SCHEMBL4675334

SCHEMBL4675334

CCCCC(CCCCc1ccc(F)cc1)c1cc[nH]c1CC(=O)C(=O)c1nn[nH]n1

nearest known ligand 0.35

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.35
NCEH1 Q6PIU2 1/20 0.35
S1PR1 P21453 1/20 0.33
AGTR2 P50052 2/20 0.32
AGTR1 P30556 1/20 0.32
CYSLTR2 Q9NS75 1/20 0.31
CYSLTR1 Q9Y271 1/20 0.31
PLA2G4A P47712 1/20 0.30
MMP2 P08253 1/20 0.30
MMP3 P08254 1/20 0.30
CYP19A1 P11511 1/20 0.30
ALDH1A1 P00352 1/20 0.30
FFAR1 O14842 1/20 0.30
FFAR4 Q5NUL3 1/20 0.30

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
SCHEMBL4678804 0.92 CES1 (0.36) CES1NCEH1S1PR1PLA2G4AMMP2
SCHEMBL4676781 0.91 CES1 (0.35) CES1NCEH1S1PR1PLA2G4AMMP2
SCHEMBL4679778 0.91 CES1 (0.45) CES1NCEH1S1PR1AGTR2AGTR1
SCHEMBL4673583 0.90 CES1 (0.35) CES1NCEH1S1PR1CYSLTR2CYSLTR1
SCHEMBL4676494 0.90 CES1 (0.35) CES1NCEH1
SCHEMBL4676356 0.90 PLA2G4A (0.36) CES1NCEH1CYSLTR2CYSLTR1PLA2G4A
SCHEMBL4678619 0.88
SCHEMBL4671586 0.86 CYSLTR2 (0.36) CES1NCEH1CYSLTR2CYSLTR1
SCHEMBL4677299 0.86 FNTA (0.33) PLA2G4ACYP19A1ALDH1A1FFAR1FFAR4
SCHEMBL4673090 0.82 CES1 (0.37) CES1NCEH1S1PR1AGTR2CYSLTR2

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 1046/4885S1PR1 3462/4885

“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.