Bioactivity | Guanethidine sesquisulfate, an antihypertensive agent, is an adrenergic neurone blocking agent. Guanethidine sesquisulfate enters noradrenergic nerve terminals by the neuronal amine carrier[1][2]. |
In Vivo | Guanethidine sesquisulfate(5-40 mg/kg;腹膜内注射;每日;4-28 天;雄性 Wistar 大鼠)以 40 mg/kg 治疗 28 天会导致不完全交感神经切除,并伴有对去甲肾上腺素的部分不可逆超敏反应,而 5 mg/kg 不会引起组织学或永久性血流动力学变化[2]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: |
CAS | 60-02-6 |
Formula | C10H22N4.1/2H2O4S |
Molar Mass | 247.34 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. Mitchell JR, et al. Antagonism of the antihypertensive action of guanethidine sulfate by desipramine hydrochloride. JAMA. 1967 Dec 4;202(10):973-6. [2]. Nielsen GD. Guanethidine induced sympathectomy in the adult rat. I. Functional effects following subacute administration. Acta Pharmacol Toxicol (Copenh). 1977 Sep;41(3):203-8. |