Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H19N5.C7H6O2 |
Molecular Weight | 391.4662 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=CC=C1.CN(C)CCC2=CNC3=CC=C(CN4C=NC=N4)C=C23
InChI
InChIKey=JPRXYLQNJJVCMZ-UHFFFAOYSA-N
InChI=1S/C15H19N5.C7H6O2/c1-19(2)6-5-13-8-17-15-4-3-12(7-14(13)15)9-20-11-16-10-18-20;8-7(9)6-4-2-1-3-5-6/h3-4,7-8,10-11,17H,5-6,9H2,1-2H3;1-5H,(H,8,9)
Molecular Formula | C7H6O2 |
Molecular Weight | 122.1213 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C15H19N5 |
Molecular Weight | 269.3449 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including
https://www.drugbank.ca/drugs/DB00953 | https://www.drugs.com/pro/rizatriptan-orally-disintegrating-tablets.html | http://reference.medscape.com/drug/maxalt-maxalt-mlt-rizatriptan-343033 | https://www.ncbi.nlm.nih.gov/pubmed/9357514
Curator's Comment: description was created based on several sources, including
https://www.drugbank.ca/drugs/DB00953 | https://www.drugs.com/pro/rizatriptan-orally-disintegrating-tablets.html | http://reference.medscape.com/drug/maxalt-maxalt-mlt-rizatriptan-343033 | https://www.ncbi.nlm.nih.gov/pubmed/9357514
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. 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. Rizatriptan acts as an agonist at serotonin 5-HT1B and 5-HT1D receptors. Rizatriptan binds with high affinity to human cloned 5-HT1B/1D receptors. Rizatriptan benzoate presumably exerts its therapeutic effects in the treatment of a migraine headache by binding to 5-HT1B/1D receptors located on intracranial blood vessels and sensory nerves of the trigeminal system. Rizatriptan is completely absorbed following oral administration. The mean oral absolute bioavailability of the rizatriptan benzoate tablet is about 45%, and mean peak plasma concentrations are reached in approximately 1-1.5 hours. The presence of a migraine headache did not appear to affect the absorption or pharmacokinetics of rizatriptan. Food has no significant effect on the bioavailability of rizatriptan but delays the time to reach peak concentration by an hour. The primary route of rizatriptan metabolism is via oxidative deamination by monoamine oxidase-A (MAO-A) to the indole acetic acid metabolite, which is not active at the 5-HT1B/1D receptor. N-mono-desmethyl-rizatriptan, a metabolite with activity similar to that of parent compound at the 5-HT1B/1D receptor, is formed to a minor degree. Plasma concentrations of N-mono-desmethyl-rizatriptan are approximately 14% of those of parent compound, and it is eliminated at a similar rate. Other minor metabolites, the N-oxide, the 6-hydroxy compound, and the sulfate conjugate of the 6-hydroxy metabolite are not active at the 5-HT1B/1D receptor.
CNS Activity
Originator
Sources: http://www.google.com/patents/EP0497512B1
Curator's Comment: # Merck Sharp and Dohme Ltd.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1898 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9986723 |
10.1 nM [Ki] | ||
Target ID: CHEMBL1983 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9986723 |
3.0 nM [EC50] | ||
Target ID: CHEMBL214 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9986723 |
140.0 nM [Ki] | ||
Target ID: CHEMBL224 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7752204 |
7.9 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | MAXALT Approved UseMAXALT is indicated for the acute treatment of migraine attacks with or without aura in adults. MAXALT is not intended for the prophylactic therapy of migraine or for use in the management of hemiplegic or basilar migraine (see CONTRAINDICATIONS). Safety and effectiveness of MAXALT have not been established for cluster headache, which is present in an older, predominantly male population. Launch Date8.9907842E11 |
|||
Primary | MAXALT Approved UseMAXALT is indicated for the acute treatment of migraine attacks with or without aura in adults. MAXALT is not intended for the prophylactic therapy of migraine or for use in the management of hemiplegic or basilar migraine (see CONTRAINDICATIONS). Safety and effectiveness of MAXALT have not been established for cluster headache, which is present in an older, predominantly male population. Launch Date8.9907842E11 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
44.8 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
6.2 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
54 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
6.1 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
12.7 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
13.2 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
27.29 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/16432269/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
28.6 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
32.1 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
127 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
16 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
161 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
19 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
33 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
42 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
68 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
69.88 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/16432269/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
72 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
84 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
97 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.1 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
