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CasNo: 5985-28-4
MF: C9H13NO2.HCl
Appearance: white powder
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Synephrine hydrochloride is white powder, while it's Molecular Formula is C9H13NO2.HCl. A α-adrenergic receptor agonist, vasoconstrictor.
The CAS number of Synephrine hydrochloride is 5985-28-4.
More information of Synephrine hydrochloride 5985-28-4 are:
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Synonyms |
Benzenemethanol,4-hydroxy-a-[(methylamino)methyl]-, hydrochloride(9CI);Benzyl alcohol, p-hydroxy-a-[(methylamino)methyl]-,hydrochloride (8CI);Oxedrine hydrochloride; |
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CAS Number |
5985-28-4 |
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Molecular Formula |
C9H13NO2.HCl |
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Molecular Weight |
203.669 |
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Melting Point |
147-150oC |
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Boiling Point |
341.1 °C at 760 mmHg |
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Flash Point |
163.4 °C |
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HS CODE |
2922199090 |
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PSA |
52.49000 |
|
LogP |
1.83790 |
(±)-Synephrine is an alkaloid with vasoconstrictor and metabolic activities. It binds to α1A-, α2A-, and α2C-adrenergic receptors (ARs; Kis = 78, 36.7, and 24.4 μM, respectively). (±)-Synephrine is an agonist of α1A-ARs in HEK293 cells (EC50 = 4 μM in a reporter assay) but not in CHO cells expressing α2A- or α2C-AR. It also acts as an antagonist of α1A-, α2A-, and α2C-ARs, inhibiting L-phenylephrine-induced activation of α1A-AR in HEK293 cells and activation of α2A- and α2C-ARs induced by the α2-AR agonist medetomidine in CHO cells (IC50s = 12.8, 26, and 27.3 μM, respectively, in reporter assays). (±)-Synephrine induces contractions in isolated rabbit aortic rings (EC50 = 6.2 μg/ml) and increases ligation-induced mean arterial pressure in rats when administered at a dose of 2 mg/kg per day. It induces lipolysis in isolated rat and human adipocytes when used at concentrations of 100 and 1,000 μg/ml. (±)-Synephrine (50 μM) increases phosphorylation of Akt and AMP-activated protein kinase (AMPK) and translocation of Glut4 to the plasma membrane, as well as increases insulin-induced glucose consumption in L6 muscle cells when used at concentrations ranging from 25 to 200 μM.
InChI:InChI=1/C9H13NO2.ClH/c1-10-6-9(12)7-2-4-8(11)5-3-7;/h2-5,9-12H,6H2,1H3;1H
Articles related to Synephrine hydrochloride:
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Article |
Source |
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Synthesis and uses of synephrine derivatives |
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