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ChemicalBook--->CAS DataBase List--->157604-55-2

157604-55-2

157604-55-2 Structure

157604-55-2 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-1-[2-[TRIS(4-METHOXYPHENYL)METHOXY]ETHYL]-3-PIPERIDINECARBOXYLIC ACID(157604-55-2)1HNMR
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