| Weight | 326.49 g/mol |
|---|---|
| Formula | C16H30CaO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Calcium valproate (33433-82-8)
Valproic Acid · Valproate · Divalproex
Score:
#1174 in Neuroscience
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#5069 in Biology
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#6556 in Chemistry
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- Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells (The EMBO Journal, 2001)
- Histone Deacetylase Is a Direct Target of Valproic Acid, a Potent Anticonvulsant, Mood Stabilizer, and Teratogen (Journal of Biological Chemistry, 2001)
- A Comparison of Valproate with Carbamazepine for the Treatment of Complex Partial Seizures and Secondarily Generalized TonicClonic Seizures in Adults (The New England Journal of Medicine, 1992)
- Polycystic ovaries and hyperandrogenism in women taking valproate for epilepsy (The New England Journal of Medicine, 1993)
- The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: an unblinded randomised controlled trial. (The Lancet, 2007)
- The mood-stabilizing agents lithium and valproate robustly increase the levels of the neuroprotective protein bcl-2 in the CNS (Journal of Neurochemistry, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Valproic Acid
- Valproate
- Divalproex
- Depakote
- Sodium Valproate
- Depakene
- Divalproex Sodium
- Valproate Sodium
- Depakine
- 2 Propylpentanoic Acid
- 2-Propylpentanoic Acid
- Valproate Calcium
- Dipropyl Acetate
- Propylisopropylacetic Acid
- Convulsofin
- Valproic Acid, Sodium Salt (2:1)
- Ergenyl
- Vupral
- Magnesium Valproate
- Semisodium Valproate
-
SMILESCCCC(CCC)C(=O)[O-].CCCC(CCC)C(=O)[O-].[Ca+2]
-
InChIKeyPIZHURYFCSGTJX-UHFFFAOYSA-L
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