Canertinib

Canertinib

SCHEMBL54837

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

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 1.00
CIT O14578 1/20 1.00
MAP2K7 O14733 1/20 1.00
GAK O14976 1/20 1.00
EPHB6 O15197 1/20 1.00
MAP3K7 O43318 1/20 1.00
RIPK2 O43353 1/20 1.00
STK17B O94768 1/20 1.00
STK10 O94804 1/20 1.00
ABL1 P00519 1/20 1.00
LCK P06239 1/20 1.00
FYN P06241 1/20 1.00
YES1 P07947 1/20 1.00
LYN P07948 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
Canertinib SCHEMBL29368458 1.00 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL29655741 1.00 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL29623482 1.00 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL2141065 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL30436576 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL2052123 0.99 EGFR (1.00) EGFRERBB2ERBB4KITSRC
Canertinib SCHEMBL731396 0.99 EGFR (0.97) EGFRERBB2ERBB4KITSRC
SCHEMBL3585133 0.93 EGFR (0.88) EGFRERBB2ERBB4KITSRC
SCHEMBL30415948 0.93 EGFR (0.88) EGFRERBB2ERBB4KITSRC
SCHEMBL13882947 0.93 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

Appears in 8083 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026103823-A1 COMBINATION OF RAS INHIBITOR AND EGFR INHIBITOR AND USE THEREOF 广州嘉越医药科技有限公司 2026-05-21 WO claimed
WO-2026107237-A1 RAS AND EGFR INHIBITORS COMBINATION THERAPY ERASCA, INC. (US) 2026-05-21 WO claimed
US-20260125490-A1 Methods for Determining the Likelihood of Survival and for Predicting Likelihood of Metastasis in Cancer Patients LABORATORY CORPORATION OF AMERICA HOLDINGS (US) 2026-05-07 US claimed
US-12618855-B2 Serum protein biomarker panel for idiopathic pulmonary fibrosis CHILDREN'S HOSPITAL MEDICAL CENTER (US) 2026-05-05 US claimed
EP-4719387-A2 COMPLEMENT ANTIBODY-DRUG CONJUGATES ADS Therapeutics LLC (US) 2026-04-08 EP claimed
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-03-17 US claimed
EP-4704832-A2 BIFUNCTIONAL SMALL MOLECULES TO TARGET THE SELECTIVE DEGRADATION OF CIRCULATING PROTEINS Biohaven Therapeutics Ltd. (VG) 2026-03-11 EP claimed
US-12569575-B2 Radiopaque particle compositions and uses thereof GUSTAVE ROUSSY TRANSFERT (FR) 2026-03-10 US claimed
US-12559800-B2 KMT2A-MAML2 fusion molecules and uses thereof FOUNDATION MEDICINE, INC. (US) 2026-02-24 US claimed
US-20260049063-A1 ALKYNYL QUINAZOLINE COMPOUNDS BLACK DIAMOND THERAPEUTICS INC (US) 2026-02-19 US claimed
WO-2003066060-A2 USE OF TYROSINE KINASE INHIBITORS FOR THE TREATMENT OF INFLAMMATORY PROCESSES BOEHRINGER INGELHEIM PHARMA GMBH & CO.KG (DE) 2003-08-14 WO claimed
US-20030149062-A1 Use of tyrosine kinase inhibitors for the treatment of inflammatory processes BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2003-08-07 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
EP-1131304-B1 N- 4-(3-CHLORO-4-FLUORO-PHENYLAMINO)-7-(3-MORPHOLIN-4-YL-PROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE, AN IRREVERSIBLE INHIBITOR OF TYROSINE KINASES WARNER LAMBERT CO (US) 2002-12-04 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
US-6344455-B1 TREATING CANCER, ATHEROSCLEROSIS, RESTENOSIS, ENDOMETRIOSIS, AND PSORIASIS WARNER-LAMBERT COMPANY 2002-02-05 US 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-1131304-A1 N- 4-(3-CHLORO-4-FLUORO-PHENYLAMINO)-7-(3-MORPHOLIN-4-YL-PROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE, AN IRREVERSIBLE INHIBITOR OF TYROSINE KINASES WARNER-LAMBERT COMPANY (US) 2001-09-12 EP claimed
WO-2000031048-A1 N-[4-(3-CHLORO-4-FLUORO-PHENYLAMINO)-7-(3-MORPHOLIN-4-YL-PROPOXY)-QUINAZOLIN-6-YL]-ACRYLAMIDE, AN IRREVERSIBLE INHIBITOR OF TYROSINE KINASES WARNER-LAMBERT COMPANY (US) 2000-06-02 WO claimed