J. Lepoittevin

W. Uter, C. Lidén, J. Johansen, 2017, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Mechanistic studies on the reactivity of sensitizing allylic hydroperoxides: investigation of the covalent modification of amino acids by carbon-radical intermediates

A. Chaintreau, J. Lepoittevin, E. Giménez-Arnau, 2014 .

Patch-testing with serial dilutions of tixocortol pivalate and potential cross-reactive substances.

A. Goossens, M. Bruze, J. Lepoittevin, 2000, Acta dermato-venereologica.

Skin sensitization to linalyl hydroperoxide: support for radical intermediates.

A. Karlberg, J. Montelius, J. Lepoittevin, 1997, Chemical research in toxicology.

Studies of the chemical selectivity of hapten, reactivity, and skin sensitization potency. 1. Synthesis and studies on the reactivity toward model nucleophiles of the (13)C-labeled skin sensitizers hex-1-ene- and hexane-1,3-sultones.

M. Barratt, J. Lepoittevin, E. Meschkat, 2001, Chemical research in toxicology.

Identification of carbon-centred radicals derived from linalyl hydroperoxide, a strong skin sensitizer: a possible route for protein modifications.

J. Lepoittevin, B. Meurer, E. Giménez-Arnau, 2005, Bioorganic & medicinal chemistry.

Identification of alkyl radicals derived from an allergenic cyclic tertiary allylic hydroperoxide by combined use of radical trapping and ESR studies

J. Lepoittevin, E. G. Arnau, L. Grossi, 2002 .

Synthesis and Allergenic Potential of a 15-Hydroperoxyabietic Acid-like Model: Trapping of Radical Intermediates

J. Lepoittevin, E. G. Arnau, V. Mutterer, 2000 .

Studies of the chemical selectivity of hapten, reactivity, and skin sensitization potency. 2. nmr studies of the covalent binding of the (13)c-labeled skin sensitizers 2-[13C]- and 3-[13C]hex-1-ene- and 3-[13C]hexane-1,3-sultones to human serum albumin.

M. Barratt, J. Lepoittevin, E. Meschkat, 2001, Chemical research in toxicology.

Deodorants on the European market: quantitative chemical analysis of 21 fragrances

P. Frosch, M. Bruze, S. Rastogi, 1998, Contact dermatitis.

Adverse Skin Reactions to Plants and Plant Products

C. Lovell, C. Lovell, J. Lepoittevin, 2020, Contact Dermatitis.

Plants and Plant Products

C. Lovell, J. Lepoittevin, E. Paulsen, 2020, Contact Dermatitis.

Allergic contact dermatitis to plants: understanding the chemistry will help our diagnostic approach.

E. Rozas-Muñoz, A. Gimenez-Arnau, J. Lepoittevin, 2012, Actas dermo-sifiliograficas.

ATPase and morphologic changes in Langerhans cells induced by epicutaneous application of a sensitizing dose of DNFB.

C. Benezra, J. Cazenave, D. Hanau, 1989, The Journal of investigative dermatology.

Patch testing with a new fragrance mix detects additional patients sensitive to perfumes and missed by the current fragrance mix

P. Frosch, W. Uter, A. Goossens, 2005, Contact dermatitis.

Patch testing with a new fragrance mix – reactivity to the individual constituents and chemical detection in relevant cosmetic products

P. Frosch, W. Uter, A. Goossens, 2005, Contact dermatitis.

The use of three-dimensional similarity in assessing the risk of cross-reactivity between carbamazepine and psychotropic drugs

G. Marcou, J. Lepoittevin, A. Barbaud, 2014, European Journal of Clinical Pharmacology.

Sensitization potential and potency of terpene hydroperoxides in the cocultured activation test method

J. Lepoittevin, J. Hennen, B. Blömeke, 2019, Contact dermatitis.

Sensitization potential and potency of terpene hydroperoxides in the COCAT method

Elena, J. Lepoittevin, J. Hennen, 2019 .

Sensitization to p-amino aromatic compounds: Study of the covalent binding of 2,5-dimethyl-p-benzoquinonediimine to a model peptide by electrospray ionization tandem mass spectrometry.

J. Lepoittevin, F. Rousset, E. Giménez-Arnau, 2008, Bioorganic & medicinal chemistry.

Mechanistic studies on the lysine-induced N-formylation of 2,5-dimethyl-p-benzoquinonediimine.

