(R)-CPP

(R)-CPP 구조식 이미지
카스 번호:
126453-07-4
상품명:
(R)-CPP
동의어(영문):
D-CPP;(R)-CCP;(R)-CPP;CPP (R)-;(R)CPP,(R) CPP;rac-(S*)-2-(2,4-Dichlorophenoxy)propanoic acid;rac-(2R*)-2-(2,4-Dichlorophenoxy)propionic acid;rac-(2R*)-2-(2,4-Dichlorophenoxy)propanoic acid;(R)-4-(3-phosphonopropyl)piperazine-2-carboxylic acid;[3-[(2R)-2-Carboxypiperazin-4-yl]propyl]phosphonic acid
CBNumber:
CB6725314
분자식:
C8H17N2O5P
포뮬러 무게:
252.2
MOL 파일:
126453-07-4.mol

(R)-CPP 속성

끓는 점
546.7±60.0 °C(Predicted)
밀도
1.408±0.06 g/cm3(Predicted)
저장 조건
Desiccate at RT
용해도
Water: 100mM
물리적 상태
백색 결정성 분말.
산도 계수 (pKa)
1.89±0.20(Predicted)
수용성
물에 100mM까지 용해됨

안전

(R)-CPP C화학적 특성, 용도, 생산

개요

(R)-CPP is an NMDA receptor antagonist (Ki = 0.14 μM). It binds to NMDA receptors containing GluN2A, GluN2B, GluN2C, and GluN2D subunits with Ki values of 0.04, 0.3, 0.6, and 2 μM, respectively. It inhibits depolarization induced by NMDA in isolated hemisected frog spinal cord (pA2 = 6.56) and NMDA-induced sodium efflux from rat brain slices (pA2 = 6.2). (R)-CPP inhibits the clonic phase of sound-induced seizures in DBA/2 mice (ED50 = 65.8 μmol/kg) and the myoclonic phase of stroboscopic-induced seizures in P. papio photosensitive baboons (ED50 = 127 μmol/kg).

용도

(R)-CPP is a piperazine derivative demonstrating highly potent NMDA receptor antagonism.

생물학적 활성

Highly potent NMDA antagonist; more active isomer. Shows some selectivity for NR2A-containing receptors (K i values are 0.041, 0.27, 0.63 and 1.99 μ M for inhibition of NR2A-, NR2B-, NR2C- and NR2D-containing recombinant NMDA receptors respectively).

(R)-CPP 준비 용품 및 원자재

원자재

준비 용품


(R)-CPP 공급 업체

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