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Key Documents

U6758

Sigma-Aldrich

UCL 2077

≥98% (HPLC), solid

Synonym(s):

(3-Triphenylmethylaminomethyl)pyridine

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About This Item

Empirical Formula (Hill Notation):
C25H22N2
CAS Number:
Molecular Weight:
350.46
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

Quality Level

assay

≥98% (HPLC)

form

solid

color

white

solubility

DMSO: soluble >20 mg/mL
H2O: insoluble

SMILES string

C(NC(c1ccccc1)(c2ccccc2)c3ccccc3)c4cccnc4

InChI

1S/C25H22N2/c1-4-12-22(13-5-1)25(23-14-6-2-7-15-23,24-16-8-3-9-17-24)27-20-21-11-10-18-26-19-21/h1-19,27H,20H2

InChI key

PQFNWDHABGBCHB-UHFFFAOYSA-N

Application

UCL 2077 has been used for slow afterhyperpolarization (sAHP) studies in thalamic paraventricular nucleus (PVT) neurons. UCL 2077 has also been used for studying its effects on the increase in excitability of hippocampal pyramidal cells.

Biochem/physiol Actions

UCL 2077 is a slow afterhyperpolarization (sAHP) channel blocker.

Preparation Note

UCL 2077 is soluble in DMSO at a concentration >20 mg/ml and is insoluble in water.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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Mala M Shah et al.
Molecular pharmacology, 70(5), 1494-1502 (2006-08-01)
The slow afterhyperpolarization (sAHP) in hippocampal neurons has been implicated in learning and memory. However, its precise role in cell excitability and central nervous system function has not been explicitly tested for 2 reasons: 1) there are, at present, no
Li Zhang et al.
Journal of neurophysiology, 104(4), 2052-2062 (2010-08-20)
Thalamic paraventricular nucleus (PVT) neurons exhibit a postburst apamin-resistant slow afterhyperpolarization (sAHP) that is unique to midline thalamus, displays activity dependence, and is abolished in tetrodotoxin. Analysis of the underlying sI(AHP) confirmed a requirement for Ca(2+) influx with contributions from
James D Angstadt et al.
Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 203(8), 613-633 (2017-05-13)
Postinhibitory rebound (PIR) responses in leech dorsal excitatory motor neurons (cell DE-3) are eliminated by Ca

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