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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
Structure of AT-7867

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)

HIDE SMILES / InChI

Molecular Formula C20H20ClN3
Molecular Weight 337.846
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
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.

Approval Year

PubMed

PubMed

TitleDatePubMed
AT7867 is a potent and oral inhibitor of AKT and p70 S6 kinase that induces pharmacodynamic changes and inhibits human tumor xenograft growth.
2010 May
Chromatin remodeling gene AT-rich interactive domain-containing protein 1A suppresses gastric cancer cell proliferation by targeting PIK3CA and PDK1.
2016 Jul 19
AT7867 Inhibits Human Colorectal Cancer Cells via AKT-Dependent and AKT-Independent Mechanisms.
2017
Patents

Sample Use Guides

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
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)
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:40:40 GMT 2023
Edited
by admin
on Sat Dec 16 15:40:40 GMT 2023
Record UNII
ERF7YL2CE2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AT-7867
Code English
PIPERIDINE, 4-(4-CHLOROPHENYL)-4-(4-(1H-PYRAZOL-4-YL)PHENYL)-
Systematic Name English
AT7867
Code English
4-(4-CHLOROPHENYL)-4-(4-(1H-PYRAZOL-4-YL)PHENYL)PIPERIDINE
Systematic Name English
Code System Code Type Description
CAS
857531-00-1
Created by admin on Sat Dec 16 15:40:40 GMT 2023 , Edited by admin on Sat Dec 16 15:40:40 GMT 2023
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PUBCHEM
11175137
Created by admin on Sat Dec 16 15:40:40 GMT 2023 , Edited by admin on Sat Dec 16 15:40:40 GMT 2023
PRIMARY
FDA UNII
ERF7YL2CE2
Created by admin on Sat Dec 16 15:40:40 GMT 2023 , Edited by admin on Sat Dec 16 15:40:40 GMT 2023
PRIMARY
DRUG BANK
DB07859
Created by admin on Sat Dec 16 15:40:40 GMT 2023 , Edited by admin on Sat Dec 16 15:40:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID00457772
Created by admin on Sat Dec 16 15:40:40 GMT 2023 , Edited by admin on Sat Dec 16 15:40:40 GMT 2023
PRIMARY