Ipatasertib

Ipatasertib
Clinical data
Routes of; administration	PO
ATC code	None;
Identifiers
	IUPAC name (S)-2-(4-Chlorophenyl)-1-(4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)-3-(isopropylamino)propan-1-one;
ChemSpider	28189084;
KEGG	D10641 ;
CompTox Dashboard (EPA)	DTXSID101025595 ;
Chemical and physical data
Formula	C24H32ClN5O2
Molar mass	458.00 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(C)NC[C@@H](C(=O)N1CCN(CC1)C1=C2[C@H](C)C[C@@H](O)C2=NC=N1)C1=CC=C(Cl)C=C1;
	InChI InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1; Key:GRZXWCHAXNAUHY-NSISKUIASA-N;

Ipatasertib (RG7440) is an experimental cancer drug in development by Roche. It is a small molecule inhibitor of Akt. It was discovered by Array Biopharma and is currently in phase II trials for treatment of breast cancer.^[1]

In vitro, ipatasertib showed activity against all three isoforms of Akt.^[2]

References

^ https://www.clinicaltrials.gov/ct2/show/NCT02301988
^ Lin K, Friedman L, Gloor S, Gross S, Liederer BM, Mitchell I, et al. Preclinical characterization of GDC-0068, a novel selective ATP competitive inhibitor of Akt. 22nd-EORTC-NCI-AACR-2010 2010; abstr. 79

[1] ttps://www.clinicaltrials.gov/ct2/show/NCT02301988

[2] Lin K, Friedman L, Gloor S, Gross S, Liederer BM, Mitchell I, et al. Preclinical characterization of GDC-0068, a novel selective ATP competitive inhibitor of Akt. 22nd-EORTC-NCI-AACR-2010 2010; abstr. 79

[1]

[2]