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Merck
모든 사진(1)

Key Documents

A251

Sigma-Aldrich

A-85380 dihydrochloride

solid

동의어(들):

3-((2S)-Azetidinylmethoxy)pyridine dihydrochloride

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About This Item

실험식(Hill 표기법):
C9H12N2O · 2HCl
Molecular Weight:
237.13
UNSPSC 코드:
12352200
PubChem Substance ID:

형태

solid

광학 활성

[α]20/D −5.2°, c = 0.5 in methanol(lit.)

색상

off-white

solubility

H2O: 10 mg/mL

SMILES string

Cl[H].Cl[H].C1C[C@H](COc2cccnc2)N1

애플리케이션

The 5-125I-analog has been used as a selective radioligand for the α4β2 nAChR subtype. Fluorinated analogs have been used for PET imaging of nAChRs.

생화학적/생리학적 작용

Potent and selective neuronal nicotinic acetylcholine receptor (nAChR) agonist.

주의사항

Hygroscopic

법적 정보

Manufactured and sold under exclusive license from Abbott Laboratories.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리 방문

J P Sullivan et al.
Neuropharmacology, 35(6), 725-734 (1996-06-01)
The in vitro pharmacological properties of a novel cholinergic channel ligand, A-85380 [3-(2(S)-azetidinylmethoxy)pyridine], were examined using tissue preparations that express different putative nAChR subtypes. In radioligand binding studies, A-85380 is shown to be a potent and selective ligand for the
A G Horti et al.
Nuclear medicine and biology, 25(7), 599-603 (1998-11-06)
The in vivo brain regional distribution of 2-[18F]fluoro-A-85380, a novel tracer for positron emission tomographic (PET) studies, followed the regional densities of brain nAChRs reported in the literature. Evidence of binding to nAChRs and high specificity of the binding in
A G Mukhin et al.
Molecular pharmacology, 57(3), 642-649 (2000-02-29)
In an effort to develop selective radioligands for in vivo imaging of neuronal nicotinic acetylcholine receptors (nAChRs), we synthesized 5-iodo-3-(2(S)-azetidinylmethoxy)pyridine (5-iodo-A-85380) and labeled it with (125)I and (123)I. Here we present the results of experiments characterizing this radioiodinated ligand in
M A Abreo et al.
Journal of medicinal chemistry, 39(4), 817-825 (1996-02-16)
Recent evidence indicating the therapeutic potential of cholinergic channel modulators for the treatment of central nervous system (CNS) disorders as well as the diversity of brain neuronal nicotine acetylcholine receptors (nAChRs) have suggested an opportunity to develop subtype-selective nAChR ligands

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