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
SMILES
CCOC(=O)C1=C(C2=CC(OC)=C(OC)C=C2)C3=C(C=C(OC)C(OC)=C3)N=C1CN4C=NC=N4
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
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.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8880222
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8880222
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
Edited
Fri Dec 15 15:28:41 GMT 2023
by
admin
on
Fri Dec 15 15:28:41 GMT 2023
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Record UNII |
W6RZK26FCB
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Record Status |
Validated (UNII)
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Record Version |
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FDA ORPHAN DRUG |
112698
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158146-85-1
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153980
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W6RZK26FCB
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admin on Fri Dec 15 15:28:41 GMT 2023 , Edited by admin on Fri Dec 15 15:28:41 GMT 2023
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