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Uperolein

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Catalog No. T80894Cas No. 55601-63-3

Uperolein, a physalaemin-like endecapeptide derived from the skin of Uperoleia rugosa and Uperoleia marmorata, exhibits spasmodic activity on the gastrointestinal tract and longitudinal muscles [1] [2] [3].

Uperolein

Uperolein

😃Good
Catalog No. T80894Cas No. 55601-63-3
Uperolein, a physalaemin-like endecapeptide derived from the skin of Uperoleia rugosa and Uperoleia marmorata, exhibits spasmodic activity on the gastrointestinal tract and longitudinal muscles [1] [2] [3].
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Product Introduction

Bioactivity
Description
Uperolein, a physalaemin-like endecapeptide derived from the skin of Uperoleia rugosa and Uperoleia marmorata, exhibits spasmodic activity on the gastrointestinal tract and longitudinal muscles [1] [2] [3].
In vitro
Uperolein, a tachykinin analogue present at concentrations of 10-100 ng/mL, induces or enhances rhythmic contractions and elevates the tone of isolated circular and longitudinal muscular layers throughout the human gastrointestinal tract, ranging from the stomach to the colon [2].
In vivo
Uperolein, administered intravenously at doses of 0.1 μg/kg and 5 μg/kg as a single injection, demonstrates significant stimulatory effects on the stomach in anesthetized rats, and induces marked spasmogenic responses throughout the entire stomach, from the fundus to the pylorus [3].
Chemical Properties
Molecular Weight1234.38
FormulaC57H79N13O16S
Cas No.55601-63-3
SmilesC([C@@H](NC(=O)[C@H]1N(C(=O)[C@@H]2CCC(=O)N2)CCC1)CC(O)=O)(=O)N3[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CC4=CC=CC=C4)C(N[C@@H](CC5=CC=C(O)C=C5)C(NCC(N[C@H](C(N[C@@H](CCSC)C(N)=O)=O)CC(C)C)=O)=O)=O)=O)C)=O)CC(N)=O)=O)CCC3
SequenceH-DL-Pyr-DL-Pro-DL-Asp-DL-Pro-DL-Asn-DL-Ala-DL-Phe-DL-Tyr-Gly-DL-Leu-DL-Met-NH2
Sequence ShortXPDPNAFYGLM
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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