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Irsogladine

From Wikipedia, the free encyclopedia
Irsogladine
Names
Preferred IUPAC name
6-(2,5-Dichlorophenyl)1,3,5-triazine-2,4-diamine
Other names
DCPDAT, Dicloguamine, MN-1695.
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
KEGG
UNII
  • InChI=1S/C9H7Cl2N5/c10-4-1-2-6(11)5(3-4)7-14-8(12)16-9(13)15-7/h1-3H,(H4,12,13,14,15,16)
    Key: ATCGGEJZONJOCL-UHFFFAOYSA-N
  • C1=CC(=C(C=C1Cl)C2=NC(=NC(=N2)N)N)Cl
Properties
C9H7Cl2N5
Molar mass256.09 g·mol−1
Pharmacology
A02BX16 (WHO)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Irsogladine is aphosphodiesterase inhibitor.[1]

Synthesis

[edit]
ChemDrug Synthesis:[2][3] Patent:[4]

2,4-Dichloro-6-(2,5-dichlorophenyl)-1,3,5-triazine [61479-79-6] (1)(2)Dicyandiamide [461-58-5] (3)2,5-Dichlorobenzonitrile [21663-61-6] (4)

References

[edit]
  1. ^Satoh, H; Amagase, K; Takeuchi, K (2013). "Mucosal protective agents prevent exacerbation of NSAID-induced small intestinal lesions caused by antisecretory drugs in rats".The Journal of Pharmacology and Experimental Therapeutics.348 (2):227–35.doi:10.1124/jpet.113.208991.PMID 24254524.S2CID 23740642.
  2. ^Serradell, MN; Blancafort, P.; Castaer, J.; MN-1695. Drugs Fut 1983, 8, 6, 502.
  3. ^Ueda F, Aratani S, Mimura K, Kimura K, Nomura A, Enomoto H. Effect of 2,4-diamino-6-(2,5-dichlorophenyl)-s-triazine maleate (MN-1695) on gastric ulcers and gastric secretion in experimental animals. Arzneimittelforschung. 1984;34(4):474-7. PMID: 654016.
  4. ^DE2506814 idem Hiromu Murai, 6 More »,U.S. patent 3,966,728 (1976 to Nippon Shinyaku Co., Ltd.).
H2 antagonists ("-tidine")
Prostaglandins (E)/
analogues ("-prost-")
Proton-pump inhibitors
("-prazole")
Potassium-competitive
acid blockers
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Others
Combinations
PDE1
PDE2
PDE3
PDE4
PDE5
PDE7
PDE9
PDE10
PDE11
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