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Details

Stereochemistry RACEMIC
Molecular Formula C20H22N2O4
Molecular Weight 354.3997
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TILNOPROFEN ARBAMEL

SMILES

CC(C(=O)OCC(=O)N(C)C)C1=CC2=C(OC3=C(C2)C=CC(C)=N3)C=C1

InChI

InChIKey=ZAKRMJAETCUYKK-UHFFFAOYSA-N
InChI=1S/C20H22N2O4/c1-12-5-6-15-10-16-9-14(7-8-17(16)26-19(15)21-12)13(2)20(24)25-11-18(23)22(3)4/h5-9,13H,10-11H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C20H22N2O4
Molecular Weight 354.3997
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/7996395

N,N-Dimethylcarbamoylmethyl alpha,2-dimethyl-5H-[1]- benzopyrano[2,3-b]pyridine-7-acetate (Y-23023/ Tilnoprofen arbamel) is a prodrug developed as a new non-steroidal anti-inflammatory drug (NSAID), by Yoshitomi and Japan Tobacco for treatment pain in Rheumatoid arthritis, but was discontinued. Y-23023 is rapidly hydrolysed to an active metabolite, alpha,2-dimethyl-5H-[1]benzopyrano[2,3-b]pyridine-7-acetic acid (TILNOPROFENIC ACID), cyclo-oxygenase inhibitor.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Inhibition by cyclo-oxygenase inhibitors of interleukin-6 production by human peripheral blood mononuclear cells.
1991
[Mechanism of analgesic action of Y-23023, a new non-steroidal anti-inflammatory drug].
1995 Oct
Patents

Patents

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
Y-9223 (TILNOPROFENIC ACID), a novel cyclo-oxygenase inhibitor, inhibited the increases in the IL-6 level in the culture medium of both mitogen-stimulated adherent cells and non-adherent cells fractionated from mononuclear cells of human peripheral blood. Northern blotting showed that the mitogen-induced increase in the expression of IL-6 mRNA was inhibited by Y-9223, indicating that this agent inhibits IL-6 biosynthesis.
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:44:43 GMT 2023
Edited
by admin
on Sat Dec 16 16:44:43 GMT 2023
Record UNII
HY45T0EF6G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TILNOPROFEN ARBAMEL
INN  
INN  
Official Name English
(±)-.ALPHA.,2-DIMETHYL-5H-(1)-BENZOPYRANO(2,3-B)PYRIDINE-7-ACETIC ACID, ESTER WITH N,N-DIMETHYLGLYCOLAMIDE
Common Name English
MEPRANOPROFEN ARBAMEL
JAN  
Common Name English
tilnoprofen arbamel [INN]
Common Name English
MEPRANOPROFEN ARBAMEL [JAN]
Common Name English
Y-23023
Code English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
Code System Code Type Description
EVMPD
SUB11055MIG
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
ChEMBL
CHEMBL1968603
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
INN
7397
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
MESH
C063558
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
PUBCHEM
164072
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
CAS
159098-79-0
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
SUPERSEDED
CAS
118635-52-2
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
SMS_ID
100000082698
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
NCI_THESAURUS
C76820
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID4048852
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
FDA UNII
HY45T0EF6G
Created by admin on Sat Dec 16 16:44:43 GMT 2023 , Edited by admin on Sat Dec 16 16:44:43 GMT 2023
PRIMARY
Related Record Type Details
METABOLITE ACTIVE -> PRODRUG
Related Record Type Details
ACTIVE MOIETY