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ChemicalBook--->CAS DataBase List--->1630936-95-6

1630936-95-6

1630936-95-6 Structure

1630936-95-6 Structure
IdentificationBack Directory
[Name]

N-[3-Chloro-4-[(5-chloro-2-pyridinyl)oxy]phenyl]-2-pyridinecarboxamide
[CAS]

1630936-95-6
[Synonyms]

ML-396
VU 0422288
ML396 >=98% (HPLC)
VU0422288 (Synonyms: ML396)
N-[3-Chloro-4-[(5-chloro-2-pyridinyl)oxy]phenyl]-2-pyridinecarboxamide
[Molecular Formula]

C17H11Cl2N3O2
[MDL Number]

MFCD28411626
[MOL File]

1630936-95-6.mol
[Molecular Weight]

360.19
Chemical PropertiesBack Directory
[Melting point ]

154-158°C
[Boiling point ]

422.6±45.0 °C(Predicted)
[density ]

1.445±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Solid
[pka]

10.42±0.70(Predicted)
[color ]

Light Red to Red
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
Hazard InformationBack Directory
[Uses]

VU 0422288 is a metabotropic glutamate receptor 7 (mGlu7) positive allosteric modulators.
[Biological Activity]

ML396 is a potent positive allosteric modulator or metabotropic glutamate receptors group III (mGlu group III PAM). ML396 was used to study the biology of mGlu7.
[in vivo]

VU0422288 (30 mg/kg; i.p.; once daily for 17 days) rescues synaptic plasticity defects and learning and memory phenotypes, reduces the number of apneas in Mecp2+/- mice, while VU0422288 has no effect in Mecp2+/+animals[2].
VU0422288 (10 mg/kg; i.p.; single dose) exhibis a plasma/brain partitioning coefficient of 1.67 in adult male Sprague-Dawley rats, with predicted unbound brain concentration of about 40 nM[2].

[IC 50]

mGluR4: 108 nM (EC50); mGluR7: 146 nM (EC50); mGluR8: 128 nM (EC50)
[storage]

Store at -20°C
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