Pazopanib

Pazopanib

SCHEMBL159487

Cc1ccc(Nc2nccc(N(C)c3ccc4c(C)n(C)nc4c3)n2)cc1S(N)(=O)=O.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CSF1RFGFR1FGFR3FLT1FLT4ITKKDRKITLCKPDGFRAPDGFRB

The experimentally established mechanism targets of Pazopanib. 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 15/20 0.98
KIT known ✓ P10721 10/20 0.98
PDGFRA known ✓ P16234 9/20 0.98
FLT1 known ✓ P17948 4/20 0.98
FLT4 known ✓ P35916 3/20 0.98
CSF1R known ✓ P07333 2/20 0.98
PDGFRB known ✓ P09619 2/20 0.98
FGFR1 known ✓ P11362 2/20 0.98
LCK known ✓ P06239 1/20 0.98
FGFR3 known ✓ P22607 1/20 0.98
ABCB11 O95342 2/20 0.98
CYP3A4 P08684 2/20 0.98
CYP2D6 P10635 2/20 0.98
CYP2C9 P11712 2/20 0.98
CYP2C19 P33261 2/20 0.98
BMPR1B O00238 1/20 0.98
PLK4 O00444 1/20 0.98
AURKA O14965 1/20 0.98
GAK O14976 1/20 0.98
EPHB6 O15197 1/20 0.98

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
Pazopanib SCHEMBL29386934 1.00 KDR (0.98) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL935692 0.99 KDR (0.97) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL588608 0.99 KDR (1.00) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL29392503 0.99 KDR (1.00) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL29520402 0.98 KDR (0.98) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL3173301 0.97 KDR (0.95) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL13025440 0.94 KDR (0.90) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL13025438 0.94 KDR (0.90) KDRKITPDGFRAFLT1FLT4
Pazopanib SCHEMBL13025441 0.93 KDR (0.89) KDRKITPDGFRAFLT1FLT4
SCHEMBL22720091 0.93 KDR (0.89) KDRKITPDGFRAFLT1FLT4

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 4628 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260124153-A1 METAL OXIDE ENCAPSULATED DRUG COMPOSITIONS AND METHODS OF PREPARING THE SAME APPLIED MATERIALS INC (US) 2026-05-07 US claimed
EP-4719365-A1 COMBINATION THERAPY WITH A MTOR INHIBITOR AND A MULTI-TYROSINE KINASE INHIBITOR FOR TREATING SOFT TISSUE SARCOMA Aadi Bioscience, Inc. (US) 2026-04-08 EP claimed
EP-4709378-A1 COMPOUNDS FOR NOS-RELATED CANCERS AND METHODS OF USE Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2026-03-18 EP claimed
US-20260069700-A1 BRUSH PRODRUGS AND USES THEREOF MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2026-03-12 US claimed
US-20260042816-A1 TYROSINE KINASE INHIBITOR AND ACTIVIN TYPE 2 RECEPTOR ANTAGONIST COMBINATION THERAPY FOR TREATING PULMONARY ARTERIAL HYPERTENSION (PAH) GB002 INC (US) 2026-02-12 US claimed
EP-4662203-A1 BINDARIT CONJUGATES, COMPOSITIONS AND METHODS FOR TREATING OCULAR DISEASES OR DISORDERS Translatum Medicus Inc. (CA) 2025-12-17 EP claimed
US-12478683-B2 Brush prodrugs and uses thereof MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2025-11-25 US claimed
EP-3957329-B1 COMPOSITION COMPRISING THE COMBINATION OF SOTAGLIFLOZIN AS THE SODIUM/GLUCOSE CO-TRANSPORTER 1 INHIBITOR (SGLT1) AND A VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 2 INHIBITOR (VEGFR2) FOR USE IN TREATING CANCER NEWISH TECH BEIJING CO LTD (CN) 2025-11-19 EP claimed
EP-4637769-A1 METHODS OF TREATING ADVANCED SOLID TUMORS Kura Oncology, Inc. (US) 2025-10-29 EP claimed
EP-4630456-A1 ANTI-CMET ANTIBODY DRUG CONJUGATES AND THERAPEUTIC USES THEREOF Mythic Therapeutics, Inc. (US) 2025-10-15 EP claimed
WO-2014066204-A1 COMBINATION GLAXOSMITHKLINE LLC (US) 2014-05-01 WO claimed
US-20130237554-A1 COMBINATION NOVARTIS PHARMA AG (CH) 2013-09-12 US claimed
EP-2608790-A1 PHARMACEUTICAL COMBINATION OF A VEGFR INHIBITOR AND A MEK INHIBITOR USEFUL FOR TREATING CANCER GlaxoSmithKline Intellectual Property Development Limited (GB) 2013-07-03 EP claimed
US-20130165456-A1 COMBINATION NOVARTIS AG (CH) 2013-06-27 US claimed
WO-2013066616-A1 PAZOPANIB FORMULATION GLAXO WELLCOME MANUFACTURING PTE LTD (SG) 2013-05-10 WO claimed
EP-2575460-A1 COMBINATION GlaxoSmithKline LLC (US) 2013-04-10 EP claimed
WO-2012027438-A1 PHARMACEUTICAL COMBINATION OF A VEGFR INHIBITOR AND A MEK INHIBITOR USEFUL FOR TREATING CANCER GLAXOSMITHKLINE LLC (US) 2012-03-01 WO claimed
US-8114885-B2 Pazopanib hydrochloride and synthesis, chemical intermediates, and dosage forms thereof; anticancer; colon cancer, breast cancer GLAXOSMITHKLINE LLC (US) 2012-02-14 US claimed
WO-2011150044-A1 COMBINATION GLAXOSMITHKLINE LLC (US) 2011-12-01 WO claimed
US-20070292513-A1 CHEMICAL COMPOUNDS NOVARTIS AG (CH) 2007-12-20 US claimed