SCHEMBL4674739

SCHEMBL4674739

CC(=O)c1ccc(Cn2cccc2C(=O)C=C(O)c2nc[nH]n2)cc1

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
CNR2 P34972 3/20 0.34
P2RY14 Q15391 2/20 0.34
HRH3 Q9Y5N1 4/20 0.33
LMNA P02545 1/20 0.33
CNR1 P21554 1/20 0.33
EPHX2 P34913 4/20 0.33
ALDH1A1 P00352 1/20 0.33
HTT P42858 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
MAOB P27338 1/20 0.33
PPARA Q07869 1/20 0.32
SCN3A Q9NY46 1/20 0.32
KDM4E B2RXH2 1/20 0.32

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
SCHEMBL4678500 0.90 CA12 (0.44) CA12CA1CA2CA9CNR2
SCHEMBL4679180 0.89 CA12 (0.44) CA12CA1CA2CA9CNR2
SCHEMBL4674377 0.89 CA12 (0.55) CA12CA1CA2CA9CNR2
SCHEMBL4674047 0.88 CA12 (0.45) CA12CA1CA2CA9LMNA
SCHEMBL4672642 0.88 CA12 (0.43) CA12CA1CA2CA9CNR2
SCHEMBL4672483 0.87 ALDH1A1 (0.36) CA12CA1CA2CA9P2RY14
SCHEMBL4673345 0.86 CA12 (0.41) CA12CA1CA2CA9CNR2
SCHEMBL4679403 0.84 CA12 (0.42) CA12CA1CA2CA9CNR2
SCHEMBL4678186 0.84 LMNA (0.35) P2RY14LMNAALDH1A1HTTSMN1; SMN2
SCHEMBL4671756 0.82 MAOB (0.34) P2RY14HRH3LMNAALDH1A1HTT

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 6 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
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.