SCHEMBL4676795

SCHEMBL4676795

CC(=O)c1ccc(Cc2sccc2CC(=O)C(=O)c2nn[nH]n2)cc1

nearest known ligand 0.39

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
XDH P47989 1/20 0.39
KMT2A Q03164 1/20 0.38
MAPK8 P45983 1/20 0.37
MAPK10 P53779 1/20 0.37
LMNA P02545 1/20 0.35
TSHR P16473 1/20 0.33
ERCC5 P28715 1/20 0.31
FEN1 P39748 1/20 0.31
CYSLTR2 Q9NS75 3/20 0.31
CYSLTR1 Q9Y271 3/20 0.31
CES1 P23141 1/20 0.30
NCEH1 Q6PIU2 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
SCHEMBL4672283 0.92 XDH (0.39) XDHKMT2AMAPK8MAPK10LMNA
SCHEMBL4674815 0.89 MAPK8 (0.36) MAPK8MAPK10CES1NCEH1
SCHEMBL4670964 0.87 MAPK8 (0.34) MAPK8MAPK10CES1NCEH1
SCHEMBL4670713 0.87 MAPK8 (0.34) MAPK8MAPK10CES1NCEH1
SCHEMBL4675661 0.87 CES1 (0.42) KMT2AMAPK8MAPK10ERCC5FEN1
SCHEMBL4677637 0.86 MAPK8 (0.49) KMT2AMAPK8MAPK10LMNATSHR
SCHEMBL4674274 0.86 MAPK8 (0.32) MAPK8MAPK10CES1NCEH1
SCHEMBL4675837 0.83 KMT2A (0.38) KMT2ALMNATSHR
SCHEMBL4676651 0.83 XDH (0.40) XDHKMT2AMAPK8MAPK10LMNA
SCHEMBL4671881 0.82 XDH (0.42) XDHKMT2ALMNATSHRERCC5

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 597/4885MAPK8 2178/4885

“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.