J. Lepoittevin, F. Rousset, E. Giménez-Arnau, 2007, Chemical research in toxicology.

Mechanistic insights on skin sensitization to linalool hydroperoxides: EPR evidence on radical intermediates formation in reconstructed human epidermis and 13C-NMR reactivity studies with thiol residues.

J. Lepoittevin, E. Giménez-Arnau, B. Vileno, 2020, Chemical research in toxicology.

Formation of methyl radicals derived from cumene hydroperoxide in reconstructed human epidermis: an EPR spin trapping confirmation by using 13C-substitution

J. Lepoittevin, E. Giménez-Arnau, B. Vileno, 2019, Free radical research.

Understanding the skin sensitization capacity of ascaridole: a combined study of chemical reactivity and activation of the innate immune system (dendritic cells) in the epidermal environment

J. Lepoittevin, B. Blömeke, E. Giménez-Arnau, 2019, Archives of Toxicology.

In situ chemical behaviour of methylisothiazolinone (MI) and methylchloroisothiazolinone (MCI) in reconstructed human epidermis: a new approach to the cross‐reactivity issue

I. Namer, F. Moussallieh, K. Elbayed, 2016, Contact dermatitis.

Nuclear magnetic resonance studies on covalent modification of amino acids thiol and amino residues by monofunctional aryl 13C-isocyanates, models of skin and respiratory sensitizers: transformation of thiocarbamates into urea adducts.

J. Lepoittevin, E. Giménez-Arnau, O. Fleischel, 2009, Chemical research in toxicology.

Methylisothiazolinone and benzisothiazolinone are widely used in paint: a multicentre study of paints from five European countries

W. Uter, R. Bossi, C. Lidén, 2015, Contact dermatitis.

In chemico evaluation of prohapten skin sensitizers: behavior of 2-methoxy-4-(¹³C)methylphenol in the peroxidase peptide reactivity assay (PPRA) as an alternative to animal testing.

G. Gerberick, J. Lepoittevin, E. Giménez-Arnau, 2013, Toxicology letters.

Mechanistic assessment of peptide reactivity assay to predict skin allergens with Kathon CG isothiazolinones.

G. Gerberick, L. Foertsch, J. Lepoittevin, 2009, Toxicology in vitro : an international journal published in association with BIBRA.

Synthesis and In Situ Behavior of 1,4- and 2,5-(13C) Isotopomers of p-Phenylenediamine in Reconstructed Human Epidermis Using High Resolution Magic Angle Spinning NMR.

F. Moussallieh, K. Elbayed, J. Lepoittevin, 2022, Chemical research in toxicology.

In Situ Alkylation of Reconstructed Human Epidermis by Methyl Methanesulfonate: A Quantitative HRMAS NMR Chemical Reactivity Mapping.

F. Moussallieh, K. Elbayed, J. Lepoittevin, 2020, Chemical research in toxicology.

In Situ Alkylation of Reconstructed Human Epidermis by Methyl Methanesulfonate: A Quantitative High Resolution Magic Angle Spinning NMR Approach

F. Moussallieh, K. Elbayed, J. Lepoittevin, 2020 .

Comparison of elicitation potential of chloroatranol and atranol – 2 allergens in oak moss absolute

M. Bruze, J. Johansen, J. Lepoittevin, 2006, Contact dermatitis.

Studies in patients with corticosteroid contact allergy. Understanding cross-reactivity among different steroids.

J. Lepoittevin, A. Dooms-Goossens, J. Drieghe, 1995, Archives of dermatology.

Hapten-Protein Interactions

Jean-Pierre Lepoittevin, David W. Roberts, D. Roberts, 1998 .

Cyclohexane analogs of poison ivy and poison oak derivatives. A totally stereoselective synthesis of trans,trans-3-alkyl-1,2-cyclohexanediols.

C. Benezra, J. Lepoittevin, 1984 .

Antitumor principles from Ginkgo biloba L.

Y. Asakawa, H. Itokawa, J. Lepoittevin, 1987, Chemical & pharmaceutical bulletin.

Isolation, structure determination and synthesis of new dihydroisocoumarins from Ginkgo biloba L.

Y. Asakawa, J. Lepoittevin, N. Choukchou-Braham, 1994 .

Synthesis and photocyclization of alpha-methylene-gamma-butyrolactone-thymine heterodimers.

