| Weight | 494.707 g/mol |
|---|---|
| Formula | C20H46N8O4S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
guanethidine sulfate (60-02-6)
Guanethidine · Ismelin · Guanethidine Monosulfate
Score:
#1225 in Neuroscience
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- A new method of destroying adrenergic nerves in adult animals using guanethidine (British Journal of Pharmacology, 1971)
- Guanethidine-sensitive release of neuropeptide Y-like immunoreactivity in the cat spleen by sympathetic nerve stimulation (Neuroscience Letters, 1984)
- INTRAVENOUS REGIONAL SYMPATHETIC BLOCK WITH GUANETHIDINE (The Lancet, 1974)
- Effects of chronic guanethidine treatment and adrenal medullectomy on plasma levels of catecholamines and corticosterone in forcibly immobilized rats. (Journal of Pharmacology and Experimental Therapeutics, 1979)
- INTERACTION OF GUANETHIDINE WITH ADRENERGIC NEURONS (Journal of Pharmacology and Experimental Therapeutics, 1965)
- Norepinephrine Depletion as a Possible Mechanism of Action of Guanethidine a New Hypotensive Agent (Experimental Biology and Medicine, 1960)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Guanethidine
- Ismelin
- Guanethidine Monosulfate
- ((2-Hexahydro-1(2H)-azocinyl)ethyl)guanidine
- Octadine
- Isobarin
- Oktadin
- Guanethidine Sulfate (1:2)
- Guanethidine Sulfate (2:1)
- Guanethidine Sulfate (2:1), 14C-Labeled
- Guanethidine Sulfate (1:1)
-
SMILESC1CCCN(CCC1)CCN=C(N)N.C1CCCN(CCC1)CCN=C(N)N.OS(=O)(=O)O
-
InChIKeyNBJGGHFXCGHTNJ-UHFFFAOYSA-N
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