SCHEMBL4673591

SCHEMBL4673591

COc1ccc(Cc2cc(C(=O)C=C(O)c3nn[nH]n3)co2)cc1

nearest known ligand 0.43

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MAPK8 P45983 1/20 0.37
MAPK10 P53779 1/20 0.37
PTGDR2 Q9Y5Y4 4/20 0.36
ERCC5 P28715 1/20 0.35
FEN1 P39748 1/20 0.35
NR4A2 P43354 1/20 0.35
ALDH1A1 P00352 2/20 0.35
TAS2R14 Q9NYV8 1/20 0.35
CYP2C8 P10632 1/20 0.35
CYP2C9 P11712 1/20 0.35
CYP2C19 P33261 1/20 0.35
XDH P47989 2/20 0.34
GPR35 Q9HC97 1/20 0.34
CXCR3 P49682 1/20 0.34
HPGD P15428 1/20 0.34

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
SCHEMBL4674709 0.89 IDH1 (0.33) PTGDR2ERCC5FEN1CYP2C19GPR35
SCHEMBL4674370 0.88 XDH (0.38) ERCC5FEN1XDH
SCHEMBL4675580 0.88 IDH1 (0.42) PTGDR2ERCC5FEN1
SCHEMBL4676741 0.87 PTGDR2 (0.33) PTGDR2ERCC5FEN1ALDH1A1GPR35
SCHEMBL4672951 0.87 IDH1 (0.33) ERCC5FEN1
SCHEMBL4672329 0.86 IDH1 (0.33) ERCC5FEN1
SCHEMBL4674403 0.85 ALDH1A1 (0.37) NR4A2ALDH1A1
SCHEMBL4678110 0.84 KDM5A (0.36) MAPK8MAPK10PTGDR2ERCC5FEN1
SCHEMBL4675745 0.84 ALDH1A1 (0.43) MAPK8MAPK10ERCC5FEN1ALDH1A1
SCHEMBL4673387 0.82 MAPK8 (0.43) MAPK8MAPK10PTGDR2ERCC5FEN1

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
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 MAPK8 2178/4885MAPK10 4133/4885PTGDR2 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.