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Oxytocin Acetate
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| Post Date: | Oct 10,2016 |
| Expiry Date: | Apr 08,2017 |
| Detailed Description: |
Cas No. :50-56-6
Quantity: 1Kilograms Price:1 USD Kilograms Payment Method: T/T Product Name Oxytocin Acetate Sequence Cas No. 50-56-6 Molecular Formula C43H66N12O12S2 Molecular Weight 1007.2 Purity (HPLC) 98.0%min. Appearance? White powder Single Impurity(HPLC)? 1.0%max Amino Acid Composition? ±10% of theoretical Peptide Content(N%) ?≥80.0% Water Content(Karl Fischer)? ≤6.0% Acetate Content(HPIC) ≤12.0% MS(ESI) Consistent Mass Balance? 95.0~105.0% Description: Oxytocin (Oxt) is a mammalian neurohypophysial hormone. Produced by the hypothalamus and stored and secreted by the posterior pituitary gland, oxytocin acts primarily as a neuromodulator in the brain. Oxytocin plays an important role in the neuroanatomy of intimacy, specifically in sexual reproduction of both sexes, in particular during and after childbirth; Its name, meaning "swift childbirth", comes from Greek, oksys "swift" and, tokos "birth. " It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, maternal bonding, and, after stimulation of the nipples, lactation. Both childbirth and milk ejection result from positive feedback mechanisms. Application: Injected oxytocin analogues are used for labor induction and to support labor in case of difficult parturition. It has largely replaced ergometrine as the principal agent to increase uterine tone in acute postpartum hemorrhage. Oxytocin is also used in veterinary medicine to facilitate birth and to stimulate milk release. The tocolyticagent atosiban (Tractocile) acts as an antagonist of oxytocin receptors; This drug is registered in many countries to suppress premature labor between 24 and 33 weeks of gestation. It has fewer side effects than drugs previously used for this purpose (ritodrine). |
| CAS Registry Number: | 50-56-6 |
| Synonyms: | ;oxytocin lyophilized;H-Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 Disulfide bond;H-Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 (Disulfide bond);oxtocin;(2s)-1-[(4r,7s,10s,13s,16s,19r)-19-amino-13-[(2s)-butan-2-yl]-10-(2-carbamoylethyl)-7-(carbamoylmethyl)-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]-n-[(1s)-1-(carbamoylmethylcarbamoyl)-3-methyl-butyl]pyrrolidine-2-carboxamide;Oxytocin Solution;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-hydroxybenzyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosan-4-yl]carbonyl}-L-prolyl-L-leucylglycinamide;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-hydroxybenzyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosan-4-yl]carbonyl}-L-prolyl-L-leucylglycinamide acetate (1:1); |
| Molecular Formula: | C43H66N12O12S2 |
| Molecular Weight: | 1007.19 |
| Molecular Structure: | 
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| Company: | Hubei Yuancheng Saichuang Technology Co.,Ltd [ China ] |
| Contact: | fion |
| Tel: | +86-027-50755967 |
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| Email: | emma@chembj.com |
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