SCHEMBL4672107

SCHEMBL4672107

O=C(C=C(O)c1nn[nH]n1)c1cc(Cc2cccc(F)c2)n[nH]1

nearest known ligand 0.42

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 3/20 0.42
FFAR2 O15552 2/20 0.39
PTGDR2 Q9Y5Y4 1/20 0.36
CES1 P23141 1/20 0.35
NCEH1 Q6PIU2 1/20 0.35
PIN1 Q13526 1/20 0.35
THRB P10828 2/20 0.35
LMNA P02545 1/20 0.35
POLB P06746 1/20 0.35
MAPT P10636 1/20 0.34
MAPK1 P28482 1/20 0.33
BRD4 O60885 1/20 0.33
NR3C2 P08235 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
SCHEMBL4671300 0.89 CA12 (0.34) PTGDR2CES1NCEH1PIN1MAPT
SCHEMBL4673085 0.84 HCAR2 (0.42) HCAR2THRBLMNAPOLBMAPK1
SCHEMBL4678660 0.83 CES1 (0.33) CES1NCEH1MAPK1
SCHEMBL4679194 0.82 HCAR3 (0.39) PTGDR2CES1NCEH1BRD4
SCHEMBL4672164 0.82 MAPT (0.36) CES1NCEH1POLBMAPTMAPK1
SCHEMBL4679659 0.82 ALPL (0.34) CES1NCEH1
SCHEMBL4679618 0.82 HCAR2 (0.48) HCAR2THRBLMNAPOLBMAPT
SCHEMBL4679142 0.81 HCAR2 (0.38) HCAR2FFAR2PTGDR2CES1NCEH1
SCHEMBL4674210 0.81 HCAR2 (0.42) HCAR2FFAR2PTGDR2CES1NCEH1
SCHEMBL4678260 0.80 XDH (0.38) CES1NCEH1LMNA

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 HCAR2 276/4885FFAR2 2618/4885PTGDR2 4591/4885

“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.