Aumolertinib

Aumolertinib

SCHEMBL17683063

C=CC(=O)Nc1cc(Nc2nccc(-c3cn(C4CC4)c4ccccc34)n2)c(OC)cc1N(C)CCN(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFR

The experimentally established mechanism targets of Aumolertinib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGFR known ✓ P00533 19/20 1.00
KCNH2 Q12809 2/20 0.82
MLNR O43193 1/20 0.82
KDM1A O60341 1/20 0.82
ABCB11 O95342 1/20 0.82
ERBB2 P04626 1/20 0.82
INSR P06213 1/20 0.82
CHRM2 P08172 1/20 0.82
HTR1A P08908 1/20 0.82
ADORA3 P0DMS8 1/20 0.82
DRD2 P14416 1/20 0.82
NQO2 P16083 1/20 0.82
ADRA2C P18825 1/20 0.82
DRD1 P21728 1/20 0.82
ERBB3 P21860 1/20 0.82
SLC6A2 P23975 1/20 0.82
HTR2A P28223 1/20 0.82
HTR2C P28335 1/20 0.82
ADORA2A P29274 1/20 0.82
SLC6A4 P31645 1/20 0.82

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Aumolertinib SCHEMBL29389482 1.00 EGFR (1.00) EGFRKCNH2MLNRKDM1AABCB11
Aumolertinib SCHEMBL30341838 0.99 EGFR (0.99) EGFRKCNH2MLNRKDM1AABCB11
Aumolertinib SCHEMBL29786118 0.97 EGFR (0.95) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL17683054 0.94 EGFR (1.00) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL30108191 0.94 EGFR (0.88) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL28942076 0.94 EGFR (0.88) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL30459752 0.93 EGFR (0.88) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL19532567 0.93 EGFR (0.88) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL17683226 0.93 EGFR (0.88) EGFRKCNH2MLNRKDM1AABCB11
SCHEMBL17683092 0.93 EGFR (0.87) EGFRKCNH2MLNRKDM1AABCB11

