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Oxytocin (acetate) Sale

(Synonyms: 醋酸催产素; 醋酸缩宫素; α-Hypophamine acetate; Oxytocic hormone acetate) 目录号 : GC44526

A peptide hormone best known for its role in reproductive biology

Oxytocin (acetate) Chemical Structure

Cas No.:6233-83-6

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥756.00
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5mg
¥446.00
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10mg
¥644.00
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50mg
¥1,188.00
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100mg
¥1,980.00
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200mg
¥3,465.00
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500mg
¥6,930.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Oxytocin is a nonapeptide hormone primarily synthesized in magnocellular neurons of the paraventricular and supraoptic nuclei of the hypothalamus. It is known best for its role in stimulating uterine contraction and lactation and is important for social memory and attachment, sexual and maternal behavior, and aggression. Also, it has been implicated in various non-social behaviors, including learning, anxiety, feeding, and pain perception.

Chemical Properties

Cas No. 6233-83-6 SDF
别名 醋酸催产素; 醋酸缩宫素; α-Hypophamine acetate; Oxytocic hormone acetate
Canonical SMILES NC(CNC([C@@H](NC([C@H]1N(C([C@@H](NC([C@H](CC(N)=O)NC([C@@H]2CCC(N)=O)=O)=O)CSSC[C@H](N)C(N[C@@H](CC3=CC=C(O)C=C3)C(N[C@]([C@@H](C)CC)([H])C(N2)=O)=O)=O)=O)CCC1)=O)CC(C)C)=O)=O.CC(O)=O
分子式 C45H70N12O14S2 分子量 1067.24
溶解度 DMF: 30 mg/ml,DMSO: 14 mg/ml,Ethanol: 5 mg/ml,PBS (pH 7.2): 5 mg/ml 储存条件 Store at -20°C,protect from light
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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1 mg 5 mg 10 mg
1 mM 0.937 mL 4.685 mL 9.37 mL
5 mM 0.1874 mL 0.937 mL 1.874 mL
10 mM 0.0937 mL 0.4685 mL 0.937 mL
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Research Update

The effect of trehalose, antioxidants, and acetate buffer concentration on Oxytocin stability

J Pept Sci 2021 Jul;27(7):e3324.PMID:33768618DOI:10.1002/psc.3324.

Oxytocin is a cyclic nonapeptide used to induce labor and prevent bleeding after childbirth. Due to its instability, storage and transport of Oxytocin formulations can be problematic in hot/tropical climates. The aim of this study was to investigate the effect of trehalose and select antioxidants (uric acid, butylated hydroxytoluene, and l-ascorbic acid) on Oxytocin stability in solution. The effect of buffer composition and acetate buffer concentration was also studied. acetate buffer was found to work better than citrate/phosphate buffer for the Oxytocin stability. Lower acetate buffer concentrations (0.025 M or less) were also found to yield improved Oxytocin stability compared to higher concentrations. Although known degradation pathways of Oxytocin include oxidation, the antioxidants uric acid and butylated hydroxytoluene had negligible effect on the Oxytocin stability while l-ascorbic acid led to significantly faster degradation. Despite trehalose's reputation as a great stabilizer for biomolecules, it also had small to negligible effect on Oxytocin stability at concentrations up to 1 M in acetate buffer. These results were surprising given the present literature on trehalose as a stabilizer for various biomolecules, including proteins and lipids.

Hormonal Contraceptives, Female Sexual Dysfunction, and Managing Strategies: A Review

J Clin Med 2019 Jun 25;8(6):908.PMID:31242625DOI:10.3390/jcm8060908.

In recent decades, hormonal contraceptives (HC) has made a difference in the control of female fertility, taking an unequivocal role in improving contraceptive efficacy. Some side effects of hormonal treatments have been carefully studied. However, the influence of these drugs on female sexual functioning is not so clear, although variations in the plasma levels of sexual hormones could be associated with sexual dysfunction. Permanent hormonal modifications, during menopause or caused by some endocrine pathologies, could be directly related to sexual dysfunction in some cases but not in all of them. HC use seems to be responsible for a decrease of circulating androgen, estradiol, and progesterone levels, as well as for the inhibition of Oxytocin functioning. Hormonal contraceptive use could alter women's pair-bonding behavior, reduce neural response to the expectation of erotic stimuli, and increase sexual jealousy. There are contradictory results from different studies regarding the association between sexual dysfunction and hormonal contraceptives, so it could be firmly said that additional research is needed. When contraceptive-related female sexual dysfunction is suspected, the recommended therapy is the discontinuation of contraceptives with consideration of an alternative method, such as levonorgestrel-releasing intrauterine systems, copper intrauterine contraceptives, etonogestrel implants, the permanent sterilization of either partner (when future fertility is not desired), or a contraceptive ring.

