Name | guanadrel |
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Synonyms |
1-(1,4-Dioxaspiro[4.5]decan-2-ylmethyl)guanidine
Guanadrel |
Description | Guanadrel is an orally active postganglionic adrenergic inhibitor of spiroketal. Guanadre can be used in anti-hypertensive studies[1]. |
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Related Catalog | |
In Vivo | Guanadrel (oral gavage, 15-400 mg/kg, every day, 6-52 weeks) has little toxicity to the nervous system in rats and dogs[1]. Animal Model: Rats, dogs[1] Dosage: 15-400 mg/kg Administration: Oral gavage; every day; 6-52 weeks Result: Showed a slight increase in the weight of the prostate and adrenal glands while loss in the kidney in rats. Decreased weight gain values in a dose-dependent manner but liver function is normal in dogs. |
References |
Density | 1.39g/cm3 |
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Boiling Point | 387.9ºC at 760 mmHg |
Melting Point | 213.5-215ºC |
Molecular Formula | C10H19N3O2 |
Molecular Weight | 213.27700 |
Flash Point | 188.4ºC |
Exact Mass | 213.14800 |
PSA | 80.36000 |
LogP | 1.73620 |
Index of Refraction | 1.618 |