SCHEMBL1203641

SCHEMBL1203641

CCN(CC)CCNC(=O)c1ccc(OC)c(Nc2ncc3c(n2)N(C2CCCC2)CCC(=O)N3C)c1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PLK1 P53350 16/20 0.67
RAD52 P43351 1/20 0.66
TTK P33981 4/20 0.58
BRD4 O60885 4/20 0.58
BRDT Q58F21 4/20 0.58
PLK3 Q9H4B4 4/20 0.54
PLK4 O00444 1/20 0.54
GAK O14976 1/20 0.54
STK33 Q9BYT3 1/20 0.54
ALK Q9UM73 1/20 0.54
PLK2 Q9NYY3 1/20 0.52
PRKD3 O94806 1/20 0.51
MAP4K4 O95819 1/20 0.51
PRKCG P05129 1/20 0.51
CLK2 P49760 1/20 0.51
RPS6KA3 P51812 1/20 0.51
NEK4 P51957 1/20 0.51
PTK2 Q05397 1/20 0.51
CAMK2G Q13555 1/20 0.51
CAMK2D Q13557 1/20 0.51

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
SCHEMBL1203787 0.95 PLK1 (0.74) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203461 0.91 PLK1 (0.71) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203986 0.91 PLK1 (0.71) PLK1RAD52TTKBRD4BRDT
SCHEMBL1202863 0.90 PLK1 (0.67) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203349 0.90 PLK1 (0.69) PLK1RAD52TTKBRD4BRDT
SCHEMBL1204132 0.89 PLK1 (0.68) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203263 0.88 PLK1 (0.67) PLK1RAD52TTKBRD4BRDT
SCHEMBL3549824 0.88 RAD52 (0.76) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203674 0.87 PLK1 (0.66) PLK1RAD52TTKBRD4BRDT
SCHEMBL1203784 0.87 PLK1 (0.73) PLK1RAD52TTKBRD4BRDT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112279806-B Organic electrode material and preparation method and application thereof 西南大学 2023-10-17 CN claimed
US-20150344486-A1 PYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS CYCLACEL LIMITED (GB) 2015-12-03 US claimed
EP-2610256-A1 Pyrimidine derivatives as protein kinase inhibitors Cyclacel Limited (GB) 2013-07-03 EP claimed
CN-101560183-B Method for preparing 5-bromo-2-methylpyridine ZHEJIANG MED XINCHANG PHARM 2011-02-02 CN claimed
CN-101560183-A Method for preparing 5-bromo-2-methylpyridine ZHEJIANG MEDICINE CO LTD (CN) 2009-10-21 CN claimed
CN-101514184-A Synthetic method of 5-bromo-2-methylpyridine NANJING UNIVERSITY OF TECHNOLOGY (CN) 2009-08-26 CN claimed
CN-100427468-C Apparatus and method for separating 5-bromo-2-methyl pyridine isomer by intermittent rectification under vacuum UNIV TIANJIN (CN) 2008-10-22 CN claimed
CN-1850803-A Apparatus and method for separating 5-bromo-2-methyl pyridine isomer by intermittent rectification under vacuum UNIV TIANJIN (CN) 2006-10-25 CN claimed
EP-2917181-B1 HETEROARYL DERIVATIVES AND USES THEREOF JACOBUS PHARMACEUTICAL COMPANY INC (US) 2019-09-25 EP disclosed
EP-2589592-B1 NOVEL NICOTINAMIDE DERIVATIVES OR SALTS THEREOF FUJIFILM CORP (JP) 2018-08-22 EP disclosed
EP-2493889-B1 IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2017-09-06 EP disclosed
EP-2545055-B1 Imidazo[1,2-a]pyrazine derivatives and their use for the prevention or treatment of neurological, psychiatric and metabolic disorders and diseases JANSSEN PHARMACEUTICA NV (BE) 2017-08-09 EP disclosed
US-9493471-B2 Pyrimidine derivatives as protein kinase inhibitors CYCLACEL LIMITED (GB) 2016-11-15 US disclosed
US-9493471-B2 Pyrimidine derivatives as protein kinase inhibitors CYCLACEL LIMITED (GB) 2016-11-15 US disclosed
EP-0508445-A1 1-Arylheteroarylalkyl substituted-1H-1,2,4-triazole compounds for treatment of circulatory disorders G.D. Searle & Co. (US) 1992-10-14 EP disclosed
EP-0508393-A1 N-arylheteroarylalkyl imidazol-2-one compounds for treatment of circulatory disorders G.D. Searle & Co. (US) 1992-10-14 EP disclosed
US-5155117-A Hypotensive agents G. D. SEARLE & CO. (US) 1992-10-13 US disclosed
WO-1992016523-A1 5-ARYLHETEROARYLALKYL-1,3,5-TRISUBSTITUTED-1,2,4-TRIAZOLE COMPOUNDS FOR TREATMENT OF CIRCULATORY DISORDERS G.D. SEARLE & CO. (US) 1992-10-01 WO disclosed
EP-0504888-A1 5-Arylheteroarylalkyl-1,3,5-trisubstituted-1,2,4-triazole compounds for treatment of circulatory disorders G.D. Searle & Co. (US) 1992-09-23 EP disclosed
CN-1032539-A The Thienoimidazole derivatives that replaces, their preparation method contains their pharmaceutical preparation and they are as the application of gastric acid secretion inhibitor HOECHST AG (DE) 1989-04-26 CN 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 (1 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-20150344486-A1 PYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS DCK, DTYMK, TK1 PLK1 23/4885RAD52 1278/4885TTK 63/4885

“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.