| Weight | 277.496 g/mol |
|---|---|
| Formula | C19H35N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
PERHEXILINE
Perhexilene
35193-73-8, 6621-47-2, 39648-48-1, 39648-47-0
Score:
#140 in Neurology
,
#634 in Neuroscience
,
#2825 in Biology
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#3539 in Chemistry
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- Metabolic Modulation With Perhexiline in Chronic Heart Failure: A Randomized, Controlled Trial of Short-Term Use of a Novel Treatment (Circulation, 2005)
- Impaired oxidation of debrisoquine in patients with perhexiline neuropathy. (BMJ, 1982)
- Metabolic Modulator Perhexiline Corrects Energy Deficiency and Improves Exercise Capacity in Symptomatic Hypertrophic Cardiomyopathy (Circulation, 2010)
- Inhibition of carnitine palmitoyltransferase-1 in rat heart and liver by perhexiline and amiodarone. (Biochemical Pharmacology, 1996)
- Impaired oxidation of debrisoquine in patients with perhexiline liver injury. (Gut, 1984)
- Efficacy and safety of perhexiline maleate in refractory angina. A double-blind placebo-controlled clinical trial of a novel antianginal agent. (Circulation, 1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Perhexilene
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SMILESC1CCC(CC1)C(CC2CCCCN2)C3CCCCC3
-
InChIKeyCYXKNKQEMFBLER-UHFFFAOYSA-N
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