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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

Molecular Formula C17H20F3N7O2
Molecular Weight 411.3816
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Phosphoinositide-3-kinase
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
766 ng/mL
80 mg 1 times / day multiple, oral
dose: 80 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
BIMIRALISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
4090 ng × h/mL
80 mg 1 times / day multiple, oral
dose: 80 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
BIMIRALISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
39.5 h
80 mg 1 times / day multiple, oral
dose: 80 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
BIMIRALISIB plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
PubMed

PubMed

TitleDatePubMed
Big Hopes with Small Molecules - PIQUR Therapeutics AG is aiming to Turn Cancer into a Manageable Disease.
2014 Dec
5-(4,6-Dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine (PQR309), a Potent, Brain-Penetrant, Orally Bioavailable, Pan-Class I PI3K/mTOR Inhibitor as Clinical Candidate in Oncology.
2017 Sep 14
PQR309 Is a Novel Dual PI3K/mTOR Inhibitor with Preclinical Antitumor Activity in Lymphomas as a Single Agent and in Combination Therapy.
2018 Jan 1
First-in human, phase 1, dose-escalation pharmacokinetic and pharmacodynamic study of the oral dual PI3K and mTORC1/2 inhibitor PQR309 in patients with advanced solid tumors (SAKK 67/13).
2018 Jun

Sample Use Guides

80 mg once-daily
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:26:58 GMT 2025
Edited
by admin
on Mon Mar 31 22:26:58 GMT 2025
Record UNII
6Z3QHB00LB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
bimiralisib [INN]
Preferred Name English
BIMIRALISIB
INN  
INN   USAN  
Official Name English
Bimiralisib [WHO-DD]
Common Name English
NC-B5
Code English
2-PYRIDINAMINE, 5-(4,6-DI-4-MORPHOLINYL-1,3,5-TRIAZIN-2-YL)-4-(TRIFLUOROMETHYL)-
Systematic Name English
NCB5
Code English
PQR-309
Code English
5-(4,6-Dimorpholin-4-yl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine
Systematic Name English
PQR309
Code English
PI3K-IN-2
Code English
BIMIRALISIB [USAN]
Common Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/17/1830
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
NCI_THESAURUS C2152
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
NCI_THESAURUS C129825
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
FDA ORPHAN DRUG 543116
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
Code System Code Type Description
SMS_ID
100000175789
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
DRUG BANK
DB14846
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
INN
10519
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
USAN
FG-92
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
NCI_THESAURUS
C111898
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
PUBCHEM
58507717
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
FDA UNII
6Z3QHB00LB
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
CAS
1225037-39-7
Created by admin on Mon Mar 31 22:26:58 GMT 2025 , Edited by admin on Mon Mar 31 22:26:58 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY