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JMV 449 acetate

Cat. No. M10171
JMV 449 acetate Structure
Synonym:

JMV449

Size Price Availability Quantity
5mg USD 870  USD870 In stock
10mg USD 1450  USD1450 In stock
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Quality Control & Documentation
Biological Activity

JMV 449 acetate is a potent neurotensin receptor agonist (IC50 = 0.15 nM for inhibition of [125I]-NT binding to neonatal mouse brain; EC50 = 1.9 nM for contraction of guinea pig ileum). JMV 449 acetate has highly potent and long-lasting hypothermic and analgesic effects in the mouse.

Chemical Information
Molecular Weight 807.03
Formula C40H70N8O9
CAS Number 139026-66-7 (free base)
Solubility (25°C) Water 90 mg/mL
Storage -20°C, sealed
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] Lars Torup, et al. Neurosci Lett. Neuroprotective effect of the neurotensin analogue JMV-449 in a mouse model of permanent middle cerebral ischaemia

[2] D Lugrin, et al. Eur J Pharmacol. Reduced peptide bond pseudopeptide analogues of neurotensin: binding and biological activities, and in vitro metabolic stability

[3] I Dubuc, et al. Eur J Pharmacol. JMV 449: a pseudopeptide analogue of neurotensin-(8-13) with highly potent and long-lasting hypothermic and analgesic effects in the mouse

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Keywords: JMV 449 acetate, JMV449 supplier, Neurotensin Receptor, inhibitors, activators


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