J. Lepoittevin, S. Mabic, E. Giménez-Arnau, 1995, Chemical research in toxicology.

A Highly Stereoselective Divergent Synthesis of Bicyclic Models of Photoreactive Sesquiterpene Lactones

J. Lepoittevin, V. Berl, Sébastien Fuchs, 2007 .

Methyl exchange on silicon during the addition of methylmagnesium iodide to a cyanohydrin O-silyl ether

J. Lepoittevin, V. Berl, C. Arbez-Gindre, 1999 .

Approach to the stereoselective synthesis of (R)- and (S)-4-methoxydalbergione via asymmetric catalytic hydrogenation

J. Lepoittevin, P. Bissel, R. Sablong, 1995 .

Direct synthesis of mono-glycosylated catechols from glycosylacetates or imidates using BF3.OEt2 as catalyst☆

C. Benezra, J. Lepoittevin, S. Mabic, 1993 .

Bihaptens with 5- and 6-methyl-substituted alkylcatechols and methylene lactone functional groups: tools for hapten (allergen or tolerogen)-protein interaction studies.

C. Benezra, J. Lepoittevin, A. Nazih, 1993, Chemical research in toxicology.

Synthesis of allylic hydroperoxides and EPR spin-trapping studies on the formation of radicals in iron systems as potential initiators of the sensitizing pathway.

A. Chaintreau, J. Lepoittevin, E. Giménez-Arnau, 2011, The Journal of organic chemistry.

Identification of radical species derived from allergenic 15-hydroperoxyabietic acid and insights into the behaviour of cyclic tertiary allylic hydroperoxides in Fe(II)/Fe(III) systems

J. Lepoittevin, E. Giménez-Arnau, L. Grossi, 2008 .

Alternative Methods for Skin Sensitisation Testing

Emanuela Corsini, Jean-Pierre Lepoittevin, Maria Ponec, 1996 .

Allergic contact cheilitis caused by polysilicone‐15 (Parsol® SLX) in a lipcare balm

J. Lepoittevin, Ludovic Martin, M. Avenel-Audran, 2014, Contact dermatitis.

Dictionary of Contact Allergens: Chemical Structures, Sources, and References

J. Lepoittevin, C. L. Coz, 2019, Contact Dermatitis.

Development of a peptide reactivity assay for screening contact allergens.

G Frank Gerberick, Jean-Pierre Lepoittevin, G. Gerberick, 2004, Toxicological sciences : an official journal of the Society of Toxicology.

The chemistry of contact allergy: why is a molecule allergenic?

David Basketter, D. Basketter, A. Karlberg, 1995, Contact dermatitis.

Tixocortol pivalate contact allergy in the GPMT: frequency and cross‐reactivity

J. Lepoittevin, K. Andersen, B. Kreilgaard, 2001, Contact dermatitis.

Occupational erythema‐multiforme‐like dermatitis from sensitization to costus resinoid, followed by flare‐up and systemic contact dermatitis from β‐cyclocostunolide in a chemistry student

J. Lepoittevin, C. Le Coz, 2001, Contact dermatitis.

Contact allergy to topical corticosteroids and systemic contact dermatitis from prednisolone with tolerance of triamcinolone.

A. Bircher, J. Lepoittevin, S. Langauer, 1995, Acta dermato-venereologica.

Deodorants: an experimental provocation study with isoeugenol

P. Frosch, A. Goossens, M. Bruze, 2005, Contact dermatitis.

Contact Allergy—Emerging Allergens and Public Health Impact

W. Uter, I. White, T. Werfel, 2020, International journal of environmental research and public health.

Patch testing with hair cosmetic series in Europe: a critical review and recommendation

P. Frosch, W. Uter, C. Lidén, 2015, Contact dermatitis.

Systemic contact dermatitis from pseudoephedrine

J. Lepoittevin, J. Foussereau, R. Tomb, 1991, Contact dermatitis.

Principles and methodology for identification of fragrance allergens in consumer products *

J. Lepoittevin, J. Camarasa, E. Giménez-Arnau, 2002, Contact dermatitis.

Chemical Modifications Induced by Phthalic Anhydride, a Respiratory Sensitizer, in Reconstructed Human Epidermis: A Combined HRMAS NMR and LC-MS/MS Proteomic Approach.

L. Kuhn, P. Hammann, J. Lepoittevin, 2021, Chemical research in toxicology.

The critical review of methodologies and approaches to assess the inherent skin sensitization potential (skin allergies) of chemicals Part I

Torkil Menné, Axel Schnuch, A. Schnuch, 2012, Contact dermatitis.

