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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=CC=C(CN3C=NC=N3)C=C12

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

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:53:26 UTC 2023
Edited
by admin
on Fri Dec 15 15:53:26 UTC 2023
Record UNII
51086HBW8G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
L-705126
Code 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 Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
NDF-RT N0000175764
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
WHO-ATC N02CC04
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
NDF-RT N0000175763
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
WHO-VATC QN02CC04
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
LIVERTOX 857
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
Code System Code Type Description
SMS_ID
100000080246
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
NCI_THESAURUS
C61930
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
MERCK INDEX
m9640
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY Merck Index
FDA UNII
51086HBW8G
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
DRUG CENTRAL
2393
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
DAILYMED
51086HBW8G
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
EVMPD
SUB10346MIG
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
LACTMED
Rizatriptan
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
MESH
C093622
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
WIKIPEDIA
Rizatriptan
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
ChEMBL
CHEMBL905
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
PUBCHEM
5078
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
DRUG BANK
DB00953
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
EPA CompTox
DTXSID2023565
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
CHEBI
48273
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
RXCUI
88014
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY RxNorm
IUPHAR
51
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
CAS
144034-80-0
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
PRIMARY
INN
7474
Created by admin on Fri Dec 15 15:53:26 UTC 2023 , Edited by admin on Fri Dec 15 15:53:26 UTC 2023
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