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1598424-76-0

1598424-76-0 Structure

1598424-76-0 Structure
IdentificationBack Directory
[Name]

(S)-methyl 3-(1-benzyl-1H-imidazol-4-yl)-2-(6-(benzyloxy)-5-methoxy-1H-indole-2-carboxamido)propanoate
[CAS]

1598424-76-0
[Synonyms]

spudl 05650
BMS466442,BMS 466442
L-Histidine, N-[[5-methoxy-6-(phenylmethoxy)-1H-indol-2-yl]carbonyl]-1-(phenylmethyl)-, methyl ester
(S)-methyl 3-(1-benzyl-1H-imidazol-4-yl)-2-(6-(benzyloxy)-5-methoxy-1H-indole-2-carboxamido)propanoate
[Molecular Formula]

C31H30N4O5
[MOL File]

1598424-76-0.mol
[Molecular Weight]

538.59
Chemical PropertiesBack Directory
[Boiling point ]

827.3±65.0 °C(Predicted)
[density ]

1.26±0.1 g/cm3(Predicted)
[storage temp. ]

-10 to -25°C
[solubility ]

Soluble to 100 mM in DMSO
[form ]

Solid
[pka]

13.15±0.46(Predicted)
[color ]

Off-white to yellow
Hazard InformationBack Directory
[Uses]

BMS-466442 is a potent and selective inhibitor of asc-1 (alanine serine cysteine transporter-1), with an IC50 of 11 nM. BMS-466442 inhibits [3H] D-serine uptake into rat brain synaptosomes, with an IC50 of 400 nM. BMS-466442 can be used for schizophrenia research[1][2].
[Biological Activity]

Potent and selective alanine serine cysteine transporter-1 (ASC-1; SLC7A10) inhibitor th at effectively blocks ASC-1-mediated cellular D-Ser uptake.



BMS-466442 is a selective alanine serine cysteine transporter-1 (ASC-1) inhibitor (D-Ser uptake IC50 = 36.8 nM and 19.7 nM using HEK human ASC-1 transfectants or primary r at embryonic cortical culturesrespectively) with good selectivity over >40 other targetsincluding LAT-2 or ASCT-2 (IC50 >10 μM).
[IC 50]

α adrenergic receptor: ≥10 μM (IC50); ASCT1: 1 nM (IC50)
[storage]

Store at -20°C
[References]

[1] Brown JM, et al. In vitro Characterization of a small molecule inhibitor of the alanine serine cysteine transporter -1 (SLC7A10). J Neurochem. 2014 Apr;129(2):275-83. DOI:10.1111/jnc.12618
[2] Torrecillas IR, et al. Inhibition of the Alanine-Serine-Cysteine-1 Transporter by BMS-466442. ACS Chem Neurosci. 2019 May 15;10(5):2510-2517. DOI:10.1021/acschemneuro.9b00019
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