Effect of 18-Crown-6 on Oxytocin Stability in Aqueous Buffer Solutions

ACS Omega 2021 Feb 15;6(8):5805-5811.PMID:33681619DOI:10.1021/acsomega.0c06248.

In this study, the effect of 18-crown-6 on the stability of Oxytocin in aqueous solution was explored. The study found that while 12-crown-4 and 15-crown-5 do not stabilize Oxytocin, 18-crown-6 does have a stabilizing effect in citrate/phosphate buffer at pH 4.5. However, in acetate buffer at the same pH, the presence of 18-crown-6 had a destabilizing effect, possibly leading to a different degradation pathway. Both the stabilizing and destabilizing effects, depending on the buffer used, are concentration dependent where a higher concentration of 18-crown-6 is linked to a stronger effect. It is hypothesized that this effect may be linked to 18-crown-6 binding to the protonated ammonium group of Oxytocin. Upon changing the mobile phase used in high-performance liquid chromatography experiments, we observed evidence supporting this binding hypothesis. When an acidic mobile phase was used (0.01% trifluoroacetic acid (TFA)), a partial shift in Oxytocin retention time was observed for samples in acetate buffers in the presence of 18-crown-6 when using a 150 mm column (C18). The amount of the peak that shifted depended on the 18-crown-6 concentration used. A similar shift in Oxytocin peak retention time was observed for samples in both acetate and citrate/phosphate buffers when using a 250 mm column (C18), but the peak completely shifted in those samples. When using an even more acidic mobile phase (0.1% TFA), the Oxytocin peaks all had the same retention time again. Ultraviolet and nuclear magnetic resonance spectroscopy experiments also showed that the presence of 18-crown-6 has an observable effect on the resulting Oxytocin spectra.

Oxytocin increases pregnancy rates after fixed time artificial insemination in Kazak ewes

Reprod Domest Anim 2021 Jun;56(6):942-947.PMID:33742456DOI:10.1111/rda.13931.

It is probable that reduced pregnancy rates in ewes after fixed time artificial insemination (FTAI) is attributable, in part, to the reduced number of normal spermatozoa that colonize the oviduct. Administration of Oxytocin stimulates both cervical dilation and uterine/oviductal contractility. The hypothesis that Oxytocin can enhance sperm transport into the uteri and the oviducts, and thereby increase pregnancy rates, was tested in the present study. Oestrus was synchronized in 199 multiparous Kazak ewes using intravaginal flurogestone-impregnated sponge. The sponge was left in the vagina for 12 days followed with an injection of 330 IU of eCG at sponge removal. Each ewe was intracervically inseminated twice at 50 hr and 62 hr after the removal of sponges using an insemination catheter containing 0.25 ml of diluted semen. Semen was collected from seven Texel rams and all the ejaculates were pooled and diluted in ultra-high temperature-treated commercial skimmed milk without (Control group, 0.05 ml of saline per mL milk, n = 144) or with Oxytocin supplement (Oxytocin group, 0.5 U of Oxytocin per ml milk, n = 55). Pregnancy status was determined by transabdominal ultrasound examination 45 days after insemination. Lambing performance was recorded at delivery. Significant differences were observed between the Oxytocin group and the Control group in terms of the pregnancy rate and the fecundity rate (85.5% and 92.7% versus 68.8% and 72.9%, respectively). In conclusion, low dose Oxytocin supplementation of semen extender significantly increased pregnancy and fecundity rates in oestrus-synchronized Kazak ewes after FTAI.

The effect of D-(+)-glucosamine, N-acetyl-D-glucosamine and tetraethylene glycol on the stability of Oxytocin in aqueous solution

Pharmazie 2021 Oct 1;76(10):480-483.PMID:34620274DOI:10.1691/ph.2021.1081.

The aim of the present study was to identify the effect of D-(+)-glucosamine, N-acetyl-D-glucosamine, tetraethyleneglycol, and the mixture of these additives on the stability of Oxytocin in phosphate and acetate buffer solutions, at pH 4.5. Our findings demonstrate that tetraethyleneglycol has a destabilizing effect on Oxytocin in both phosphate buffer and acetate buffer. D-(+)-Glucosamine hydrochloride had small to negligible effect at low concentrations, yielding a slight improvement lower concentrations of the additive in the presence of the buffers used, but at higher concentrations it increased the rate of degradation. N-Acetyl-D-glucosamine showed a possibly slight improvement to the stability of Oxytocin. It is hypothesized that the different effect of N-acetyl-D-glucosamine compared to D-(+)-glucosamine is a consequence of the free amine group in D-(+)-glucosamine promoting a faster degradation, while the amino group is acetylated in N-acetyl-D-glucosamine and therefore no longer reactive in the same way. While it remains unclear why tetraethyleneglycol has a destabilizing effect on Oxytocin, the D-(+)-glucosamine results aid in deepening our understanding of the degradation mechanism of Oxytocin.