The critical review of methodologies and approaches to assess the inherent skin sensitization potential (skin allergies) of chemicals Part III

A. Schnuch, J. Thyssen, T. Menné, 2012, Contact dermatitis.

Synthesis and Photoreaction of a‐Methylene‐γ‐Butyrolactone‐Psoralen Heterodimers

J. Lepoittevin, E. Giménez-Arnau, Cécile Bussey, 1997 .

Ectopic contact dermatitis from ethyl cyanoacrylate instant adhesives

J. Lepoittevin, E. Grosshans, R. Tomb, 1993, Contact dermatitis.

Alpha-methylene-gamma-butyrolactones: versatile skin bioactive natural products.

J. Lepoittevin, V. Berl, E. Giménez-Arnau, 2009, Chemical record.

Content of oak moss allergens atranol and chloroatranol in perfumes and similar products

R. Bossi, S. Rastogi, J. Johansen, 2004, Contact dermatitis.

Contact allergy caused by isothiazolinone derivatives: an overview of non-cosmetic and unusual cosmetic sources

J. Lepoittevin, J. Lambert, A. Goossens, 2017, European Journal of Dermatology.

Preservatives in cosmetics: reactivity of allergenic formaldehyde‐releasers towards amino acids through breakdown products other than formaldehyde *

J. Lepoittevin, E. Giménez-Arnau, Mustapha Kireche, 2010, Contact dermatitis.

Chloroatranol, an extremely potent allergen hidden in perfumes: a dose‐response elicitation study

M. Bruze, S. Rastogi, J. Johansen, 2003, Contact dermatitis.

Deodorants: an experimental provocation study with cinnamic aldehyde.

P. Frosch, S. Wakelin, M. Bruze, 2003, Journal of the American Academy of Dermatology.

The time-dose-response relationship for elicitation of contact dermatitis in isoeugenol allergic individuals.

A Goossens, P. Frosch, A. Goossens, 2001, Toxicology and applied pharmacology.

Risk Assessment of Dimethylfumarate Residues in Dwellings Following Contamination by Treated Furniture

R. Garnier, A. Lefranc, C. Rousselle, 2014, Risk analysis : an official publication of the Society for Risk Analysis.

The critical review of methodologies and approaches to assess the inherent skin sensitization potential (skin allergies) of chemicals Part II

Jean-Pierre Lepoittevin, Torkil Menné, Axel Schnuch, 2012, Contact dermatitis.

Hapten-peptide-T cell receptor interactions: molecular basisfor the recognition of haptens by T lymphocytes

J. Lepoittevin, I. Leblond, 2000 .

Sensitization properties of acetophenone azine, a new skin sensitizer identified in textile

C. Rousselle, J. Lepoittevin, C. Solal, 2022, Contact dermatitis.

Dictionary of Occupational Allergens: Chemical Structures, Sources and References

C. Le Coz, J P Lepoittevin, J. Lepoittevin, 2000 .

Sesquiterpene lactone mix is not an adequate screen for Compositae allergy

J. Lepoittevin, R. Tomb, 1995, Contact dermatitis.

Presence of resin acids in "Oakmoss" patch test material: a source of misdiagnosis?

J. Lepoittevin, S. Huygens, E. Meschkat, 2000, The Journal of investigative dermatology.

Evidence for [2+2] Photoreaction of α‐Methylene‐γ‐Butyrolactones with Thymine: An Explanation for Chronic Actinic Dermatitis to Sesquiterpene Lactones?

J. Lepoittevin, V. Berl, 1999 .

Dendritic Cells as a Tool for the Predictive Identification of Skin Sensitisation Hazard

Valérie Zuang, Silvia Casati, Thomas Hartung, 2005, Alternatives to laboratory animals : ATLA.

The Report and Recommendations of ECVAM Workshop 51 1,2

T. Hartung, D. Basketter, A. Cavani, 2005 .

Deodorants: an experimental provocation study with hydroxycitronellal

P. Frosch, A. Goossens, M. Bruze, 2003, Contact dermatitis.

Molecular Aspects of Fragrance Sensitisation

J. Lepoittevin, V. Mutterer, 1998 .

Skin sensitization to eugenol and isoeugenol in mice: possible metabolic pathways involving ortho-quinone and quinone methide intermediates.

D W Roberts, D A Basketter, D. Roberts, 1997, Chemical research in toxicology.

