| Weight | 335.473 g/mol |
|---|---|
| Formula | C17H25N3O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
Almotriptan (181183-52-8, 154323-57-6)
Score:
#105 in Neurology
,
#504 in Neuroscience
,
#2344 in Biology
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- Early vs. non-early intervention in acute migraineAct when Mild (AwM). A double-blind, placebo-controlled trial of almotriptan (Cephalalgia, 2008)
- WithinPatient Early Versus Delayed Treatment of Migraine Attacks With Almotriptan: The Sooner the Better (Headache, 2002)
- Consistent efficacy and tolerability of almotriptan in the acute treatment of multiple migraine attacks: results of a large, randomized, double-blind, placebo-controlled study (Cephalalgia, 2000)
- Efficacy and Tolerability of Almotriptan in Adolescents: A Randomized, Double-Blind, Placebo-Controlled Trial (Headache, 2008)
- Early intervention with almotriptan improves sustained pain-free response in acute migraine. (Headache, 2003)
- Almotriptan is an effective and well-tolerated treatment for migraine pain: results of a randomized, double-blind, placebo-controlled clinical trial (Cephalalgia, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN(C)CCC1=CNC2=C1C=C(C=C2)CS(=O)(=O)N3CCCC3
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- Pubchem - Almotriptan
- Wikipedia - almotriptan
Almotriptan (trade name Axert and others) is a triptan drug discovered and developed by Almirall for the treatment of heavy migraine headache.
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Almotriptan
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