ORG 24598 LITHIUM SALT

ORG 24598 LITHIUM SALT 구조식 이미지
카스 번호:
722456-08-8
상품명:
ORG 24598 LITHIUM SALT
동의어(영문):
ORG 24598 LITHIUM SALT;KEGXIIFRCYASEJ-ZEECNFPPSA-N;R-(-)-N-METHYL-N-[3-[(4-TRIFLUOROMETHYL)PHENOXY]-3-PHENYL-PROPYL]GLYCINE LITHIUM SALT
CBNumber:
CB9827439
분자식:
C19H21F3LiNO3
포뮬러 무게:
375.32
MOL 파일:
Mol file
MSDS 파일:
SDS

ORG 24598 LITHIUM SALT 속성

저장 조건
2-8°C
용해도
H2O: >2mg/mL
물리적 상태
고체
물리적 상태
단단한 모양
색상
흰색에서 황백색까지

안전

WGK 독일 3

ORG 24598 LITHIUM SALT C화학적 특성, 용도, 생산

용도

Org 24598 Lithium Salt is a selective glycine transporter-1 (GlyT-1) inhibitor.

Biochem/physiol Actions

Org 24598 is a selective, potent inhibitor of glial GlyT (GlyT1, glycine transporter type 1). In rats (P12-P16) and in the presence of kynurenic acid, 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and bicuculline, ORG 24598 at a concentration of 10 μM induced a mean inward current of -10/-50 pA at -60 mV and increased significantly the decay time constants of miniature (mIPSCs), spontaneous (sIPSCs) and electrically evoked glycinergic (eIPSCs) inhibitory postsynaptic currents. Replacing extracellular sodium with N-methyl-d-glucamine or superfusing the slice with micromolar concentrations of glycine also increased the decay time constant of glycinergic IPSCs. Glycine (1-5 μM and d-serine (10 μM) increased the amplitude of eEPSCs whereas l-serine had no effect. Org 24598 increased significantly the amplitude of NMDA receptor-mediated eEPSCs without affecting the amplitude of non-NMDA receptor-mediated eEPSCs. This brings conclusion that blocking glial glycine transporter by Org 24598 increased the level of glycine in spinal cord slices, which in turn prolonged the duration of glycinergic synaptic current and potentiated the NMDA-mediated synaptic response.

ORG 24598 LITHIUM SALT 준비 용품 및 원자재

원자재

준비 용품


ORG 24598 LITHIUM SALT 공급 업체

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