SCHEMBL2338264

SCHEMBL2338264

Fc1c(Cl)c(-c2ccccc2)cc2c(NCc3ccc(OC(F)(F)F)cc3)n[nH]c12

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 2/20 0.54
CDK1 P06493 1/20 0.54
CDK2 P24941 1/20 0.54
MAPK8 P45983 1/20 0.46
MAPK10 P53779 1/20 0.46
NTRK1 P04629 1/20 0.44
MAP2K4 P45985 2/20 0.39
KCNN3 Q9UGI6 1/20 0.39
PPARA Q07869 1/20 0.39
METAP2 P50579 1/20 0.39
CTNNB1 P35222 1/20 0.39
TCF7L2 Q9NQB0 1/20 0.39
P2RX7 Q99572 1/20 0.39
HTT P42858 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
USP1 O94782 3/20 0.38
WDR48 Q8TAF3 3/20 0.38
FGFR1 P11362 1/20 0.38
MEN1 O00255 1/20 0.37
LMNA P02545 1/20 0.37

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
SCHEMBL2336207 0.88 GSK3B (0.58) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL2338045 0.87 GSK3B (0.62) GSK3BCDK1CDK2MAP2K4USP1
SCHEMBL1375621 0.87 GSK3B (0.64) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL6528915 0.87 GSK3B (0.57) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL2338742 0.87 GSK3B (0.57) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL1378926 0.86 GSK3B (0.61) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL2360847 0.86 GSK3B (0.61) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL1378107 0.83 GSK3B (0.49) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL4502817 0.83 MAPK8 (0.51) GSK3BCDK1CDK2MAPK8MAPK10
SCHEMBL1375685 0.82 GSK3B (0.57) GSK3BCDK1CDK2NTRK1MAP2K4

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1572200-B1 AMINOINDAZOLE DERIVATIVES AND USE THEREOF AS KINASE INHIBITORS AVENTIS PHARMA SA (FR) 2011-08-17 EP claimed
CN-101979382-A Aminoindazole derivatives and use thereof as kinase inhibitors AVENTIS PHARMA SA 2011-02-23 CN claimed
US-7629374-B2 Use of aminoindazole derivatives for the inhibition of tau phosphorylation AVENTIS PHARMA SA (FR) 2009-12-08 US claimed
US-20080261997-A1 USE OF AMINOINDAZOLE DERIVATIVES FOR THE INHIBITION OF TAU PHOSPHORYLATION AVENTIS PHARMA S.A. (FR) 2008-10-23 US claimed
US-7019011-B2 Aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2006-03-28 US claimed
CN-1713909-A Aminoindazole derivatives and their use as kinase inhibitors AVENTIS PHARMA SA (FR) 2005-12-28 CN claimed
US-20040132794-A1 Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2004-07-08 US claimed
EP-1572200-B1 AMINOINDAZOLE DERIVATIVES AND USE THEREOF AS KINASE INHIBITORS AVENTIS PHARMA SA (FR) 2011-08-17 EP disclosed
CN-101979382-A Aminoindazole derivatives and use thereof as kinase inhibitors AVENTIS PHARMA SA 2011-02-23 CN disclosed
US-7629374-B2 Use of aminoindazole derivatives for the inhibition of tau phosphorylation AVENTIS PHARMA SA (FR) 2009-12-08 US disclosed
US-20080261997-A1 USE OF AMINOINDAZOLE DERIVATIVES FOR THE INHIBITION OF TAU PHOSPHORYLATION AVENTIS PHARMA S.A. (FR) 2008-10-23 US disclosed
US-7407981-B2 Aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2008-08-05 US disclosed
US-20070155735-A1 NOVEL AMINOINDAZOLE DERIVATIVES AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM AVENTIS PHARMA S.A. (FR) 2007-07-05 US disclosed
US-7196109-B2 Aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA SA (FR) 2007-03-27 US disclosed
US-20060074122-A1 Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2006-04-06 US disclosed
US-7019011-B2 Aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2006-03-28 US disclosed
CN-1713909-A Aminoindazole derivatives and their use as kinase inhibitors AVENTIS PHARMA SA (FR) 2005-12-28 CN disclosed
EP-1572200-A1 AMINOINDAZOLE DERIVATIVES AND USE THEREOF AS KINASE INHIBITORS Aventis Pharma S.A. (FR) 2005-09-14 EP disclosed
WO-2004062662-A1 AMINOINDAZOLE DERIVATIVES AND USE THEREOF AS KINASE INHIBITORS AVENTIS PHARMA S.A. (FR) 2004-07-29 WO disclosed
US-20040132794-A1 Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them AVENTIS PHARMA S.A. (FR) 2004-07-08 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 (4 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-20080261997-A1 USE OF AMINOINDAZOLE DERIVATIVES FOR THE INHIBITION OF TAU PHOSPHORYLATION OXSR1, CBR1, OXER1 GSK3B 159/4885CDK1 63/4885CDK2 549/4885
US-20040132794-A1 Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them SIGMAR1, CYP2C8, CNR1 GSK3B 3595/4885CDK1 2123/4885CDK2 2237/4885
US-20070155735-A1 NOVEL AMINOINDAZOLE DERIVATIVES AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM CNR1, SUCNR1, CBR1 GSK3B 3542/4885CDK1 1006/4885CDK2 1855/4885
US-20060074122-A1 Novel aminoindazole derivatives as medicaments and pharmaceutical compositions including them CNR1, SUCNR1, CBR1 GSK3B 3542/4885CDK1 1006/4885CDK2 1855/4885

“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.