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Home > Encyclopedia > 1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1)

1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1)

pharmaceutical raw materials
1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1) structure

1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1) 

structure
  • CAS No:

    84504-69-8

  • Formula:

    C9H7Cl2N5.C4H4O4

  • Chemical Name:

    1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1)

  • Synonyms:

    1,3,5-Triazine-2,4-diamine,6-(2,5-dichlorophenyl)-,(2Z)-2-butenedioate (1:1);1,3,5-Triazine-2,4-diamine,6-(2,5-dichlorophenyl)-,(Z)-2-butenedioate (1:1);MN 1695;2,4-Diamino-6-(2,5-dichlorophenyl)-s-triazine maleate;Irsogladine maleate;Gaslon;Gaslon N

  • Categories:

    Active Pharmaceutical Ingredients  >  Digestive System Drugs

Description

Irsogladine is a PDE4 inhibitor and muscarinic acetylcholine receptor binder.Target: PDE4; mACHRIrsogladine treatment (300 and 500 mg/kg/day) resulted in a dose-dependent reduction of angiogenesis in wild-type mice by 21 and 45.3% (P < 0.02, P < 0.001), in tPA-deficient mice by 42.6 and 46% (P < 0.001, P < 0.001), and in uPA-deficient mice by 27.2 and 46% (P < 0.05, p < 0.001), respectively. Irsogladine inhibits bFGF-induced angiogenesis in wild-type, tPA-knockout, and uPA-knockout mice

1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1) Basic Attributes

372.16

371.018799

2933699090

Characteristics

165

2.88400

205 °C (decomp)

552.2ºC at 760 mmHg

287.8ºC

Desiccate at RT

LD50 in male, female mice, rats (mg/kg): 6035, 5697, 3898, 2917 orally; 2841, 3216, 1600, 1524 s.c.; 775, 1006, 558, 545 i.p. (Ueda, 1984 p 474)

Safety Information

NONH for all modes of transport

XY5930000

P201, P202, P281, P308+P313, P405, P501

H361

1,3,5-Triazine-2,4-diamine, 6-(2,5-dichlorophenyl)-, (2Z)-2-butenedioate (1:1) Use and Manufacturing

antiulcerative;selective PDE4 inhibitor which also enhances gap junction intercellular communication

Drug Function and Efficacy

It has anti-ulcer effect, can strengthen the combination between gastric mucosal epithelial cells, enhance the stability of the mucosa itself, play a cellular defense role, and increase the blood flow of gastric mucosa; it does not affect the basic gastric acid secretion, and does not stimulate acid secretion. It shows the inhibitory or curative effect of dosage compliance on experimental gastritis.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

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