ChemicalBook--->CAS DataBase List--->1260533-36-5

1260533-36-5

1260533-36-5 Structure

1260533-36-5 Structure
IdentificationBack Directory
[Name]

TAS-116
[CAS]

1260533-36-5
[Synonyms]

TAS-116
TAS 116;TAS116
Des-iPr-TAS-116
3-ethyl-4-{3-isopropyl-4-(4-(1-methyl-1H-pyrazol-4-yl)-1H-imidazol-1-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}benzamide
Benzamide, 3-ethyl-4-[3-(1-methylethyl)-4-[4-(1-methyl-1H-pyrazol-4-yl)-1H-imidazol-1-yl]-1H-pyrazolo[3,4-b]pyridin-1-yl]-
[Molecular Formula]

C25H26N8O
[MDL Number]

MFCD28502196
[MOL File]

1260533-36-5.mol
[Molecular Weight]

454.53
Chemical PropertiesBack Directory
[Boiling point ]

661.7±55.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: soluble
[form ]

A solid
[pka]

15.43±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Biological Activity]

TAS-116 is a novel small molecule inhibitor of HSP90 with Ki values of 34.7 nmol/L and 21.3 nmol/L for HSP90α and HSP90β, respectively. It does not inhibit other ATPases such as HSP70 (IC50 >200 μmol/L).
[in vitro]

TAS-116 is a selective inhibitor of HSP90α and HSP90β in the cytoplasm, but has no inhibitory effect on endoplasmic reticulum GRP94 or mitochondrial TRAP1. Treatment of HCT116 cells with 0.3 μM of TAS-1116 for 8 hours resulted in a decrease in DDR1 levels and induction of HSP70.

[in vivo]

In a mouse model with human xenograft tumors, oral administration of TAS-116 induced tumor shrinkage accompanied by depletion of HSP90. In a rat model, TAS-116 was more distributed in subcutaneously xenografted NCI-H1975 non-small cell lung cancer tumors than in the retina. TAS-116 was also active in orthotopically transplanted NCI-H1975 lung tumors.
[target]

TargetValue
HSP90β
(Cell-free assay)
21.3 nM(Ki)
HSP90α
(Cell-free assay )
34.7 nM(Ki)
[storage]

Store at -20°C
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