Patch test reactions to Biobans in metalworkers are often weak and not reproducible

J. Geier, P. Frosch, J. Lepoittevin, 2002, Contact dermatitis.

Understanding the skin sensitization capacity of ascaridole: a combined study of chemical reactivity and activation of the innate immune system (dendritic cells) in the epidermal environment

J. Lepoittevin, B. Blömeke, E. Giménez-Arnau, 2019, Archives of Toxicology.

A murine in vitro model of allergic contact dermatitis to sesquiterpene α-methylene-γ-butyrolactones

C. Benezra, J. Lepoittevin, R. Fraginals, 2004, Archives of Dermatological Research.

A murine in vitro model of allergic contact dermatitis to sesquiterpene alpha-methylene-gamma-butyrolactones.

C. Benezra, J. Lepoittevin, R. Fraginals, 1992, Archives of dermatological research.

ATPase and morphologic changes induced by UVB on Langerhans cells in guinea pigs.

C. Benezra, D. Hanau, J. Lepoittevin, 1985, The Journal of investigative dermatology.

Contact allergy to oak moss: search for sensitizing molecules using combined bioassay-guided chemical fractionation, GC-MS, and structure-activity relationship analysis

A. Goossens, S. Rastogi, S. Heydorn, 2003, Archives of Dermatological Research.

The incorporation of lysine into the peroxidase peptide reactivity assay for skin sensitization assessments.

Petra S Kern, G Frank Gerberick, Jean-Pierre Lepoittevin, 2011, Toxicological sciences : an official journal of the Society of Toxicology.

Synthesis and reactivity toward nucleophilic amino acids of 2,5-[13C]-dimethyl-p-benzoquinonediimine.

Joan Eilstein, Jean-Pierre Lepoittevin, Daniel Duché, 2006, Chemical research in toxicology.

A murine model of contact dermatitis to sesquiterpene α‐methylene‐α‐butyrolactones *

C. Benezra, J. Lepoittevin, R. Fraginals, 1992 .

13C-enriched methyl alkanesulfonates: New lipophilic methylating agents for the identification of nucleophilic amino acids of proteins by NMR.

C. Benezra, J. Lepoittevin, 1992 .

Comments on Conformational Studies of Monoglycosylated 3-N-Alkylcatechols

J. Lepoittevin, T. Grindley, Glen D. Rockwell, 1999 .

Mono-Glycosylated 3-N-Alkylcatechols: Direct Synthesis from Glycosylacetates, 1H Nmr Analysis and Conformational Studies

J. Lepoittevin, S. Mabic, 1996 .

Synthesis and interaction studies of 13C labeled lactone derivatives with a model protein using 13C NMR.

C. Benezra, J. Lepoittevin, C. Franot, 1993, Bioorganic & medicinal chemistry.

Investigation of peptide reactivity of pro-hapten skin sensitizers using a peroxidase-peroxide oxidation system.

G Frank Gerberick, Jean-Pierre Lepoittevin, Carsten Goebel, 2009, Toxicological sciences : an official journal of the Society of Toxicology.

Chronic Actinic Dermatitis to Sesquiterpene Lactones: [2+2] Photoreaction Toward Thymidine of (+) and (−) α‐Methylene‐Hexahydrobenzofuranone with a cis Ring Junction

J. Lepoittevin, V. Berl, Sébastien Fuchs, 2010, Photochemistry and photobiology.

Air oxidation of 17-hydroxycorticosteroids catalyzed by cupric acetate: formation of hemiacetal dimers

J. Lepoittevin, V. Berl, C. Arbez-Gindre, 2003, Steroids.

Regioselective bromination of O-β-glycosylated aromatics

J. Lepoittevin, S. Mabic, 1995 .

Occupational allergic contact dermatitis from ethyl cyanoacrylate

M. Bruze, J. Lepoittevin, B. Björkner, 1995, Contact dermatitis.

The Practical Approach

D. Basketter, A. Goossens, A. Karlberg, 1998 .

Novel predictive assay for contact allergens using human skin explant cultures.

P. Das, J. Bos, M. Kapsenberg, 1996, The American journal of pathology.

Structure–activity relationships for selected fragrance allergens

G. Patlewicz, D. Basketter, J. Lepoittevin, 2002, Contact dermatitis.

New Syntheses of the Benzoquinone Primin and its Water-Soluble Analog Primin Acid via Heck Reactions

C. Benezra, J. Lepoittevin, S. Mabic, 1999 .

Molecular Aspects in Allergic and Irritant Contact Dermatitis

Jean-Pierre Lepoittevin, J. Lepoittevin, 2020, Contact Dermatitis.

