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ChemicalBook--->CAS DataBase List--->924537-98-4

924537-98-4

924537-98-4 Structure

924537-98-4 Structure
IdentificationBack Directory
[Name]

319H6
[CAS]

924537-98-4
[Synonyms]

319H6
BT 13 NEW
BT-13 (RET agonist BT13)
Benzenesulfonamide, N,N-diethyl-3-[4-[4-fluoro-2-(trifluoromethyl)benzoyl]-1-piperazinyl]-4-methoxy-
[Molecular Formula]

C23H27F4N3O4S
[MOL File]

924537-98-4.mol
[Molecular Weight]

517.54
Chemical PropertiesBack Directory
[Boiling point ]

637.0±65.0 °C(Predicted)
[density ]

1.326±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 25 mg/mL (48.31 mM)
[form ]

Solid
[pka]

0.42±0.20(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Biological Activity]

BT-13 is a potent, selective agonist of the glial cell-derived neurotrophic factor (GDNF) receptor RET (acts independently of GDNF ligands), promotes sensory neuron neurite outgrowth in vitro, and alleviates neuropathy in rats happened.
[in vitro]

BT-13 stimulates phosphorylation of RET, as well as RET-dependent intracellular signaling, but activated neither NGF receptor TrkA nor BDNF receptor TrkB nor intracellular signaling in the absence of RET.

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[in vivo]

BT-13 (20 and 25mg/kg in rats induced by ligation of left L5 and L6 spinal nerves) has a slight antinociceptive/antihyperalgesic effect and protected DRG neurons in rats with surgery-induced neuropathy.

Animal Model: Rats induced by ligation of left L5 and L6 spinal nerves.
Dosage: 5-25 mg/kg, dissolved in sesame oil containing 5% DMSO.
Administration: Subcutaneous injections on post-surgical days 1, 3, 5, 8, 10, and 12.
Result: 20 and 25mg/kg decreased mechanical hypersensitivity and normalized expression of sensory neuron markers in dorsal root ganglia.
[target]

GDNF receptor RET.

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