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Details

Stereochemistry ACHIRAL
Molecular Formula C17H20F3N7O2
Molecular Weight 411.3816
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BIMIRALISIB

SMILES

NC1=NC=C(C2=NC(=NC(=N2)N3CCOCC3)N4CCOCC4)C(=C1)C(F)(F)F

InChI

InChIKey=ADGGYDAFIHSYFI-UHFFFAOYSA-N
InChI=1S/C17H20F3N7O2/c18-17(19,20)12-9-13(21)22-10-11(12)14-23-15(26-1-5-28-6-2-26)25-16(24-14)27-3-7-29-8-4-27/h9-10H,1-8H2,(H2,21,22)

HIDE SMILES / InChI

Description

PQR-309 is an orally bioavailable pan inhibitor of phosphoinositide-3-kinases (PI3K) and inhibitor of the mammalian target of rapamycin (mTOR), with potential antineoplastic activity. PI3K/mTOR kinase inhibitor PQR-309 inhibits the PI3K kinase isoforms alpha, beta, gamma and delta and, to a lesser extent, mTOR kinase, which may result in tumor cell apoptosis and growth inhibition in cells overexpressing PI3K/mTOR. By inhibiting mTOR to a lesser extent than PI3K, PQR-309 does not interfere with the mTOR-mediated negative feedback loop on PI3K signaling. Blocking the negative feedback loop would potentially increase PI3K signaling and decrease therapeutic efficacy. PQR-309 is in phase II clinical trial for the treatment of glioblastoma, head and neck cancer, lymphoma and breast cancer. Common adverse events included fatigue, hyperglycemia, nausea, diarrhea, constipation, rash, anorexia and vomiting.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Cmax

ValueDoseCo-administeredAnalytePopulation
766 ng/mL
80 mg 1 times / day multiple, oral
BIMIRALISIB plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
4090 ng × h/mL
80 mg 1 times / day multiple, oral
BIMIRALISIB plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
39.5 h
80 mg 1 times / day multiple, oral
BIMIRALISIB plasma
Homo sapiens

PubMed

Sample Use Guides

In Vivo Use Guide
80 mg once-daily
Route of Administration: Oral