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E8534

Sigma-Aldrich

E3330

≥98% (HPLC)

Synonym(e):

(2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene]-undecanoic acid

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5 MG
CHF 338.00
25 MG
CHF 1’010.00

CHF 338.00

Voraussichtliches Versanddatum01. Juni 2025

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5 MG
CHF 338.00
25 MG
CHF 1’010.00

About This Item

Empirische Formel (Hill-System):
C21H30O6
CAS-Nummer:
136164-66-4
Molekulargewicht:
378.46
MDL-Nummer:
MFCD00901331
UNSPSC-Code:
12352200
PubChem Substanz-ID:
329799080
NACRES:
NA.77

CHF 338.00

Voraussichtliches Versanddatum01. Juni 2025

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Qualitätsniveau

100

Assay

≥98% (HPLC)

Form

powder

Farbe

red to orange

Löslichkeit

DMSO: >20 mg/mL

Lagertemp.

2-8°C

SMILES String

CCCCCCCCC\C(=C/C1=C(C)C(=O)C(OC)=C(OC)C1=O)C(O)=O

InChI

1S/C21H30O6/c1-5-6-7-8-9-10-11-12-15(21(24)25)13-16-14(2)17(22)19(26-3)20(27-4)18(16)23/h13H,5-12H2,1-4H3,(H,24,25)/b15-13+

InChIKey

AALSSIXXBDPENJ-FYWRMAATSA-N

Anwendung

E3330 has been used in the inhibition of endothelial cancer cells[1] and apurinic/apyrimidinic endodeoxyribonuclease 1 (APEX1).[2]

Biochem./physiol. Wirkung

E3330 is a specific inhibitor of AP endonuclease 1 redox domain. E3330 inhibits APE-1 regulation of transcription factors, but does not affect Ape1 DNA repair activity. AP endonuclease 1 (APE1; also known as REF-1) is a multifunctional protein with dual functions in DNA repair and redox regulation of transcription factors. It is involved in apurinic/apyrimidinic endonuclease DNA base excision repair activity, in proofreading exonuclease activity, and in modulating DNA binding activity of several transcription factors including NF-κB, Egr-1, p53, AP-1, CREB, HIF-α, and members of the Pax family. APE1 is overexpressed in several human cancers, and disruption of APE1 function has detrimental effects on cancer cell viability. E3330 significantly reduces the growth of human pancreatic cancer cells in vitro and inhibits pancreatic cancer cell migration.
E3330 is a specific inhibitor of AP endonuclease 1 redox domain; inhibits APE-1 regulation of transcription factors, but does not affect Ape1 DNA repair activity.

H-Sätze

H413

P-Sätze

P273 - P501

Gefahreneinstufungen

Aquatic Chronic 4

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000141776
0000054904
0000054904
0000141776
0000100171

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Mark R Kelley et al.
Antioxidants & redox signaling, 14(8), 1387-1401 (2010-09-30)
APE1 is a multifunctional protein possessing DNA repair and redox activation of transcription factors. Blocking these functions leads to apoptosis, antiangiogenesis, cell-growth inhibition, and other effects, depending on which function is blocked. Because a selective inhibitor of the APE redox
Brittney A Manvilla et al.
Biochemistry, 50(48), 10540-10549 (2011-10-29)
AP endonuclease 1 (APE1) is a multifaceted protein with essential roles in DNA repair and transcriptional regulation. APE1 (ref-1) activates many transcription factors (TF), including AP-1 and NF-κB. While the mechanism of APE1 redox activity remains unknown, it may involve
K Murata et al.
Hepato-gastroenterology, 48(40), 1022-1027 (2001-08-09)
We demonstrated that partial splenic embolization for hematological disorders in cirrhotic patients also improved liver function. Therefore, we investigated the mechanism of the beneficial effects of splenectomy on a rat cirrhotic model. 1) Rats were administered DMN (dimethylnitrosamine) after splenectomy
Dian Su et al.
Biochemistry, 50(1), 82-92 (2010-12-02)
Apurinic/apyrimidinic endonuclease (APE1) is an essential base excision repair protein that also functions as a reduction and oxidation (redox) factor in mammals. Through a thiol-based mechanism, APE1 reduces a number of important transcription factors, including AP-1, p53, NF-κB, and HIF-1α.
Melissa L Fishel et al.
Molecular cancer therapeutics, 10(9), 1698-1708 (2011-06-28)
Pancreatic cancer is especially a deadly form of cancer with a survival rate less than 2%. Pancreatic cancers respond poorly to existing chemotherapeutic agents and radiation, and progress for the treatment of pancreatic cancer remains elusive. To address this unmet
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