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ChemicalBook--->CAS DataBase List--->1353644-70-8

1353644-70-8

1353644-70-8 Structure

1353644-70-8 Structure
IdentificationBack Directory
[Name]

(3aR,6aR)-N-(4-((3-ethynylphenyl)amino)-7-methoxyquinazolin-6-yl)-1-methylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxamide
[CAS]

1353644-70-8
[Synonyms]

HMPL309
HMPL-309
HMPL 309
EOS-61583
Theliatinib
Theliatinib (HMPL-309)
ThTheliatinib (HMPL-309)
HMPL-309;HMPL 309;HMPL309
(3aR,6aR)-N-(4-((3-ethynylphenyl)amino)-7-methoxyquinazolin-6-yl)-1-methylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxamide
[Molecular Formula]

C25H26N6O2
[MDL Number]

MFCD32173988
[MOL File]

1353644-70-8.mol
[Molecular Weight]

442.51
Chemical PropertiesBack Directory
[Boiling point ]

675.6±55.0 °C(Predicted)
[density ]

1.35±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 5 mg/mL (11.30 mM)
[form ]

Solid
[pka]

13.59±0.20(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Biological Activity]

Theliatinib (HMPL-309) is a potent EGFR inhibitor with a Ki value of 0.05 nM for EGFR and IC50 values of 3 nM and 22 nM for EGFR and EGFR T790M/L858R mutant, respectively. It is more than 50-fold selective for EGFR over 72 other kinases.
[in vitro]

Compared with erlotinib or gefitnib, theliatinib has stronger binding affinity to wild-type EGFR and is more difficult to be replaced by ATP, which makes theliatinib have better target binding effect, and the EGFR-activated tumors have stronger antitumor activity.
[in vivo]

Theliatinib has concentration-dependent antitumor activity in a series of patient-derived esophageal cancer xenograft models. But aberrant activation or genetic mutation of other targets such as PI3K and FGFR attenuates the antitumor activity of EGFR inhibitors, especially theliatinib.

[target]

< td style="border-bottom: 1px dotted #ccc;padding: 5px;"> 3 nM
TargetValue
WT EGFR
(Cell-free assay)
EGFR T790M/L858R
(Cell-free assay)
22 nM
[storage]

Store at -20°C
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