75 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
26
Discovery of a Potent and Selective Sphingosine Kinase 1 Inhibitor through the Molecular Combination of Chemotype-Distinct Screening Hits.

Pfizer
60
A benzo[b]thiophene-based selective type 4 S1P receptor agonist.

Harvard Medical School
2
Identification and Preclinical Pharmacology of BMS-986104: A Differentiated S1P1 Receptor Modulator in Clinical Trials.

Bristol-Myers Squibb
65
Novel S1P1 receptor agonists - Part 4: Alkylaminomethyl substituted aryl head groups.

Actelion Pharmaceuticals
38
Discovery of Tetrahydropyrazolopyridine as Sphingosine 1-Phosphate Receptor 3 (S1P3)-Sparing S1P1 Agonists Active at Low Oral Doses.

Glaxosmithkline
19
Discovery of novel S1P2 antagonists, part 3: Improving the oral bioavailability of a series of 1,3-bis(aryloxy)benzene derivatives.

Ono Pharmaceutical
55
Late-stage optimization of a tercyclic class of S1P3-sparing, S1P1 receptor agonists.

Boehringer Ingelheim Pharmaceuticals
14
Discovery of novel S1P2 antagonists. Part 2: Improving the profile of a series of 1,3-bis(aryloxy)benzene derivatives.

Ono Pharmaceutical
25
Discovery of novel S1P2 antagonists. Part 1: discovery of 1,3-bis(aryloxy)benzene derivatives.

Ono Pharmaceutical
32
Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptor.

Arena Pharmaceuticals
11
(7-Benzyloxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic Acids as S1P1 Functional Antagonists.

Arena Pharmaceuticals
19
Discovery of APD334: Design of a Clinical Stage Functional Antagonist of the Sphingosine-1-phosphate-1 Receptor.

Arena Pharmaceuticals
23
Discovery of a novel class of zwitterionic, potent, selective and orally active S1P1 direct agonists.

RhôNe-Poulenc Rorer
7
An oral sphingosine 1-phosphate receptor 1 (S1P(1)) antagonist prodrug with efficacy in vivo: discovery, synthesis, and evaluation.

Novartis Pharma
12
Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease.

Arena Pharmaceuticals
10
4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1.

TBA
6
Constrained azacyclic analogues of the immunomodulatory agent FTY720 as molecular probes for sphingosine 1-phosphate receptors.

University of Montreal
11
Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: discovery of potent S1P1 receptor agonists.

University of Virginia
8
Synthesis of benzimidazole based analogues of sphingosine-1-phosphate: discovery of potent, subtype-selective S1P4 receptor agonists.

University of Virginia
19
Design and synthesis of conformationally constrained 3-(N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors.

Merck Research Laboratories
12
Synthesis of para-alkyl aryl amide analogues of sphingosine-1-phosphate: discovery of potent S1P receptor agonists.

University of Virginia
3
Synthesis and evaluation of CS-2100, a potent, orally active and S1P(3)- sparing S1P(1) agonist.

Daiichi Sankyo
2
Discovery of CS-0777: A Potent, Selective, and Orally Active S1P1 Agonist.

TBA
41
Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P¿? agonists.

Arena Pharmaceuticals
31
Discovery, synthesis and SAR analysis of novel selective small molecule S1P4-R agonists based on a (2Z,5Z)-5-((pyrrol-3-yl)methylene)-3-alkyl-2-(alkylimino)thiazolidin-4-one chemotype.

The Scripps Research Institute
9
Discovery of a brain-penetrant S1P3-sparing direct agonist of the S1P¿? and S1P5 receptors efficacious at low oral dose.

Glaxosmithkline
10
SAR analysis of innovative selective small molecule antagonists of sphingosine-1-phosphate 4 (S1P4) receptor.

The Scripps Research Institute
41
Discovery, design and synthesis of the first reported potent and selective sphingosine-1-phosphate 4 (S1P4) receptor antagonists.

The Scripps Research Institute
11
Structure-activity relationship studies of sphingosine-1-phosphate receptor agonists with N-cinnamyl-ß-alanine moiety.

Ono Pharmaceutical
16
Discovery of AMG 369, a Thiazolo[5,4-
b]pyridine Agonist of S1P
1 and S1P
5
TBA
69
2-imino-thiazolidin-4-one derivatives as potent, orally active S1P1 receptor agonists.

Actelion Pharmaceuticals
15
Exploration of amino alcohol derivatives as novel, potent, and highly selective sphingosine-1-phosphate receptor subtype-1 agonists.

Praecis Pharmaceuticals
8
Stereochemistry-activity relationship of orally active tetralin S1P agonist prodrugs.

Biogen Idec
11
S1P receptor mediated activity of FTY720 phosphate mimics.

Novartis Institutes For Biomedical Research
53
Discovery of a novel series of potent S1P1 agonists.

Merck Serono
15
Pyrazole derived from (+)-3-carene; a novel potent, selective scaffold for sphingosine-1-phosphate (S1P(1)) receptor agonists.

