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Details

Stereochemistry ACHIRAL
Molecular Formula C19H22N2
Molecular Weight 278.3914
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of TRIPROLIDINE

SMILES

CC1=CC=C(C=C1)C(=C/CN2CCCC2)\C3=CC=CC=N3

InChI

InChIKey=CBEQULMOCCWAQT-WOJGMQOQSA-N
InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+

HIDE SMILES / InChI
Molecular Formula C19H22N2
Molecular Weight 278.3914
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:19:58 UTC 2023
Edited
by admin
on Fri Dec 15 15:19:58 UTC 2023
Record UNII
2L8T9S52QM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIPROLIDINE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
TRIPROLIDINE [MI]
Common Name English
Triprolidine [WHO-DD]
Common Name English
TRIPROLIDINE [VANDF]
Common Name English
TRIPROLIDINE [HSDB]
Common Name English
triprolidine [INN]
Common Name English
Classification Tree Code System Code
LIVERTOX NBK548164
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
WHO-VATC QR06AX07
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
WHO-ATC R06AX07
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
Code System Code Type Description
EVMPD
SUB11323MIG
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
DRUG BANK
DB00427
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
WIKIPEDIA
TRIPROLIDINE
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
DRUG CENTRAL
2763
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID3023718
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-627-0
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
IUPHAR
1228
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL855
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
CHEBI
84116
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
NCI_THESAURUS
C61992
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
SMS_ID
100000076950
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
FDA UNII
2L8T9S52QM
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
RXCUI
10849
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY RxNorm
MESH
D014311
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
DAILYMED
2L8T9S52QM
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
PUBCHEM
5282443
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
CAS
486-12-4
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
HSDB
6316
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
MERCK INDEX
m11192
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY Merck Index
INN
502
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
LACTMED
Triprolidine
Created by admin on Fri Dec 15 15:19:58 UTC 2023 , Edited by admin on Fri Dec 15 15:19:58 UTC 2023
PRIMARY
Related Record Type Details
HISTAMINE H1 RECEPTOR
TARGET -> INHIBITOR
Structure of TRIPROLIDINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Structure of TRIPROLIDINE HYDROCHLORIDE ANHYDROUS
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of TRIPROLIDINE
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