Afatinib

Afatinib

SCHEMBL232772

CN(C)C/C=C/C(=O)Nc1cc2c(Nc3ccc(F)c(Cl)c3)ncnc2cc1O[C@H]1CCOC1

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 Afatinib. 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 10/20 1.00
ERBB4 known ✓ Q15303 2/20 1.00
GAK O14976 2/20 1.00
ABL1 P00519 2/20 1.00
LCK P06239 2/20 1.00
MET P08581 2/20 1.00
PHKG2 P15735 2/20 1.00
BLK P51451 2/20 1.00
IRAK1 P51617 2/20 1.00
DYRK1A Q13627 2/20 1.00
HIPK4 Q8NE63 2/20 1.00
EPHA6 Q9UF33 2/20 1.00
CIT O14578 1/20 1.00
EPHB6 O15197 1/20 1.00
RIPK2 O43353 1/20 1.00
STK10 O94804 1/20 1.00
LYN P07948 1/20 1.00
RET P07949 1/20 1.00
CHRM2 P08172 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
Afatinib SCHEMBL28567422 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL2269415 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL29733662 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL2865630 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL231072 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL185621 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL2865634 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL185786 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL231073 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK
Afatinib SCHEMBL28409673 1.00 EGFR (1.00) EGFRERBB2GAKABL1LCK

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 16838 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4746970-A1 EGFR ANTAGONISTS FOR THE TREATMENT OF DISEASES INVOLVING UNWANTED MIGRATION, PROLIFERATION, AND/OR METAPLASIA OF RETINAL PIGMENT EPITHELIUM (RPE) CELLS Jonas, Jost B. (DE) 2026-05-27 EP claimed
EP-4747285-A1 MONOCLONAL ANTIBODIES AGAINST PCDH7 FOR LUNG CANCER THERAPY The Board of Regents of the University of Texas System (US) 2026-05-27 EP claimed
CN-122075497-A Use of NLRP3 agonist for tumor treatment 2026-05-26 CN claimed
CN-122075716-A Medicine for treating tumor by combining recombinant oncolytic virus and small-molecule anticancer medicine 2026-05-26 CN claimed
CN-122074043-A Combination therapy with KRAS modulators 光达治疗公司 2026-05-22 CN claimed
US-20260137678-A1 METHODS FOR TREATING OR PREVENTING NEUROENDOCRINE TUMOR FORMATION USING XPO1 INHIBITORS MEMORIAL SLOAN-KETTERING CANCER CENTER (US) 2026-05-21 US claimed
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-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
WO-2026107237-A1 RAS AND EGFR INHIBITORS COMBINATION THERAPY ERASCA, INC. (US) 2026-05-21 WO claimed
US-20050203088-A1 Medicament combinations based on scopine- or tropene acid esters with EGFR-kinase inhibitors BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-09-15 US claimed
US-20050165013-A1 Pharmaceutical compositions containing anticholinergics and EGFR kinase inhibitors BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-07-28 US claimed
US-20050148562-A1 Pharmaceutical compositions based on anticholinergics and additional active ingredients BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-07-07 US claimed
US-20050085495-A1 Process for preparing amino crotonyl compounds BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-04-21 US claimed
US-20050043233-A1 Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-02-24 US claimed
US-20040048887-A1 Pharmaceutical compositions based on anticholinergics and EGFR kinase inhibitors BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2004-03-11 US claimed
US-20030225079-A1 Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH)/prostatic hypertrophy BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2003-12-04 US claimed
US-20030158196-A1 Pharmaceutical compositions based on anticholinergics and EGFR kinase inhibitors BOEHRINGER INGELHEIM PHARMA GMBH CO. KG (DE) 2003-08-21 US 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
US-20020173509-A1 Quinazoline derivatives and phamaceutical compositions containing them BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2002-11-21 US claimed