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Details

Stereochemistry ACHIRAL
Molecular Formula C12H11N7
Molecular Weight 253.2626
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIAMTERENE

SMILES

NC1=NC2=C(N=C(C3=CC=CC=C3)C(N)=N2)C(N)=N1

InChI

InChIKey=FNYLWPVRPXGIIP-UHFFFAOYSA-N
InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)

HIDE SMILES / InChI

Molecular Formula C12H11N7
Molecular Weight 253.2626
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 Sat Dec 16 04:48:13 UTC 2023
Edited
by admin
on Sat Dec 16 04:48:13 UTC 2023
Record UNII
WS821Z52LQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIAMTERENE
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
DYAZIDE COMPONENT TRIAMTERENE
Common Name English
SK&F 8542
Code English
TRIAMTERENE [USP MONOGRAPH]
Common Name English
2,4,7-PTERIDINETRIAMINE, 6-PHENYL-
Systematic Name English
TRIAMTERENE COMPONENT OF DYAZIDE
Common Name English
NSC-639359
Code English
TRIAMTERENE [ORANGE BOOK]
Common Name English
TRIAMTERENE [JAN]
Common Name English
TRIAMTERENE [USAN]
Common Name English
TRIAMTERENE [IARC]
Common Name English
TRIAMTERENE [USP IMPURITY]
Common Name English
TRIAMTERENE [USP-RS]
Common Name English
TRIAMTERENE [MART.]
Common Name English
triamterene [INN]
Common Name English
SK-8542
Code English
MAXZIDE COMPONENT TRIAMTERENE
Common Name English
2,4,7-Triamino-6-phenylpteridine
Systematic Name English
NSC-77625
Code English
TRIAMTERENE [HSDB]
Common Name English
SK&F-8542
Code English
TRIAMTERENE [MI]
Common Name English
TRIAMTERENE [VANDF]
Common Name English
TRIAMTERENE COMPONENT OF MAXZIDE
Common Name English
TRIAMTERENE [EP MONOGRAPH]
Common Name English
Triamterene [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC C03DB02
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
NDF-RT N0000175418
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
NCI_THESAURUS C49186
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
LIVERTOX NBK547859
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
NDF-RT N0000175359
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
WHO-VATC QC03DB02
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
NDF-RT N0000008859
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
Code System Code Type Description
NSC
77625
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
RS_ITEM_NUM
1680007
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
ChEMBL
CHEMBL585
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
CAS
396-01-0
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
PUBCHEM
5546
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
DRUG BANK
DB00384
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
LACTMED
Triamterene
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
SMS_ID
100000092570
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
WIKIPEDIA
TRIAMTERENE
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
NCI_THESAURUS
C29519
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
RXCUI
10763
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY RxNorm
NSC
639359
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
HSDB
3405
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
EVMPD
SUB11256MIG
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
DRUG CENTRAL
2728
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
EPA CompTox
DTXSID6021373
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
MESH
D014223
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
MERCK INDEX
m11030
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY Merck Index
IUPHAR
4329
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
INN
1266
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
ECHA (EC/EINECS)
206-904-3
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
DAILYMED
WS821Z52LQ
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
CHEBI
9671
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
FDA UNII
WS821Z52LQ
Created by admin on Sat Dec 16 04:48:13 UTC 2023 , Edited by admin on Sat Dec 16 04:48:13 UTC 2023
PRIMARY
Related Record Type Details
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
BINDER->LIGAND
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
USP
Related Record Type Details
METABOLITE ACTIVE -> PARENT
METABOLITE ACTIVE -> PARENT
Related Record Type Details
IMPURITY -> PARENT
For the calculation of contents, multiply the peak areas by 1.5
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
For the calculation of contents, multiply the peak areas by 1.8
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
EP
Related Record Type Details
ACTIVE MOIETY