Weight | 143.23 g/mol |
---|---|
Formula | C8H17NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
Valpromide (2430-27-5)
valproic acid amide · dipropylacetamide · Depamide
Score:
#214 in Neurology
,
#977 in Neuroscience
,
#4290 in Biology
,
#5412 in Chemistry
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- Inhibition of human liver microsomal epoxide hydrolase by valproate and valpromide: In vitro/in vivo correlation (Clinical Pharmacology & Therapeutics, 1989)
- Clinical Pharmacology of Valpromide (Clinical Pharmacokinectics, 1991)
- StructurePharmacokinetic Relationships in a Series of Valpromide Derivatives with Antiepileptic Activity (Pharmaceutical Research, 1989)
- Valnoctamide, valpromide and valnoctic acid are much less teratogenic in mice than valproic acid (Epilepsy Research, 1998)
- Sodium Valproate and Valpromide: Differential Interactions with Carbamazepine in Epileptic Patients (Epilepsia, 1986)
- Valproic acid amide in the treatment of affective and schizoaffective disorders (Journal of Affective Disorders, 1984)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - valproic acid amide
- dipropylacetamide
- Depamide
-
SMILESCCCC(CCC)C(=O)N
-
InChIKeyOMOMUFTZPTXCHP-UHFFFAOYSA-N
- Pubchem - Valpromide
- Wikipedia - valpromide
Valpromide (marketed as Depamide by Sanofi-Aventis) is a carboxamide derivative of valproic acid used in the treatment of epilepsy and some affective disorders. It is rapidly metabolised (80%) to valproic acid (another anticonvulsant) but has anticonvulsant properties itself. It may produce more stable plasma levels than valproic acid or sodium valproate and may be more effective at preventing febrile seizures.
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