| Identification | Back Directory | [Name]
N-[2-[3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-2-quinoxalinecarboxamide | [CAS]
925434-55-5 | [Synonyms]
SRT1720 free base/ STR1720 HCl salt
SRT1720 - CAS 925434-55-5 - Calbiochem
N-[2-[3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl]phenyl]-2-quinoxalinecarboxamide
N-(2-(3-(piperazin-1-ylmethyl)imidazo[2,1-b]thiazol-6-yl)phenyl)quinoxaline-2-carboxamide
2-QuinoxalinecarboxaMide, N-[2-[3-(1-piperazinylMethyl)iMidazo[2,1-b]thiazol-6-yl]phenyl]-
N-[2-[3-(piperazin-1-ylmethyl)imidazo[2,1-b][1,3]thiazol-6-yl]phenyl]quinoxaline-2-carboxamide
Quinoxaline-2-carboxylic acid [2-(3-piperazin-1-ylmethyl-imidazo[2,1-b]thiazol-6-yl)-phenyl]-amide | [Molecular Formula]
C25H23N7OS | [MDL Number]
MFCD14584468 | [MOL File]
925434-55-5.mol | [Molecular Weight]
469.56 |
| Chemical Properties | Back Directory | [Melting point ]
221℃ | [density ]
1.46 | [storage temp. ]
-20C | [solubility ]
DMSO:5.0(Max Conc. mg/mL);10.65(Max Conc. mM) | [form ]
Yellow solid | [pka]
11.19±0.70(Predicted) | [color ]
Light yellow to yellow |
| Hazard Information | Back Directory | [General Description]
A cell-permeable quinolinecarboxamide compound that is shown to inhibit the mitochondrial SIRT3 in a substrate AceCS2-competitive (Ki = 0.56 μM; Km = 2.44 μM), but NAD+-uncompetitive (Ki = 0.34 μM; Km = 280 μM), manner. Also reported to decrease cellular p53 Lys382 acetylation (Effective conc. = 10 μM in U2OS and MEF cultures) and inhibit p300 HAT activity (IC50 = 9 μM) in vitro, as well as offer therapeutic benefits in several murine and rodent type 2 diabetes models (100 mg/kg/dayl p.o.) in vivo. Whether and how SRT1720 activates SIRT1 activity remains uncertain. Also available as a 25 mM solution in DMSO (Cat. No. 530748). | [storage]
Store at -20°C |
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