Oxytocin
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- Concentration
- 5 mg per vial
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Molecular Formula | C43H66N12O12S2 |
Molecular Weight | 1007.2 |
Monoisotopic Mass | 1006.43645793 |
Polar Area | 450 |
Complexity | 1870 |
XLogP | -2.6 |
Heavy Atom Count | 69 |
Hydrogen Bond Donor Count | 12 |
Hydrogen Bond Acceptor Count | 15 |
Rotatable Bond Count | 17 |
Physical Appearance | Fine White Lyophilized Powder |
Stability | Lyophilized protein is to be stored at -20°C. It is recommended to aliquot the reconstituted (dissolved) protein into several discrete vials in order to avoid repeated freezing and thawing. Reconstituted protein can be stored at 4°C |
PubChem LCSS | Oxytocin Laboratory Chemical Safety Summary |
Property | Property Value |
---|---|
CID | 439302 |
CAS | 50-56-6 |
InChI | InChI=1S/C43H66N12O12S2/c1-5-22(4)35-42(66)49-26(12-13-32(45)57)38(62)51-29(17-33(46)58)39(63)53-30(20-69-68-19-25(44)36(60)50-28(40(64)54-35)16-23-8-10-24(56)11-9-23)43(67)55-14-6-7-31(55)41(65)52-27(15-21(2)3)37(61)48-18-34(47)59/h8-11, 21-22, 25-31, 35, 56H, 5-7, 12-20, 44H2, 1-4H3, (H2, 45, 57)(H2, 46, 58)(H2, 47, 59)(H, 48, 61)(H, 49, 66)(H, 50, 60)(H, 51, 62)(H, 52, 65)(H, 53, 63)(H, 54, 64)/t22-, 25-, 26-, 27-, 28-, 29-, 30-, 31-, 35-/m0/s1 |
InChIKey | XNOPRXBHLZRZKH-DSZYJQQASA-N |
Isomeric SMILES | CC[C@H](C)[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@H](C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)N3CCC[C@H]3C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N |
Canonical SMILES | CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)N)C(=O)N3CCCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N |
IUPAC Name | (2S)-1-[(4R, 7S, 10S, 13S, 16S, 19R)-19-amino-7-(2-amino-2-oxoethyl)-10-(3-amino-3-oxopropyl)-13-[(2S)-butan-2-yl]-16-[(4-hydroxyphenyl)methyl]-6, 9, 12, 15, 18-pentaoxo-1, 2-dithia-5, 8, 11, 14, 17-pentazacycloicosane-4-carbonyl]-N-[(2S)-1-[(2-amino-2-oxoethyl)amino]-4-methyl-1-oxopentan-2-yl]pyrrolidine-2-carboxamide |
Generated by Extreme Peptide with Open Babel, version 2.3.1, http://openbabel.org (accessed May 20, 2024)
Oxytocin is a synthetic analogue of a naturally occurring peptide bearing the same name that is typically produced in hypothalamus nerve cells and then stored in the posterior pituitary gland1. Oxytocin is a neuromodulating agent in the brain with significant action throughout the process of mammalian sexual reproduction2. From stimulating sexual attraction3 to intensifying sexual climax4 to diminishing pain sensitivity and relaxing a mother’s muscles during childbirth5, oxytocin is present and integral to all stages of procreation, earning it the colloquial name ‘The Love Hormone’.
Oxytocin has been extensively researched as an agent for initiating a state of calm, a sense of trust, and a more relaxed mode for interpersonal connection and social interaction6. Animal subjects have been observed to act more boldly and with reduced anxiety following administration of oxytocin, as opposed to the evolutionary urge to keep others at a distance7. Complementary to the emotional state of calm, oxytocin has been shown to release muscle tension, to slow heart rate, and to reduce blood pressure8.
Oxytocin has also been observed to be a positive effector of quick wound healing9 as a result of fibroblast recruitment and an inhibition of the inflammatory response10. Research in animal subjects has demonstrated that oxytocin also has a peripheral role in stimulating growth hormone release11 and in inducing digestion, leading to enhanced metabolic efficiency.
Oxytocin’s action in enhancing libido, reducing social anxiety, and allowing for sensations of romantic attachment make it attractive as a potential remedy for subjects receiving necessary treatment that may inhibit these functions through side effects.
Oxytocin Acetate, 3-Isoleucine-8-leucine vasopressin; Alpha-hypophamine; Atonin O; Di-sipidin; Endopituitrina; Hyphotocin; Intertocine S; Perlacton; Pitocin; Piton S; Presoxin;Synpitan;
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