Name | A6770 |
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Synonyms |
MFCD28675904
1-[5-(Hydroxymethyl)-1H-imidazol-2-yl]ethanone A6770 Ethanone, 1-[5-(hydroxymethyl)-1H-imidazol-2-yl]- |
Description | A6770 is an orally active, potent sphingosine 1-phosphate (S1P) lyase (S1PL) inhibitor. A6770 is phosphorylated and the phosphorylated form directly inhibits S1P lyased.A6770, a potential key metabolite of THI, induces a [3H]dhS1P increase[1][2]. |
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Related Catalog | |
In Vitro | A6770 causes concentration-dependent increases in [3H] dhS1P with the EC50 ranging from 30 to 200 μM under the normal condition[1]. A6770 leads to S1PL inhibition rather than SPHK activation or SPP inhibition[2]. |
In Vivo | A6770 (1, 10, 100mg/kg; po; single dose) induces reductions in peripheral lymphocyte number in rats[2] |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 384.1±34.0 °C at 760 mmHg |
Molecular Formula | C6H8N2O2 |
Molecular Weight | 140.140 |
Flash Point | 186.1±25.7 °C |
Exact Mass | 140.058578 |
LogP | -1.64 |
Vapour Pressure | 0.0±0.9 mmHg at 25°C |
Index of Refraction | 1.577 |