Orantinib

Orantinib

SCHEMBL900355

Cc1[nH]c(/C=C2/C(=O)Nc3ccccc32)c(C)c1CCC(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FGFR1FGFR2FGFR3FGFR4KDRPDGFRAPDGFRB

The experimentally established mechanism targets of Orantinib. 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
FGFR1 known ✓ P11362 16/20 1.00
KDR known ✓ P35968 16/20 1.00
PDGFRB known ✓ P09619 16/20 1.00
FGFR3 known ✓ P22607 1/20 1.00
FLT1 P17948 3/20 1.00
AURKA O14965 2/20 1.00
RET P07949 2/20 1.00
FLT3 P36888 2/20 1.00
MAP4K2 Q12851 2/20 1.00
STK3 Q13188 2/20 1.00
AURKB Q96GD4 2/20 1.00
ZAP70 P43403 2/20 1.00
GAK O14976 1/20 1.00
RPS6KA5 O75582 1/20 1.00
RPS6KA4 O75676 1/20 1.00
LATS1 O95835 1/20 1.00
CSNK2A2 P19784 1/20 1.00
MAP2K2 P36507 1/20 1.00
MAP2K1 Q02750 1/20 1.00
STK4 Q13043 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
Orantinib SCHEMBL134662 1.00 FGFR1 (1.00) FGFR1KDRPDGFRBFLT1AURKA
Orantinib SCHEMBL134661 1.00 FGFR1 (1.00) FGFR1KDRPDGFRBFLT1AURKA
Orantinib SCHEMBL29354645 1.00 FGFR1 (1.00) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL12020869 0.91 KDR (0.84) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL25717271 0.90 KDR (0.82) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL26023377 0.88 KDR (0.79) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL13497857 0.88 KDR (0.79) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL4408686 0.88 KDR (1.00) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL29678231 0.88 KDR (1.00) FGFR1KDRPDGFRBFLT1AURKA
SCHEMBL30676938 0.88 KDR (1.00) FGFR1KDRPDGFRBFLT1AURKA

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

Claimed or disclosed in 133 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210213037-A1 METHODS FOR TREATING FIBROSIS CHILDREN'S HOSPITAL MEDICAL CENTER (US) 2021-07-15 US claimed
EP-3752161-A1 METHODS FOR TREATING FIBROSIS Children's Hospital Medical Center (US) 2020-12-23 EP claimed
WO-2019161000-A1 METHODS FOR TREATING FIBROSIS CHILDREN'S HOSPITAL MEDICAL CENTER (US) 2019-08-22 WO claimed
EP-2994130-A1 FGF MODULATION OF IN VIVO ANTIBODY PRODUCTION AND HUMORAL IMMUNITY Bush, Andrew B. (US) 2016-03-16 EP claimed
WO-2014182277-A1 FGF MODULATION OF IN VIVO ANTIBODY PRODUCTION AND HUMORAL IMMUNITY BUSH ANDREW B (US) 2014-11-13 WO claimed
WO-2014175444-A1 ANTI-NLRR1 ANTIBODY 千葉県 (JP) 2014-10-30 WO claimed
US-20130236483-A1 FGF MODULATION OF IN VIVO ANTIBODY PRODUCTION AND HUMORAL IMMUNITY BUSH ANDREW B (US) 2013-09-12 US claimed
EP-4743106-A1 METHODS OF USING THE BRAIN-DERIVED OSTEOGENIC FACTOR CCN3 FOR TREATMENT OF BONE AND CARTILAGE DEGENERATION The Regents of University of California (US) 2026-05-20 EP disclosed
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION ERESINA LLC (US) 2026-04-16 US disclosed
EP-3954436-B1 METHOD FOR PRODUCING BIOTISSUE-LIKE STRUCTURE ORIZURU THERAPEUTICS INC (JP) 2026-01-07 EP disclosed
WO-2025101807-A1 TREATMENT OF GLIOMAS WITH CHIMERIC ANTIGEN RECEPTOR T CELLS THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2025-05-15 WO disclosed
US-12268715-B2 Method for producing biological tissue-like structure Orizuru Therapeutics, Inc. (JP) 2025-04-08 US disclosed
US-20250074981-A1 COMBINATION THERAPY WITH DEXAMETHASONE AND TUMOR-SPECIFIC T CELL ENGAGING MULTI-SPECIFIC ANTIBODIES FOR TREATING CANCER NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2025-03-06 US disclosed
WO-2008132153-A1 NOVEL TETRAHYDROCARBAZOLE DERIVATIVES AS LIGANDS OF G-PROTEIN COUPLED RECEPTORS ÆTERNA ZENTARIS GMBH (DE) 2008-11-06 WO disclosed
EP-1988098-A1 Novel Tetrahydrocarbazole Derivatives as Ligands of G-protein Coupled Receptors AEterna Zentaris GmbH (DE) 2008-11-05 EP disclosed
EP-1976529-A2 ANG2 AND VEGF INHIBITOR COMBINATIONS Amgen Inc. (US) 2008-10-08 EP disclosed
EP-1915151-A2 COMBINATIONS FOR THE TREATMENT OF CANCER COMPRISING ANTI-EGFR ANTIBODY AND VEGFR INHIBITORS Amgen, Inc (US) 2008-04-30 EP disclosed
WO-2007089445-A2 ANG2 AND VEGF INHIBITOR COMBINATIONS AMGEN INC. (US) 2007-08-09 WO disclosed
WO-2006102504-A2 COMBINATIONS FOR THE TREATMENT OF CANCER COMPRISING ANTI-EGFR ANTIBODY AND VEGFR INHIBITORS AMGEN INC (US) 2006-09-28 WO disclosed
US-20060216288-A1 Combinations for the treatment of cancer AMGEN INC (US) 2006-09-28 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060216288-A1 Combinations for the treatment of cancer TP53, VHL, FOLR2 FGFR1 646/4885KDR 2043/4885PDGFRB 737/4885
US-20130236483-A1 FGF MODULATION OF IN VIVO ANTIBODY PRODUCTION AND HUMORAL IMMUNITY FGF2, FGF1, FGFR2 FGFR1 4/4885KDR 130/4885PDGFRB 59/4885
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION COL2A1, COLGALT1, PLOD3 FGFR1 3001/4885KDR 4542/4885PDGFRB 2435/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.