Synthesis and photocytotoxic activity of new α-methylene-γ-butyrolactone-psoralen heterodimers

P. Bischoff, J. Lepoittevin, V. Berl, 2004 .

Synthesis and Photoreaction of 5‐Aikenyloxypsoralen Derivatives

J. Lepoittevin, E. Giménez-Arnau, 1996 .

Intramolecular photocyclization of 5-geranoxy psoralen (bergamottin)

J. Lepoittevin, S. Mabic, E. Giménez-Arnau, 1994 .

Double-headed molecules based on linear or angular psoralen and α-methylene-ψ-butyrolactone: a search for non-phototoxic potential antiproliferative compounds

C. Benezra, J. Lepoittevin, Cécile Bussey, 1993 .

Allergic contact dermatitis to Ginkgo biloba L.: relationship with urushiol

C. Benezra, Y. Asakawa, J. Lepoittevin, 2004, Archives of Dermatological Research.

Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects

A. M. Api, H. Maibach, A. Schnuch, 2011, Cellular and Molecular Life Sciences.

Isothiazolinones are still widely used in paints purchased in five European countries: a follow‐up study

W. Uter, R. Bossi, C. Lidén, 2018, Contact dermatitis.

[Physiopathology of contact eczema].

J. Lepoittevin, B. Cribier, 1998, Annales de dermatologie et de venereologie.

Patch testing with serial dilutions of budesonide, its R and S diastereomers, and potentially cross-reacting substances.

A. Goossens, M. Bruze, J. Lepoittevin, 2001, American Journal of Contact Dermatitis.

Thymoquinone as a causative allergen in Nigella sativa oil contact dermatitis with cross‐reactivity to tert‐butylhydroquinone

J. Lepoittevin, A. Barbaud, F. Chasset, 2020, Contact dermatitis.

Allergic contact dermatitis caused by naturally occurring quinones

Jean-Pierre Lepoittevin, C. Benezra, J. Lepoittevin, 1991, Pharmaceutisch Weekblad.

Molecular Basis of Allergic Contact Dermatitis

J. Lepoittevin, V. Berl, 2004 .

Molecular Aspects of Allergic Contact Dermatitis

J. Lepoittevin, 2001 .

Chemical reactivity measurement and the predicitve identification of skin sensitisers. The report and recommendations of ECVAM Workshop 64.

Silvia Casati, David Basketter, Petra Kern, 2008, Alternatives to laboratory animals : ATLA.

Effect of glutathione on the covalent binding of the 13C-labeled skin sensitizer 5-chloro-2-methylisothiazol-3-one to human serum albumin: identification of adducts by nuclear magnetic resonance, matrix-assisted laser desorption/ionization mass spectrometry, and nanoelectrospray tandem mass spectrom

D. Basketter, A. Dell, H. Morris, 2004, Chemical Research in Toxicology.

Modifications induced by chemical skin allergens on the metabolome of reconstructed human epidermis: A pilot high‐resolution magic angle spinning nuclear magnetic resonance study

F. Moussallieh, K. Elbayed, E. Moss, 2020 .

Further evaluation of quantitative structure–activity relationship models for the prediction of the skin sensitization potency of selected fragrance allergens

G. Patlewicz, D. Roberts, D. Basketter, 2004, Contact dermatitis.

Studies of chemical selectivity of hapten, reactivity, and skin sensitization potency. 3. Synthesis and studies on the reactivity toward model nucleophiles of the 13C-labeled skin sensitizers, 5-chloro-2-methylisothiazol-3-one (MCI) and 2-methylisothiazol-3-one (MI).

Jean-Pierre Lepoittevin, David Basketter, Camilla Pease, 2003, Chemical research in toxicology.

Covalent binding of the 13C-labeled skin sensitizers 5-chloro-2-methylisothiazol-3-one (MCI) and 2-methylisothiazol-3-one (MI) to a model peptide and glutathione.

D. Basketter, J. Lepoittevin, C. Pease, 2004, Bioorganic & medicinal chemistry letters.

Synthesis of a water-soluble analog of 6-methyl-3-N-alkyl catechol labeled with carbon 13: NMR approach to the reactivity of poison ivy/oak sensitizers toward proteins.

