SCHEMBL4674667

SCHEMBL4674667

Nc1ccc(Cn2cc(CCc3ccccc3)c(C(=O)C=C(O)c3nn[nH]n3)c2)cc1

nearest known ligand 0.39

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.39
NCEH1 Q6PIU2 1/20 0.39
PLA2G4A P47712 2/20 0.34
MAOA P21397 2/20 0.33
MAOB P27338 2/20 0.33
S1PR1 P21453 1/20 0.31
S1PR5 Q9H228 1/20 0.31
MMEL1 Q495T6 1/20 0.31
TSHR P16473 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
HPGD P15428 1/20 0.31
KLKB1 P03952 1/20 0.31
HTT P42858 1/20 0.31

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
SCHEMBL4676460 0.94 CES1 (0.43) CES1NCEH1PLA2G4AS1PR1S1PR5
SCHEMBL4679350 0.91 CES1 (0.39) CES1NCEH1PLA2G4AMMEL1
SCHEMBL4674328 0.91 CES1 (0.39) CES1NCEH1PLA2G4A
SCHEMBL4674218 0.90 CES1 (0.40) CES1NCEH1PLA2G4ASMN1; SMN2
SCHEMBL4675233 0.89 CES1 (0.38) CES1NCEH1PLA2G4A
SCHEMBL4676235 0.88 CDK5 (0.38) CES1NCEH1PLA2G4A
SCHEMBL4675686 0.85 CES1 (0.38) CES1NCEH1PLA2G4A
SCHEMBL4673650 0.85 MAOA (0.33) PLA2G4AMAOAMAOBS1PR1S1PR5
SCHEMBL4673837 0.85 CES1 (0.39) CES1NCEH1PLA2G4AMMEL1
SCHEMBL5899412 0.84 CES1 (0.39) CES1NCEH1PLA2G4ATSHRSMN1; SMN2

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 CES1 445/4885NCEH1 1046/4885PLA2G4A 4868/4885

“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.