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Details

Stereochemistry ACHIRAL
Molecular Formula C15H19N5
Molecular Weight 269.3449
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIZATRIPTAN

SMILES

CN(C)CCC1=CNC2=C1C=C(CN3C=NC=N3)C=C2

InChI

InChIKey=ULFRLSNUDGIQQP-UHFFFAOYSA-N
InChI=1S/C15H19N5/c1-19(2)6-5-13-8-17-15-4-3-12(7-14(13)15)9-20-11-16-10-18-20/h3-4,7-8,10-11,17H,5-6,9H2,1-2H3

HIDE SMILES / InChI

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

Description
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.

Originator

Curator's Comment: # Merck Sharp and Dohme Ltd.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
10.1 nM [Ki]
3.0 nM [EC50]
140.0 nM [Ki]
7.9 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
MAXALT

Approved Use

MAXALT 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 Date

1998
Primary
MAXALT

Approved Use

MAXALT 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 Date

1998
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
6.2 ng/mL
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
12.7 ng/mL
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
28.6 ng/mL
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
44.8 ng/mL
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
6.1 ng/mL
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
13.2 ng/mL
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
32.1 ng/mL
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
54 ng/mL
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
27.29 ng/mL
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
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
16 ng × h/mL
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
33 ng × h/mL
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
72 ng × h/mL
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
127 ng × h/mL
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
19 ng × h/mL
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
42 ng × h/mL
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
97 ng × h/mL
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
161 ng × h/mL
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
68 ng × h/mL
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
84 ng × h/mL
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
69.88 ng × h/mL
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
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
2.1 h
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
2.2 h
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
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
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
2.2 h
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
2.4 h
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
2.6 h
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
2.4 h
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
2.9 h
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
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
Doses

Doses

DosePopulationAdverse events​
10 mg single, oral
Recommended
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 17 years
Health Status: unhealthy
Age Group: 17 years
Sex: F
Sources:
Other AEs: Jaundice...
Other AEs:
Jaundice
Sources:
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
Health Status: unhealthy
Age Group: 25 years
Sex: M
Sources:
Other AEs: Syncope, Incontinence...
Other AEs:
Syncope (1 patient)
Incontinence (1 patient)
Sources:
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25-29 years
Health Status: unhealthy
Age Group: 25-29 years
Sex: M+F
Sources:
Other AEs: Dizziness...
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
Health Status: unhealthy
Age Group: 29 years
Sex: F
Sources:
Other AEs: Vomiting, Bradycardia...
Other AEs:
Vomiting (1 patient)
Bradycardia (1 patient)
Sources:
10 mg 2 times / day multiple, oral
Recommended
Dose: 10 mg, 2 times / day
Route: oral
Route: multiple
Dose: 10 mg, 2 times / day
Sources:
unhealthy, 43 years
Health Status: unhealthy
Age Group: 43 years
Sex: M
Sources:
Disc. AE: Transient ischemic attack...
AEs leading to
discontinuation/dose reduction:
Transient ischemic attack
Sources:
AEs

AEs

AESignificanceDosePopulation
Jaundice
10 mg single, oral
Recommended
Dose: 10 mg
Route: oral
Route: single
Dose: 10 mg
Sources:
unhealthy, 17 years
Health Status: unhealthy
Age Group: 17 years
Sex: F
Sources:
Incontinence 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
Health Status: unhealthy
Age Group: 25 years
Sex: M
Sources:
Syncope 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25 years
Health Status: unhealthy
Age Group: 25 years
Sex: M
Sources:
Dizziness 2 patients
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 25-29 years
Health Status: unhealthy
Age Group: 25-29 years
Sex: M+F
Sources:
Bradycardia 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
Health Status: unhealthy
Age Group: 29 years
Sex: F
Sources:
Vomiting 1 patient
80 mg single, oral
Overdose
Dose: 80 mg
Route: oral
Route: single
Dose: 80 mg
Sources:
unhealthy, 29 years
Health Status: unhealthy
Age Group: 29 years
Sex: F
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
Sources:
unhealthy, 43 years
Health Status: unhealthy
Age Group: 43 years
Sex: M
Sources:
PubMed

