Structure of Osimertinib mesylate
CAS No.: 1421373-66-1
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Osimertinib mesylate (AZD9291 mesylate) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. It overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
Synonyms: AZD-9291 mesylate; Mereletinib mesylate
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Batch number can be found on the product's label following the word 'Batch'.
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CAS No. : | 1421373-66-1 |
Formula : | C29H37N7O5S |
M.W : | 595.71 |
SMILES Code : | C=CC(NC1=CC(NC2=NC=CC(C3=CN(C)C4=C3C=CC=C4)=N2)=C(OC)C=C1N(CCN(C)C)C)=O.CS(=O)(O)=O |
Synonyms : |
AZD-9291 mesylate; Mereletinib mesylate
|
MDL No. : | MFCD28137994 |
InChI Key : | FUKSNUHSJBTCFJ-UHFFFAOYSA-N |
Pubchem ID : | 78357807 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Description |
Osimertinib mesylate (AZD9291 mesylate) is a covalent, orally active, irreversible EGFR inhibitor selective for mutant forms, with an IC50 of 12 nM against the L858R mutation and 1 nM against the L858R/T790M mutation. Otherwise, Osimertinib overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer[1].
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Target |
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In Vitro:
Cell Line
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Concentration | Treated Time | Description | References |
PC9 | 1uM | 24 h | To evaluate the effect of Osimertinib on EGFR, AKT, and ERK signaling pathways, results showed that in resistant cells, EGFR signaling was suppressed, but ERK and AKT signaling was enhanced, and apoptosis was reduced. | PMC6324945 |
H1975 | 1uM | 24 h | To evaluate the effect of Osimertinib on EGFR, AKT, and ERK signaling pathways, results showed that in resistant cells, EGFR signaling was suppressed, but ERK and AKT signaling was enhanced, and apoptosis was reduced. | PMC6324945 |
HCC827 | 0.01–2 µM | 3 days | To observe the acute treatment response of HCC827 cells to Osimertinib, it was found that a subpopulation of tumor cells survived the initial treatment. | PMC6750230 |
HCC827 | 160 nM | 2–3 weeks | To observe the survival of HCC827 cells under continuous exposure to 160 nM Osimertinib, it was found that a small percentage of cells could survive for more than 2-3 weeks. | PMC6750230 |
NCI-H1975 | 12 nM | 72 h | To evaluate the antiproliferation activity of ASK120067 on tumor cells harboring EGFR T790M mutation, the results showed that ASK120067 has potent antiproliferation activity on NCI-H1975 cells. | PMC7218543 |
PC-9 | 6 nM | 72 h | To evaluate the antiproliferation activity of ASK120067 on tumor cells harboring EGFR T790M mutation, the results showed that ASK120067 has potent antiproliferation activity on PC-9 cells. | PMC7218543 |
HCC827 | 2 nM | 72 h | To evaluate the antiproliferation activity of ASK120067 on tumor cells harboring EGFR T790M mutation, the results showed that ASK120067 has potent antiproliferation activity on HCC827 cells. | PMC7218543 |
H1975 cells | 0.1 μM | 72 h | Osimertinib inhibited the growth of H1975 cells by 28 ± 13% | PMC8419812 |
EGFR-mutant lung adenocarcinoma cells | 0.1 μM | 72 h | Osimertinib inhibited the growth of EGFR-mutant lung adenocarcinoma cells by 81 ± 15% | PMC8419812 |
PC9, H1975, HCC827, HCC2935 | 500 nM | 21 days | RNA-seq analysis revealed significant changes in gene expression regulation in osimertinib DTPs, particularly upregulation of EMT-related pathways and downregulation of cell cycle and MAPK signaling pathways. | PMC9794691 |
PC9, H1975, HCC827, HCC2935 | 500 nM | 24 days | ATAC-seq analysis revealed significant changes in chromatin accessibility in osimertinib DTPs, particularly upregulation of EMT-related pathways and downregulation of tyrosine kinase signaling pathways. | PMC9794691 |
PC9 cells | 2 μM | 9 days | To evaluate the role of YAP in drug tolerance, an increase in YAP nuclear localization was observed. | PMC11068778 |
H1975 cells | 2 μM | 9 days | To evaluate the role of YAP in drug tolerance, an increase in YAP nuclear localization was observed. | PMC11068778 |
HCC4006 | 100 nM | 48 h | To evaluate the synergistic effect of AZ1366 with EGFR inhibitors, results showed that AZ1366 enhanced the anti-proliferative effect of gefitinib. | PMC5354947 |
HCC4006 | 100 nM | 7 days | To evaluate the long-term anti-proliferative effect of AZ1366 in combination with gefitinib, results showed that AZ1366 enhanced the anti-proliferative effect of gefitinib. | PMC5354947 |
HCC4006 | 100 nM | 24 h | To evaluate the effect of AZ1366 in combination with gefitinib on transcriptional changes, results showed that AZ1366 significantly enhanced the transcriptional changes induced by gefitinib. | PMC5354947 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | PC9-OR cell xenograft model | Oral | 5mg/kg | Once daily for 71 days | To evaluate the effect of Osimertinib in combination with Aurora kinase inhibitor MLN8237 on tumor growth, results showed that the combination significantly suppressed tumor growth. | PMC6324945 |
Mice | Non-small cell lung cancer xenograft model | Oral | 5 mg/kg | Once daily for 95 days | To investigate the resistance mechanisms of Osimertinib in EGFR L858R and T790M mutant non-small cell lung cancer xenograft models. The results showed that continuous Osimertinib treatment led to the emergence of BRAF G7V and PIK3C2A A86fs mutations, along with a decrease in the frequency of EGFR L858R and T790M mutations, resulting in drug resistance. | PMC5993147 |
BALB/cA nude mice | NCI-H1975 xenograft model | Oral | 1, 5, 10 mg/kg | Once daily for 21 days | To evaluate the in vivo antitumor activity of ASK120067 in the NCI-H1975 xenograft model, the results showed that ASK120067 dose-dependently inhibited tumor growth and caused significant tumor shrinkage at the dose of 10 mg/kg. | PMC7218543 |
mice | H1975 xenograft model | orally | 5 mg/kg | 5 days a week for 3 consecutive weeks | To evaluate the effect of Osimertinib on tumor volume in vivo, a significant reduction in tumor volume was observed. | PMC11068778 |
Mice | Orthotopic NSCLC model | Oral | 3.125 mg/kg | Once daily, 5/7 days | To evaluate the effect of osimertinib in combination with AZ1366 on tumor growth and survival, results showed that the combination treatment did not significantly improve survival. | PMC5354947 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT06530719 | Lung Neoplasms|Lung Cancer, No... More >>nsmall Cell Less << | PHASE2 | NOT_YET_RECRUITING | 2025-05-28 | - |
Tags: Osimertinib mesylate | AZD-9291 | Mereletinib | AZD9291 | AZD 9291 | EGFR | L858R | Epidermal growth factor receptor | ErbB-1 | HER1 | EGFR inhibitor | T790M resistance | NSCLC | EGFR mutations | irreversible | IC50 | 1421373-66-1
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H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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