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Merck

E1905

(+)-Etomoxir sodium salt hydrate

≥98% (HPLC), powder, CPT-1 inhibitor

동의어(들):

R(+)-2-[6-(4-Chlorophenoxy)hexyl]-oxirane-2-carboxylic acid sodium salt hydrate

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C15H18ClO4 · Na · H2O
CAS 번호:
Molecular Weight:
338.76
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
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제품 이름

(+)-Etomoxir sodium salt hydrate, ≥98% (HPLC), powder

SMILES string

O.[Na+].[O-]C(=O)[C@@]2(CCCCCCOc1ccc(Cl)cc1)CO2

InChI key

WENJLJJSJDAJDN-QCUBGVIVSA-M

InChI

1S/C15H19ClO4.Na.H2O/c16-12-5-7-13(8-6-12)19-10-4-2-1-3-9-15(11-20-15)14(17)18;;/h5-8H,1-4,9-11H2,(H,17,18);;1H2/q;+1;/p-1/t15-;;/m1../s1

assay

≥98% (HPLC)

form

powder

color

white

solubility

H2O: freely soluble

storage temp.

2-8°C

Quality Level

Application

(+)-Etomoxir sodium salt hydrate has been used as an inhibitor of carnitine palmitoyltransferase 1 (CPT-1) in breast tumor cell lines and mice tumor. It has also been used as an inhibitor of fatty acid oxidation in human primary prostate epithelial cells and lymphocytes.

Biochem/physiol Actions

Irreversible O-carnitine palmitoyltransferase-1 (CPT-1) inhibitor; PPARα activator

General description

(+)-Etomoxir sodium salt hydrate belongs to oxirane carboxylic acid group of compounds and mediates metabolic channeling of fatty acid precursors. It favors oxidative stress in T cells and prevents T cell differentiation. It inhibits fatty acid oxidation and promotes hunger and food intake. Etomoxir impairs myeloid-derived suppressor cells mediated tumor and could have potential therapeutic potential.

Packaging

Store tightly sealed, protected from exposure to light

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

저장 등급

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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문서 라이브러리 방문

Etomoxir mediates differential metabolic channeling of fatty acid and glycerol precursors into cardiolipin in H9c2 cells
Xu FY, et al.
Journal of Lipid Research, 44(2), 415-423 (2003)
The CPT1a inhibitor, etomoxir induces severe oxidative stress at commonly used concentrations
OConnor RS, et al.
Scientific Reports, 8(1), 6289-6289 (2018)
Organoids model distinct Vitamin E effects at different stages of prostate cancer evolution
Njoroge RN, et al.
Scientific Reports, 7(1), 16285-16285 (2017)
Etomoxir actions on regulatory and memory T cells are independent of Cpt1a-mediated fatty acid oxidation
Raud B, et al.
Cell Metabolism, 28(3), 504-515 (2018)
Ibrutinib Resistance Is Reduced By Fatty Acid Oxidation Inhibition In Primary CLL Lymphocytes
Galicia-Vazquez G and Aloyz R
Frontiers in Oncology, 8, 411-411 (2018)

문서

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Discover Bioactive Small Molecules for Lipid Signaling Research

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