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Details

Stereochemistry ACHIRAL
Molecular Formula C12H16N2S
Molecular Weight 220.334
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XYLAZINE

SMILES

CC1=CC=CC(C)=C1NC2=NCCCS2

InChI

InChIKey=BPICBUSOMSTKRF-UHFFFAOYSA-N
InChI=1S/C12H16N2S/c1-9-5-3-6-10(2)11(9)14-12-13-7-4-8-15-12/h3,5-6H,4,7-8H2,1-2H3,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C12H16N2S
Molecular Weight 220.334
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 15:47:44 UTC 2023
Edited
by admin
on Fri Dec 15 15:47:44 UTC 2023
Record UNII
2KFG9TP5V8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XYLAZINE
INN   MART.   MI   USP   USP-RS  
INN  
Official Name English
xylazine [INN]
Common Name English
XYLAZINE [USP-RS]
Common Name English
XYLAZINE [USP MONOGRAPH]
Common Name English
XYLAZINE [MART.]
Common Name English
XYLAZINE [MI]
Common Name English
NSC-758142
Code English
Tranq component xylazine
Common Name English
XYLAZINE [GREEN BOOK]
Common Name English
5,6-Dihydro-2-(2,6-xylidino)-4H-1,3-thiazine
Systematic Name English
CHANAZINE
Brand Name English
Classification Tree Code System Code
WHO-VATC QN05CM92
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
CFR 21 CFR 522.2662
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
NCI_THESAURUS C29709
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
Code System Code Type Description
NSC
758142
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
CAS
7361-61-7
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL297362
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
FDA UNII
2KFG9TP5V8
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
MESH
D014991
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
EVMPD
SUB00120MIG
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
MERCK INDEX
m11547
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB11477
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
ECHA (EC/EINECS)
230-902-1
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
NCI_THESAURUS
C75049
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
CHEBI
92386
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
EPA CompTox
DTXSID3040643
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
WIKIPEDIA
XYLAZINE
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
PUBCHEM
5707
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
INN
2663
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
SMS_ID
100000079362
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
DAILYMED
2KFG9TP5V8
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
RXCUI
1099660
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY RxNorm
RS_ITEM_NUM
1720407
Created by admin on Fri Dec 15 15:47:44 UTC 2023 , Edited by admin on Fri Dec 15 15:47:44 UTC 2023
PRIMARY
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SALT/SOLVATE -> PARENT
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MAJOR
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IMPURITY -> PARENT
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ACTIVE MOIETY