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SIB 1757

Cat. No. M20686
SIB 1757 Structure
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Biological Activity

SIB 1757 is a highly selective, noncompetitive antagonist of metabotropic glutamate receptor type 5 (mGluR5) with IC50 of 0.4 μM at hmGluR5 compared with >30 µM at hmGluR1b, hmGluR2, hmGluR4, hmGluR6, hmGluR7 and hmGluR8.

Chemical Information
Molecular Weight 213.24
Formula C12H11N3O
CAS Number 31993-01-8
Solubility (25°C) DMSO 22 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Hilary Highfield Nickols, et al. Neurobiol Dis. Development of allosteric modulators of GPCRs for treatment of CNS disorders

[2] V Bruno, et al. J Cereb Blood Flow Metab. Metabotropic glutamate receptor subtypes as targets for neuroprotective drugs

[3] F Micheli. Curr Opin Investig Drugs. Methylphenylethynylpyridine (MPEP) Novartis

[4] A Dogrul, et al. Neurosci Lett. Peripheral and spinal antihyperalgesic activity of SIB-1757, a metabotropic glutamate receptor (mGLUR(5)) antagonist, in experimental neuropathic pain in rats

[5] M A Varney, et al. J Pharmacol Exp Ther. SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5

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