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
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)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18849971Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/20622997
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18849971
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.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2842 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18849971 |
8.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26885449
Mice: intraperitoneal injections of 5 mg/Kg in 30% PEG 400
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18849971
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 | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |
ACTIVE MOIETY