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AB141111

TPEN, Metal ion chelator

TPEN, Metal ion chelator

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(1 Publication)

MW 424.5 Da, Purity >99%. Metal ion chelator. Decreases intracellular zinc levels. Induces apoptosis. Causes defects in oocyte maturation. Modulates hippocampal neurogenesis following seizure. Cell permeable. Active in vivo and in vitro.

別名を表示する

AI838772, AW493413, FLJ11090, MGC104252, MGC112732, RP24-311F12.2, SCAN1, TYDP, TYDP1_HUMAN, Tyr-DNA phosphodiesterase 1, Tyrosyl-DNA phosphodiesterase 1

1 Images
Chemical Structure - TPEN, Metal ion chelator (AB141111)
  • Chemical Structure

Lab

Chemical Structure - TPEN, Metal ion chelator (AB141111)

2D chemical structure image of ab141111, TPEN, Metal ion chelator

Key facts

CAS番号

16858-02-9

精製度

>99%

製品の状態

Solid

form

分子量

424.5 Da

分子式

C<sub>2</sub><sub>6</sub>H<sub>2</sub><sub>8</sub>N<sub>6</sub>

PubChem

5519

由来

Synthetic

溶解性

Soluble in DMSO to 25 mM

Soluble in ethanol to 100 mM

化学名

N,N,N',N'-Tetrakis(2-pyridylmethyl)ethylenediamine

生物学的記述

Metal ion chelator. Decreases intracellular zinc levels. Induces apoptosis. Causes defects in oocyte maturation. Modulates hippocampal neurogenesis following seizure. Cell permeable. Active in vivo and in vitro.

Canonical smiles

C1=CC=NC(=C1)CN(CCN(CC2=CC=CC=N2)CC3=CC=CC=N3)CC4=CC=CC=N4

InChi

InChI=1S/C26H28N6/c1-5-13-27-23(9-1)19-31(20-24-10-2-6-14-28-24)17-18-32(21-25-11-3-7-15-29-25)22-26-12-4-8-16-30-26/h1-16H,17-22H2

InChiKey

CVRXLMUYFMERMJ-UHFFFAOYSA-N

IUPAC名

N,N,N',N'-tetrakis(pyridin-2-ylmethyl)ethane-1,2-diamine

出荷温度及び保存条件

出荷温度
Ambient - Can Ship with Ice
短期保存温度
+4°C
長期保存温度
+4°C
保管に関する情報
The product can be stored for up to 12 months

補足情報

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

TDP1 short for Tyrosyl-DNA Phosphodiesterase 1 is an enzyme involved in the repair of DNA damage. Also known as SCAN1 protein this enzyme has a mass of approximately 60 kDa and is expressed in a variety of tissues with higher levels seen in the brain and heart. It plays a mechanical role by hydrolyzing the phosphodiester bond between a DNA 3'-phosphate and a tyrosine residue an important step in resolving topoisomerase I-DNA crosslinks during the repair of stalled replication forks.
Biological function summary

TDP1 contributes significantly to the maintenance of genomic stability. It functions primarily as a DNA repair enzyme acting independently rather than as part of a protein complex. TDP1's ability to cleave phosphotyrosyl bonds makes it integral to processes that safeguard against DNA strand breaks induced by oxidative stress or other exogenous factors. Though not part of a complex its function is supported by the interaction with proteins like DNA polymerase which aids in the subsequent steps of DNA repair synthesis.

Pathways

TDP1 is involved in the DNA damage response and repair pathways. It collaborates heavily with the Base Excision Repair (BER) and the Single-Strand Break Repair (SSBR) pathways. TDP1 works alongside proteins like PARP1 facilitating the repair of single-strand DNA breaks which is critical for cell survival and prevention of mutations. Aphidicolin a known inhibitor of DNA polymerase can affect DNA synthesis steps that follow TDP1 activity indicating how interconnected these pathways are.

TDP1 has notable associations with certain neurodegenerative diseases and cancer. Mutations or dysregulation in TDP1 have been implicated in the autosomal recessive disorder known as Spinocerebellar Ataxia with Axonal Neuropathy (SCAN1). Additionally due to its role in DNA repair TDP1 may influence cancer progression as cells with impaired DNA repair capabilities accumulate mutations that could lead to tumorigenesis. The interaction with methotrexate a chemotherapeutic agent can also affect cancer treatment outcomes given methotrexate's influence on folate metabolism and DNA synthesis.

製品プロトコール

文献 (1)

Recent publications for all applications. Explore the full list and refine your search

Nature communications 6:7168 PubMed25981743

2015

Trans-synaptic zinc mobilization improves social interaction in two mouse models of autism through NMDAR activation.

Applications

Unspecified application

Species

Unspecified reactive species

Eun-Jae Lee,Hyejin Lee,Tzyy-Nan Huang,Changuk Chung,Wangyong Shin,Kyungdeok Kim,Jae-Young Koh,Yi-Ping Hsueh,Eunjoon Kim
View all publications

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