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146-04-3

146-04-3 Structure

146-04-3 Structure
IdentificationBack Directory
[Name]

Oosponol
[CAS]

146-04-3
[Synonyms]

Oosponol
Lenzitin
Brn 1287762
4-Glycolyl-8-hydroxyisocoumarin
Isocoumarin, 4-glycolyl-8-hydroxy-
4-(1-Oxo-2-hydroxyethyl)-8-hydroxyisocoumarin
8-Hydroxy-4-(hydroxyacetyl)-1H-2-benzopyran-1-one
[MDL Number]

MFCD01718127
[MOL File]

146-04-3.mol
Chemical PropertiesBack Directory
[LogP]

0.789 (est)
Hazard InformationBack Directory
[Uses]

Oosponol is a dopamine beta-hydroxylase inhibitor exhibiting hypotensive effects.Oospongol has strong antifungal activity against many antagonistic fungi[1][2].
[in vivo]

Oosponol (6.25 mg/kg, 3.1 mg/kg, ip, Once) can lower blood pressure in spontaneously hypertensive rats model[1].

Animal Model:Spontaneously hypertensive rats[1]
Dosage:6.25 mg/kg, 3.1 mg/kg
Administration:Intraperitoneal injection, once.
Result:The intraperitoneal injection of 6.25 mg/kg lowered the pressure from 186 mm to 138~112 mm, the intraperitoneal injection of 3.1 mg/kg lowered the pressure from 185 mm to 164~131 mm[1].
Animal Model:Spontaneously hypertensive rats[1]
Dosage:6.25 mg/kg, 3.1 mg/kg
Administration:Intraperitoneal injection, once.
Result:The intraperitoneal injection of 6.25 mg/kg lowered the pressure from 186 mm to 138~112 mm, the intraperitoneal injection of 3.1 mg/kg lowered the pressure from 185 mm to 164~131 mm.
[References]

[1] Umezawa H, et al.. Dopamine -hydroxylase inhibitor produced by Gloeophyllum striatum and its identity with oosponol. J Antibiot (Tokyo). 1972 Apr;25(4):239-42. DOI:10.7164/antibiotics.25.239
[2] Sonnenbichler J,et al. Influence of the Gloeophyllum metabolite oosponol and some synthetic analogues on protein and RNA synthesis in target cells. Eur J Biochem. 1997 May 15;246(1):45-9. DOI:10.1111/j.1432-1033.1997.t01-2-00045.x
Safety DataBack Directory
[Toxicity]

LD50 oral in rat: 250mg/kg
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