On the public citation graph

QSAR Analyses of Skin Penetration Enhancers

https://doi.org/10.1021/ci700051e
0 signed · 36 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/9780470057339.vaa008openalex-snapshot
Multivariate Adaptive Regression Splines
inferredcites →https://doi.org/10.1007/s11095-005-7416-4openalex-snapshot
Investigation of Iminosulfuranes as Novel Transdermal Penetration Enhancers: Enhancement Activity and Cytotoxicity
inferredcites →https://doi.org/10.1016/0168-3659(87)90066-6openalex-snapshot
Mode of action of penetration enhancers in human skin
inferredcites →https://doi.org/10.1016/0378-5173(93)90025-bopenalex-snapshot
In vitro evaluation of a series of Azone analogs as dermal penetration enhancers. II. (Thio) amides
inferredcites →https://doi.org/10.1016/0378-5173(93)90424-eopenalex-snapshot
In vitro evaluation of a series of Azone analogs as dermal penetration enhancers. I
inferredcites →https://doi.org/10.1016/0378-5173(94)00294-fopenalex-snapshot
In vitro evaluation of a series of Azone analogs as dermal penetration enhancers: IV. Amines
inferredcites →https://doi.org/10.1016/0378-5173(94)90245-3openalex-snapshot
In vitro evaluation of a series of azone analogs as dermal penetration enhancers: III. Acyclic amides
inferredcites →https://doi.org/10.1016/s0168-3659(96)01573-8openalex-snapshot
Effect of novel penetration enhancers on the transdermal delivery of hydrocortisone: an in vitro species comparison
inferredcites →https://doi.org/10.1016/s0378-5173(97)00349-9openalex-snapshot
In vitro evaluation of azone analogs as dermal penetration enhancers
inferredcites →https://doi.org/10.1016/s0378-5173(98)00060-xopenalex-snapshot
Synthesis and investigation of urea compounds as transdermal penetration enhancers
inferredcites →https://doi.org/10.1021/ci049898sopenalex-snapshot
4D-Fingerprints, Universal QSAR and QSPR Descriptors
inferredcites →https://doi.org/10.1021/js950331nopenalex-snapshot
Synthesis and in Vitro Transdermal Penetration Enhancing Activity of Lactam N-Acetic Acid Esters
inferredcites →https://doi.org/10.1081/ddc-100102251openalex-snapshot
Influence of Drug Lipophilicity on Terpenes as Transdermal Penetration Enhancers
inferredcites →https://doi.org/10.3109/10717549509031359openalex-snapshot
Investigation of enhancer structure activity relationships in congeners of 2-(1-nonyl)-1,3-dioxolane

What points at this work

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

inferred← citeshttps://doi.org/10.1002/9783527628766.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/cem.2415openalex-snapshot
Novel algorithm to select basis functions in spline regression: applications in quantitative structure–activity relationship studies
inferred← citeshttps://doi.org/10.1002/chin.200734206openalex-snapshot
QSAR Analyses of Skin Penetration Enhancers.
inferred← citeshttps://doi.org/10.1002/med.20227openalex-snapshot
Azone analogues: classification, design, and transdermal penetration principles
inferred← citeshttps://doi.org/10.1007/978-3-662-47039-8_4openalex-snapshot
Structure-Activity Relationship of Chemical Penetration Enhancers
inferred← citeshttps://doi.org/10.1007/978-3-662-47039-8_6openalex-snapshot
Azone® and Its Analogues as Penetration Enhancers
inferred← citeshttps://doi.org/10.1007/s10822-011-9511-4openalex-snapshot
The great descriptor melting pot: mixing descriptors for the common good of QSAR models
inferred← citeshttps://doi.org/10.1007/s12247-023-09757-yopenalex-snapshot
Classification of Potent and Weak Penetration Enhancers Using Multiple Feature Selection Methods and Machine Learning Models
inferred← citeshttps://doi.org/10.1016/j.chemolab.2012.05.013openalex-snapshot
QSAR model for chemical penetration enhancers containing long hydrocarbon chain
inferred← citeshttps://doi.org/10.1016/j.ejps.2021.105924openalex-snapshot
An integrated biophysical model for predicting the clinical pharmacokinetics of transdermally delivered compounds
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2009.12.028openalex-snapshot
A skin permeability model of insulin in the presence of chemical penetration enhancer
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2013.01.015openalex-snapshot
Effect of unsaturated menthol analogues on the in vitro penetration of 5-fluorouracil through rat skin
inferred← citeshttps://doi.org/10.1016/j.ijpx.2025.100468openalex-snapshot
Research progress of penetration enhancers in transdermal drug delivery systems: Multidimensional exploration from mechanisms to clinical application
inferred← citeshttps://doi.org/10.1016/j.mineng.2012.06.001openalex-snapshot
QSAR analysis of selectivity in flotation of chalcopyrite from pyrite for xanthate derivatives: Xanthogen formates and thionocarbamates
inferred← citeshttps://doi.org/10.1016/j.tox.2017.06.008openalex-snapshot
Quantitative structure-skin permeability relationships
inferred← citeshttps://doi.org/10.1021/bk-2016-1222.ch014openalex-snapshot
Steps Toward a Virtual Rat: Predictive Absorption, Distribution, Metabolism, and Toxicity Models
inferred← citeshttps://doi.org/10.1021/ci8000277openalex-snapshot
Membrane-Interaction Quantitative Structure−Activity Relationship (MI-QSAR) Analyses of Skin Penetration Enhancers
inferred← citeshttps://doi.org/10.1021/ci9002427openalex-snapshot
3D Pharmacophore Mapping Using 4D QSAR Analysis for the Cytotoxicity of Lamellarins Against Human Hormone-Dependent T47D Breast Cancer Cells
inferred← citeshttps://doi.org/10.1021/tx700392bopenalex-snapshot
Identification of Possible Sources of Nanotoxicity from Carbon Nanotubes Inserted into Membrane Bilayers Using Membrane Interaction Quantitative Structure−Activity Relationship Analysis
inferred← citeshttps://doi.org/10.1080/10717544.2018.1561764openalex-snapshot
Permeation-enhancing effects and mechanisms of O-acylterpineol on isosorbide dinitrate: mechanistic insights based on ATR-FTIR spectroscopy, molecular modeling, and CLSM images
inferred← citeshttps://doi.org/10.3390/ph17020177openalex-snapshot
Model-Informed Drug Development: In Silico Assessment of Drug Bioperformance following Oral and Percutaneous Administration
inferred← citeshttps://doi.org/10.3390/pharmaceutics4030343openalex-snapshot
Design of Skin Penetration Enhancers Using Replacement Methods for the Selection of the Molecular Descriptors
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.