SCHEMBL578750

SCHEMBL578750

CC(C)NC(=O)[C@H]1CCC[C@H]1Nc1nc(Nc2ccc(C(=O)N(C)C3CCN(C)CC3)cc2)ncc1Cl

nearest known ligand 0.50

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SYK P43405 4/20 0.50
KDR P35968 3/20 0.50
AURKB Q96GD4 3/20 0.50
PTK2 Q05397 3/20 0.47
INSR P06213 4/20 0.47
ALK Q9UM73 4/20 0.47
JAK2 O60674 2/20 0.44
JAK1 P23458 2/20 0.44
AXL P30530 3/20 0.43
NTRK1 P04629 1/20 0.42

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
SCHEMBL578749 1.00 SYK (0.50) SYKKDRAURKBPTK2INSR
SCHEMBL579032 0.92 SYK (0.51) SYKAURKBPTK2JAK2JAK1
SCHEMBL579033 0.92 SYK (0.51) SYKAURKBPTK2JAK2JAK1
SCHEMBL578928 0.91 AURKA (0.53) SYKAURKBPTK2JAK2JAK1
SCHEMBL578929 0.91 AURKA (0.53) SYKAURKBPTK2JAK2JAK1
SCHEMBL578714 0.90 PTK2 (0.57) SYKPTK2ALKNTRK1
SCHEMBL12174633 0.90 PTK2 (0.57) SYKPTK2ALKNTRK1
SCHEMBL578672 0.90 PTK2 (0.57) SYKPTK2ALKNTRK1
SCHEMBL578671 0.90 PTK2 (0.57) SYKPTK2ALKNTRK1
SCHEMBL13808220 0.88 PTK2 (0.55) SYKPTK2ALKNTRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4115907-B1 COMBINATION DRUG OF KINASE INHIBITORS FOR USE IN THE TREATMENT OF PANCREATIC CANCER UNIV HOKKAIDO NAT UNIV CORP (JP) 2026-05-06 EP claimed
CN-114207437-B Method for screening anticancer agent and combination drug of kinase inhibitor for treating pancreatic cancer 国立大学法人北海道大学 2024-05-28 CN claimed
EP-4115907-A1 METHOD FOR SCREENING ANTICANCER AGENT AND COMBINATION DRUG OF KINASE INHIBITORS FOR TREATMENT OF PANCREATIC CANCER National University Corporation Hokkaido University (JP) 2023-01-11 EP claimed
US-20220387630-A1 METHOD FOR SCREENING ANTICANCER AGENT AND COMBINATION DRUG OF KINASE INHIBITORS FOR TREATMENT OF PANCREATIC CANCER NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2022-12-08 US claimed
CN-114207437-A Method of screening anticancer agent and combination drug of kinase inhibitor for treating pancreatic cancer 国立大学法人北海道大学 2022-03-18 CN claimed
EP-2027107-B1 2, 4 -DIAMINO PYRIMIDINES AS CELL CYCLE KINASE INHIBITORS BOEHRINGER INGELHEIM INT (DE) 2012-02-15 EP claimed
EP-4115907-B1 COMBINATION DRUG OF KINASE INHIBITORS FOR USE IN THE TREATMENT OF PANCREATIC CANCER UNIV HOKKAIDO NAT UNIV CORP (JP) 2026-05-06 EP disclosed
CN-114207437-B Method for screening anticancer agent and combination drug of kinase inhibitor for treating pancreatic cancer 国立大学法人北海道大学 2024-05-28 CN disclosed
CN-116334024-A Aurora kinase B gene K85 and K87 mutation and application thereof 北京大学 2023-06-27 CN disclosed
CN-116004567-A Aurora kinase B gene K202 mutation and application thereof 北京大学 2023-04-25 CN disclosed
EP-4115907-A1 METHOD FOR SCREENING ANTICANCER AGENT AND COMBINATION DRUG OF KINASE INHIBITORS FOR TREATMENT OF PANCREATIC CANCER National University Corporation Hokkaido University (JP) 2023-01-11 EP disclosed
US-20220387630-A1 METHOD FOR SCREENING ANTICANCER AGENT AND COMBINATION DRUG OF KINASE INHIBITORS FOR TREATMENT OF PANCREATIC CANCER NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2022-12-08 US disclosed
CN-114207437-A Method of screening anticancer agent and combination drug of kinase inhibitor for treating pancreatic cancer 国立大学法人北海道大学 2022-03-18 CN disclosed
US-20130289014-A1 Combination therapy in treatment of oncological and fibrotic diseases BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-10-31 US disclosed
US-20120107304-A1 Combination therapy in treatment of oncological and fibrotic diseases BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-05-03 US disclosed
EP-2027107-B1 2, 4 -DIAMINO PYRIMIDINES AS CELL CYCLE KINASE INHIBITORS BOEHRINGER INGELHEIM INT (DE) 2012-02-15 EP disclosed
WO-2011134898-A1 NEW COMBINATION THERAPY IN TREATMENT OF ONCOLOGICAL AND FIBROTIC DISEASES BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2011-11-03 WO disclosed
US-20090163467-A1 New compounds BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-06-25 US disclosed
US-20090163467-A1 New compounds BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-06-25 US disclosed
WO-2007132010-A1 2, 4 -DIAMINO PYRIMIDINES AS CELL CYCLE KINASE INHIBITORS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-11-22 WO 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-20120107304-A1 Combination therapy in treatment of oncological and fibrotic diseases AURKB, AURKC, AURKA SYK 926/4885KDR 45/4885AURKB 1/4885
US-20130289014-A1 Combination therapy in treatment of oncological and fibrotic diseases AURKB, AURKC, AURKA SYK 926/4885KDR 45/4885AURKB 1/4885
US-20090163467-A1 New compounds CCNA1, MKI67, CCNT1 SYK 3650/4885KDR 1793/4885AURKB 1454/4885

“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.