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Merck

SML0400

Sigma-Aldrich

ML204

≥98% (HPLC)

Synonym(e):

4-Methyl-2-(1-piperidinyl)-quinoline

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About This Item

Empirische Formel (Hill-System):
C15H18N2
CAS-Nummer:
Molekulargewicht:
226.32
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥98% (HPLC)

Form

powder

Farbe

white to beige

Löslichkeit

DMSO: 5 mg/mL at warmed (clear solution)

Lagertemp.

2-8°C

SMILES String

Cc1cc(nc2ccccc12)N3CCCCC3

InChI

1S/C15H18N2/c1-12-11-15(17-9-5-2-6-10-17)16-14-8-4-3-7-13(12)14/h3-4,7-8,11H,2,5-6,9-10H2,1H3

InChIKey

USYRQXDHKXGTCK-UHFFFAOYSA-N

Anwendung

4-methyl-2-(1- piperidinyl)-quinoline (ML204) has been used to attenuate Ewing sarcoma (EWS)-FLI1 activity in TC32 cells. It has also been used to attenuate scratching behavior evoked by α-Me-5HT in mice.

Biochem./physiol. Wirkung

ML204 is a potent and selective TRPC4 channel inhibitor.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

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Lee SH, et al.
The Journal of Allergy and Clinical Immunology, 142(4), 1349-1352 (2018)
Stephanie D Jones et al.
Zoology (Jena, Germany), 118(6), 439-445 (2015-08-25)
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Domingos M S Pereira et al.
Oxidative medicine and cellular longevity, 2018, 4904696-4904696 (2018-07-10)
Thioredoxin plays an essential role in bacterial antioxidant machinery and virulence; however, its regulatory actions in the host are less well understood. Reduced human Trx activates transient receptor potential canonical 5 (TRPC5) in inflammation, but there is no evidence of
Englerin A inhibits EWS-FLI1 DNA binding in Ewing sarcoma cells
Caropreso V, et al.
The Journal of Biological Chemistry, 291(19), 10058-10066 (2016)

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