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BMS 193885

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Catalog No. T22608Cas No. 679839-66-8
Alias BMS193885

BMS 193885 is a selective and competitive neuropeptide Y(1) receptor antagonist with affinity of 3.3 nM.

BMS 193885

BMS 193885

😃Good
Catalog No. T22608Alias BMS193885Cas No. 679839-66-8
BMS 193885 is a selective and competitive neuropeptide Y(1) receptor antagonist with affinity of 3.3 nM.
Pack SizePriceAvailabilityQuantity
10 mg$84035 days
50 mg$3,36035 days
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Product Introduction

Bioactivity
Description
BMS 193885 is a selective and competitive neuropeptide Y(1) receptor antagonist with affinity of 3.3 nM.
In vitro
BMS 193885 increases the Kd of [(125)I]PeptideYY from 0.35 nM to 0.65 nM without changing the Bmax (0.16 pmol/mg of protein) in SK-N-MC cells that endogenously express the neuropeptide Y(1) receptor[1]. BMS 193885 is a full antagonist with an apparent Kb of 4.5 nM measured by reversal of forskolin-stimulated inhibition of cAMP production by neuropeptide Y[1].
In vivo
BMS 193885 (10 mg/kg; i.p.) reduces one-hour neuropeptide Y-induced food intake in satiated rats, as well as spontaneous overnight food consumption. Chronic administration of BMS 193885 (10 mg/kg) i.p. for 44 days significantly reduces food intake and the rate of body weight gain compared to vehicle treated control without developing tolerance or affecting water intake[1].
AliasBMS193885
Chemical Properties
Molecular Weight680.79
FormulaC36H48N4O9
Cas No.679839-66-8
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: <13.62 mg/mL
DMSO: 63 mg/mL (92.5 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.4689 mL7.3444 mL14.6888 mL73.4441 mL
5 mM0.2938 mL1.4689 mL2.9378 mL14.6888 mL
10 mM0.1469 mL0.7344 mL1.4689 mL7.3444 mL
20 mM0.0734 mL0.3672 mL0.7344 mL3.6722 mL
50 mM0.0294 mL0.1469 mL0.2938 mL1.4689 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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