SCHEMBL4676641

SCHEMBL4676641

CC(=O)c1ccc(Cc2cscc2C(=O)C=C(O)c2nn[nH]n2)cc1

nearest known ligand 0.38

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
XDH P47989 1/20 0.38
KMT2A Q03164 1/20 0.36
LMNA P02545 1/20 0.36
ERCC5 P28715 1/20 0.32
FEN1 P39748 1/20 0.32
TSHR P16473 1/20 0.32
CYSLTR2 Q9NS75 6/20 0.32
CYSLTR1 Q9Y271 6/20 0.32
PTGER4 P35408 1/20 0.32
PTGER2 P43116 1/20 0.32
CES1 P23141 1/20 0.31
NCEH1 Q6PIU2 1/20 0.31
TBXAS1 P24557 2/20 0.31
AGTR1 P30556 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
SCHEMBL4672195 0.90 CES1 (0.32) PTGER4CES1NCEH1
SCHEMBL4671521 0.88 CES1 (0.41) ERCC5FEN1PTGER4PTGER2CES1
SCHEMBL4672589 0.88 MMEL1 (0.32) CES1NCEH1
SCHEMBL4680244 0.88 CES1 (0.32) CES1NCEH1
SCHEMBL4671442 0.87 MAPK8 (0.37) LMNAERCC5FEN1CYSLTR2CYSLTR1
SCHEMBL4676165 0.86 CES1 (0.33) CES1NCEH1
SCHEMBL4671272 0.84 KMT2A (0.36) KMT2ALMNATSHRPTGER4PTGER2
SCHEMBL4675834 0.84 XDH (0.38) XDHKMT2ALMNAERCC5FEN1
SCHEMBL4676788 0.82 XDH (0.38) XDHKMT2ALMNAERCC5FEN1
SCHEMBL4672278 0.82 XDH (0.38) XDHKMT2ALMNAERCC5FEN1

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 XDH 112/4885KMT2A 597/4885LMNA 659/4885

“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.