ChemicalBook--->CAS DataBase List--->2070015-10-8

2070015-10-8

2070015-10-8 Structure

2070015-10-8 Structure
IdentificationBack Directory
[Name]

ML 204
[CAS]

2070015-10-8
[Molecular Formula]

C15H19ClN2
[MDL Number]

MFCD30377212
[MOL File]

2070015-10-8.mol
[Molecular Weight]

262.78
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
Hazard InformationBack Directory
[Biological Activity]

ML204 is a potent and selective inhibitor of TRPC4/TRPC5 channels with 20-fold selectivity over TRPC6, without affecting other TRP channels and voltage-gated sodium, potassium or Ca2+ channels.
[in vitro]

ML204 inhibits TRPC4β-mediated intracellular Ca 2+ rise with an IC 50 value of 0.96 μM (HEK293 cells) and exhibits 19-fold selectivity against muscarinic receptor-coupled TRPC6 channel activation.
It blocks TRPC4β activity induced through either G i/o stimulation by μ-opioid, 5HT 1A serotonin, and M 2 muscarinic receptors or G q/11 stimulation by the endogenous M 3 -like muscarinic receptors.
It blocks LPS-induced TRPC5 channel activity.

[in vivo]

ML204 (1 mg/kg; sc; twice a day; for 5 days) causes mortality associated with exacerbated hypothermia and decreases peritoneal leukocyte numbers and cytokines in LPS-injected mice.

< td class="col2"> Subcutaneous injection, twice a day, for 5 days (prior to LPS injection) < td class="col2"> Induces mortality associated with increased hypothermia in mice with LPS-induced systemic inflammatory response.
Animal Model: Nonfasted male C57BL/6 (2-3 months)
Dosage: 1 mg/kg
Administration:
Result:
[target]

TRPC4

TRPC5

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