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 | C15H19N5 |
Molecular Weight | 269.3449 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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 |
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 Date1998 |
|||
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 Date1998 |
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 |
---|---|---|
Characterisation of the 5-HT receptor binding profile of eletriptan and kinetics of [3H]eletriptan binding at human 5-HT1B and 5-HT1D receptors. | 1999 Mar 5 |
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Rizatriptan: pharmacological differences from sumatriptan and clinical results. | 2001 |
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Sumatriptan: pharmacological basis and clinical results. | 2001 |
|
Comparison of preference for rizatriptan 10-mg wafer versus sumatriptan 50-mg tablet in migraine. | 2001 |
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[Current topics: expectation for new triptans]. | 2001 Apr 10 |
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Rizatriptan wafer--sublingual vs. placebo at the onset of acute migraine. | 2001 Feb |
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Influence of beta-adrenoceptor antagonists on the pharmacokinetics of rizatriptan, a 5-HT1B/1D agonist: differential effects of propranolol, nadolol and metoprolol. | 2001 Jul |
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Establishing a standard of speed for assessing the efficacy of the serotonin(1B/1D) agonists (triptans). | 2001 Jul |
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Acute treatment of migraine and the role of triptans. | 2001 Mar |
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Evidence-based migraine therapy. | 2001 Nov |
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[Cost effectiveness of treatment with triptanes in Spain]. | 2001 Nov 16-30 |
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Pharmacokinetics of rizatriptan in healthy elderly subjects. | 2001 Oct |
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Effect of rizatriptan and other triptans on the nausea symptom of migraine: a post hoc analysis. | 2001 Sep |
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What matters is not the differences between triptans, but the differences between patients. | 2001 Sep |
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Restoring migraine sufferers' ability to function normally: a comparison of rizatriptan and other triptans in randomized trials. | 2002 |
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Rizatriptan: an update of its use in the management of migraine. | 2002 |
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[Satisfaction and recovery of normal activity with rizatriptan 10 mg. Results from the open, prospective, observational 4M study]. | 2002 Dec |
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Rizatriptan 5 mg for the acute treatment of migraine in adolescents: a randomized, double-blind, placebo-controlled study. | 2002 Jan |
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[Treatment of migraine in patients with hypertension and ischemic heart disease]. | 2002 Jan 20 |
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Mechanisms of action of the 5-HT1B/1D receptor agonists. | 2002 Jul |
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The effect of rizatriptan, ergotamine, and their combination on human peripheral arteries: a double-blind, placebo-controlled, crossover study in normal subjects. | 2002 Jul |
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Gateways to Clinical Trials. June 2002. | 2002 Jun |
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Rizatriptan combined with rofecoxib vs. rizatriptan for the acute treatment of migraine: an open label pilot study. | 2002 May |
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CNS effects of sumatriptan and rizatriptan in healthy female volunteers. | 2002 May |
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Triptans (serotonin, 5-HT1B/1D agonists) in migraine: detailed results and methods of a meta-analysis of 53 trials. | 2002 Oct |
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[New onset headache. Which patients should be sent for CT imaging?]. | 2002 Oct 24 |
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Comparison of rizatriptan and other triptans on stringent measures of efficacy. | 2002 Sep 10 |
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Coprescription of triptans with potentially interacting medications: a cohort study involving 240,268 patients. | 2003 Jan |
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[New therapeutic recommendations for severe migraine. High beginning dosage rather than slow dosage increase]. | 2003 Jan 30 |
|
Safety profile of the triptans. | 2003 Mar |
|
Real-world experiences in migraine therapy with rizatriptan. | 2003 Mar |
|
[Highly selective beginning. Associated symptoms and side effects in retrospect]. | 2003 May 26 |
|
Cost-effectiveness of almotriptan and rizatriptan in the treatment of acute migraine. | 2003 Nov |
|
Triptans for treatment of acute pediatric migraine: a systematic literature review. | 2003 Nov |
|
Investigation of the effects of naratriptan, rizatriptan, and sumatriptan on jugular venous oxygen saturation in anesthetized pigs: implications for their mechanism of acute antimigraine action. | 2003 Oct |
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Naratriptan for the treatment of acute migraine: meta-analysis of randomised controlled trials. | 2004 Feb |
|
Evaluating triptan usage. | 2004 Feb |
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Productivity cost benefit to employers of treating migraine with rizatriptan: a specific worksite analysis and model. | 2004 Jan |
|
Defeating migraine pain with triptans: a race against the development of cutaneous allodynia. | 2004 Jan |
|
Neuronal expression and regulation of CGRP promoter activity following viral gene transfer into cultured trigeminal ganglia neurons. | 2004 Jan 30 |
|
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
by
admin
on
Edited
Fri Dec 15 16:30:39 GMT 2023
by
admin
on
Fri Dec 15 16:30:39 GMT 2023
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Record UNII |
WR978S7QHH
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Record Status |
Validated (UNII)
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C47794
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237082
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HH-46
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CHEMBL905
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DB00953
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758919
Created by
admin on Fri Dec 15 16:30:40 GMT 2023 , Edited by admin on Fri Dec 15 16:30:40 GMT 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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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |