Gefitinib

Gefitinib

SCHEMBL7866

COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN1CCOCC1

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 Gefitinib. 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 18/20 1.00
KDR P35968 3/20 1.00
BRAF P15056 2/20 1.00
EPHB4 P54760 2/20 1.00
FLT4 P35916 2/20 1.00
CIT O14578 1/20 1.00
GAK O14976 1/20 1.00
EPHB6 O15197 1/20 1.00
ABCC4 O15439 1/20 1.00
DAPK3 O43293 1/20 1.00
RIPK2 O43353 1/20 1.00
NR1I2 O75469 1/20 1.00
RPS6KA4 O75676 1/20 1.00
STK17B O94768 1/20 1.00
STK10 O94804 1/20 1.00
PRKD3 O94806 1/20 1.00
ABCB11 O95342 1/20 1.00
MAP4K4 O95819 1/20 1.00
CHEK2 O96017 1/20 1.00
ABL1 P00519 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
Gefitinib SCHEMBL465143 1.00 EGFR (1.00) EGFRKDRBRAFEPHB4FLT4
SCHEMBL1734701 1.00 EGFR (1.00) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL29351336 1.00 EGFR (1.00) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL29351046 1.00 EGFR (1.00) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL28098790 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL29371159 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL2770155 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL28097850 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL11776 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4
Gefitinib SCHEMBL30887946 0.99 EGFR (0.98) EGFRKDRBRAFEPHB4FLT4

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 127784 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
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-116209439-B Cereblon protein modulators Saint Jude Children's Research Hospital Ltd. (US) 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-20260137685-A1 SOLID PHARMACEUTICAL FORMULATION OF PARP INHIBITORS AND USE THEREOF IMPACT THERAPEUTICS SHANGHAI INC (CN) 2026-05-21 US claimed
US-20260137686-A1 SOLID PHARMACEUTICAL FORMULATION OF PARP INHIBITORS AND USE THEREOF IMPACT THERAPEUTICS SHANGHAI INC (CN) 2026-05-21 US claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO 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-2002056692-A1 METHODS FOR MODULATING TUMOR GROWTH AND METASTASIS BRISTOL-MYERS SQUIBB COMPANY (US) 2002-07-25 WO claimed
EP-1225233-A2 Means and methods for treatment evaluation Amsterdam Support Diagnostics B.V. (NL) 2002-07-24 EP claimed
WO-2002045717-A1 LOMETREXOL COMBINATION THERAPY TULARIK INC. (US) 2002-06-13 WO claimed
US-20020061304-A1 Combined treatment with keratinocyte growth factor and epidermal growth factor inhibitor PFIZER PRODUCTS INC. & OSI PHARMACEUTICALS, INC. 2002-05-23 US claimed
WO-2002018368-A1 TRICYCLIC ANTITUMOR COMPOUNDS BEING FARNESYL PROTEIN TRANSFERASE INHIBITORS SCHERING CORPORATION (US) 2002-03-07 WO claimed
US-20020002162-A1 Synergistic methods and compositions for treating cancer BRISTOL-MYERS SQUIBB COMPANY 2002-01-03 US claimed
WO-2001072721-A2 SYNERGISTIC METHODS AND COMPOSITIONS FOR TREATING CANCER BRISTOL-MYERS SQUIBB COMPANY (US) 2001-10-04 WO claimed
WO-2001070255-A2 COMBINED TREATMENT WITH KERATINOCYTE GROWTH FACTOR AND EPIDERMAL GROWTH FACTOR INHIBITOR PFIZER PRODUCTS, INC. (US) 2001-09-27 WO claimed
EP-0823900-B1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2000-12-27 EP claimed
US-5770599-A RECEPTOR TYROSINE KINASE INHIBITORS including 4-(3'-chloro-4'-fluoroanilino)-7-methoxy-6-(2-morpholinoethoxy)quinazoline (gefitinib) ZENECA LIMITED (GB) 1998-06-23 US claimed