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Details

Stereochemistry ACHIRAL
Molecular Formula C30H26F6N4O2
Molecular Weight 588.5435
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ANTRAFENINE

SMILES

FC(F)(F)C1=CC2=C(C=C1)C(NC3=C(C=CC=C3)C(=O)OCCN4CCN(CC4)C5=CC(=CC=C5)C(F)(F)F)=CC=N2

InChI

InChIKey=NWGGKKGAFZIVBJ-UHFFFAOYSA-N
InChI=1S/C30H26F6N4O2/c31-29(32,33)20-4-3-5-22(18-20)40-14-12-39(13-15-40)16-17-42-28(41)24-6-1-2-7-25(24)38-26-10-11-37-27-19-21(30(34,35)36)8-9-23(26)27/h1-11,18-19H,12-17H2,(H,37,38)

HIDE SMILES / InChI
Antrafenine (SL 73033 or 2-[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]ethyl 2-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoate) showed marked analgesic activity, long duration of action, and excellent tolerance in pharmacological and toxicological studies. Antrafenine exerts anti-inflammatory effects. It has been studied in the treatment of osteoarthritis.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Ionized fluorine in the plasma and urine of subjects treated with organofluorine drugs prescribed in rheumatology].
1979 Feb
Synthesis and analgesic activities of some (4-substituted phenyl-1-piperazinyl)alkyl 2-aminobenzoates and 2-aminonicotinates.
1979 May
A double blind study of antrafenine, naproxen and placebo in osteoarthrosis.
1983
Antrafenine, naproxen and placebo in osteoarthritis: a comparative study.
1983 May
Antrafenine: anti-inflammatory activity with respect to oedema and leucocyte infiltration in the rat.
1984 Feb
In-vivo metabolism in the rat and mouse of antrafenine to 1-m-trifluoromethylphenylpiperazine.
1985 Jan
[Identification of a metabolite of floctafenine in urinary calculi].
1987
Name Type Language
ANTRAFENINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
antrafenine [INN]
Common Name English
Antrafenine [WHO-DD]
Common Name English
ANTRAFENINE [MI]
Common Name English
2-(4-(.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-M-TOLYL)-1-PIPERAZINYL)ETHYL N-(7-(TRIFLUOROMETHYL)-4-QUINOLYL)ANTHRANILATE
Systematic Name English
ANTRAFENINE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
Code System Code Type Description
INN
3939
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID60203833
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
PUBCHEM
68723
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL345524
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
MESH
C017014
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
MERCK INDEX
m52
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
ANTRAFENINE
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
CAS
55300-29-3
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
DRUG CENTRAL
3677
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
DRUG BANK
DB01419
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
NCI_THESAURUS
C72107
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
EVMPD
SUB05530MIG
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
SMS_ID
100000086973
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY
FDA UNII
21FS93Y6OE
Created by admin on Fri Dec 15 15:28:58 UTC 2023 , Edited by admin on Fri Dec 15 15:28:58 UTC 2023
PRIMARY