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Stereochemistry–activity relationship of orally active tetralin S1P agonist prodrugs
- Source :
- Bioorganic & Medicinal Chemistry Letters. 20:2264-2269
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- Modifying FTY720, an immunosuppressant modulator, led to a new series of well phosphorylated tetralin analogs as potent S1P1 receptor agonists. The stereochemistry effect of tetralin ring was probed, and (−)-(R)-2-amino-2-((S)-6-octyl-1,2,3,4-tetrahydronaphthalen-2-yl) propan-1-ol was identified as a good SphK2 substrate and potent S1P1 agonist with good oral bioavailability.
- Subjects :
- Models, Molecular
Agonist
Multiple Sclerosis
Tetrahydronaphthalenes
medicine.drug_class
Stereochemistry
Clinical Biochemistry
Administration, Oral
Pharmaceutical Science
Crystallography, X-Ray
Biochemistry
Article
Mice
Structure-Activity Relationship
chemistry.chemical_compound
Lymphopenia
Drug Discovery
medicine
Animals
Structure–activity relationship
Prodrugs
Tetralin
Phosphorylation
Molecular Biology
S1p1 receptor
Organic Chemistry
Substrate (chemistry)
Prodrug
Bioavailability
Phosphotransferases (Alcohol Group Acceptor)
Receptors, Lysosphingolipid
Orally active
chemistry
Molecular Medicine
Immunosuppressive Agents
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....0c0bd28d957e3d66454e8b25926b1272
- Full Text :
- https://doi.org/10.1016/j.bmcl.2010.02.006