15 mg single, oral dose: 15 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
2.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
2.5 mg single, oral dose: 2.5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
2.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
2.9 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
4 mg single, intravenous dose: 4 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
2.6 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10233200/ |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
RIZATRIPTAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
10 mg single, oral Recommended |
unhealthy, 17 years n = 1 Health Status: unhealthy Age Group: 17 years Sex: F Population Size: 1 Sources: |
Other AEs: Jaundice... |
80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 25 years n = 2 Health Status: unhealthy Age Group: 25 years Sex: M Population Size: 2 Sources: |
Other AEs: Syncope, Incontinence... Other AEs: Syncope (1 patient) Sources: Incontinence (1 patient) |
80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 25-29 years n = 2 Health Status: unhealthy Age Group: 25-29 years Sex: M+F Population Size: 2 Sources: |
Other AEs: Dizziness... Other AEs: Dizziness (2 patients) Sources: |
80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 29 years n = 2 Health Status: unhealthy Age Group: 29 years Sex: F Population Size: 2 Sources: |
Other AEs: Vomiting, Bradycardia... Other AEs: Vomiting (1 patient) Sources: Bradycardia (1 patient) |
10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Co-administed with:: tacrolimus(8.5 mg/day; oral) Sources: |
unhealthy, 43 years n = 1 Health Status: unhealthy Age Group: 43 years Sex: M Population Size: 1 Sources: |
Disc. AE: Transient ischemic attack... AEs leading to discontinuation/dose reduction: Transient ischemic attack Sources: |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Jaundice | 10 mg single, oral Recommended |
unhealthy, 17 years n = 1 Health Status: unhealthy Age Group: 17 years Sex: F Population Size: 1 Sources: |
|
Incontinence | 1 patient | 80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 25 years n = 2 Health Status: unhealthy Age Group: 25 years Sex: M Population Size: 2 Sources: |
Syncope | 1 patient | 80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 25 years n = 2 Health Status: unhealthy Age Group: 25 years Sex: M Population Size: 2 Sources: |
Dizziness | 2 patients | 80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 25-29 years n = 2 Health Status: unhealthy Age Group: 25-29 years Sex: M+F Population Size: 2 Sources: |
Bradycardia | 1 patient | 80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 29 years n = 2 Health Status: unhealthy Age Group: 29 years Sex: F Population Size: 2 Sources: |
Vomiting | 1 patient | 80 mg single, oral Overdose Dose: 80 mg Route: oral Route: single Dose: 80 mg Sources: |
unhealthy, 29 years n = 2 Health Status: unhealthy Age Group: 29 years Sex: F Population Size: 2 Sources: |
Transient ischemic attack | Disc. AE | 10 mg 2 times / day multiple, oral Recommended Dose: 10 mg, 2 times / day Route: oral Route: multiple Dose: 10 mg, 2 times / day Co-administed with:: tacrolimus(8.5 mg/day; oral) Sources: |
unhealthy, 43 years n = 1 Health Status: unhealthy Age Group: 43 years Sex: M Population Size: 1 Sources: |
PubMed
Title | Date | PubMed |
---|---|---|
Triptans in migraine: a comparative review of pharmacology, pharmacokinetics and efficacy. | 2000 Dec |
|
Comparative aspects of triptans in treating migraine. | 2001 |
|
Comparison of preference for rizatriptan 10-mg wafer versus sumatriptan 50-mg tablet in migraine. | 2001 |
|
Pharmacokinetics and pharmacodynamics of the triptan antimigraine agents: a comparative review. | 2001 |
|
[Current topics: expectation for new triptans]. | 2001 Apr 10 |
|
The anti-migraine 5-HT(1B/1D) agonist rizatriptan inhibits neurogenic dural vasodilation in anaesthetized guinea-pigs. | 2001 Aug |
|
A systematic review of the use of triptans in acute migraine. | 2001 Feb |
|
Influence of beta-adrenoceptor antagonists on the pharmacokinetics of rizatriptan, a 5-HT1B/1D agonist: differential effects of propranolol, nadolol and metoprolol. | 2001 Jul |
|
Establishing a standard of speed for assessing the efficacy of the serotonin(1B/1D) agonists (triptans). | 2001 Jul |
|
Migraine treatment outcomes with rizatriptan in triptan-naive patients: a naturalistic study. | 2001 Jun |
|
Meta-analysis of rizatriptan efficacy in randomized controlled clinical trials. | 2001 Mar |
|
Efficacy and tolerability of rizatriptan 10 mg in migraine: experience with 70 527 patient episodes. | 2001 Mar |
|
Oral triptans (serotonin 5-HT(1B/1D) agonists) in acute migraine treatment: a meta-analysis of 53 trials. | 2001 Nov 17 |
|
Triptans in the treatment of basilar migraine and migraine with prolonged aura. | 2001 Nov-Dec |
|
Effect of rizatriptan and other triptans on the nausea symptom of migraine: a post hoc analysis. | 2001 Sep |
|
[Satisfaction and recovery of normal activity with rizatriptan 10 mg. Results from the open, prospective, observational 4M study]. | 2002 Dec |
|
Impact of migraine symptoms on health care use and work loss in Canada in patients randomly assigned in a phase III clinical trial. | 2002 Fall |
|
Migraine: diagnosis, management, and new treatment options. | 2002 Feb |
|
Molecular cloning and expression of the porcine trigeminal ganglion cDNA encoding a 5-ht(1F) receptor. | 2002 Feb 1 |
|
[Treatment of migraine in patients with hypertension and ischemic heart disease]. | 2002 Jan 20 |
|
