SCHEMBL4671000

SCHEMBL4671000

O=C(Cc1cocc1Cc1ccc(F)cc1)C(=O)c1nn[nH]n1

nearest known ligand 0.33

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.33
TDP1 Q9NUW8 1/20 0.33
MMEL1 Q495T6 1/20 0.32
CES1 P23141 1/20 0.32
NCEH1 Q6PIU2 1/20 0.32
MPO P05164 1/20 0.32
PTGDR2 Q9Y5Y4 1/20 0.32
CXCR3 P49682 1/20 0.32
HSP90AA1 P07900 1/20 0.32
HTT P42858 1/20 0.32
PIN1 Q13526 1/20 0.31
ACHE P22303 1/20 0.31
HCAR2 Q8TDS4 1/20 0.31
MME P08473 1/20 0.31
RET P07949 1/20 0.31
KDR P35968 1/20 0.31
NPSR1 Q6W5P4 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
SCHEMBL4675479 0.88 CES1 (0.32) MMEL1CES1NCEH1
SCHEMBL4676779 0.88 CES1 (0.32) MAPTMMEL1CES1NCEH1HSP90AA1
SCHEMBL4676550 0.88 CES1 (0.43) MMEL1CES1NCEH1HTTHCAR2
SCHEMBL4675567 0.87 CYP11B1 (0.34) CES1NCEH1
SCHEMBL4672911 0.87 FFAR2 (0.40) MAPTCES1NCEH1MPOPTGDR2
SCHEMBL4675844 0.86 XDH (0.40) CES1NCEH1
SCHEMBL4676121 0.86 PTGDR2 (0.35) MAPTTDP1MMEL1CES1NCEH1
SCHEMBL4674717 0.85 MAPK8 (0.41) MPOPTGDR2CXCR3HTT
SCHEMBL4672590 0.84 CXCR3 (0.34) MAPTTDP1MMEL1CES1NCEH1
SCHEMBL4670733 0.83 AR (0.36) MMEL1CES1NCEH1MPOPTGDR2

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 MAPT 205/4885TDP1 306/4885MMEL1 1144/4885

“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.