TAS-116
TAS-116 Basic information
- Product Name:
- TAS-116
- Synonyms:
-
- TAS 116;TAS116
- 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
- TAS-116
- 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]-
- Des-iPr-TAS-116
- Pimitespib (TAS-116)
- Pimitespib
- inhibit,HSP,TAS 116,TAS116,Pimitespib,Heat shock proteins,Inhibitor
- CAS:
- 1260533-36-5
- MF:
- C25H26N8O
- MW:
- 454.53
- Mol File:
- 1260533-36-5.mol
TAS-116 Chemical Properties
- 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)
- color
- White to off-white
TAS-116 Usage And Synthesis
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
Target | Value |
HSP90β (Cell-free assay) | 21.3 nM(Ki) |
HSP90α (Cell-free assay ) | 34.7 nM(Ki) | tr>
TAS-116Supplier
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