SCHEMBL597105

SCHEMBL597105

COc1cc2c(Nc3ccc(NC(=O)c4ccccc4)cc3)ncnc2cc1OCCCN1CCOCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGFR P00533 11/20 1.00
KDR P35968 11/20 1.00
AURKA O14965 7/20 1.00
AURKB Q96GD4 5/20 1.00
SRC P12931 2/20 1.00
ROCK2 O75116 1/20 1.00
ALDH1A1 P00352 1/20 1.00
LCK P06239 1/20 1.00
FYN P06241 1/20 1.00
RET P07949 1/20 1.00
MET P08581 1/20 1.00
MAPT P10636 1/20 1.00
PDGFRA P16234 1/20 1.00
LTK P29376 1/20 1.00
TTK P33981 1/20 1.00
MAP2K2 P36507 1/20 1.00
MAP2K1 Q02750 1/20 1.00
BTK Q06187 1/20 1.00
TYRO3 Q06418 1/20 1.00
TNK2 Q07912 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
SCHEMBL29377224 1.00 EGFR (1.00) EGFRKDRAURKAAURKBSRC
SCHEMBL6949133 0.91 EGFR (0.82) EGFRKDRAURKAAURKBSRC
SCHEMBL15519470 0.90 HDAC1 (1.00) EGFRKDRAURKAAURKBSRC
SCHEMBL13529060 0.89 SRC (0.84) EGFRKDRAURKAAURKBSRC
Hydrochloric Acid SCHEMBL3535974 0.89 EGFR (0.80) EGFRKDRAURKAAURKBSRC
SCHEMBL3578284 0.89 KDR (0.98) EGFRKDRAURKAAURKBSRC
SCHEMBL13497826 0.88 EGFR (0.80) EGFRKDRAURKAAURKBSRC
SCHEMBL12694312 0.88 EGFR (0.79) EGFRKDRAURKAAURKBSRC
SCHEMBL6704281 0.88 EGFR (0.80) EGFRKDRAURKAAURKBSRC
SCHEMBL31167326 0.86 EGFR (0.78) EGFRKDRAURKAAURKBSRC

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 173 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
US-20200181284-A1 EPIGENETIC INHIBITORS FOR SENSITIZING HEMATOLOGIC OR OTHER MALIGNANCIES TO GLUCOCORTICOID THERAPY UNIVERSITY OF SOUTHERN CALIFORNIA (US) 2020-06-11 US claimed
EP-3638268-A1 COMPOSITIONS AND METHODS FOR TREATING A CLINICAL CONDITION THROUGH THE USE OF HEMATOPOIETIC STEM CELLS Indiana University Research & Technology Corporation (US) 2020-04-22 EP claimed
US-20200054681-A1 COMPOSITIONS AND METHODS FOR TREATING A CLINICAL CONDITION THROUGH THE USE OF HEMATOPOIETIC STEM CELLS INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION (US) 2020-02-20 US claimed
WO-2019161000-A1 METHODS FOR TREATING FIBROSIS CHILDREN'S HOSPITAL MEDICAL CENTER (US) 2019-08-22 WO claimed
WO-2018232272-A1 COMPOSITIONS AND METHODS FOR TREATING A CLINICAL CONDITION THROUGH THE USE OF HEMATOPOIETIC STEM CELLS INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION (US) 2018-12-20 WO claimed
EP-2788504-B1 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS PALACKY UNIVERSITY OLOMOUC (CZ) 2016-08-17 EP claimed
US-20140336073-A1 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS PALACKY UNIVERSITY, OLOMOUC (CZ) 2014-11-13 US claimed
EP-2788504-A2 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS Palacky University, Olomouc (CZ) 2014-10-15 EP claimed
WO-2013083098-A2 METHOD OF DETERMINATION OF CANCER CELL DRUG SENSITIVITY TOWARDS AURORA KINASE INHIBITORS PALACKY UNIVERSITY, OLOMOUC (CZ) 2013-06-13 WO claimed
EP-2602330-A1 Method of determination of cancer cell drug sensitivity towards Aurora kinase inhibitors and overcoming their resistance Palacky University, Olomouc (CZ) 2013-06-12 EP claimed
EP-4541381-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2026-02-04 EP disclosed
US-20250381202-A1 PRODRUG KIT FOR MULTI-PRONGED CHEMOTHERAPY ZOUNEK ALEX (DE) 2025-12-18 US disclosed
EP-4545101-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
EP-4541380-B1 STABLE, CONCENTRATED RADIONUCLIDE COMPLEX SOLUTIONS ADVANCED ACCELERATOR APPLICATIONS S A (FR) 2025-12-10 EP disclosed
US-7563787-B2 Substituted pyrazole compounds MIIKANA THERAPEUTICS, INC. (US) 2009-07-21 US disclosed
US-20090029992-A1 SUBSTITUTED PYRAZOLE COMPOUNDS MIIKANA THERAPEUTICS, INC. 2009-01-29 US disclosed
US-20080200485-A1 Kinase Inhibitors MIIKANA THERAPEUTICS, INC. 2008-08-21 US disclosed
US-20070142368-A1 Substituted pyrazole compounds MIIKANA THERAPEUTICS, INC. 2007-06-21 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 (5 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-20200181284-A1 EPIGENETIC INHIBITORS FOR SENSITIZING HEMATOLOGIC OR OTHER MALIGNANCIES TO GLUCOCORTICOID THERAPY NR3C1, EZH2, MECP2 EGFR 3808/4885KDR 3256/4885AURKA 1971/4885
US-20250381202-A1 PRODRUG KIT FOR MULTI-PRONGED CHEMOTHERAPY KIT, CTSL, PAICS EGFR 358/4885KDR 328/4885AURKA 27/4885
US-20080200485-A1 Kinase Inhibitors AURKC, AURKA, AURKB EGFR 1016/4885KDR 2378/4885AURKA 2/4885
US-20070142368-A1 Substituted pyrazole compounds AURKC, AURKA, AURKB EGFR 1774/4885KDR 2577/4885AURKA 2/4885
US-20090029992-A1 SUBSTITUTED PYRAZOLE COMPOUNDS AURKC, AURKA, AURKB EGFR 1774/4885KDR 2577/4885AURKA 2/4885

“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.