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AB141134

Nisoxetine hydrochloride, norepinephrine reuptake (NET) inhibitor

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MW 307.8 Da, Purity >99%. Potent and selective norepinephrine reuptake (NET) inhibitor (Ki values are 0.46, 158 and 505 nM for NET, SERT and DAT, respectively).

View Alternative Names

AI838772, AW493413, Eag-related protein 1, Ether a go go related potassium channel protein, Ether-a-go-go-related gene potassium channel 1, Ether-a-go-go-related protein 1, FLJ11090, H-ERG, KCNH2_HUMAN, Kv11.1, LQT 2, MGC104252, MGC112732, Potassium channel HERG, Potassium voltage gated channel subfamily H (eag related) member 2, Potassium voltage-gated channel subfamily H member 2, RP24-311F12.2, SCAN1, SQT1, TYDP, TYDP1_HUMAN, Tyr-DNA phosphodiesterase 1, Tyrosyl-DNA phosphodiesterase 1, Voltage gated potassium channel, subfamily H, member 2, Voltage-gated potassium channel subunit Kv11.1, eag homolog, hERG-1

1 Images
Chemical Structure - Nisoxetine hydrochloride, norepinephrine reuptake (NET) inhibitor (AB141134)
  • Chemical Structure

Lab

Chemical Structure - Nisoxetine hydrochloride, norepinephrine reuptake (NET) inhibitor (AB141134)

2D chemical structure image of ab141134, Nisoxetine hydrochloride, norepinephrine reuptake (NET) inhibitor

Key facts

CAS number

57754-86-6

Purity

>99%

Form

Solid

form

Molecular weight

307.8 Da

Molecular formula

C<sub>1</sub><sub>7</sub>H<sub>2</sub><sub>2</sub>ClNO<sub>2</sub>

PubChem

134453

Nature

Synthetic

Solubility

Soluble in water to 100 mM

Biochemical name

Nisoxetine hydrochloride

Biological description

Potent and selective norepinephrine reuptake (NET) inhibitor (Ki values are 0.46, 158 and 505 nM for NET, SERT and DAT, respectively).

Canonical smiles

CNCCC(C1=CC=CC=C1)OC2=CC=CC=C2OC.Cl

InChi

InChI=1S/C17H21NO2.ClH/c1-18-13-12-15(14-8-4-3-5-9-14)20-17-11-7-6-10-16(17)19-2;/h3-11,15,18H,12-13H2,1-2H3;1H

InChiKey

LCEURBZEQJZUPV-UHFFFAOYSA-N

IUPAC Name

3-(2-methoxyphenoxy)-N-methyl-3-phenylpropan-1-amine;hydrochloride

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

TDP1 also known as tyrosyl-DNA phosphodiesterase 1 is an important protein involved in DNA repair. It weighs around 66 kDa. TDP1 repairs damaged DNA by hydrolyzing phosphodiester bonds at DNA termini. It mainly expresses in the nucleus of proliferating cells where DNA damage frequently occurs due to cellular division and environmental stress. TDP1 activity is critical in resolving stalled topoisomerase I-DNA complexes created during transcription and replication.
Biological function summary

TDP1 functions to maintain genomic stability by participating in the single-strand break repair (SSBR) mechanism. It is not known to be part of a larger protein complex but interacts with several other proteins to fulfill its role. This protein’s function in DNA repair mechanisms suggests that its activity prevents the accumulation of DNA lesions which could potentially result in genomic instability if left unchecked.

Pathways

TDP1 plays an essential role in the DNA repair pathways. The single-strand DNA break repair pathway is one primary pathway involving TDP1. This pathway is important for maintaining DNA integrity after damaging events such as oxidative stress. TDP1 collaborates with proteins like XRCC1 in these pathways to facilitate efficient DNA repair processes.

Disruptions in TDP1 activity have links with neurodegenerative diseases like spinocerebellar ataxia with axonal neuropathy (SCAN1). Inefficient DNA repair due to TDP1 mutations can lead to accumulated DNA damage contributing to this disorder. Moreover TDP1 might interact with altered PARP1 function in conditions where DNA repair defects underlie the pathophysiology. The study of TDP1 gives insight into mechanisms by which DNA repair deficiencies contribute to diseases.

Product protocols

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