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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

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