U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C16H16N6O
Molecular Weight 308.3378
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PP-242

SMILES

CC(C)N1N=C(C2=CC3=C(N2)C=CC(O)=C3)C4=C(N)N=CN=C14

InChI

InChIKey=MFAQYJIYDMLAIM-UHFFFAOYSA-N
InChI=1S/C16H16N6O/c1-8(2)22-16-13(15(17)18-7-19-16)14(21-22)12-6-9-5-10(23)3-4-11(9)20-12/h3-8,20,23H,1-2H3,(H2,17,18,19)

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/20622997

PP-242 is a selective mTOR inhibitor with IC50 of 8 nM. mTOR has emerged as an important drug target, and PP-242 is the first selective and ATP competitive inhibitor of mTOR that has been described. Unlike rapamycin, PP-242 inhibits both mTORC1 and mTORC2. PP-242 suppresses bladder cancer cell proliferation and migration through deactivating the mammalian target of rapamycin complex 2/AKT1 signaling pathway. PP242 also inhibits several protein kinases including PKC, RET and JAK2 kinases. PP-242 shows strong antitumor activity in a pheochromocytoma PC12 cell tumor model. PP-242 suppresses cell proliferation, metastasis, and angiogenesis of gastric cancer through inhibition of the PI3K/AKT/mTOR pathway. PP-242 induces apoptosis in AML cells under conditions mimicking the bone marrow microenvironment.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
8.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Activation state-dependent binding of small molecule kinase inhibitors: structural insights from biochemistry.
2010 Nov 24
Comprehensive analysis of kinase inhibitor selectivity.
2011 Oct 30
Patents

Sample Use Guides

Mice: intraperitoneal injections of 5 mg/Kg in 30% PEG 400
Route of Administration: Intraperitoneal
In BT549 cells, PP-242 treatment (0.04-10 uM) inhibits the phosphorylation of Akt, the mTOR substrate p70S6K, and its downstream target S6 in a dose-dependent manner.
Name Type Language
PP-242
Common Name English
PP242
Code English
1H-INDOL-5-OL, 2-(4-AMINO-1-(1-METHYLETHYL)-1H-PYRAZOLO(3,4-D)PYRIMIDIN-3-YL)-
Systematic Name English
2-(4-AMINO-1-ISOPROPYL-1H-PYRAZOLO(3,4-D)PYRIMIDIN-3-YL)-1H-INDOL-5-OL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID5048685
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
CHEBI
90679
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
CAS
1092351-67-1
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
FDA UNII
H5669VNZ7V
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
NCI_THESAURUS
C128632
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY
PUBCHEM
135565635
Created by admin on Sat Dec 16 10:31:23 GMT 2023 , Edited by admin on Sat Dec 16 10:31:23 GMT 2023
PRIMARY