Novartis Institutes For Biomedical Research
20
Synthesis and evaluation of arylalkoxy- and biarylalkoxy-phenylamide and phenylimidazoles as potent and selective sphingosine-1-phosphate receptor subtype-1 agonists.

Praecis Pharmaceuticals
6
Synthesis and evaluation of alkoxy-phenylamides and alkoxy-phenylimidazoles as potent sphingosine-1-phosphate receptor subtype-1 agonists.

Praecis Pharmaceuticals
12
Synthesis and biological evaluation of gamma-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists.

University of Virginia
28
Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypes.

Merck Research Laboratories
41
Highly selective and potent agonists of sphingosine-1-phosphate 1 (S1P1) receptor.

Merck
11
2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors.

Merck Research Laboratories
11
2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists.

Merck Research Laboratories
4
Novel immunomodulator FTY720 is phosphorylated in rats and humans to form a single stereoisomer. Identification, chemical proof, and biological characterization of the biologically active species and its enantiomer.

Novartis Institutes For Biomedical Research
30
Synthesis and evaluation of highly selective quinazoline-2,4-dione ligands for sphingosine-1-phosphate receptor 2.

Washington University
41
Rational Design, Synthesis, and Biological Evaluation of Novel S1PR2 Antagonists for Reversing 5-FU-Resistance in Colorectal Cancer.

Ocean University of China
23
A rational utilization of high-throughput screening affords selective, orally bioavailable 1-benzyl-3-carboxyazetidine sphingosine-1-phosphate-1 receptor agonists.

Merck Research Laboratories
13
Discovery of Potent Selective Nonzinc Binding Autotaxin Inhibitor BIO-32546.

Biogen
4
Identification and Preclinical Pharmacology of ((1 R,3 S)-1-Amino-3-(( S)-6-(2-methoxyphenethyl)-5,6,7,8-tetrahydronaphthalen-2-yl)cyclopentyl)methanol (BMS-986166): A Differentiated Sphingosine-1-phosphate Receptor 1 (S1P

Bristol-Myers Squibb Research and Development
4
Bicyclic Ligand-Biased Agonists of S1P

Bristol Myers Squibb Research & Early Development
29
Novel Potent Selective Orally Active S1P5 Receptor Antagonists.

Biogen
4
Small-molecule agents for the treatment of inflammatory bowel disease.

Gilead Sciences
28
Discovery and Structure-Activity Relationship (SAR) of a Series of Ethanolamine-Based Direct-Acting Agonists of Sphingosine-1-phosphate (S1P1).

Bristol-Myers Squibb
29
Design, synthesis, and in vitro bioactivity evaluation of fluorine-containing analogues for sphingosine-1-phosphate 2 receptor.

Washington University
55
Discovery of A-971432, An Orally Bioavailable Selective Sphingosine-1-Phosphate Receptor 5 (S1P5) Agonist for the Potential Treatment of Neurodegenerative Disorders.

Abbvie Bioresearch Center
3
Discovery of Clinical Candidate GSK1842799 As a Selective S1P1 Receptor Agonist (Prodrug) for Multiple Sclerosis.

Praecis Pharmaceuticals
28
Discovery, design and synthesis of a selective S1P(3) receptor allosteric agonist.

The Scripps Research Institute
6
Modulators of the Sphingosine 1-phosphate receptor 1.

The Scripps Research Institute
5
NBD-labeled derivatives of the immunomodulatory drug FTY720 as tools for metabolism and mode of action studies.

Novartis Institutes For Biomedical Research
22
Discovery of a 1-Methyl-3,4-dihydronaphthalene-Based Sphingosine-1-Phosphate (S1P) Receptor Agonist Ceralifimod (ONO-4641). A S1P

Ono Pharmaceutical
639
Compounds for modulating S1P1 activity and methods of using the same

Trevena
4
Amino alcohol derivative, pharmaceutical composition and application thereof

Beijing Foreland Pharma
366
Sphinogosine-1 -phosphate receptor modulators for treatment of cardiopulmonary disorders

The Scripps Research Institute
42
Spiro-cyclic amine derivatives as S1P modulators

Abbvie
25
Tetrahydronaphthalene derivative

Ono Pharmaceutical
58
Compositions for binding sphingosine-1-phosphate receptor 1 (S1P1), imaging of S1P1, and methods of use thereof

Washington University
365
Sphinogosine-1-phosphate receptor modulators for treatment of cardiopulmonary disorders

The Scripps Research Institute
21
Sphingosine 1-phosphate receptor antagonists

Arroyo Biosciences
42
Spiro-cyclic amine derivatives as S1P modulators

Abbvie
21
Fused heterocyclic derivatives as S1P modulators

Abbvie
4
Asymmetric synthesis and biological evaluation of the enantiomeric isomers of the immunosuppressive FTY720-phosphate.

Mitsubishi Pharma
8
SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties.

Merck Research Laboratories
20
Discovery of potent 3,5-diphenyl-1,2,4-oxadiazole sphingosine-1-phosphate-1 (S1P1) receptor agonists with exceptional selectivity against S1P2 and S1P3.

Merck Research Laboratories