J. Lepoittevin, G. Goetz, E. Meschkat, 1999, Bioorganic & medicinal chemistry letters.

Adverse cutaneous drug reaction to alendronate

P. Frosch, J. Lepoittevin, T. Brinkmeier, 2007, Contact dermatitis.

Isothiazolinones in commercial products at Danish workplaces

J. Bonde, M. Flyvholm, J. Johansen, 2014, Contact dermatitis.

Modifications induced by chemical skin allergens on the metabolome of reconstructed human epidermis: A pilot HRMAS NMR study.

F. Moussallieh, K. Elbayed, E. Moss, 2019, Contact dermatitis.

[Contact allergy to beta blockaders in eye drops: cross allergy?].

J. Bazex, J. Lepoittevin, F. Giordano‐Labadie, 1997, Annales de dermatologie et de venereologie.

Can contact allergy to p‐phenylenediamine explain the high rates of terpene hydroperoxide allergy? – An epidemiological study based on consecutive patch test results

J. Johansen, J. Lepoittevin, N. H. Bennike, 2017, Contact dermatitis.

Synthesis of a Water-Soluble Analogue of 6-Methyl-3-n-Alkyl Catechol Labeled with Carbon-13. NMR Approach to the Reactivity of Poison Ivy/Oak Sensitizers Toward Proteins.

J. Lepoittevin, G. Goetz, E. Meschkat, 1999 .

Structure-activity relationships for contact allergenic potential of gamma,gamma-dimethyl-gamma-butyrolactone derivatives. 1. Synthesis and electrophilic reactivity studies of alpha-(omega-substituted-alkyl)-gamma,gamma-dimethyl-gamma-butyrolacton es and correlation of skin sensitization potential a

D. Roberts, D. Basketter, C. Benezra, 1994, Chemical research in toxicology.

Structure-activity relationships for contact allergenic potential of gamma,gamma-dimethyl-gamma-butyrolactone derivatives. 2. Quantitative structure-skin sensitization relationships for alpha-substituted-alpha-methyl-gamma,gamma-dimethyl-gamma-butyrolactone s.

D W Roberts, D A Basketter, C Benezra, 1994, Chemical research in toxicology.

13C‐Enriched Methyl Alkanesulfonates: New Lipophilic Methylating Agents for the Identification of Nucleophilic Amino Acids of Proteins by NMR.

C. Benezra, J. Lepoittevin, 1992 .

Is a low content in atranol/chloroatranol safe in oak moss‐sensitized individuals?

A. Goossens, J. Lepoittevin, E. Giménez-Arnau, 2009, Contact dermatitis.

Identification of Allergens in Complex Mixtures and Products

V. Mahler, J. Lepoittevin, Johansen, 2021 .

A liquid chromatography-mass spectrometric method for the determination of oak moss allergens atranol and chloroatranol in perfumes.

R. Bossi, S. Rastogi, J. Johansen, 2004, Journal of separation science.

Sensitizing capacity of three methyl alkanesulphonates: a murine in vivo and in vitro model of allergic contact dermatitis

C. Benezra, J. Lepoittevin, R. Fraginals, 2004, Archives of Dermatological Research.

Interactions of allergenic hydroperoxides with proteins: a radical mechanism?

A. Karlberg, J. Lepoittevin, 1994, Chemical research in toxicology.

A successful murine model for contact sensitization to a sesquiterpene-α-methylene-γ-butyrolactone: Sensitization to alantolactone in four strains of mice

C. Benezra, J. Lepoittevin, R. Fraginals, 1991 .

Development of a peptide reactivity assay for screening contact allergens.

G. Gerberick, J. Vassallo, J. Chaney, 2004, Toxicological sciences : an official journal of the Society of Toxicology.

Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects

A. M. Api, T. L. Diepgen, D. A. Basketter, 2011, Cellular and Molecular Life Sciences.

Mechanism of allergic contact dermatitis from propacetamol: sensitization to activated N,N‐diethylglycine

J. Lepoittevin, A. Barbaud, V. Berl, 1998, Contact dermatitis.

Regulatory classification of substances oxidized to skin sensitizers on exposure to air

D. Basketter, A. Goossens, A. Karlberg, 1999, Contact dermatitis.

Contact Allergy to Fragrances

W. Uter, J. Lepoittevin, J. D. Johansen, 2020, Contact Dermatitis.

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