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 81 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220370448-A1 PHARMACEUTICAL COMPOSITION COMPRISING THIRD GENERATION SMALL MOLECULE EGFR INHIBITOR AND PREPARATION METHOD THEREOF JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2022-11-24 US claimed
US-11155534-B2 EGFR inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2021-10-26 US claimed
EP-3795157-A1 PHARMACEUTICAL COMPOSITION COMPRISING SMALL MOLECULE EGFR INHIBITOR AND PREPARATION METHOD THEREFOR Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (CN) 2021-03-24 EP claimed
US-20210069190-A1 PHARMACEUTICAL COMPOSITION COMPRISING SMALL MOLECULE EGFR INHIBITOR AND PREPARATION METHOD THEREFOR JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2021-03-11 US claimed
EP-3434673-B1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION JIANGSU HANSOH PHARMACEUTICAL GROUP CO LTD (CN) 2021-02-17 EP claimed
US-20200361909-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION SHANGHAI HANSOH BIOMEDICAL CO., LTD. (CN) 2020-11-19 US claimed
US-10759782-B2 EGFR inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2020-09-01 US claimed
US-20190077791-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2019-03-14 US claimed
EP-3434673-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (CN) 2019-01-30 EP claimed
US-20260137681-A1 EPIDERMAL GROWTH FACTOR RECEPTOR TYROSINE KINASE INHIBITORS IN COMBINATION WITH HGF-RECEPTOR INHIBITORS FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2026-05-21 US disclosed
US-20250325543-A1 EGFR TKIs FOR USE IN THE TREATMENT OF NON-SMALL LUNG CANCER ASTRAZENECA AB (SE) 2025-10-23 US disclosed
US-20250275968-A1 INHIBITORS OF TAU PROTEINS DEUTSCHES ZENTRUM FÜR NEURODEGENERATIVE ERKRANKUNGEN E.V. (DE) 2025-09-04 US disclosed
US-20250214995-A1 CONDENSED BICYCLIC HETEROAROMATIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2025-07-03 US disclosed
US-20250205233-A1 EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) TYROSINE KINASE INHIBITORS IN COMBINATION WITH AN AKT INHIBITOR FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2025-06-26 US disclosed
US-20170313714-A1 EGFR INHIBITOR, PREPARATION METHOD AND USE THEREOF SHANGHAI HANSOH BIOMEDICAL CO., LTD. (CN) 2017-11-02 US disclosed
US-20170313714-A1 EGFR INHIBITOR, PREPARATION METHOD AND USE THEREOF SHANGHAI HANSOH BIOMEDICAL CO., LTD. (CN) 2017-11-02 US disclosed
WO-2017161937-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION 江苏豪森药业集团有限公司 2017-09-28 WO disclosed
EP-3205650-A1 EGFR INHIBITOR, AND PREPARATION AND APPLICATION THEREOF Shanghai Hansoh Biomedical Co., Ltd. (CN) 2017-08-16 EP disclosed
EP-3205650-A1 EGFR INHIBITOR, AND PREPARATION AND APPLICATION THEREOF Shanghai Hansoh Biomedical Co., Ltd. (CN) 2017-08-16 EP disclosed
WO-2016054987-A1 EGFR INHIBITOR, AND PREPARATION AND APPLICATION THEREOF 上海翰森生物医药科技有限公司 2016-04-14 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (12 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250275968-A1 INHIBITORS OF TAU PROTEINS MAPT, PSEN2, PSEN1 EGFR 4305/4885KCNH2 4624/4885MLNR 4599/4885
US-10759782-B2 EGFR inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application EGFR, WEE1, SLC38A7 EGFR 1/4885KCNH2 1883/4885MLNR 801/4885
US-20170313714-A1 EGFR INHIBITOR, PREPARATION METHOD AND USE THEREOF EGFR, ERBB2, ERBB4 EGFR 1/4885KCNH2 4088/4885MLNR 166/4885
US-20200361909-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION EGFR, WEE1, SLC38A7 EGFR 1/4885KCNH2 1883/4885MLNR 801/4885
US-20190077791-A1 EGFR INHIBITOR FREE BASE OR ACID SALT POLYCRYSTALLINE FORM, PREPARATION METHOD THEREFOR, AND APPLICATION EGFR, WEE1, SLC38A7 EGFR 1/4885KCNH2 1883/4885MLNR 801/4885
US-20250205233-A1 EPIDERMAL GROWTH FACTOR RECEPTOR (EGFR) TYROSINE KINASE INHIBITORS IN COMBINATION WITH AN AKT INHIBITOR FOR THE TREATMENT OF CANCER EGFR, ERBB2, ERBB3 EGFR 1/4885KCNH2 4834/4885MLNR 678/4885
US-20220370448-A1 PHARMACEUTICAL COMPOSITION COMPRISING THIRD GENERATION SMALL MOLECULE EGFR INHIBITOR AND PREPARATION METHOD THEREOF EGFR, ERBB3, ERBB2 EGFR 1/4885KCNH2 3776/4885MLNR 185/4885
US-20260137681-A1 EPIDERMAL GROWTH FACTOR RECEPTOR TYROSINE KINASE INHIBITORS IN COMBINATION WITH HGF-RECEPTOR INHIBITORS FOR THE TREATMENT OF CANCER MET, HGF, EGFR EGFR 3/4885KCNH2 4499/4885MLNR 1925/4885
US-20250325543-A1 EGFR TKIs FOR USE IN THE TREATMENT OF NON-SMALL LUNG CANCER EGFR, ERBB2, ERBB4 EGFR 1/4885KCNH2 4306/4885MLNR 865/4885
US-20250214995-A1 CONDENSED BICYCLIC HETEROAROMATIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, TP53, SDHA EGFR 894/4885KCNH2 3918/4885MLNR 3168/4885
US-11155534-B2 EGFR inhibitor free base or acid salt polycrystalline form, preparation method therefor, and application EGFR, WEE1, SLC38A7 EGFR 1/4885KCNH2 1883/4885MLNR 801/4885
US-20210069190-A1 PHARMACEUTICAL COMPOSITION COMPRISING SMALL MOLECULE EGFR INHIBITOR AND PREPARATION METHOD THEREFOR EGFR, ERBB2, ERBB3 EGFR 1/4885KCNH2 4168/4885MLNR 266/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.