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UFP-101 acetate

🥰Excellent
Catalog No. TP2105L
Alias UFP-101 acetate(849024-68-6 free base)

UFP-101 acetate is a selective and competitive antagonist of the NOP receptor (pKi = 10.24) with >3000-fold selectivity over δ, μ, and κ opioid receptors.

UFP-101 acetate

UFP-101 acetate

🥰Excellent
Purity: 95.92%
Catalog No. TP2105LAlias UFP-101 acetate(849024-68-6 free base)
UFP-101 acetate is a selective and competitive antagonist of the NOP receptor (pKi = 10.24) with >3000-fold selectivity over δ, μ, and κ opioid receptors.
Pack SizePriceAvailabilityQuantity
1 mg$317In Stock
2 mg$573In Stock
5 mg$897In Stock
10 mg$1,230In Stock
25 mg$1,820In Stock
50 mg$2,460In Stock
100 mg$3,290In Stock
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Purity:95.92%
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Product Introduction

Bioactivity
Description
UFP-101 acetate is a selective and competitive antagonist of the NOP receptor (pKi = 10.24) with >3000-fold selectivity over δ, μ, and κ opioid receptors.
In vivo
In mice submitted to the forced swimming test, UFP-101 acetate elicits a pronounced acute and dose-dependent antidepressant-like effect[2].
AliasUFP-101 acetate(849024-68-6 free base)
Chemical Properties
Molecular Weight1968.23
FormulaC84H142N32O23
SmilesCC(O)=O.O=C(N)[C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC(CNC([C@@H](NC([C@@H](NC(CNC(CNC(CNCC1=CC=CC=C1)=O)=O)=O)CC2=CC=CC=C2)=O)[C@H](O)C)=O)=O)C)=O)CCCNC(N)=N)=O)CCCCN)=O)CO)=O)C)=O)CCCNC(N)=N)=O)CCCCN)=O)CCCNC(N)=N)=O)CCCCN)=O)CC(N)=O)=O)CCC(N)=O
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 83.3 mg/mL (42.3 mM)
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM0.5081 mL2.5404 mL5.0807 mL25.4035 mL
5 mM0.1016 mL0.5081 mL1.0161 mL5.0807 mL
10 mM0.0508 mL0.2540 mL0.5081 mL2.5404 mL
20 mM0.0254 mL0.1270 mL0.2540 mL1.2702 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.
1 Enter information below:
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2 Enter the in vivo formulation:
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