Canertinib

Canertinib

SCHEMBL2052123

C=CC(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3)ncnc2cc1OCCCN1CCOCC1.Cl.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFRERBB2ERBB4

The experimentally established mechanism targets of Canertinib. 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 20/20 1.00
ERBB2 known ✓ P04626 9/20 1.00
ERBB4 known ✓ Q15303 3/20 1.00
KIT P10721 2/20 1.00
SRC P12931 2/20 1.00
ERBB3 P21860 2/20 1.00
BMPR1B O00238 1/20 0.99
CIT O14578 1/20 0.99
MAP2K7 O14733 1/20 0.99
GAK O14976 1/20 0.99
EPHB6 O15197 1/20 0.99
MAP3K7 O43318 1/20 0.99
RIPK2 O43353 1/20 0.99
STK17B O94768 1/20 0.99
STK10 O94804 1/20 0.99
ABL1 P00519 1/20 0.99
LCK P06239 1/20 0.99
FYN P06241 1/20 0.99
YES1 P07947 1/20 0.99
LYN P07948 1/20 0.99

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
Canertinib SCHEMBL2141065 1.00 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL30436576 1.00 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL29623482 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL54837 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL29655741 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL29368458 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL731396 0.98 EGFR (0.97) EGFRERBB2ERBB4KITSRC
SCHEMBL3585133 0.93 EGFR (0.88) EGFRERBB2ERBB4KITSRC
SCHEMBL30415948 0.93 EGFR (0.88) EGFRERBB2ERBB4KITSRC
SCHEMBL13153156 0.92 EGFR (0.86) EGFRERBB2ERBB4KITSRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240182864-A1 NOVEL CHEMICAL COMBINATIONS AND METHODS OF USE THEREOF, TOWARDS DIFFERENTIATION OF HUMAN PROGENITOR CELLS INTO FUNCTIONAL BETA CELLS SALK INSTITUTE FOR BIOLOGICAL STUDIES 2024-06-06 US claimed
US-20230190748-A1 COMPOSITIONS FOR TREATMENT OF AGED DISEASES GERO PTE LTD (SG) 2023-06-22 US claimed
CN-109071622-B Peptides with anticancer activity IDP研发制药有限公司(ES) 2023-01-13 CN claimed
WO-2022204377-A1 NOVEL CHEMICAL COMBINATIONS AND METHODS OF USE THEREOF, TOWARDS DIFFERENTIATION OF HUMAN PROGENITOR CELLS INTO FUNCTIONAL β CELLS SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 2022-09-29 WO claimed
US-20040034022-A1 Polymorphic forms/hydrates of n-[4-(3-chloro-4-fluorophenylamino)-7-(3-morpholin-4-ylpropoxy)-quinazolin-6-yl]-acrylamide dihydrochloride GODECKE GMBH (DE) 2004-02-19 US claimed
EP-1299363-A1 POLYMORPHIC FORMS/HYDRATES OF N- 4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE GÖDECKE GMBH (DE) 2003-04-09 EP claimed
US-20020169176-A1 Method for inhibiting retinoid skin damage ELDER JAMES T (US) 2002-11-14 US claimed
EP-1230919-A2 Use of a composition comprising a retinoid and an erb inhibitor in the preparation of a medicament for the treatment of retinoid skin damage WARNER-LAMBERT COMPANY (US) 2002-08-14 EP claimed
WO-2002000630-A1 POLYMORPHIC FORMS/HYDRATES OF N-[4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE Gödecke GmbH (DE) 2002-01-03 WO claimed
EP-4748453-A2 METHODS OF TREATING LOCALLY ADVANCED OR METASTATIC BREAST CANCERS USING PD-1 AXIS BINDING ANTAGONISTS AND TAXANES F. Hoffmann-La Roche AG (CH) 2026-05-27 EP disclosed
EP-4747408-A1 DIAGNOSTIC AND THERAPEUTIC METHODS FOR CANCER GENENTECH, INC. (US) 2026-05-27 EP disclosed
CN-122081247-A Oncolytic vaccinia virus and recombinant viruses and methods of use thereof 2026-05-26 CN disclosed
US-20260139315-A1 DIAGNOSTIC AND THERAPEUTIC METHODS FOR CANCER GENENTECH, INC. (US) 2026-05-21 US disclosed
US-20260139061-A1 TREATMENT OF CANCER USING HUMANIZED ANTI-EGFRvIII CHIMERIC ANTIGEN RECEPTOR NOVARTIS AG (CH) 2026-05-21 US disclosed
EP-1299363-A1 POLYMORPHIC FORMS/HYDRATES OF N- 4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE GÖDECKE GMBH (DE) 2003-04-09 EP disclosed
EP-1299363-A1 POLYMORPHIC FORMS/HYDRATES OF N- 4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE GÖDECKE GMBH (DE) 2003-04-09 EP disclosed
US-20020169176-A1 Method for inhibiting retinoid skin damage ELDER JAMES T (US) 2002-11-14 US disclosed
EP-1230919-A2 Use of a composition comprising a retinoid and an erb inhibitor in the preparation of a medicament for the treatment of retinoid skin damage WARNER-LAMBERT COMPANY (US) 2002-08-14 EP disclosed
WO-2002000630-A1 POLYMORPHIC FORMS/HYDRATES OF N-[4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE Gödecke GmbH (DE) 2002-01-03 WO disclosed
WO-2002000630-A1 POLYMORPHIC FORMS/HYDRATES OF N-[4-(3-CHLORO-4-FLUOROPHENYLAMINO)-7-(3-MORPHOLIN-4-YLPROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE DIHYDROCHLORIDE Gödecke GmbH (DE) 2002-01-03 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 (5 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-20230190748-A1 COMPOSITIONS FOR TREATMENT OF AGED DISEASES AGER, CKMT1A; CKMT1B, GLA EGFR 1153/4885ERBB2 1599/4885ERBB4 1657/4885
US-20020169176-A1 Method for inhibiting retinoid skin damage RARB, EBP, RXRA EGFR 47/4885ERBB2 183/4885ERBB4 110/4885
US-20260139061-A1 TREATMENT OF CANCER USING HUMANIZED ANTI-EGFRvIII CHIMERIC ANTIGEN RECEPTOR EGFR, ERBB2, HAVCR2 EGFR 1/4885ERBB2 2/4885ERBB4 6/4885
US-20260139315-A1 DIAGNOSTIC AND THERAPEUTIC METHODS FOR CANCER APOL1, PDCD1LG2, PRSS1 EGFR 264/4885ERBB2 1515/4885ERBB4 2040/4885
US-20040034022-A1 Polymorphic forms/hydrates of n-[4-(3-chloro-4-fluorophenylamino)-7-(3-morpholin-4-ylpropoxy)-quinazolin-6-yl]-acrylamide dihydrochloride TP53, ABL1, PRKDC EGFR 1887/4885ERBB2 234/4885ERBB4 347/4885

“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.