For laboratory research use only. Not for human consumption.
Oxytocin is a synthetic mammalian nonapeptide hormone (Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 with a 1-6 disulfide bridge) engineered for neuro-endocrine, smooth muscle contraction, and central neuropeptidergic research. By selectively activating the Gq-coupled Oxytocin Receptor (OXTR), Oxytocin stimulates intracellular calcium mobilization via the Phospholipase C (PLC) pathway.
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Oxytocin is a naturally occurring cyclic nonapeptide neuropeptide synthesized within the paraventricular and supraoptic nuclei of the hypothalamus. Characterized by its conserved nine amino acid sequence (Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2) with a modern intramolecular disulfide bridge between Cysteine-1 and Cysteine-6, Oxytocin serves as a foundational neuro-endocrine signal across mammalian physiology. Operating primarily through the G-protein coupled Oxytocin Receptor (OXTR), Oxytocin regulates peripheral myoepithelial and vascular smooth muscle tone while modulating central social affiliation, stress attenuation, and reward pathways in limbic brain structures. Batch-tested for high analytical purity at Modern Aminos, Oxytocin is offered in a standardized laboratory format:
Laboratories investigating neuro-endocrine receptor kinetics, smooth muscle excitation-contraction coupling, and central behavioral signaling evaluate Oxytocin alongside complementary neuropeptide and melanocortinergic reference standards available on the site, such as PT-141 (Bremelanotide), Melanotan II, and Kisspeptin-10.
| Compound Name | Oxytocin (Hypothalamic Nonapeptide) |
|---|---|
| Quantity / Formats Offered | 5MG Lyophilized Powder (2R Glass Vial) | 10MG Lyophilized Powder (2R Glass Vial) |
| Peptide Sequence | Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 (Disulfide Bridge: Cys1–Cys6) |
| Synonyms / Alt Names | Alpha-hypophamine, Pitocin, Oxytocic Hormone, OXT |
| CAS Number | 50-56-6 |
| Chemical Formula | C43H66N12O12S2 |
| Molecular Weight | 1007.19 g/mol |
| IUPAC Name | 1-({(4R,7S,10S,13S,16S,19R)-19-amino-7-(2-amino-2-oxoethyl)-10-(3-amino-3-oxopropyl)-13-[(1S)-1-methylpropyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacyclohenicosan-16-yl}carbonyl)-L-prolyl-L-leucylglycinamide |
| InChIKey | XAHKRIXOARWGHG-DMYRUZCASA-N |
| SMILES Code | CCC(C)C1C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)NC(CCC(=O)N)C(=O)NC(CC(=O)N)C(=O)N3CCCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)O |
The biochemical pathways and cellular targets of Oxytocin in laboratory research include:
When evaluating research efficacy and published scientific literature for Oxytocin:
To evaluate receptor selectivity, signal transduction, and physiological targets, researchers compare Oxytocin against alternative neuropeptide reference standards available at Modern Aminos:
While both compounds are investigated for their roles in central nervous system signaling and autonomic neuro-endocrine responses, Oxytocin and PT-141 (Bremelanotide) operate through entirely distinct molecular receptor families:
| Compound / Reference | Chemical Class & Structure | Primary Receptor Target | Research Focus & Profile |
|---|---|---|---|
| Oxytocin | Cyclic Nonapeptide (1–6 Disulfide Bridge) | Oxytocin Receptor (OXTR) [Gq/11-Coupled] | Focuses on intracellular calcium mobilization, smooth muscle contraction, and central oxytocinergic bonding/stress attenuation |
| PT-141 (Bremelanotide) | Synthetic Cyclic Heptapeptide | Melanocortin MC3R & MC4R [Gs-Coupled] | Focuses on central hypothalamic melanocortinergic signaling, adenylate cyclase/cAMP activation, and autonomic arousal pathways |
| Melanotan II | Synthetic Cyclic Lactam Analogue | Non-selective MC1R, MC3R, MC4R, MC5R | Focuses on melanogenesis, skin pigmentation models, and non-selective central melanocortin receptor activation |
| Kisspeptin-10 | Decapeptide Fragment (Kiss-1) | GPR54 (KISS1R) [Gq/11-Coupled] | Focuses on hypothalamic GnRH pulse generation, pituitary gonadotropin (LH/FSH) release, and HPG axis regulation |
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2. An intramolecular disulfide bond links the cysteine residues at positions 1 and 6, forming a 6-amino-acid cyclic ring with a 3-amino-acid C-terminal tail.DISCLAIMER: All compounds and research materials supplied by Modern Aminos are intended exclusively for in vitro laboratory research by qualified professionals. They are not medicinal products and have not been authorised by the European Medicines Agency or any national competent authority for human or veterinary use. They are not foods, food supplements, cosmetics or medical devices. Products must not be administered to humans or animals by any route and must not be used for in vivo experimentation or any other non-laboratory purpose. We will refuse or cancel orders, and may close accounts, where there is any indication of human or animal use. By purchasing, you confirm that products will be used only in a controlled laboratory environment by appropriately qualified personnel, in line with all applicable laws.
All products are sold in powder (lyophilized) form and require reconstitution with a suitable diluent for research purposes only. Research supplies (e.g., syringes, bacteriostatic water) are not included. No dosing instructions are provided. We adhere to all local and state laws around Research Only Chemical sales. We are not a pharmacy, nor do we promote or provide any advice for human or animal consumption. Please review our terms and conditions carefully before making a purchase on our website.
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