| Weight | 291.138 g/mol |
|---|---|
| Formula | C10H12Cl2N4O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Wytensin (23256-50-0)
Guanabenz · Guanabenz Acetate · BR 750
Score:
#508 in Neuroscience
,
#885 in Biochemistry
,
#2360 in Biology
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#2924 in Chemistry
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- Antihypertensive drug guanabenz is active in vivo against both yeast and mammalian prions. (PLOS ONE, 2008)
- Guanabenz. A review of its pharmacodynamic properties and therapeutic efficacy in hypertension. (Drugs, 1983)
- Guanabenz-mediated Inactivation and Enhanced Proteolytic Degradation of Neuronal Nitric-oxide Synthase (Journal of Biological Chemistry, 2000)
- Guanabenz, guanochlor, guanoxan and idazoxan bind with high affinity to non-adrenergic sites in pig kidney membranes (European Journal of Pharmacology, 1989)
- Studies on the centrally mediated hypotensive activity of guanabenz. (European Journal of Pharmacology, 1976)
- Renal effects of the antihypertensive, guanabenz, in the dog. (Journal of Pharmacology and Experimental Therapeutics, 1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Guanabenz
- Guanabenz Acetate
- BR 750
- BR-750
- 2,6-Dichlorobenzylideneaminoguanidine
- BR750
- Wyeth Ayerst of Guanabenz Acetate
- WY-8678
- WY 8678
- 2,6 Dichlorobenzylideneaminoguanidine
- Wyeth-Ayerst of Guanabenz Acetate
- Guanabenz Monoacetate
- WY8678
- Guanabenz Acetate Wyeth-Ayerst
-
SMILESCC(=O)[O-].C1=CC(=C(C(=C1)Cl)C=NN=C([NH3+])N)Cl
-
InChIKeyMCSPBPXATWBACD-UHFFFAOYSA-N
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