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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Information
Domperidone is an oraldopamine D2 receptorantagonist, used to treat nausea and vomiting.
In vitro
Domperidone (a D2R antagonist) inhibits Equilibrative NT1 (ENT1) activity more in the presence than in the absence of Bromocriptine and displays an IC50 value lower than that of Bromocriptine or Ergovaline in Madin-Darby bovine kidney (MDBK) cells.
In vivo
Domperidone (0.1 mg/kg) results in a significant decrease in feeding behavior and stimulation of basal metabolism, but has no effect on locomotor activity of rats in a Phenomaster system. Domperidone (1.1 mg/kg and 5.5 mg/kg, oral) significantly increases laminar microvascular blood flow (LMBF) in horses, compared with baseline values, beginning 4 hours after administration, and this effect persisted for at least 8 hours. Domperidone (0.2 mg/kg, i.v.) significantly increases laminar microvascular blood flow (LMBF) in horses, compared with baseline values, at 10 and 12 hours after administration. Domperidone can ameliorate deleterious reproductive effects and reduce weight gain associated with fescue toxicosis in heifers. Domperidone-treated mares have shorter gestation duration and foaled closer to their expected parturition date than did control mares. Domperidone-treated mares have higher Mammary gland scores and serum prolactin concentration. Domperidone (5 mg/kg, oral) increases peak plasma acetaminophen concentration and area under the curve in rats, indicating increased gastric emptying. Domperidone decreases the dopamine-induced contractile activity of midjejunal longitudinal muscle strips in rats.
Cell Data
cell lines:SET-2 and TEL-JAK Ba/F3 cells
Concentrations:
Incubation Time:
Powder Purity:≥98%
| ALogP | 3.9 |
|---|
| Isómeros SMILES | C1CN(CCC1N2C3=C(C=C(C=C3)Cl)NC2=O)CCCN4C5=CC=CC=C5NC4=O |
|---|---|
| WGK Alemania | 3 |
| RTECS | DE2275900 |
| Peso molecular | 425.91 |
| Reaxy-Rn | 903774 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=903774&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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| Solubilidad | Solubility (25°C) In vitro 5%TFA 3.06 mg/mL (17.37 mM); DMSO: 0.1 mg/mL (0.56 mM); Water: Insoluble; |
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| Punto de fusión (°C) | 243°C |
| 1. Yang Zhou, Lei Guo, Zhiheng Zhao, Sisi Zheng, Yue Xu, Bin Xiang, Savaş Kaya. (2018) Anticorrosion potential of domperidone on copper in different concentration of hydrochloric acid solution. JOURNAL OF ADHESION SCIENCE AND TECHNOLOGY, [PMID:] [10.1080/01694243.2018.1426542] |
| 2. Yanxia Liu, Xiuquan Yao, Chunlin Liu, Xiaofang Luo, Chao Guo, Wei Du. (2023) The Drug Domperidone as a Corrosion Inhibitor for X60 Steel in Hydrochloric Acid Solution. International Journal of Electrochemical Science, [PMID:] [10.20964/2022.04.55] |
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