SCHEMBL4675749

SCHEMBL4675749

COc1ccc(Cc2ccc(CC(=O)C(=O)c3nn[nH]n3)o2)cc1

nearest known ligand 0.48

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.42
LMNA P02545 2/20 0.42
TP53 P04637 2/20 0.42
HPGD P15428 1/20 0.42
MAPK8 P45983 1/20 0.42
MAPK10 P53779 1/20 0.42
CXCR3 P49682 1/20 0.37
TSHR P16473 1/20 0.36
HTT P42858 1/20 0.36
XDH P47989 2/20 0.36
TAS2R14 Q9NYV8 1/20 0.36
PTGDR2 Q9Y5Y4 1/20 0.36
GPR35 Q9HC97 1/20 0.35
SAE1 Q9UBE0 1/20 0.35
UBA2 Q9UBT2 1/20 0.35

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
SCHEMBL4673270 0.87 ALDH1A1 (0.39) ALDH1A1LMNATP53HPGDHTT
SCHEMBL4673272 0.85 XDH (0.41) ALDH1A1LMNATSHRXDH
SCHEMBL4674477 0.85 CES1 (0.33) ALDH1A1TSHR
SCHEMBL3228436 0.85 CXCR3 (0.34) TP53CXCR3PTGDR2
SCHEMBL4671114 0.85 CES1 (0.44) HTT
SCHEMBL4678112 0.84 MAPK8 (0.40) MAPK8MAPK10CXCR3XDHTAS2R14
SCHEMBL4673593 0.84 MAPK8 (0.40) ALDH1A1LMNATP53HPGDMAPK8
SCHEMBL4677023 0.84 CYP11B1 (0.34) LMNATSHRHTT
SCHEMBL4675237 0.83 ALDH1A1 (0.43) ALDH1A1LMNATP53HPGDTSHR
SCHEMBL4673736 0.82 MAPK8 (0.44) ALDH1A1LMNATP53HPGDMAPK8

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 ALDH1A1 980/4885LMNA 659/4885TP53 999/4885

“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.