| Identification | Back Directory | [Name]
INO5042 | [CAS]
14782-19-5 | [Synonyms]
INO5042
Naphtho[2,3-d]thiazole-4,9-dione, 2-(2-furanyl)- | [Molecular Formula]
C15H7NO3S | [MDL Number]
MFCD31544375 | [MOL File]
14782-19-5.mol | [Molecular Weight]
281.29 |
| Chemical Properties | Back Directory | [Boiling point ]
504.1±42.0 °C(Predicted) | [density ]
1.481±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO: 2 mg/mL (7.11 mM; ultrasonic and adjust pH to 3 with HCl) | [form ]
Solid | [pka]
-1.80±0.20(Predicted) | [color ]
Yellow to orange |
| Hazard Information | Back Directory | [Uses]
INO5042, a thiazole fused 1,4-naphthoquinone compound, and exhibits anti-inflammation activity[1][2]. | [References]
[1] Renard M, et al. Induced changes of leukocyte slow rolling in an in flow pharmacological model of adhesion to endothelial cells. Biorheology. 2003;40(1-3):173-8. PMID:12454402
[2] Fosse C, et, al. Parameters and mechanistic studies on the oxidative ring cleavage of synthetic heterocyclic naphthoquinones by Streptomyces strains. Appl Microbiol Biotechnol. 2004 Sep;65(4):446-56. DOI:10.1007/s00253-004-1588-4 |
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