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Details

Stereochemistry ACHIRAL
Molecular Formula C17H12Cl2N4
Molecular Weight 343.21
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIAZOLAM

SMILES

CC1=NN=C2CN=C(C3=C(Cl)C=CC=C3)C4=C(C=CC(Cl)=C4)N12

InChI

InChIKey=JOFWLTCLBGQGBO-UHFFFAOYSA-N
InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3

HIDE SMILES / InChI

Molecular Formula C17H12Cl2N4
Molecular Weight 343.21
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 15:22:47 UTC 2023
Edited
by admin
on Fri Dec 15 15:22:47 UTC 2023
Record UNII
1HM943223R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIAZOLAM
HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
USAN   INN  
Official Name English
TRIAZOLAM [HSDB]
Common Name English
N05CD05
Code English
TRIAZOLAM [JAN]
Common Name English
U-33,030
Code English
TRIAZOLAM [MART.]
Common Name English
TRIAZOLAM [VANDF]
Common Name English
4H-(1,2,4)TRIAZOLO(4,3-A)(1,4)BENZODIAZEPINE, 8-CHLORO-6-(2-CHLOROPHENYL)-1-METHYL-
Systematic Name English
Triazolam [WHO-DD]
Common Name English
TRIAZOLAM [MI]
Common Name English
U-33030
Code English
triazolam [INN]
Common Name English
TRIAZOLAM [USAN]
Common Name English
TRIAZOLAM [ORANGE BOOK]
Common Name English
TRIAZOLAM [USP MONOGRAPH]
Common Name English
8-CHLORO-6-(O-CHLOROPHENYL)-1-METHYL-4H-S-TRIAZOLO(4,3-A)(1,4)BENZODIAZEPINE
Common Name English
TRIAZOLAM CIV [USP-RS]
Common Name English
HALCION
Brand Name English
TRIAZOLAM CIV
USP-RS  
Common Name English
Classification Tree Code System Code
WHO-VATC QN05CD05
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
NDF-RT N0000007542
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
NCI_THESAURUS C1012
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
NDF-RT N0000175694
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
LIVERTOX NBK547843
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
DEA NO. 2887
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
WHO-ATC N05CD05
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
Code System Code Type Description
FDA UNII
1HM943223R
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
HSDB
6759
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
DRUG CENTRAL
2729
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
DRUG BANK
DB00897
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
EPA CompTox
DTXSID6046763
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
MERCK INDEX
m11035
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY Merck Index
SMS_ID
100000092518
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
ECHA (EC/EINECS)
249-307-3
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
WIKIPEDIA
TRIAZOLAM
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
ChEMBL
CHEMBL646
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
PUBCHEM
5556
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
CAS
28911-01-5
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
INN
3409
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
MESH
D014229
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
RXCUI
10767
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY RxNorm
IUPHAR
7313
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
LACTMED
Triazolam
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
RS_ITEM_NUM
1680506
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
NCI_THESAURUS
C29520
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
CHEBI
9674
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
EVMPD
SUB11258MIG
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
DAILYMED
1HM943223R
Created by admin on Fri Dec 15 15:22:47 UTC 2023 , Edited by admin on Fri Dec 15 15:22:47 UTC 2023
PRIMARY
Related Record Type Details
BINDER->LIGAND
BINDING
METABOLIC ENZYME -> SUBSTRATE
METABOLIC ENZYME -> SUBSTRATE
Related Record Type Details
METABOLITE -> PARENT
METABOLITE -> PARENT
METABOLITE ACTIVE -> PARENT
METABOLITE ACTIVE -> PARENT
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC