GUANETHIDINE SULFATE

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1.What is the GUANETHIDINE SULFATE ?

Antihypertensive.

2.What is the CAS number for GUANETHIDINE SULFATE ?

The CAS number of GUANETHIDINE SULFATE is 645-43-2.

More information of GUANETHIDINE SULFATE 645-43-2 are:

3.What are another words for GUANETHIDINE SULFATE ?

Synonyms?for?GUANETHIDINE SULFATE 645-43-2:2-(Octahydro-1-azocinyl)ethyl guanidine sulphate;Heptamethylenimine, 1-(2-guanidinoethyl)-;Guanethidine monosulfate [USAN];N-(2-Perhydroazocin-1-ylethyl)guanidine;Azocine, 1-((2-(aminoiminomethyl)amino)ethyl)octahydro-;(2-(Hexahydro-(2H)-azocin-1-yl)ethyl)guanidinium sulphate;Azocine, 1-(2-guanidinoethyl)octahydro-;Guanidine,[2-(hexahydro-1(2H)-azocinyl)- ethyl]-,sulfate (1:1);2-[2-(azocan-1-yl)ethyl]guanidine;Abapresin;Oktadin;Dopom;N-(2-Guanidino ethyl)heptamethylenimine sulfate;Eutensol;Esimil;Dopam;2-(1-N,N-Heptamethyleneimino)ethylguanidine;Guanidine, (2-(hexahydro-1(2H)-azocinyl)ethyl)-, sulfate (1:1);Guanethidinum [INN-Latin];Oktatenzin;Oktatensin;Ismelin(TN);Guanidine, (2-(hexahydro-1(2H)-azocinyl)ethyl)-;Guanetidina [INN-Spanish];Octatensine;(2-(Hexahydro-1(2H)-azocinyl)ethyl) guanidine hydrogen sulfate;Sanotensin;2-[2-(azocan-1-yl)ethyl]guanidine; sulfuric acid;2-(1-Azacyclooctyl)ethylguanidine;Ismelin sulfate;Guanethidine sulfate;(2-(Octahydro-1-azocinyl)ethyl)guanidine;Ismelin;(2-(Hexahydro-1(2H)-azocinyl)ethyl)guanidine sulfate (1:1);

4.What is the molecular formula of GUANETHIDINE SULFATE?

The chemical formula of ?GUANETHIDINE SULFATE is?C10H22N4•H2O4S which containing 10 Carbon atoms,24 Hydrogen atoms,1 Nitrogen atoms,4 Oxygen atoms and 1 Sulfur atoms,and the molecular weight of??GUANETHIDINE SULFATE?is 296.44.

5.What is GUANETHIDINE SULFATE (645-43-2) used for?

Guanethidine is an antihypertensive compound that competes with norepinephrine for transport into presynaptic terminals of adrenergic neurons by the norepinephrine transporter. Once guanethidine has entered the nerve, it becomes concentrated in synaptic vesicles, depleting endogenous norepinephrine, and thus, reducing the release of norepinephrine in response to action potentials. Guanethidine’s actions are restricted to peripheral nerve terminals because its basic guanidine group does not allow passage through the blood brain barrier. Its use has been explored in the relief of chronic pain caused by complex regional pain syndrome.

InChI:InChI=1/C10H22N4.H2O4S/c11-10(12)13-6-9-14-7-4-2-1-3-5-8-14;1-5(2,3)4/h1-9H2,(H4,11,12,13);(H2,1,2,3,4)

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