Poziotinib

Poziotinib

SCHEMBL29375341

C=CC(=O)N1CCC(Oc2cc3c(Nc4ccc(Cl)c(Cl)c4F)ncnc3cc2OC)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFRERBB2ERBB3ERBB4

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

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
EGFR known ✓ P00533 20/20 1.00
ERBB2 known ✓ P04626 5/20 1.00
KCNH2 Q12809 2/20 1.00
RIPK2 O43353 1/20 1.00
RET P07949 1/20 1.00
MET P08581 1/20 1.00
EPHB2 P29323 1/20 1.00
TEC P42680 1/20 1.00
EPHB4 P54760 1/20 1.00
EPHA4 P54764 1/20 1.00
BTK Q06187 1/20 1.00
TNK1 Q13470 1/20 1.00
RIPK3 Q9Y572 1/20 1.00

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
Poziotinib SCHEMBL3391764 1.00 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
Poziotinib SCHEMBL29453260 1.00 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
Poziotinib SCHEMBL14841985 0.99 EGFR (0.98) EGFRERBB2KCNH2RIPK2RET
SCHEMBL22598558 0.95 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
SCHEMBL29751974 0.95 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
SCHEMBL3390837 0.95 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
SCHEMBL14786610 0.94 EGFR (0.88) EGFRERBB2KCNH2RIPK2RET
SCHEMBL3391925 0.94 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET
SCHEMBL21613670 0.93 EGFR (0.87) EGFRERBB2KCNH2RIPK2RET
SCHEMBL29444156 0.93 EGFR (1.00) EGFRERBB2KCNH2RIPK2RET

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12595297-B2 Methods and compositions for inhibition of EGF/EGFR pathway in combination with tyrosine kinase inhibitors IN3BIO LTD. (BM) 2026-04-07 US claimed
US-20240269136-A1 EGFR INHIBITOR AND PERK ACTIVATOR IN COMBINATION THERAPY AND THEIR USE FOR TREATING CANCER GENENTECH, INC. (US) 2024-08-15 US claimed
EP-4392423-A1 QUINAZOLINE COMPOUNDS FOR TREATMENT OF DISEASE Arthrosi Therapeutics, Inc. (US) 2024-07-03 EP claimed
EP-4355330-A1 EGFR INHIBITOR AND PERK ACTIVATOR IN COMBINATION THERAPY AND THEIR USE FOR TREATING CANCER Genentech, Inc. (US) 2024-04-24 EP claimed
CN-117479943-A EGFR inhibitors and PERK activators in combination therapies and use thereof for treating cancer 基因泰克公司 2024-01-30 CN claimed
WO-2023028054-A1 QUINAZOLINE COMPOUNDS FOR TREATMENT OF DISEASE ARTHROSI THERAPEUTICS, INC. (US) 2023-03-02 WO claimed
WO-2022265950-A1 EGFR INHIBITOR AND PERK ACTIVATOR IN COMBINATION THERAPY AND THEIR USE FOR TREATING CANCER GENENTECH, INC. (US) 2022-12-22 WO claimed
CN-122074043-A Combination therapy with KRAS modulators 光达治疗公司 2026-05-22 CN disclosed
US-20250243171-A1 QUINAZOLINE COMPOUNDS FOR TREATMENT OF DISEASE ARTHROSI THERAPEUTICS, INC. 2025-07-31 US disclosed
WO-2025106901-A1 COMBINATION CANCER THERAPIES WITH A KRAS MODULATOR AND AN RTK-MAPK PATHWAY INHIBITOR QUANTA THERAPEUTICS, INC. (US) 2025-05-22 WO disclosed
WO-2025034919-A1 COMBINATION THERAPIES WITH KRAS MODULATORS QUANTA THERAPEUTICS, INC. (US) 2025-02-13 WO disclosed
US-20240269136-A1 EGFR INHIBITOR AND PERK ACTIVATOR IN COMBINATION THERAPY AND THEIR USE FOR TREATING CANCER GENENTECH, INC. (US) 2024-08-15 US disclosed
EP-4412717-A1 COMBINATION THERAPIES OF KRAS G12D INHIBITORS WITH PAN ERBB FAMILY INHIBITORS Mirati Therapeutics, Inc. (US) 2024-08-14 EP disclosed
EP-4017495-A1 POZIOTINIB COMBINATION WITH VEGFR2 INHIBITORS AND METHODS OF USE THEREOF Spectrum Pharmaceuticals, Inc. (US) 2022-06-29 EP disclosed
US-11365189-B2 Heterocyclic inhibitors of tyrosine kinase BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-06-21 US disclosed
WO-2022043923-A1 SYNTHESIS OF POZIOTINIB DERIVATIVE HANMI SCIENCE CO., LTD. (KR) 2022-03-03 WO disclosed
EP-3956035-A1 COMPOUNDS AGAINST CANCER BEARING TYROSINE KINASE INHIBITOR RESISTANT EGFR MUTATIONS Board of Regents, The University of Texas System (US) 2022-02-23 EP disclosed
EP-3946632-A1 COMPOUNDS WITH ANTI-TUMOR ACTIVITY AGAINST CANCER CELLS BEARING HER2 EXON 21 INSERTIONS Board of Regents, The University of Texas System (US) 2022-02-09 EP disclosed
EP-3946293-A1 COMPOUNDS WITH ANTI-TUMOR ACTIVITY AGAINST CANCER CELLS BEARING EGFR OR HER2 EXON 20 INSERTIONS Board of Regents, The University of Texas System (US) 2022-02-09 EP disclosed
WO-2022026442-A1 TREATMENT OF NON-SMALL CELL LUNG CANCER WITH POZIOTINIB SPECTRUM PHARMACEUTICALS, INC. (US) 2022-02-03 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 (4 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-20250243171-A1 QUINAZOLINE COMPOUNDS FOR TREATMENT OF DISEASE EGFR, ABL1, ERBB2 EGFR 1/4885ERBB2 3/4885KCNH2 3824/4885
US-12595297-B2 Methods and compositions for inhibition of EGF/EGFR pathway in combination with tyrosine kinase inhibitors EGFR, ERBB2, ERBB3 EGFR 1/4885ERBB2 2/4885KCNH2 3216/4885
US-20240269136-A1 EGFR INHIBITOR AND PERK ACTIVATOR IN COMBINATION THERAPY AND THEIR USE FOR TREATING CANCER EGFR, ERBB2, ERBB4 EGFR 1/4885ERBB2 2/4885KCNH2 4876/4885
US-11365189-B2 Heterocyclic inhibitors of tyrosine kinase ERBB2, ERBB3, EGFR EGFR 3/4885ERBB2 1/4885KCNH2 4678/4885

“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.