Metoclopramide hydrochloride hydrate
CAS No. 54143-57-6
Metoclopramide hydrochloride hydrate( AHR-3070-C, Maxolon, Metoclopramide HCl, Metoclopramide monohydrochloride monohydrate, Metozolv, Reglan )
Catalog No. M14937 CAS No. 54143-57-6
A potent dopamine D2 receptor antagonist with Ki of 28 nM; also is a mixed 5-HT3 receptor antagonist/5-HT4 receptor agonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
100MG | 67 | Get Quote |
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200MG | 88 | Get Quote |
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500MG | 133 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameMetoclopramide hydrochloride hydrate
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NoteResearch use only, not for human use.
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Brief DescriptionA potent dopamine D2 receptor antagonist with Ki of 28 nM; also is a mixed 5-HT3 receptor antagonist/5-HT4 receptor agonist.
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DescriptionA potent dopamine D2 receptor antagonist with Ki of 28 nM; also is a mixed 5-HT3 receptor antagonist/5-HT4 receptor agonist; commonly used to treat nausea and vomiting caused by chemotherapy.Chemotherapeutic Agents Phase 2 Discontinued(In Vitro):Metoclopramide (0.01-10 μM) hydrochloride hydrate stimulates aldosterone release in isolated perfused rat zona glomerulosa cells.Metoclopramide hydrochloride hydrate results in prokinesis by four mechanisms: inhibition of presynaptic D2 receptors and stimulation of presynaptic excitatory 5-HT4 receptors, thereby allowing acetylcholine (ACh) release from intrinsic cholinergic motor neurons; inhibition of D2 postsynaptic receptors; and antagonism of the presynaptic inhibition of muscarinic receptors, leading to further augmentation of ACh release.(In Vivo):Metoclopramide (6.7 μg/g; s.c. daily for 50 days) hydrochloride hydrate significantly increases the number and the volume of lactotroph cells of the pituitary gland during all phases of the estrous cycle.Metoclopramide (5-40 mg/kg; i.p.) hydrochloride hydrate induces catalepsy and antagonizes Apomorphine induced cage climbing behaviour in mice.Metoclopramide (1.25-2.5 mg/kg; i.p.) hydrochloride hydrate induces stereotyped cage climbing behaviour in mice.
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In VitroMetoclopramide (0.01-10 μM) hydrochloride hydrate stimulates aldosterone release in isolated perfused rat zona glomerulosa cells.Metoclopramide hydrochloride hydrate results in prokinesis by four mechanisms: inhibition of presynaptic D2 receptors and stimulation of presynaptic excitatory 5-HT4 receptors, thereby allowing acetylcholine (ACh) release from intrinsic cholinergic motor neurons; inhibition of D2 postsynaptic receptors; and antagonism of the presynaptic inhibition of muscarinic receptors, leading to further augmentation of ACh release.
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In VivoMetoclopramide (6.7 μg/g; s.c. daily for 50 days) hydrochloride hydrate significantly increases the number and the volume of lactotroph cells of the pituitary gland during all phases of the estrous cycle.Metoclopramide (5-40 mg/kg; i.p.) hydrochloride hydrate induces catalepsy and antagonizes Apomorphine induced cage climbing behaviour in mice.Metoclopramide (1.25-2.5 mg/kg; i.p.) hydrochloride hydrate induces stereotyped cage climbing behaviour in mice. Animal Model:Adult, virgin female mice of the Swiss EPM-1 strainDosage:6.7 μg/g Administration:S.c. daily for 50 days Result:Increased the number but also stimulated the metabolic activity of lactotrophs.
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SynonymsAHR-3070-C, Maxolon, Metoclopramide HCl, Metoclopramide monohydrochloride monohydrate, Metozolv, Reglan
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PathwayGPCR/G Protein
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TargetDopamine Receptor
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RecptorDopamine Receptor
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Research AreaCancer
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IndicationChemotherapeutic
Chemical Information
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CAS Number54143-57-6
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Formula Weight354.2726
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Molecular FormulaC14H25Cl2N3O3
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO.Cl.CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC
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Chemical NameBenzamide, 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxy-, hydrochloride, hydrate (1:1:1)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Matsui A, et al. J Pharmacol Exp Ther. 1998 Nov;287(2):725-32.
2. Tonini M, et al. Pharmacol Res. 1995 May;31(5):257-60.
3. Bateman DN, et al. Br J Clin Pharmacol. 1978 Nov;6(5):401-7.
molnova catalog
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