Pelitinib

Pelitinib

SCHEMBL29349785

CCOc1cc2ncc(C#N)c(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)/C=C/CN(C)C

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 Pelitinib. 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 P04626 14/20 1.00
STK25 O00506 1/20 1.00
CIT O14578 1/20 1.00
CHEK1 O14757 1/20 1.00
GAK O14976 1/20 1.00
DAPK3 O43293 1/20 1.00
JAK2 O60674 1/20 1.00
STK17B O94768 1/20 1.00
STK10 O94804 1/20 1.00
MAP4K4 O95819 1/20 1.00
ABL1 P00519 1/20 1.00
LCK P06239 1/20 1.00
FYN P06241 1/20 1.00
FES P07332 1/20 1.00
CSF1R P07333 1/20 1.00
YES1 P07947 1/20 1.00
LYN P07948 1/20 1.00
MET P08581 1/20 1.00
HCK P08631 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
Pelitinib SCHEMBL29623744 1.00 EGFR (1.00) EGFRERBB2STK25CITCHEK1
Pelitinib SCHEMBL29385637 1.00 EGFR (1.00) EGFRERBB2STK25CITCHEK1
Pelitinib SCHEMBL29352012 1.00 EGFR (1.00) EGFRERBB2STK25CITCHEK1
Pelitinib SCHEMBL93756 1.00 EGFR (1.00) EGFRERBB2STK25CITCHEK1
Pelitinib SCHEMBL93757 1.00 EGFR (1.00) EGFRERBB2STK25CITCHEK1
SCHEMBL8132957 0.93 EGFR (1.00) EGFRERBB2STK25CITCHEK1
SCHEMBL6382792 0.93 EGFR (1.00) EGFRERBB2STK25CITCHEK1
SCHEMBL12641715 0.92 EGFR (1.00) EGFRERBB2STK25CITCHEK1
SCHEMBL10108217 0.92 EGFR (0.85) EGFRERBB2STK25CITCHEK1
SCHEMBL14944414 0.92 EGFR (0.85) EGFRERBB2STK25CITCHEK1

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 4724 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107237-A1 RAS AND EGFR INHIBITORS COMBINATION THERAPY ERASCA, INC. (US) 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
CN-122005813-A Targeted treatment of cancers with deregulated fibroblast growth factor receptor signaling 法码科思莫斯控股有限公司 2026-05-12 CN claimed
EP-4363043-B1 COMPOSITIONS FOR USE IN METHODS FOR INCREASING CANCER CELL SENSITIVITY TO ALTERNATING ELECTRIC FIELDS NOVOCURE GMBH (CH) 2026-04-22 EP claimed
EP-4724151-A1 A 1,5-DIHYDRO-4H-PYRROLO[3,2-C] PYRIDIN-4-ONE FOR USE IN THE TREATMENT OF CANCER Antares Therapeutics, Inc. (US) 2026-04-15 EP claimed
EP-4724150-A1 A 1,5-DIHYDRO-4H-PYRROLO[3,2-C] PYRIDIN-4-ONE FOR USE IN THE TREATMENT OF CANCER Antares Therapeutics, Inc. (US) 2026-04-15 EP claimed
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields NOVOCURE GMBH (CH) 2026-04-07 US claimed
US-20260091021-A1 COMBINATION THERAPIES COMPRISING PANOBINOSTAT FOR THE TREATMENT OF CHOLANGIOCARCINOMA SEALD AS (NO) 2026-04-02 US 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
CN-110325212-B Farnesyl transferase inhibitors for use in methods of treating cancer 库拉肿瘤学公司 2022-03-22 CN claimed
EP-3965896-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER The United States Government as Represented by the Department of Veterans Affairs (US) 2022-03-16 EP claimed
EP-3964513-A1 COMBINATION PRODUCTS WITH TYROSINE KINASE INHIBITORS AND THEIR USE Novartis AG (CH) 2022-03-09 EP claimed
EP-3955928-A1 COMPOUNDS WITH ANTI-TUMOR ACTIVITY AGAINST CANCER CELLS BEARING TYROSINE KINASE INHIBITOR RESISTANT EGFR MUTATIONS Board of Regents, The University of Texas System (US) 2022-02-23 EP claimed
WO-2022029628-A1 COMPOSITIONS AND METHODS FOR INCREASING CANCER CELL SENSITIVITY TO ALTERNATING ELECTRIC FIELDS NOVOCURE GMBH (CH) 2022-02-10 WO claimed
US-20220041704-A1 METHODS AND COMPOSITIONS FOR INHIBITION OF EGF/EGFR PATHWAY IN COMBINATION WITH TYROSINE KINASE INHIBITORS IN3BIO LTD. (BM) 2022-02-10 US claimed
CN-113975393-A Methods of treating gefitinib resistant cancers 综合医院公司 2022-01-28 CN claimed
EP-3942045-A1 A DBAIT MOLECULE IN COMBINATION WITH KINASE INHIBITOR FOR THE TREATMENT OF CANCER ONXEO (FR) 2022-01-26 EP claimed
CN-113952338-A Methods of treating gefitinib resistant cancers 综合医院公司 2022-01-21 CN claimed
CN-113952459-A Methods of treating gefitinib resistant cancers 综合医院公司 2022-01-21 CN claimed