19 articles for LF Hennequin
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Identification of novel TACE inhibitors compatible with topical application.

Nestl�
Discovery of phenoxyindazoles and phenylthioindazoles as ROR¿ inverse agonists.

Galderma R & D
Discovery of AZD8931, an Equipotent, Reversible Inhibitor of Signaling by EGFR, HER2, and HER3 Receptors.

Astrazeneca
Neutral 5-substituted 4-anilinoquinazolines as potent, orally active inhibitors of erbB2 receptor tyrosine kinase.

Astrazeneca
Inhibitors of epidermal growth factor receptor tyrosine kinase: optimisation of potency and in vivo pharmacokinetics.

Astrazeneca
Novel 4-anilinoquinazolines with C-6 carbon-linked side chains: synthesis and structure-activity relationship of a series of potent, orally active, EGF receptor tyrosine kinase inhibitors.

Astrazeneca
Inhibitors of epidermal growth factor receptor tyrosine kinase: Novel C-5 substituted anilinoquinazolines designed to target the ribose pocket.

Astrazeneca
5-Substituted 4-anilinoquinazolines as potent, selective and orally active inhibitors of erbB2 receptor tyrosine kinase.

Astrazeneca
Impact of Minor Structural Modifications on Properties of a Series of mTOR Inhibitors.

Nestl�
Design and synthesis of potent non-polyglutamatable quinazoline antifolate thymidylate synthase inhibitors.

Astrazeneca
Quinazoline antifolates thymidylate synthase inhibitors: lipophilic analogues with modification to the C2-methyl substituent.

Zeneca Pharma
Squaramides as novel class I and IIB histone deacetylase inhibitors for topical treatment of cutaneous t-cell lymphoma.

Nestle Skin Health R&D
Sulfoximines as potent RORγ inverse agonists.

Nestle Skin Health
Discovery and process development of a novel TACE inhibitor for the topical treatment of psoriasis.

Nestle Skin Health
Rational Drug Design of Topically Administered Caspase 1 Inhibitors for the Treatment of Inflammatory Acne.

Nestl�
Azapeptides as CD36 binding compounds

Valorisation-Recherche, Limited Partnership
Selective octahydro-cyclopenta[C] pyrrole negative modulators of NR2B

Cadent Therapeutics
C17-aryl substituted betulinic acid analogs

Viiv Healthcare UK (NO.5)
Tyrosine kinase inhibitors. 1. Structure-activity relationships for inhibition of epidermal growth factor receptor tyrosine kinase activity by 2,3-dihydro-2-thioxo-1H-indole-3-alkanoic acids and 2,2'-dithiobis(1H-indole-3-alkanoic acids).

University of Auckland