SCHEMBL3216951

SCHEMBL3216951

O=C(COc1c(F)c(F)cc(F)c1F)COc1c(F)c(F)cc(F)c1F

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.50
KDM4E B2RXH2 2/20 0.50
ALDH1A1 P00352 2/20 0.50
HTT P42858 1/20 0.50
MAPK1 P28482 1/20 0.49
CTSV O60911 1/20 0.41
CTSL P07711 1/20 0.41
CTSB P07858 1/20 0.41
CTSH P09668 1/20 0.41
CTSS P25774 1/20 0.41
CTSK P43235 1/20 0.41
CTSF Q9UBX1 1/20 0.41
CA1 P00915 2/20 0.40
CA2 P00918 2/20 0.40
CA4 P22748 2/20 0.40
TSHR P16473 2/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
CASP3 P42574 5/20 0.39
CASP7 P55210 1/20 0.39
CASP6 P55212 1/20 0.39

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
SCHEMBL4289806 0.89 MAPT (0.43) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL22308325 0.88 MAPT (0.49) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL3410954 0.87 MAPT (0.48) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL29503795 0.85 MAPT (0.43) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL13382341 0.85 TSHR (0.56) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL22307313 0.84 MAPT (0.56) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL22307834 0.84 MAPT (0.46) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL18215408 0.84 KDM4E (0.49) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL8063168 0.83 MAPT (0.48) MAPTKDM4EALDH1A1HTTMAPK1
SCHEMBL26623341 0.83 MAPT (0.48) MAPTKDM4EALDH1A1HTTMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2010059418-A1 SUBSTITUTED TRIAZINE AND PURINE COMPOUNDS, METHODS OF INHIBITING CRUZAIN AND RHODESAIN AND METHODS OF TREATING CHAGAS DISEASE AND AFRICAN TRYPANOSOMIASIS THE GOVERNMENT OF THE U.S.A. AS REPRESENTED BY THE SECRETARY OF THE DEPT. OF HEALTH & HUMAN SERVICES (US) 2010-05-27 WO disclosed
US-20100041661-A1 CASPASE INHIBITORS BASED ON PYRIDAZINONE SCAFFOLD LG LIFE SCIENCES LTD. (KR) 2010-02-18 US disclosed
WO-2009075778-A3 NONPEPTIDIC INHIBITORS OF CRUZAIN THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-10-15 WO disclosed
EP-2079710-A1 CASPASE INHIBITORS BASED ON PYRIDAZINONE SCAFFOLD LG Life Sciences Ltd. (KR) 2009-07-22 EP disclosed
WO-2009075778-A2 NONPEPTIDIC INHIBITORS OF CRUZAIN THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-06-18 WO disclosed
WO-2008056897-A1 CASPASE INHIBITORS BASED ON PYRIDAZINONE SCAFFOLD LG LIFE SCIENCES LTD. (KR) 2008-05-15 WO disclosed
WO-2006033551-A1 CASPASE INHIBITORS CONTAINING DICARBONYLAMINO-ISOXAZOLINE LG LIFE SCIENCES LTD. (KR) 2006-03-30 WO disclosed
WO-2005035497-A1 CASPASE INHIBITOR COMPRISING 2-ALKYL-4-OXOBUTANOYL GROUP AND PHARMACEUTICAL COMPOSITION THEREOF LG LIFE SCIENCES LTD. (KR) 2005-04-21 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 (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-20100041661-A1 CASPASE INHIBITORS BASED ON PYRIDAZINONE SCAFFOLD CASP1, CASP2, CASP5 MAPT 944/4885KDM4E 1498/4885ALDH1A1 3666/4885

“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.