SCHEMBL4676065

SCHEMBL4676065

O=C(C=C(O)c1nn[nH]n1)c1cccn1Cc1cccc(F)c1

nearest known ligand 0.43

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CA12 O43570 2/20 0.43
CA1 P00915 2/20 0.43
CA2 P00918 2/20 0.43
CA9 Q16790 2/20 0.43
KDM4E B2RXH2 2/20 0.42
ALDH1A1 P00352 2/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
FFAR2 O15552 1/20 0.39
CNR2 P34972 4/20 0.38
CNR1 P21554 1/20 0.37
DBH P09172 1/20 0.37
PTGDR2 Q9Y5Y4 1/20 0.36
MKNK1 Q9BUB5 1/20 0.35
MKNK2 Q9HBH9 1/20 0.35
NTRK1 P04629 1/20 0.35
CES1 P23141 1/20 0.35
NCEH1 Q6PIU2 1/20 0.35
HCAR2 Q8TDS4 1/20 0.35

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
SCHEMBL4671562 0.90 CA12 (0.55) CA12CA1CA2CA9KDM4E
SCHEMBL4673175 0.88 CA12 (0.44) CA12CA1CA2CA9KDM4E
SCHEMBL4677008 0.88 KDM4C (0.40) ALDH1A1FFAR2DBHPTGDR2NTRK1
SCHEMBL4675435 0.85 PTGDR2 (0.39) KDM4EALDH1A1L3MBTL1FFAR2PTGDR2
SCHEMBL5899410 0.85 CES1 (0.39) KDM4EALDH1A1L3MBTL1FFAR2PTGDR2
SCHEMBL4676080 0.84 FFAR2 (0.39) FFAR2PTGDR2NTRK1CES1NCEH1
SCHEMBL5899386 0.84 CA12 (0.43) CA12CA1CA2CA9KDM4E
SCHEMBL4674956 0.84 POLB (0.38) KDM4EALDH1A1L3MBTL1FFAR2DBH
SCHEMBL4676597 0.83 KDM4C (0.37) ALDH1A1FFAR2DBHPTGDR2MKNK1
SCHEMBL4679614 0.83 CA12 (0.41) CA12CA1CA2CA9KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1142872-B1 AROMATIC HETEROCYCLE COMPOUNDS HAVING HIV INTEGRASE INHIBITING ACTIVITIES SHIONOGI & CO (JP) 2008-10-15 EP disclosed
US-7098201-B2 Heteroaromatic derivatives having an inhibitory activity against HIV integrase SHIONOGI & CO., LTD. (JP) 2006-08-29 US disclosed
US-20040002485-A1 Heteroaromatic derivatives having an inhibitory activity against HIV integrase FUJISHITA TOSHIO (JP) 2004-01-01 US disclosed
US-6645956-B1 1-(5-(4-fluorobenzyl)furan-2-yl)-3-hydroxy-3-(1H-1,2,4-triazol-3 -yl)-propenone; viricides; AIDS treatment SHIONOGI & CO., LTD. (JP) 2003-11-11 US disclosed
US-6620841-B1 Furan or benzofuran derivatives substituted with triazole; acquired immunodeficiency syndrome (AIDS) SHIONOGI & CO., LTD. (JP) 2003-09-16 US disclosed
CN-1335834-A Aromatic heterocyclic compounds having HIV integrase inhibitory activity SHIONOGI & CO (JP) 2002-02-13 CN disclosed
EP-1142872-A1 AROMATIC HETEROCYCLE COMPOUNDS HAVING HIV INTEGRASE INHIBITING ACTIVITIES SHIONOGI & CO., LTD. (JP) 2001-10-10 EP 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-20040002485-A1 Heteroaromatic derivatives having an inhibitory activity against HIV integrase RCOR1, BCOR, CYP8B1 CA12 4245/4885CA1 3590/4885CA2 2384/4885

“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.