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ChemicalBook--->CAS DataBase List--->1203494-49-8

1203494-49-8

1203494-49-8 Structure

1203494-49-8 Structure
IdentificationBack Directory
[Name]

DASA-58
[CAS]

1203494-49-8
[Synonyms]

DASA-58
CS-1563
DASA58; DASA 58
3-[[4-[(2,3-Dihydro-1,4-benzodioxin-6-yl)sulfonyl]hexahydro-1H-1,4-diazepin-1-yl]sulfonyl]benzenamine
Benzenamine, 3-[[4-[(2,3-dihydro-1,4-benzodioxin-6-yl)sulfonyl]hexahydro-1H-1,4-diazepin-1-yl]sulfonyl]-
[Molecular Formula]

C19H23N3O6S2
[MDL Number]

MFCD29472280
[MOL File]

1203494-49-8.mol
[Molecular Weight]

453.53
Chemical PropertiesBack Directory
[Boiling point ]

681.5±65.0 °C(Predicted)
[density ]

1.453±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[solubility ]

insoluble in EtOH; insoluble in H2O; ≥127.2 mg/mL in DMSO
[form ]

solid
[pka]

3.35±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Description]

DASA-58 is a selective activator of pyruvate kinase M2 (PKM2; AC50 = 38 nM in vitro, EC50 = 19.6 μM in cells). DASA-58 converts PKM2 to a constitutively active enzyme state that is resistant to inhibition by tyrosine-phosphorylated proteins. Through its effects on PKM2, DASA-58 blocks the induction of HIF-1α by lipopolysaccharide in bone marrow-derived macrophages, suppressing the expression of several HIF-1α-dependent targets, including IL-1β. It also impairs metastatic dissemination of prostate cancer PCa cells in SCID mice.
[Uses]

DASA-58 is a potential pyruvate kinase isozyme (PKM2) allosteric activator. DASA-58 can be used for the research of metabolism and kinds of cancer[1].
[Definition]

ChEBI: 3-[[4-(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)-1,4-diazepan-1-yl]sulfonyl]aniline is a member of benzenes and a sulfonamide.
[References]

[1]. anastasiou d, yu y, israelsen wj, et al. pyruvate kinase m2 activators promote tetramer formation and suppress tumorigenesis. nature chemical biology, 2012, 8(10): 839-847.
Spectrum DetailBack Directory
[Spectrum Detail]

DASA-58(1203494-49-8)1HNMR
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