm approach

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Development of an in Vitro Rat Intestine Segmental Perfusion Model to Investigate Permeability and Predict Oral Fraction Absorbed

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The Role of Permeability in Drug ADME/PK, Interactions and Toxicity—Presentation of a Permeability-Based Classification System (PCS) for Prediction of ADME/PK in Humans

inferredcites →https://doi.org/10.1016/0005-2736(90)90261-lopenalex-snapshot

Transport of a large neutral amino acid (phenylalanine) in a human intestinal epithelial cell line: Caco-2

inferredcites →https://doi.org/10.1016/j.ejpb.2004.03.001openalex-snapshot

Classification of orally administered drugs on the World Health Organization Model list of Essential Medicines according to the biopharmaceutics classification system

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PAMPA—a drug absorption in vitro model

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Impact of carriers in oral absorption: Permeation across Caco-2 cells for the organic anions estrone-3-sulfate and glipizide

inferredcites →https://doi.org/10.1016/j.ejps.2010.10.006openalex-snapshot

Structure-based in silico model profiles the binding constant of poorly soluble drugs with β-cyclodextrin

inferredcites →https://doi.org/10.1016/j.ijpharm.2009.02.002openalex-snapshot

Theoretical investigation of passive intestinal membrane permeability using Monte Carlo method to generate drug-like molecule population

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Structural and functional characteristics and tissue distribution pattern of rat OCTN1, an organic cation transporter, cloned from placenta

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Interaction of digoxin with antihypertensive drugs via MDR1

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OATP and P-Glycoprotein Transporters Mediate the Cellular Uptake and Excretion of Fexofenadine

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Effect of colchicine and heat shock on multidrug resistance gene and P-glycoprotein expression in rat liver

inferredcites →https://doi.org/10.1016/s0169-409x(00)00129-0openalex-snapshot

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings 1PII of original article: S0169-409X(96)00423-1. The article was originally published in Advanced Drug Delivery Reviews 23 (1997) 3–25. 1

inferredcites →https://doi.org/10.1016/s0169-409x(02)00004-2openalex-snapshot

Prediction of intestinal permeability

inferredcites →https://doi.org/10.1016/s0378-5173(03)00161-3openalex-snapshot

Prediction of human intestinal permeability using artificial membrane permeability

inferredcites →https://doi.org/10.1016/s1093-3263(02)00163-8openalex-snapshot

Hydrogen bonding descriptors in the prediction of human in vivo intestinal permeability

inferredcites →https://doi.org/10.1021/ci600343xopenalex-snapshot

ADME Evaluation in Drug Discovery. 7. Prediction of Oral Absorption by Correlation and Classification

inferredcites →https://doi.org/10.1021/jm011027bopenalex-snapshot

Descriptors, Physical Properties, and Drug-Likeness

inferredcites →https://doi.org/10.1021/jm020017nopenalex-snapshot

Molecular Properties That Influence the Oral Bioavailability of Drug Candidates

inferredcites →https://doi.org/10.1021/jm049661nopenalex-snapshot

In Silico Prediction of Membrane Permeability from Calculated Molecular Parameters

inferredcites →https://doi.org/10.1021/jm901846topenalex-snapshot

How Well Can the Caco-2/Madin−Darby Canine Kidney Models Predict Effective Human Jejunal Permeability?

inferredcites →https://doi.org/10.1021/jm9810102openalex-snapshot

Correlation of Human Jejunal Permeability (in Vivo) of Drugs with Experimentally and Theoretically Derived Parameters. A Multivariate Data Analysis Approach

inferredcites →https://doi.org/10.1021/mp0600182openalex-snapshot

A Provisional Biopharmaceutical Classification of the Top 200 Oral Drug Products in the United States, Great Britain, Spain, and Japan

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pH-Dependent Solubility and Permeability Criteria for Provisional Biopharmaceutics Classification (BCS and BDDCS) in Early Drug Discovery

inferredcites →https://doi.org/10.1021/mp300140hopenalex-snapshot

The Fraction Dose Absorbed, in Humans, and High Jejunal Human Permeability Relationship

inferredcites →https://doi.org/10.1021/mp300502mopenalex-snapshot

Establishing the Pharmaceutical Quality of Chinese Herbal Medicine: A Provisional BCS Classification

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Increased Understanding of Intestinal Drug Permeability Determined by the LOC-I-GUT Approach Using Multislice Computed Tomography

inferredcites →https://doi.org/10.1023/a:1007692622216openalex-snapshot

Influence of Passive Permeability on Apparent P-glycoprotein Kinetics

inferredcites →https://doi.org/10.1023/a:1011916329863openalex-snapshot

Jejunal Absorption and Metabolism of R/S-Verapamil in Humans

inferredcites →https://doi.org/10.1023/a:1014264614637openalex-snapshot

Comparative Inhibitory Effects of Different Compounds on Rat Oatp1 (Slc21a1)- and Oatp2 (Slc21a5)-Mediated Transport

inferredcites →https://doi.org/10.1023/a:1016065715308openalex-snapshot

Comparison Between Permeability Coefficients in Rat and Human Jejunum

inferredcites →https://doi.org/10.1023/a:1016220428705openalex-snapshot

Does Fluid Flow Across the Intestinal Mucosa Affect Quantitative Oral Drug Absorption? Is It Time for a Reevaluation?

inferredcites →https://doi.org/10.1023/a:1020483911355openalex-snapshot

Comparison of Human Duodenum and Caco-2 Gene Expression Profiles for 12,000 Gene Sequences Tags and Correlation with Permeability of 26 Drugs

inferredcites →https://doi.org/10.1038/nrd1470openalex-snapshot

Can the pharmaceutical industry reduce attrition rates?

