U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C13H11ClN2O2S
Molecular Weight 294.757
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NUCLOMEDONE

SMILES

ClC1=CC=C(CC2C(=O)N=C3SCCN3C2=O)C=C1

InChI

InChIKey=QSKVYHYMQQQAFS-UHFFFAOYSA-N
InChI=1S/C13H11ClN2O2S/c14-9-3-1-8(2-4-9)7-10-11(17)15-13-16(12(10)18)5-6-19-13/h1-4,10H,5-7H2

HIDE SMILES / InChI

Molecular Formula C13H11ClN2O2S
Molecular Weight 294.757
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Nuclomedone (TEI-3096), a thiazolopyrimidine compound has been shown to suppress adjuvant arthritis in rats without any effect on conventional inflammation. TEI-3096 also enhanced the delayed type hypersensitivity in mice and rats. These results suggests that TEI-3096 restores the abnormal immune response. Nuclomedone was discovered by Teijin and investigated as a potential treatment for rheumatoid arthritis and inflammatory disorders.

Approval Year

PubMed

PubMed

TitleDatePubMed
Immunopharmacological profile of TEI-3096: a new immunomodulator.
1982-1983
Inhibitory effect of TI-31 on autoimmune nephritis in NZB/NZW F1 mice through regulation of the immune response.
1987 Apr
Anti-arthritic and immunoregulatory effects of TI-31 on collagen-induced arthritis.
1987 Nov
Characterization of immunomodulating action of TI-31 on antibody response in mice.
1991 Aug
Patents

Patents

Sample Use Guides

Oral Nuclomedone (TI-31) treatment in doses of 10 and 50 mg/kg daily for 7 days prior to collagen immunization depressed the development of arthritis in rats.
Route of Administration: Oral
In Vitro Use Guide
Nuclomedone (TI-31), at concentrations of 10 and 100 uM, suppressed the antibody response to T cell-dependent (sheep red blood cells, SRBC) and -independent antigens (trinitrophenyl-lipopolysaccharide, TNP-LPS and TNP-Ficoll).
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:48:30 GMT 2023
Edited
by admin
on Sat Dec 16 15:48:30 GMT 2023
Record UNII
MR28U787Z2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NUCLOMEDONE
INN  
INN  
Official Name English
TEI-3096
Code English
TI-31
Code English
nuclomedone [INN]
Common Name English
5H-THIAZOLO(3,2-A)PYRIMIDINE-5,7(6H)-DIONE, 6-((4-CHLOROPHENYL)METHYL)-2,3-DIHYDRO-
Systematic Name English
NUCLOMEDONE [JAN]
Common Name English
(±)-6-(P-CHLOROBENZYL)-2,3-DIHYDRO-5H-THIAZOLO(3,2-A)PYRIMIDINE-5,7(6H)-DIONE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
Code System Code Type Description
CAS
75963-52-9
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
NCI_THESAURUS
C72930
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
SMS_ID
100000083626
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
PUBCHEM
128798
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
EVMPD
SUB09388MIG
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106465
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID2046208
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
FDA UNII
MR28U787Z2
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
INN
6122
Created by admin on Sat Dec 16 15:48:30 GMT 2023 , Edited by admin on Sat Dec 16 15:48:30 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY