| Weight | 337.573 g/mol |
|---|---|
| Formula | C20H35NOS |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 12 |
suloctidil (54767-75-8, 54063-56-8)
Suloctidil Hydrochloride · CP-556S
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- A secondary prevention, randomized trial of suloctidil in patients with a recent history of thromboembolic stroke. (Stroke, 1985)
- Suloctidil: A novel inhibitor of platelet aggregation in human beings (Thrombosis Research, 1976)
- Antiplatelet and antithrombogenic effects of suloctidil (European Journal of Pharmacology, 1976)
- A doubleblind trial of suloctidil v. Placebo in intermittent claudication (British Journal of Surgery, 1982)
- Evaluation of antithrombotic properties of suloctidil in comparison with aspirin and dipyridamole (Thrombosis Research, 1976)
- Controlled trial of suloctidil in intermittent claudication (Journal of Cardiovascular Pharmacology, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Suloctidil Hydrochloride
- CP-556S
-
SMILESCCCCCCCCNC(C)C(C1=CC=C(C=C1)SC(C)C)O
-
InChIKeyBFCDFTHTSVTWOG-UHFFFAOYSA-N
- Pubchem - suloctidil
- Wikipedia - 2-(octylamino)-1-[4-(propan-2-ylthio)phenyl]-1-propanol
Suloctidil was a sulfer-containing aminoalcohol that was brought to market in the early 1970s as a vasodilator by Continental Pharma, a Belgian company. Continental was bought by Monsanto in 1984, primarily on the promise of sales of suloctidil, which was approved in Europe at the time, but not in the US. However, in 1985 Monsanto halted development and withdrew the drug worldwide following reports of liver toxicity.
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