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LN-939026

GDC-0077 , 0.99summer , 2060571-02-8

CAS NO.:2060571-02-8

Empirical Formula: C18H19F2N5O4

Molecular Weight: 407.37

MDL number:

Update time: 2023-04-23

PRODUCT Properties

Boiling point: 698.0±65.0 °C(Predicted)
Density  1.63±0.1 g/cm3(Predicted)
storage temp.  Store at -20°C
solubility  DMSO:110.0(Max Conc. mg/mL);245.47(Max Conc. mM)
pka 15.89±0.50(Predicted)
form  Solid
color  Off-white to yellow
InChIKey SGEUNORSOZVTOL-CABZTGNLSA-N
SMILES C(N)(=O)[C@@H](NC1C=C2OCCN3C=C(N4[C@H](C(F)F)COC4=O)N=C3C2=CC=1)C

Description and Uses

Inavolisib, or GDC-0077, is a potent and selective PI3K inhibitor. GDC-0077 blocks an enzyme involved in cancer growth called PI3K. GDC0077 binds to and inhibits various members of the PI3K family, including activating mutations in the catalytic alpha isoform PIK3CA. PI3K inhibition prevents the activation of the PI3K-mediated signaling pathway and inhibits the growth and survival of PI3K-overexpressing tumor cells. The IUPAC name of this compound is (S)-2-((2-((S)-4-(difluoromethyl)-2-oxooxazolidin-3-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl)amino)propanamide.

Inavolisib (GDC-0077) is a potent, orally active, and selective PI3Kα inhibitor (IC50=0.038 nM). Inavolisib exerts its activity by binding to the ATP binding site of PI3K, thereby inhibiting the phosphorylation of PIP2 to PIP3. Inavolisib is more selective for mutant versus wild-type PI3Kα. Inavolisib can be used for the study of breast cancer[1].

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