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SML0023

Sigma-Aldrich

5-Iodo-A-85380 dihydrochloride hydrate

≥98% (HPLC)

Sinónimos:

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

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About This Item

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

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to tan

solubility

H2O: ≥22 mg/mL

storage temp.

−20°C

SMILES string

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

InChI key

DCVONLXGZUKNSI-CZDIJEQGSA-N

Application

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

Biochem/physiol Actions

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.

Features and Benefits

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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «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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