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ChemicalBook--->CAS DataBase List--->1257093-40-5

1257093-40-5

1257093-40-5 Structure

1257093-40-5 Structure
IdentificationBack Directory
[Name]

TC-SP 14
[CAS]

1257093-40-5
[Synonyms]

TC-SP 14
1-[[3-Fluoro-4-[5-[(2-fluorophenyl)Methyl]-2-benzothiazolyl]phenyl]Methyl]-3-azetidinecarboxylic Acid
3-Azetidinecarboxylic acid, 1-[[3-fluoro-4-[5-[(2-fluorophenyl)methyl]-2-benzothiazolyl]phenyl]methyl]-
[Molecular Formula]

C25H20F2N2O2S
[MDL Number]

MFCD22683814
[MOL File]

1257093-40-5.mol
[Molecular Weight]

450.5
Chemical PropertiesBack Directory
[Boiling point ]

608.1±65.0 °C(Predicted)
[density ]

1.396±0.06 g/cm3(Predicted)
[storage temp. ]

Desiccate at RT
[solubility ]

<22.52mg/ml in DMSO
[form ]

solid
[pka]

2.65±0.20(Predicted)
[color ]

Off-white
Hazard InformationBack Directory
[Uses]

1-[[3-Fluoro-4-[5-[(2-fluorophenyl)methyl]-2-benzothiazolyl]phenyl]methyl]-3-azetidinecarboxylic Acid is a potent Sphingosine-1-Phosphate Receptor 1 (S1P1) agonist with minimal activity at S1P3. It has been shown to attenuate DTH response to antigen challenge while significantly reducing blood lymphocyte counts.
[Biological Activity]

ec50: 0.042 μm for hs1p1tc-sp 14 is an agonist of sphingosine-1-phosphate receptor 1 (s1p1).studies have revealed that the lysophospholipid sphingosine-1-phosphate (s1p1) is a pleiotropic modulator of diverse cellular processes. such effects are reported to be mediated by the interactions of s1p with a set of paralogous g proteincoupled receptors, which are widely expressed in the immune, central nervous and cardiovascular systems.
[in vitro]

as a small lipophilic substituent proved equally effective to a larger substituent in reducing s1p3 activity, tc-sp 14 was screened. tc-sp 14 was found to be a potent s1p1 agonist (ec50 = 0.042 μm) with reduced activity for s1p3 (ec50 = 3.47 μm) [1].
[in vivo]

in lewis rats, tc-sp 14 produced a dose-dependent reduction in circulating blood lymphocytes, which was consistent with s1p1 agonism. moreover, statistical significance was shown at a dose of 0.3 mg/kg, and the dose fo 3.0 mg/kg led to near maximal lymphopenia. tc-sp 14 was subsequently investigated in a dth antigen challenge model. results showed a statistically significant reduction in ear swelling at doses of 0.3 mg/kg and higher. in addition, reduced ear swelling was found to closely track circulating lymphocyte counts [1].
[IC 50]

S1PR1: 0.042 μM (EC50); S1PR3: 3.47 μM (EC50)
[References]

[1] lanman ba,cee vj,cheruku sr et al. discovery of a potent, s1p3-sparing benzothiazole agonist of sphingosine-1-phosphate receptor 1 (s1p1). acs med chem lett.2010 nov 9;2(2):102-6.
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