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Oxytocin

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Catalog No. T5026Cas No. 50-56-6
Alias α-Hypophamine, Oxytocin (Syntocinon), Oxytocic hormone

Oxytocin (Syntocinon) is a mammalian neuropituitary hormone, a pleiotropic hypothalamic peptide and ligand for the oxytocin receptor, which contributes to labor, lactation, and pro-social behavior. Oxytocin has the ability to stimulate mammary secretion of breast milk, promote contraction of uterine smooth muscle during labor, and facilitate mothering.

Oxytocin

Oxytocin

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Purity: 99.87%
Catalog No. T5026Alias α-Hypophamine, Oxytocin (Syntocinon), Oxytocic hormoneCas No. 50-56-6
Oxytocin (Syntocinon) is a mammalian neuropituitary hormone, a pleiotropic hypothalamic peptide and ligand for the oxytocin receptor, which contributes to labor, lactation, and pro-social behavior. Oxytocin has the ability to stimulate mammary secretion of breast milk, promote contraction of uterine smooth muscle during labor, and facilitate mothering.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$40-In Stock
10 mg$57-In Stock
25 mg$94-In Stock
50 mg$138-In Stock
100 mg$209-In Stock
200 mg$325-In Stock
500 mg$593-In Stock
1 g$945InquiryInquiry
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.87%
Appearance:Solid
Color:White
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Product Introduction

Oxytocin AI Summary
Oxytocin exhibits a variety of bioactivities, including high binding affinity to the oxytocin receptor (OTR) and vasopressin receptors in different tissues. It acts as an oxytocin receptor antagonist in rat uterine strips both in vitro and in vivo, showing uterotonic activity with varying potency in the presence and absence of Mg2+, and displaying milk ejection activity. The compound demonstrates vasopressor activity and antidiuretic activity in rat models, affecting urinary volume, and electrolyte excretion. It has an EC50 of 0.4 nM for the oxytocin receptor in human cells and shows a preference for the vasopressin V1a receptor with an EC50 of 0.08 nM compared to higher values for the V2 receptor. Oxytocin also shows agonist activity at human vasopressin and oxytocin receptors, affecting intracellular calcium levels in assays. It demonstrates stability in gastric fluid but lower stability in intestinal fluid, indicating potential challenges in oral bioavailability. Additionally, it exhibits good pharmacokinetic properties such as high binding affinity and short half-life in different species, with no significant adverse effects on liver cells. The compound's multifunctional profile, including potent agonist and antagonist activities, makes it a candidate for further exploration in modulating hormonal pathways related to oxytocin and vasopressin receptors..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Oxytocin (Syntocinon) is a mammalian neuropituitary hormone, a pleiotropic hypothalamic peptide and ligand for the oxytocin receptor, which contributes to labor, lactation, and pro-social behavior. Oxytocin has the ability to stimulate mammary secretion of breast milk, promote contraction of uterine smooth muscle during labor, and facilitate mothering.
Targets&IC50
CHO cells:24.5 nM (EC50), CHO-K1 cells:2.3 nM (EC50), COS-1 cells:15 nM (EC50)
In vitro
METHODS: KGN, MA-10 and C18-4 cells were treated with Tris(2,4-di-tert-butylphenyl)phosphate (0.1-100 µM) for 48 h. Cell counts were measured by Hoechst 33342 stained.
RESULTS: Tris(2,4-di-tert-butylphenyl)phosphate was not cytotoxic to any of the 3 cell lines. [1]
In vivo
METHODS: To assay acute anti-inflammatory activity in vivo, Tris(2,4-di-tert-butylphenyl)phosphate (50-70 mg/kg, 0.1% sodium carboxymethyl cellulose in 1M phosphate buffer pH 7.2) was administered to a carrageenan-induced rat foot-plantar edema model.
RESULTS: Tris(2,4-di-tert-butylphenyl)phosphate at the doses of 50 mg/kg and 70 mg/kg showed significant anti-inflammatory activity in the carrageenan-induced foot-plantar edema model. Tris(2,4-di-tert-butylphenyl)phosphate significantly reduced the volume of raw paw edema. [2]
Synonymsα-Hypophamine, Oxytocin (Syntocinon), Oxytocic hormone
Chemical Properties
Molecular Weight1007.19
FormulaC43H66N12O12S2
Cas No.50-56-6
SmilesCC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)NCC(N)=O
Relative Density.1.27 g/cm3
Storage & Solubility Information
Storagekeep away from moisture,keep away from direct sunlight,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 100 mg/mL (99.29 mM), Sonication is recommended.
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM0.9929 mL4.9643 mL9.9286 mL49.6431 mL
5 mM0.1986 mL0.9929 mL1.9857 mL9.9286 mL
10 mM0.0993 mL0.4964 mL0.9929 mL4.9643 mL
20 mM0.0496 mL0.2482 mL0.4964 mL2.4822 mL
50 mM0.0199 mL0.0993 mL0.1986 mL0.9929 mL

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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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