Linifanib

Linifanib

SCHEMBL93804

Cc1ccc(F)c(NC(=O)Nc2ccc(-c3cccc4[nH]nc(N)c34)cc2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CSF1RFLT1FLT3FLT4KDRPDGFRAPDGFRB

The experimentally established mechanism targets of Linifanib. 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
KDR known ✓ P35968 19/20 1.00
FLT3 known ✓ P36888 16/20 1.00
CSF1R known ✓ P07333 10/20 1.00
FLT4 known ✓ P35916 10/20 1.00
FLT1 known ✓ P17948 9/20 1.00
PDGFRB known ✓ P09619 1/20 1.00
PDGFRA known ✓ P16234 1/20 1.00
KIT P10721 14/20 1.00
LYN P07948 7/20 1.00
SRC P12931 6/20 1.00
BLK P51451 6/20 1.00
AURKA O14965 5/20 1.00
AURKB Q96GD4 5/20 1.00
PLK4 O00444 4/20 1.00
ROCK2 O75116 4/20 1.00
MET P08581 4/20 1.00
PRKACA P17612 4/20 1.00
RPS6KB1 P23443 4/20 1.00
CSNK1D P48730 4/20 1.00
STK3 Q13188 4/20 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
Linifanib SCHEMBL29375368 1.00 KDR (1.00) KDRFLT3KITCSF1RFLT4
Linifanib SCHEMBL1880038 0.99 KDR (0.98) KDRFLT3KITCSF1RFLT4
Linifanib SCHEMBL2239943 0.97 KDR (0.94) KDRFLT3KITCSF1RFLT4
SCHEMBL421934 0.90 KDR (0.82) KDRFLT3KITCSF1RFLT4
SCHEMBL420765 0.90 KDR (1.00) KDRFLT3KITCSF1RFLT4
SCHEMBL1662335 0.89 KDR (0.81) KDRFLT3KITCSF1RFLT4
SCHEMBL423705 0.89 KDR (0.80) KDRFLT3KITCSF1RFLT4
SCHEMBL1659063 0.89 KDR (0.79) KDRFLT3KITCSF1RFLT4
SCHEMBL424019 0.89 KDR (0.79) KDRFLT3KITCSF1RFLT4
SCHEMBL6073436 0.89 KDR (0.79) KDRFLT3KITCSF1RFLT4

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 4138 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260142007-A1 DIGITAL THERAPEUTICS AND COMBINATION THERAPY FOR THE TREATMENT OF TENOSYNOVIAL GIANT CELL TUMOR (TGCT) REMEPY HEALTH LTD (IL) 2026-05-21 US claimed
EP-4735120-A2 CHEMICALLY INDUCED REPROGRAMMING TO REVERSE AGING President and Fellows of Harvard College (US) 2026-05-06 EP claimed
EP-4729519-A1 CRYSTAL FORM OF ENPP1 INHIBITOR CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. (CN) 2026-04-22 EP claimed
EP-4719387-A2 COMPLEMENT ANTIBODY-DRUG CONJUGATES ADS Therapeutics LLC (US) 2026-04-08 EP claimed
US-20260076943-A1 METHOD FOR IMPROVING SKELETAL HEALTH UNIV INDIANA TRUSTEES (US) 2026-03-19 US claimed
US-20260076872-A1 POLYMER VIALS WITH SUBSTANTIALLY FLAT BOTTOMS AND INJECTION STRETCH BLOW MOLDING METHODS FOR MAKING THE SAME SIO2 MEDICAL PRODUCTS LLC (US) 2026-03-19 US claimed
WO-2026041394-A1 A CSF1R INHIBITOR AND A BONE MARROW CELL POPULATION FOR THE REPLACEMENT OF MICROGLIA AND CENTRAL NERVOUS SYSTEM-ASSOCIATED MACROPHAGES IN CENTRAL NERVOUS SYSTEM DISEASES Albert-Ludwigs-Universität Freiburg, Körperschaft des öffentlichen Rechts (DE) 2026-02-26 WO claimed
US-20260028587-A1 COMPOSITIONS AND METHODS FOR MICROGLIA REPLACEMENT THERAPY NOVOGLIA, INC. 2026-01-29 US claimed
US-12522873-B2 ALK and NTRK1 fusion molecules and uses thereof FOUNDATION MEDICINE, INC. (US) 2026-01-13 US claimed
US-12491183-B2 Compositions and methods of using nintedanib for treating ocular diseases with abnormal neovascularization ADS THERAPEUTICS LLC (US) 2025-12-09 US claimed
US-20070148225-A1 PHARMACEUTICAL FORMULATION FOR DELIVERY OF RECEPTOR TYROSINE KINASE INHIBITING (RTKi) COMPOUNDS TO THE EYE ALCON, INC. (US) 2007-06-28 US claimed
EP-1797877-A1 JOINT USE OF SULFONAMIDE BASED COMPOUND WITH ANGIOGENESIS INHIBITOR Eisai Co., Ltd. (JP) 2007-06-20 EP claimed
US-20070104780-A1 Formulation comprising a drug of low water solubility and method of use thereof ABBVIE INC. 2007-05-10 US claimed
WO-2006091801-A2 METHODS FOR TREATING OCULAR ANGIOGENESIS, RETINAL EDEMA, RETINAL ISCHEMIA, AND DIABETIC RETINOPATHY USING SELECTIVE RTK INHIBITORS ALCON, INC. (CH) 2006-08-31 WO claimed
US-20060189608-A1 Methods for treating ocular angiogenesis, retinal edema, retinal ischemia, and diabetic retinopathy using selective RTK inhibitors ALCON, INC. 2006-08-24 US claimed
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors EISAI CO., LTD. (JP) 2006-06-22 US claimed
EP-1638941-A1 INDAZOLE, BENZISOXAZOLE, AND BENZISOTHIAZOLE KINASE INHIBITORS ABBOTT LABORATORIES (US) 2006-03-29 EP claimed
US-20050020603-A1 Indazole, benzisoxazole, and benzisothiazole kinase inhibitors ABBVIE INC. 2005-01-27 US claimed
WO-2004113304-A1 INDAZOLE, BENZISOXAZOLE, AND BENZISOTHIAZOLE KINASE INHIBITORS ABBOTT LABORATORIES (US) 2004-12-29 WO claimed
US-20040235892-A1 Indazole and benzisoxazole kinase inhibitors ABBOTT LABORATORIES 2004-11-25 US claimed