Identification | Back Directory | [Name]
(S)-1-[2-[TRIS(4-METHOXYPHENYL)METHOXY]ETHYL]-3-PIPERIDINECARBOXYLIC ACID | [CAS]
157604-55-2 | [Synonyms]
(S)-SP5114 (S)-SNAP 5114 SNAP 5114 (S)- (S)-SNAP-5114 >=98% (HPLC), solid S)-1-[2-[TRIS(4-METHOXYPHENYL)METHOXY]ETHYL]-3-PIP (S)-1-[2-[TRIS(4-METHOXYPHENYL)METHOXY]ETHYL]-3-PIPERIDINECARBOXYLIC ACID 1-[2-[TRIS(4-METHOXYPHENYL)METHOXY]ETHYL]-(S)-3-PIPERIDINECARBOXYLIC ACID 3-Piperidinecarboxylic acid, 1-[2-[tris(4-methoxyphenyl)methoxy]ethyl]-, (3S)- | [Molecular Formula]
C30H35NO6 | [MDL Number]
MFCD06799500 | [MOL File]
157604-55-2.mol | [Molecular Weight]
505.6 |
Chemical Properties | Back Directory | [Boiling point ]
643.9±55.0 °C(Predicted) | [density ]
1.175±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
H2O: insoluble
| [form ]
solid
| [pka]
3.85±0.20(Predicted) | [color ]
white
|
Hazard Information | Back Directory | [Uses]
(S)-SNAP 5114 is a GABA, GAT3 inhibitor. | [Biological Activity]
GABA transport inhibitor, showing selectivity for GAT-3 and GAT-2 (IC 50 values are 5, 21 and 388 μ M for hGAT-3, rGAT-2 and hGAT-1 respectively). Increases thalamic GABA levels and is an anticonvulsant following systemic administration in vivo . | [storage]
Store at -20°C | [References]
[1]. borden la, dhar tg, smith ke, et al. cloning of the human homologue of the gaba transporter gat-3 and identification of a novel inhibitor with selectivity for this site. receptors channels, 1994, 2(3): 207-213. [2]. pabel j, faust m, prehn c, et al. development of an (s)-1-{2-[tris(4-methoxyphenyl)methoxy]ethyl}piperidine-3-carboxylic acid [(s)-snap-5114] carba analogue inhibitor for murine γ-aminobutyric acid transporter type 4. chemmedchem, 2012, 7(7): 1245-1255. [3]. dalby no. gaba-level increasing and anticonvulsant effects of three different gaba uptake inhibitors. neuropharmacology, 2000, 39(12): 2399-2407. [4]. kataoka k, hara k, haranishi y, et al. the antinociceptive effect of snap5114, a gamma-aminobutyric acid transporter-3 inhibitor, in rat experimental pain models. anesth analg, 2013, 116(5): 1162-1169. |
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BOC Sciences
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Energy Chemical
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