Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H20ClN3 |
Molecular Weight | 337.846 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C1)C2(CCNCC2)C3=CC=C(C=C3)C4=CNN=C4
InChI
InChIKey=LZMOSYUFVYJEPY-UHFFFAOYSA-N
InChI=1S/C20H20ClN3/c21-19-7-5-18(6-8-19)20(9-11-22-12-10-20)17-3-1-15(2-4-17)16-13-23-24-14-16/h1-8,13-14,22H,9-12H2,(H,23,24)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 | https://www.ncbi.nlm.nih.gov/pubmed/28081222Curator's Comment: Description was created based on several sources, including
https://astx.com/wp-content/uploads/2016/11//ASTX_News_2010_4_13_General_Releases.pdf
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 | https://www.ncbi.nlm.nih.gov/pubmed/28081222
Curator's Comment: Description was created based on several sources, including
https://astx.com/wp-content/uploads/2016/11//ASTX_News_2010_4_13_General_Releases.pdf
AT7867 is a novel and potent inhibitor of both AKT and the downstream kinase p70 S6 kinase (p70S6K) and also of protein kinase A. This ATP-competitive small molecule potently inhibits both AKT and p70S6K activity at the cellular level, as measured by inhibition of GSK3beta and S6 ribosomal protein phosphorylation, and also causes growth inhibition in a range of human cancer cell lines as a single agent. AT7867 inhibited survival and proliferation of established (HT-29, HCT116 and DLD-1 lines) and primary human CRC cells. In vivo, intraperitoneal injection of AT7867 inhibited HT-29 xenograft tumor growth in nude mice. AKT activation was also inhibited in AT7867-treated HT-29 tumors. Together, the preclinical results suggest that AT7867 inhibits CRC cells via AKT-dependent and -independent mechanisms.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
17.0 nM [IC50] | |||
Target ID: CHEMBL4282 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 |
32.0 nM [IC50] | ||
Target ID: CHEMBL4816 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 |
47.0 nM [IC50] | ||
Target ID: CHEMBL2094138 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 |
20.0 nM [IC50] | ||
Target ID: CHEMBL2111330 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992 |
85.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992
Mice: a single dose of AT7867 was administered to BALB/c mice at 5mg/kg intravenously (i.v.) and 20mg/kg per os (p.o.). To assess the pharmacokinetic (PK) and pharmacodynamic (PD) profile, a single dose of
AT7867 (90mg/kg p.o. or 20mg/kg i.p.) was given to mice bearing MES-SA tumor xenografts.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20423992
AT7867 appeared to be most potent at inhibiting
proliferation in MES-SA uterine, MDA-MB-468 and MCF-7 breast, and HCT116 and HT29
colon lines (IC50 values range from 0.9-3 uM)
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857531-00-1
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11175137
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ERF7YL2CE2
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DB07859
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DTXSID00457772
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SUBSTANCE RECORD