16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Optimization of spirocyclic proline tryptophan hydroxylase-1 inhibitors.

Karos Pharmaceuticals
Discovery of acyl guanidine tryptophan hydroxylase-1 inhibitors.

Karos Pharmaceuticals
Discovery of spirocyclic proline tryptophan hydroxylase-1 inhibitors.

Karos Pharmaceuticals
Tryptophan hydroxylase 1 (Tph-1)-targeted bone anabolic agents for osteoporosis.

Nanjing University
Substituted 3-(4-(1,3,5-triazin-2-yl)-phenyl)-2-aminopropanoic acids as novel tryptophan hydroxylase inhibitors.

Lexicon Pharmaceuticals
Modulation of peripheral serotonin levels by novel tryptophan hydroxylase inhibitors for the potential treatment of functional gastrointestinal disorders.

Lexicon Pharmaceuticals
Structure-Based Design of Xanthine-Imidazopyridines and -Imidazothiazoles as Highly Potent and In Vivo Efficacious Tryptophan Hydroxylase Inhibitors.

Leibniz-Fmp
Synthesis and biological evaluation of xanthine derivatives with phenacyl group as tryptophan hydroxylase 1 (TPH1) inhibitors for obesity and fatty liver disease.

Gwangju Institute of Science and Technology
A decade of approved first-in-class small molecule orphan drugs: Achievements, challenges and perspectives.

China Pharmaceutical University
Structure-Based Design of Xanthine-Benzimidazole Derivatives as Novel and Potent Tryptophan Hydroxylase Inhibitors.

Leibniz-Forschungsinstitut F�R Molekulare Pharmakologie (Fmp)
Peripheral Selective Oxadiazolylphenyl Alanine Derivatives as Tryptophan Hydroxylase 1 Inhibitors for Obesity and Fatty Liver Disease.

Gwangju Institute of Science and Technology
Pyrido[3,2-d]pyrimidine compounds as immunomodulators

Incyte
1H-pyrazolo[4,3-b]pyridines as PDE1 inhibitors

H. Lundbeck
(S)-5-ethynyl-anabasine, derivatives thereof, and related compositions and methods of making and using

Iowa State University Research Foundation
Quinuclidine derivatives and medicinal compositions containing the same

Almirall
Ligand Discovery for a Peptide-Binding GPCR by Structure-Based Screening of Fragment- and Lead-Like Chemical Libraries.

Stockholm University