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SML0023

Sigma-Aldrich

5-Iodo-A-85380 dihydrochloride hydrate

≥98% (HPLC)

Sinônimo(s):

3-((2S)-2-Azetidinylmethoxy)-5-iodo-pyridine dihydrochloride hydrate

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About This Item

Fórmula empírica (Notação de Hill):
C9H11IN2O · 2HCl · xH2O
Número CAS:
213550-82-4
Peso molecular:
363.02 (anhydrous basis)
Número MDL:
MFCD20488048
Código UNSPSC:
12352202
ID de substância PubChem:
329825095
NACRES:
NA.77

Ensaio

≥98% (HPLC)

forma

powder

condição de armazenamento

desiccated

cor

white to tan

solubilidade

H2O: ≥22 mg/mL

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

O.Cl.Cl.Ic1cncc(OC[C@@H]2CCN2)c1

InChI

1S/C9H11IN2O.2ClH.H2O/c10-7-3-9(5-11-4-7)13-6-8-1-2-12-8;;;/h3-5,8,12H,1-2,6H2;2*1H;1H2/t8-;;;/m0.../s1

chave InChI

DCVONLXGZUKNSI-CZDIJEQGSA-N

Aplicação

5-Iodo-A-85380 dihydrochloride hydrate may be used in nicotinic acetylcholine receptor-mediated signaling studies.

Ações bioquímicas/fisiológicas

5-Iodo-A-85380 increases the influx of extracellular Ca+2 in rat cortical neurons and exhibits protective effects against glutamate-induced neurotoxicity. Studies reveal that it also activates α6β2 nicotinic acetylcholine receptors.
5-Iodo-A-85380 is a highly selective α4β2 nicotinic receptor agonist. The Ki values for binding to the human and rat receptors are 12 and 10 pM, respectively.

Características e benefícios

This compound is featured on the Acetylcholine Receptors (Nicotinic) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H318

Classificações de perigo

Acute Tox. 4 Oral - Eye Dam. 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Marwa Y Sallam et al.
European journal of pharmacology, 834, 36-44 (2018-07-17)
The cholinergic antiinflammatory pathway favorably influences end organ damage induced by inflammatory conditions. Here, we hypothesized that α7 and/or α4β2-nicotinic acetylcholine receptors (nAChRs) protect against cardiovascular and autonomic imbalances induced by endotoxemia in rats. We assessed dose-effect relationships of i.v.
Adrian J Mogg et al.
Neuropharmacology, 47(6), 848-859 (2004-11-06)
The novel compound 5-iodo-A-85380 binds with higher affinity to alpha4beta2* nicotinic acetylcholine receptors (nAChR), compared with other nAChR subtypes (Mukhin et al., 2000). In the present study, we have confirmed that in competition binding assays for three major nAChR subtypes
Masashi Ueda et al.
Brain research, 1199, 46-52 (2008-02-14)
5-iodo-3-(2(S)-azetidinylmethoxy)pyridine (5-iodo-A-85380, 5IA) has very high affinity and selectivity to nicotinic acetylcholine receptor (nAChR) alpha 4 beta 2 subtype, and a relative safe profile. To assess whether 5IA has neuroprotective properties, we examined the effect of 5IA on glutamate (Glu)-induced
Helena Montanuy et al.
Orphanet journal of rare diseases, 15(1), 170-170 (2020-07-02)
Fanconi anemia is a rare disease clinically characterized by malformations, bone marrow failure and an increased risk of solid tumors and hematologic malignancies. The only therapies available are hematopoietic stem cell transplantation for bone marrow failure or leukemia, and surgical

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