SCHEMBL4675485

SCHEMBL4675485

CC(=O)c1ccc(Cc2cc(C(=O)C=C(O)c3nn[nH]n3)cs2)cc1

nearest known ligand 0.38

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
XDH P47989 1/20 0.38
TSHR P16473 1/20 0.37
KMT2A Q03164 1/20 0.36
LMNA P02545 2/20 0.36
ERCC5 P28715 1/20 0.32
FEN1 P39748 1/20 0.32
ALDH1A1 P00352 1/20 0.31
GLA P06280 1/20 0.31
CES1 P23141 1/20 0.31
NCEH1 Q6PIU2 1/20 0.31
PARP1 P09874 2/20 0.31
CREBBP Q92793 1/20 0.31
DAO P14920 2/20 0.30
MAPK8 P45983 1/20 0.30
MAPK10 P53779 1/20 0.30
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
SCHEMBL4676673 0.91 PTGER4 (0.33) CES1NCEH1PARP1DAO
SCHEMBL4673886 0.89 CES1 (0.40) ERCC5FEN1CES1NCEH1DAO
SCHEMBL4673198 0.89 CES1 (0.32) ERCC5FEN1CES1NCEH1DAO
SCHEMBL4674439 0.89 PTGDR2 (0.33) ERCC5FEN1ALDH1A1CES1NCEH1
SCHEMBL4673387 0.88 MAPK8 (0.43) XDHKMT2AERCC5FEN1PARP1
SCHEMBL4675363 0.88 PARP1 (0.35) ERCC5FEN1CES1NCEH1PARP1
SCHEMBL4671043 0.84 TSHR (0.39) TSHRKMT2ALMNAALDH1A1GLA
SCHEMBL4671210 0.84 MAPT (0.41) XDHTSHRKMT2ALMNAERCC5
SCHEMBL4679021 0.83 HDAC1 (0.38) XDHKMT2ALMNAALDH1A1
SCHEMBL4671694 0.82 TSHR (0.40) XDHTSHRKMT2ALMNAERCC5

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 XDH 112/4885TSHR 1614/4885KMT2A 597/4885

“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.