inferredcites →https://doi.org/10.1080/00498250701704819openalex-snapshot

Intestinal permeability and its relevance for absorption and elimination

inferredcites →https://doi.org/10.1111/j.1365-2125.1993.tb05691.xopenalex-snapshot

The effect of L‐leucine on the absorption of levodopa, studied by regional jejunal perfusion in man.

inferredcites →https://doi.org/10.1201/9780824741969.axhopenalex-snapshot

Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System

inferredcites →https://doi.org/10.1210/en.2008-0188openalex-snapshot

Competitive Inhibition of Organic Anion Transporting Polypeptide 1c1-Mediated Thyroxine Transport by the Fenamate Class of Nonsteroidal Antiinflammatory Drugs

inferredcites →https://doi.org/10.1248/bpb1978.7.452openalex-snapshot

Intestinal absorption mechanism of amino-.BETA.-lactam antibiotics. III. Kinetics of carrier-mediated transport across the rat small intestine in situ.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/bdd.2152openalex-snapshot

Integrating theoretical and experimental permeability estimations for provisional biopharmaceutical classification: Application to the WHO essential medicines

inferred← citeshttps://doi.org/10.1007/s00216-019-02336-6openalex-snapshot

Dynamic in vitro intestinal barrier model coupled to chip-based liquid chromatography mass spectrometry for oral bioavailability studies

inferred← citeshttps://doi.org/10.1016/b978-0-12-802447-8.00012-1openalex-snapshot

Oral Drug Absorption

inferred← citeshttps://doi.org/10.1016/b978-0-323-91111-5.00002-0openalex-snapshot

In silico, in situ, in vitro, and in vivo predictive methods for modeling formulation performance

inferred← citeshttps://doi.org/10.1016/j.addr.2016.02.005openalex-snapshot

Computational prediction of formulation strategies for beyond-rule-of-5 compounds

inferred← citeshttps://doi.org/10.1016/j.ejps.2017.06.033openalex-snapshot

Comparison of segmental-dependent permeability in human and in situ perfusion model in rat

inferred← citeshttps://doi.org/10.1016/j.ejps.2018.07.057openalex-snapshot

A physiologically based pharmacokinetic model for valacyclovir established based on absolute expression quantity of hPEPT1 and its application

inferred← citeshttps://doi.org/10.1016/j.ejps.2021.106098openalex-snapshot

Best practices in current models mimicking drug permeability in the gastrointestinal tract - An UNGAP review

inferred← citeshttps://doi.org/10.1016/j.ejps.2025.107212openalex-snapshot

Precipitation as key parameter for early oral drug absorption predictions, Part II: Development of a predictive model

inferred← citeshttps://doi.org/10.1016/j.ejps.2026.107576openalex-snapshot

Synergistic impact of 3D multicellular architecture and capillary-like flow on intestinal drug permeability

inferred← citeshttps://doi.org/10.1016/j.ijpharm.2024.124958openalex-snapshot

Quantitative analysis of excipients to the permeability of BCS class III drugs

inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.11.048openalex-snapshot

All layers matter: Innovative three-dimensional epithelium-stroma-endothelium intestinal model for reliable permeability outcomes

inferred← citeshttps://doi.org/10.1016/j.xphs.2018.10.005openalex-snapshot

Formation of a Bile Salt-Drug Hydrogel to Predict Human Intestinal Absorption

inferred← citeshttps://doi.org/10.1016/j.xphs.2020.08.008openalex-snapshot

A Retrospective Biopharmaceutical Analysis of >800 Approved Oral Drug Products: Are Drug Properties of Solid Dispersions and Lipid-Based Formulations Distinctive?

inferred← citeshttps://doi.org/10.1021/acs.analchem.3c01749openalex-snapshot

Biomimetic Dispersive Solid-Phase Microextraction: A Novel Concept for High-Throughput Estimation of Human Oral Absorption of Organic Compounds

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.1c00669openalex-snapshot

Global Analysis of Models for Predicting Human Absorption: QSAR, In Vitro , and Preclinical Models

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.0c00023openalex-snapshot

Effect of Common Excipients on Intestinal Drug Absorption in Wistar Rats

inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.2c01117openalex-snapshot

Artificial Intelligence-Based Quantitative Structure–Property Relationship Model for Predicting Human Intestinal Absorption of Compounds with Serotonergic Activity

inferred← citeshttps://doi.org/10.1038/s41598-017-18012-7openalex-snapshot

Entropy and Polarity Control the Partition and Transportation of Drug-like Molecules in Biological Membrane

inferred← citeshttps://doi.org/10.1080/1062936x.2016.1216010openalex-snapshot

Structure-based model profiles affinity constant of drugs with hPEPT1 for rapid virtual screening of hPEPT1’s substrate

inferred← citeshttps://doi.org/10.1080/17425247.2020.1813108openalex-snapshot

Effect of excipients on oral absorption process according to the different gastrointestinal segments

inferred← citeshttps://doi.org/10.1166/jbn.2020.30041755openalex-snapshot

Mixed Micelles with Galactose Ligands for the Oral Delivery of Berberine to Enhance Its Bioavailability and Hypoglycemic Effects

inferred← citeshttps://doi.org/10.1517/17460441.2014.877881openalex-snapshot

Selecting oral bioavailability enhancing formulations during drug discovery and development

inferred← citeshttps://doi.org/10.18433/j3ks4popenalex-snapshot

Crystal-liquid Fugacity Ratio as a Surrogate Parameter for Intestinal Permeability

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A Physiologically Based Pharmacokinetic (PBPK) Study to Assess the Adjuvanticity of Three Peptides in an Oral Vaccine

inferred← citeshttps://doi.org/10.56028/aetr.13.1.873.2025openalex-snapshot

Review of current techniques analysing interactions between cell-penetrating peptides and lipid membranes

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.