Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C23H26N4O3 |
Molecular Weight | 406.4775 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[C@@H](C)CN1C(=O)N(C)C2=C1C3=CC(=CC=C3N=C2)C4=CC(=CN=C4)C(C)(C)O
InChI
InChIKey=ACCFLVVUVBJNGT-AWEZNQCLSA-N
InChI=1S/C23H26N4O3/c1-14(30-5)13-27-21-18-9-15(16-8-17(11-24-10-16)23(2,3)29)6-7-19(18)25-12-20(21)26(4)22(27)28/h6-12,14,29H,13H2,1-5H3/t14-/m0/s1
Molecular Formula | C23H26N4O3 |
Molecular Weight | 406.4775 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/27439478Curator's Comment: Description was created using several sources including: http://www.lillyoncologypipeline.com/molecule/pi-3-k-m-tor-dual-inhibitor/overview;
https://www.google.com/patents/WO2012097039A1|https://clinicaltrials.gov/ct2/show/NCT02407054|https://clinicaltrials.gov/ct2/show/NCT02443337|https://clinicaltrials.gov/ct2/show/NCT02549989
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478
Curator's Comment: Description was created using several sources including: http://www.lillyoncologypipeline.com/molecule/pi-3-k-m-tor-dual-inhibitor/overview;
https://www.google.com/patents/WO2012097039A1|https://clinicaltrials.gov/ct2/show/NCT02407054|https://clinicaltrials.gov/ct2/show/NCT02443337|https://clinicaltrials.gov/ct2/show/NCT02549989
LY3023414, an investigational drug, is a small molecule that that demonstrates activity against PI3K, mTOR, and DNA-PK in tumor cells, thereby inducing cell-cycle effects and inhibiting cancer cell viability. As shown in vitro LY3023414 inhibits the ability of PI3K and mTOR to phosphorylate substrates in the PI3K/mTOR pathway, one of the most frequently mutated pathways in cancer, leading to cancer progression and resistance to existing treatments. Downstream target inhibition by LY3023414 occurs rapidly via an intermittent “on/off” mechanism that may enhance the drug's clinical tolerability, which may in turn allow LY3023414 to overcome some of the toxicities associated with PI3K/mTOR inhibitors and potentially reduce the emergence of feedback mechanisms leading to resistance. The physicochemical and absorption properties of LY3023414 are favorable, as evidenced by the molecule's high solubility across a wide pH range and high oral bioavailability. On the basis of these findings, LY3023414 is currently being evaluated in clinical trials in patients with advanced cancer such as metastatic prostate cancer and non-small cell lung cancer in combination with other chemotherapeutic agents and in endometrial cancer as a monotherapy.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478
Curator's Comment: # Eli Lilly
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: 1.04295552E8 Gene Symbol: PIK3CA Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478 |
6.07 nM [IC50] | ||
Target ID: 1.00017328E8 Gene Symbol: PIK3CB Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478 |
77.6 nM [IC50] | ||
Target ID: CHEMBL3142 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478 |
4.24 nM [IC50] | ||
Target ID: CHEMBL2221341 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478 |
165.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
weak | yes (co-administration study) Comment: Increased midazolam AUCinf by 46%. Sources: https://pubmed.ncbi.nlm.nih.gov/29636360/ |
|||
yes [IC50 0.6513 uM] |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
major | ||||
minor | ||||
yes | ||||
yes | ||||
yes |
PubMed
Title | Date | PubMed |
---|---|---|
Genomic profiling is predictive of response to cisplatin treatment but not to PI3K inhibition in bladder cancer patient-derived xenografts. | 2016 Nov 22 |
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Characterization of LY3023414, a Novel PI3K/mTOR Dual Inhibitor Eliciting Transient Target Modulation to Impede Tumor Growth. | 2016 Oct |
|
PI3K/mTOR Dual Inhibitor, LY3023414, Demonstrates Potent Antitumor Efficacy Against Esophageal Adenocarcinoma in a Rat Model. | 2017 Jul |
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT02549989
200 mg LY3023414 twice daily in patients with recurrent or persistent endometrial cancer
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27439478
The ability of LY3023414 to inhibit cancer cell proliferation was evaluated in 32 human cancer cell lines from different tumor types in culture after LY3023414 treatment for 2 to 3 cell doublings in dose–response studies.LY3023414 demonstrated potent single-agent activity and IC50 values below 122 nmol/L in half of the cell lines tested. Among the more sensitive cell lines were ones originating from breast cancer (4 of 4 tested) and mesothelioma (5 of 6 tested), whereas none of the lung or colon cancer cell lines tested appeared to be highly sensitive.
Substance Class |
Chemical
Created
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admin
on
Edited
Sat Dec 16 08:10:00 GMT 2023
by
admin
on
Sat Dec 16 08:10:00 GMT 2023
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Record UNII |
C88817F47Y
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Record Status |
Validated (UNII)
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Record Version |
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C1404
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CHEMBL3544999
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100000177957
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