1. GPCR/G Protein Neuronal Signaling Immunology/Inflammation
  2. Histamine Receptor Serotonin Transporter
  3. Dimephosphon

Dimephosphon is an anti-inflammatory agent with antihistamine and antiserotonin activities. Dimephosphon helps maintain the conduction function of the spinal cord and reduces the excitability of spinal motor neurons in the area surrounding the lesion. Dimephosphon directly activates lymphatic vessel movement and improves lymphatic circulation. Dimephosphon can be used for the study of inflammatory edema, acute spinal cord injury and lymphatic circulation disorders.

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Dimephosphon

Dimephosphon Chemische Struktur

CAS. Nr. : 14394-26-4

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Beschreibung

Dimephosphon is an anti-inflammatory agent with antihistamine and antiserotonin activities. Dimephosphon helps maintain the conduction function of the spinal cord and reduces the excitability of spinal motor neurons in the area surrounding the lesion. Dimephosphon directly activates lymphatic vessel movement and improves lymphatic circulation. Dimephosphon can be used for the study of inflammatory edema, acute spinal cord injury and lymphatic circulation disorders[1][2][3].

In Vivo

The antihistamine and antiserotonin activity of Dimephosphon is shown on models of paw edema caused by subplantar administration of mediators and modulators of inflammation[1].
Dimephosphon (2.5 % Dimephosphon Solution, 1 mL, daily for 10 days) promotes the recovery of spinal cord conduction function, and its mechanism may be related to anti-edema, vascular protection and reduction of neuronal hyperexcitability, in hybrid dogs with spinal cord injury[2].
Dimephosphon (50 mg/kg, i.p, once dose) enhances lymphatic circulation by directly activating lymphatic vessel contraction (stimulating vessel wall and valve muscle cells) in rats[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Albino rats (200-230 g)[3]
Dosage: 50 mg/kg
Administration: Intraperitoneal injection (i.p.), once dose
Result: Increased the thoracic duct (TLD) lymph flow rate to 1.4 times that of the control group, and enhanced the contraction activity of lymphatic vessels. Increased the number of functional lymphatic vessels and the number of mesenteric lymphatic vessels by 1.5 times
Molekulargewicht

208.19

Formel

C8H17O4P

CAS. Nr.
SMILES

O=C(CC(C)(P(OC)(OC)=O)C)C

Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

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