The effect of rizatriptan, ergotamine, and their combination on human peripheral arteries: a double-blind, placebo-controlled, crossover study in normal subjects. | 2002 Jul |
|
Gateways to Clinical Trials. June 2002. | 2002 Jun |
|
Pharmacological treatments for acute migraine: quantitative systematic review. | 2002 Jun |
|
Rizatriptan combined with rofecoxib vs. rizatriptan for the acute treatment of migraine: an open label pilot study. | 2002 May |
|
[New meta-analysis of triptanes. Concrete help, so the choice doesn't become overwhelming]. | 2002 May 6 |
|
Further evaluation of rizatriptan in menstrual migraine: retrospective analysis of long-term data. | 2002 Oct |
|
Triptans (serotonin, 5-HT1B/1D agonists) in migraine: detailed results and methods of a meta-analysis of 53 trials. | 2002 Oct |
|
[New onset headache. Which patients should be sent for CT imaging?]. | 2002 Oct 24 |
|
Comparison of rizatriptan and other triptans on stringent measures of efficacy. | 2002 Sep 10 |
|
Newer formulations of the triptans: advances in migraine management. | 2003 |
|
Crossover comparison of efficacy and preference for rizatriptan 10 mg versus ergotamine/caffeine in migraine. | 2003 |
|
Migraine headache recurrence: relationship to clinical, pharmacological, and pharmacokinetic properties of triptans. | 2003 Apr |
|
Coprescription of triptans with potentially interacting medications: a cohort study involving 240,268 patients. | 2003 Jan |
|
Meta-analysis of oral triptan therapy for migraine: number needed to treat and relative cost to achieve relief within 2 hours. | 2003 Jan-Feb |
|
Eletriptan metabolism by human hepatic CYP450 enzymes and transport by human P-glycoprotein. | 2003 Jul |
|
Almotriptan versus rizatriptan in patients with migraine in Spain. | 2003 Jul-Aug |
|
Safety profile of the triptans. | 2003 Mar |
|
Real-world experiences in migraine therapy with rizatriptan. | 2003 Mar |
|
Triptans for treatment of acute pediatric migraine: a systematic literature review. | 2003 Nov |
|
An in vitro interethnic comparison of monoamine oxidase activities between Japanese and Caucasian livers using rizatriptan, a serotonin receptor 1B/1D agonist, as a model drug. | 2003 Nov |
|
[It impairs quality of life and work time. Migraine therapy should not be left to the patients!]. | 2003 Nov 27 |
|
Endothelium-dependent relaxant responses to selective 5-HT(1B/1D) receptor agonists in the isolated middle cerebral artery of the rat. | 2003 Nov-Dec |
|
Naratriptan for the treatment of acute migraine: meta-analysis of randomised controlled trials. | 2004 Feb |
|
Evaluating triptan usage. | 2004 Feb |
|
Defeating migraine pain with triptans: a race against the development of cutaneous allodynia. | 2004 Jan |
|
CNS effects of sumatriptan and rizatriptan. | 2004 Jan |
|
Fast onset medications through thermally generated aerosols. | 2004 May |
Sample Use Guides
5-10 mg PO at onset of symptoms; repeat dose after 2 hours if necessary; not to exceed 30 mg/24 hr
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9357514
Rizatriptan intrinsic efficacy, expressed as percent of the maximal 5-HT response, was measured in cloned human 5-HT1D and 5-HT1B receptors stably expressed in CHO cells using agonist-induced [35S]GTPγS binding. In this assay, interaction of the agonist-occupied receptor with the G-protein results in dissociation of GDP from the G-protein R-subunit and the binding of a molecule of GTP. Under normal conditions the R-subunit dissociates from the âγ-subunits and, following modulation of its effector, intrinsic R-subunit GTPase hydrolyzes the GTP to GDP. Because [35S]GTPγS is resistant to this GTPase, it accumulates in the membrane and it can be measured by virtue of its radiolabel
Substance Class |
Chemical
Created
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admin
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Record UNII |
WR978S7QHH
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C47794
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145202-66-0
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DTXSID20162937
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237082
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HH-46
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CHEMBL905
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C47708
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WR978S7QHH
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WR978S7QHH
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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100000090268
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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1604880
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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M9640
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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PRIMARY | Merck Index | ||
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DB00953
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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758919
Created by
admin on Wed Jul 05 23:56:30 UTC 2023 , Edited by admin on Wed Jul 05 23:56:30 UTC 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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LABELED -> NON-LABELED | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
EP
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
USP
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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||
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |