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Details

Stereochemistry ACHIRAL
Molecular Formula C25H26N4O6
Molecular Weight 478.4971
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TAK-603

SMILES

CCOC(=O)C1=C(CN2C=NC=N2)N=C3C=C(OC)C(OC)=CC3=C1C4=CC=C(OC)C(OC)=C4

InChI

InChIKey=CLQRMSBSMHXMMC-UHFFFAOYSA-N
InChI=1S/C25H26N4O6/c1-6-35-25(30)24-18(12-29-14-26-13-27-29)28-17-11-22(34-5)21(33-4)10-16(17)23(24)15-7-8-19(31-2)20(9-15)32-3/h7-11,13-14H,6,12H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C25H26N4O6
Molecular Weight 478.4971
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

TAK-603 is a quinoline derivative, originally developed as a anti-rheumatic drug. TAK-603 selectively suppresses Th1 cytokine production. In animal models TAK-603 has the ability to suppress the immune system and protect cartilage from destruction. The development of TAK-603 has been discontinued.

Approval Year

Sample Use Guides

In adjuvant arthritic (AA) rats, TAK-603 inhibited the hind paw swelling and the body weight loss. The minimum effective dose was 3.13 mg/kg/day (p.o.).
Route of Administration: Oral
In Vitro Use Guide
TAK-603 suppressed the mitogen-induced proliferation of mouse lymphocytes and the ConA-induced IFN-gamma and IL-2 production by rat lymphocytes at 0.1 to 10 uM
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:58:25 GMT 2025
Edited
by admin
on Mon Mar 31 17:58:25 GMT 2025
Record UNII
W6RZK26FCB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TAK-603
Common Name English
3-QUINOLINECARBOXYLIC ACID, 4-(3,4-DIMETHOXYPHENYL)-6,7-DIMETHOXY-2-(1H-1,2,4-TRIAZOL-1-YLMETHYL)-, ETHYL ESTER
Preferred Name English
ETHYL 4-(3,4-DIMETHOXYPHENYL)-6,7-DIMETHOXY-2-(1,2,4-TRIAZOL-1-YLMETHYL)QUINOLINE-3-CARBOXYLATE
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 112698
Created by admin on Mon Mar 31 17:58:25 GMT 2025 , Edited by admin on Mon Mar 31 17:58:25 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID30166380
Created by admin on Mon Mar 31 17:58:25 GMT 2025 , Edited by admin on Mon Mar 31 17:58:25 GMT 2025
PRIMARY
CAS
158146-85-1
Created by admin on Mon Mar 31 17:58:25 GMT 2025 , Edited by admin on Mon Mar 31 17:58:25 GMT 2025
PRIMARY
PUBCHEM
153980
Created by admin on Mon Mar 31 17:58:25 GMT 2025 , Edited by admin on Mon Mar 31 17:58:25 GMT 2025
PRIMARY
FDA UNII
W6RZK26FCB
Created by admin on Mon Mar 31 17:58:25 GMT 2025 , Edited by admin on Mon Mar 31 17:58:25 GMT 2025
PRIMARY