PubMed

TitleDatePubMed
Fast onset medications through thermally generated aerosols.
2004-05
Naratriptan for the treatment of acute migraine: meta-analysis of randomised controlled trials.
2004-02
Evaluating triptan usage.
2004-02
Neuronal expression and regulation of CGRP promoter activity following viral gene transfer into cultured trigeminal ganglia neurons.
2004-01-30
Productivity cost benefit to employers of treating migraine with rizatriptan: a specific worksite analysis and model.
2004-01
Defeating migraine pain with triptans: a race against the development of cutaneous allodynia.
2004-01
CNS effects of sumatriptan and rizatriptan.
2004-01
[It impairs quality of life and work time. Migraine therapy should not be left to the patients!].
2003-11-27
Meta-analysis of oral triptan therapy for migraine: number needed to treat and relative cost to achieve relief within 2 hours.
2003-11-14
Cost-effectiveness of almotriptan and rizatriptan in the treatment of acute migraine.
2003-11
Patient-reported benefits of rizatriptan compared with usual non-triptan therapy for migraine in a primary care setting.
2003-11
Triptans for treatment of acute pediatric migraine: a systematic literature review.
2003-11
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.
2003-11
Rizatriptan RPD for severe migraine in the emergency department--a multicenter study.
2003-10
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.
2003-10
Migraine: diagnosis and management.
2003-09-27
Almotriptan versus rizatriptan in patients with migraine in Spain.
2003-08-02
Migraine treatment patterns and patient satisfaction with prior therapy: a substudy of a multicenter trial of rizatriptan effectiveness.
2003-07
Eletriptan metabolism by human hepatic CYP450 enzymes and transport by human P-glycoprotein.
2003-07
[Highly selective beginning. Associated symptoms and side effects in retrospect].
2003-05-26
Migraine headache recurrence: relationship to clinical, pharmacological, and pharmacokinetic properties of triptans.
2003-04
Safety profile of the triptans.
2003-03
Real-world experiences in migraine therapy with rizatriptan.
2003-03
[New therapeutic recommendations for severe migraine. High beginning dosage rather than slow dosage increase].
2003-01-30
Endothelium-dependent relaxant responses to selective 5-HT(1B/1D) receptor agonists in the isolated middle cerebral artery of the rat.
2003-01-22
Coprescription of triptans with potentially interacting medications: a cohort study involving 240,268 patients.
2003-01
Newer formulations of the triptans: advances in migraine management.
2003
Pharmacological approaches to migraine.
2003
Crossover comparison of efficacy and preference for rizatriptan 10 mg versus ergotamine/caffeine in migraine.
2003
[Satisfaction and recovery of normal activity with rizatriptan 10 mg. Results from the open, prospective, observational 4M study].
2002-12
[New onset headache. Which patients should be sent for CT imaging?].
2002-10-24
Further evaluation of rizatriptan in menstrual migraine: retrospective analysis of long-term data.
2002-10
Determinants of migraine-specific quality of life.
2002-10
Sum of Pain Intensity Differences (SPID) in migraine trials. A comment based on four rizatriptan trials.
2002-10
Triptans (serotonin, 5-HT1B/1D agonists) in migraine: detailed results and methods of a meta-analysis of 53 trials.
2002-10
Comparison of rizatriptan and other triptans on stringent measures of efficacy.
2002-09-10
Comparison of rizatriptan and other triptans on stringent measures of efficacy.
2002-09-10
Rizatriptan 5mg is not efficacious for migraine in adolescents.
2002-09
Mechanisms of action of the 5-HT1B/1D receptor agonists.
2002-07
The effect of rizatriptan, ergotamine, and their combination on human peripheral arteries: a double-blind, placebo-controlled, crossover study in normal subjects.
2002-07
Gateways to Clinical Trials. June 2002.
2002-06
Rizatriptan combined with rofecoxib vs. rizatriptan for the acute treatment of migraine: an open label pilot study.
2002-05
[Treatment of migraine in patients with hypertension and ischemic heart disease].
2002-01-20
An introduction to migraine: from ancient treatment to functional pharmacology and antimigraine therapy.
2002
Impact of migraine symptoms on health care use and work loss in Canada in patients randomly assigned in a phase III clinical trial.
2002
Restoring migraine sufferers' ability to function normally: a comparison of rizatriptan and other triptans in randomized trials.
2002
Spotlight on rizatriptan in migraine.
2002
Comparative aspects of triptans in treating migraine.
2001
Rizatriptan: pharmacological differences from sumatriptan and clinical results.
2001
Sumatriptan: pharmacological basis and clinical results.
2001
Patents

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
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 Mon Mar 31 18:12:13 GMT 2025
Edited
by admin
on Mon Mar 31 18:12:13 GMT 2025
Record UNII
51086HBW8G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
L-705126
Preferred Name English
RIZATRIPTAN
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
RIZATRIPTAN [MI]
Common Name English
MK-462 FREE BASE
Code English
Rizatriptan [WHO-DD]
Common Name English
rizatriptan [INN]
Common Name English
RIZATRIPTAN [VANDF]
Common Name English
1H-INDOLE-3-ETHANAMINE, N,N-DIMETHYL-5-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-
Systematic Name English
Classification Tree Code System Code
NDF-RT N0000175765
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
NCI_THESAURUS C47794
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
NDF-RT N0000175764
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
WHO-ATC N02CC04
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
NDF-RT N0000175763
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
WHO-VATC QN02CC04
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
LIVERTOX 857
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
Code System Code Type Description
SMS_ID
100000080246
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
NCI_THESAURUS
C61930
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
MERCK INDEX
m9640
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY Merck Index
FDA UNII
51086HBW8G
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
DRUG CENTRAL
2393
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
DAILYMED
51086HBW8G
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
EVMPD
SUB10346MIG
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
LACTMED
Rizatriptan
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
MESH
C093622
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
WIKIPEDIA
Rizatriptan
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
ChEMBL
CHEMBL905
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
PUBCHEM
5078
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
DRUG BANK
DB00953
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID2023565
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
CHEBI
48273
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
RXCUI
88014
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY RxNorm
IUPHAR
51
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
CAS
144034-80-0
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
INN
7474
Created by admin on Mon Mar 31 18:12:13 GMT 2025 , Edited by admin on Mon Mar 31 18:12:13 GMT 2025
PRIMARY
Related Record Type Details
EXCRETED UNCHANGED
Approximately 26 and 14% of i.v. and oral rizatriptan doses, respectively, were excreted in urine as intact parent drug
URINE
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SOLVATE->ANHYDROUS
Related Record Type Details
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
after oral (10-mg)
URINE
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
The mono N-desmethyl metabolite has intrinsic potency that is about 3-fold lower. Its contribution to in vivo efficacy is probably very low or negligible, since circulating concentrations are about one-tenth those of the parent drug
METABOLITE -> PARENT
after i.v. (3-mg)
URINE
Related Record Type Details
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
Tmax PHARMACOKINETIC ORAL ADMINISTRATION