| Weight | 269.352 g/mol |
|---|---|
| Formula | C15H19N5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 5 |
rizatriptan (145202-66-0, 144034-80-0)
Score:
#113 in Neurology
,
#537 in Neuroscience
,
#2456 in Biology
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#3059 in Chemistry
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- Oral Rizatriptan Versus Oral Sumatriptan: A Direct Comparative Study in the Acute Treatment of Migraine (Headache, 1998)
- Crossover Comparison of Rizatriptan 5 mg and 10 mg Versus Sumatriptan 25 mg and 50 mg in Migraine (Headache, 1998)
- Rizatriptan has central antinociceptive effects against durally evoked responses (European Journal of Pharmacology, 1997)
- A placebo-controlled crossover study of rizatriptan in the treatment of multiple migraine attacks (Neurology, 1998)
- The novel anti-migraine agent rizatriptan inhibits neurogenic dural vasodilation and extravasation (European Journal of Pharmacology, 1997)
- Rizatriptan 5 mg for the acute treatment of migraine in adolescents: A randomized, double-blind, placebo-controlled study (Headache, 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)CN3C=NC=N3
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InChIKeyULFRLSNUDGIQQP-UHFFFAOYSA-N
- Pubchem - rizatriptan
- Wikipedia - rizatriptan
Rizatriptan (trade name Maxalt) is a 5-HT1 receptor agonist of the triptan class of drugs developed by Merck & Co. for the treatment of migraine headaches. It is available in strengths of 5 and 10 mg as tablets and orally disintegrating tablets (Maxalt-MLT).
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