DUP-697 Chemical Properties

storage temp. 

2-8°C

solubility 

DMF: 54 mg/ml; DMF:PBS (pH 7.2) (1:1): 0.5 mg/ml; DMSO: 15 mg/ml; Ethanol: 7 mg/ml

form 

White to off-white solid.

color 

White to off-white

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-36

DUP-697 Usage And Synthesis

Description

DuP-697 is a member of the diaryl heterocycle group of selective COX-2 inhibitors which includes MK-966 (rofecoxib), SC-58125, and celecoxib. DuP-697 is a potent and time-dependent inhibitor of COX-2. When tested on isolated recombinant enzymes, DuP-697 is at least 50 times more potent in the inhibition of COX-2 than COX-1. The IC₅₀ values for human recombinant COX-2 are 80 and 40 nM at 5 and 10 minutes, respectively. The IC₅₀ for the inhibition of human recombinant COX-1 after the same time intervals is 9 μM. DuP-697 also attenuates the COX-1 inhibitory activity of non-selective COX inhibitors such as indomethacin.

Uses

DuP-697 is a thiophene that inhibits COX-2 and acts as a NSAID.

Definition

ChEBI: DuP 697 is a member of thiophenes.

Biological Activity

Potent and selective inhibitor of cyclooxygenase-2 (IC 50 values are 10 and 800 nM for COX-2 and COX-1 respectively). Inhibits prostaglandin synthesis and is anti-inflammatory in vivo . Orally active.

storage

Store at +4°C

DUP-697(88149-94-4)Related Product Information

• NS-398
• Indometacin
• Piroxicam
• (S)-(+)-Ibuprofen
• Ibuprofen
• Phenidone
• (R)-(-)-IBUPROFEN
• 4-[5-(4-CHLOROPHENYL)-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-1-YL]BENZENESULFONAMIDE
• Meloxicam
• Naproxen
• MECLOFENAMATE SODIUM
• SC-560
• Sulindac sulfide
• APHS
• N-(2-PHENYLETHYL)-INDOMETHACIN AMIDE
• 2-(4-Fluorophenyl)-thiophene
• DUP-697
• 2-BROMO-5-PHENYLTHIOPHENE