SCHEMBL4673282

SCHEMBL4673282

CC(=O)c1ccc(CCCCCc2cc[nH]c2CC(=O)C(=O)c2nn[nH]n2)cc1

nearest known ligand 0.42

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.42
NCEH1 Q6PIU2 1/20 0.42
XDH P47989 1/20 0.37
HSD17B10 Q99714 1/20 0.36
CYSLTR2 Q9NS75 7/20 0.33
CYSLTR1 Q9Y271 7/20 0.33
THRA P10827 1/20 0.33
THRB P10828 1/20 0.33
S1PR1 P21453 1/20 0.32
PLA2G7 Q13093 1/20 0.32
FAAH O00519 2/20 0.32
MGLL Q99685 1/20 0.32
HRH3 Q9Y5N1 1/20 0.31
KMT2A Q03164 1/20 0.31

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
SCHEMBL4678575 0.88 CES1 (0.43) CES1NCEH1S1PR1FAAHMGLL
SCHEMBL4675211 0.88 XDH (0.40) XDHCYSLTR2CYSLTR1KMT2A
SCHEMBL4676036 0.88 CES1 (0.56) CES1NCEH1FAAHMGLL
SCHEMBL4671699 0.84 HRH3 (0.38) HSD17B10THRATHRBPLA2G7HRH3
SCHEMBL4675331 0.83 XDH (0.40) CES1NCEH1XDHCYSLTR2CYSLTR1
SCHEMBL4673583 0.82 CES1 (0.35) CES1NCEH1XDHHSD17B10CYSLTR2
SCHEMBL4673089 0.81 CES1 (0.36) CES1NCEH1XDHHSD17B10CYSLTR2
SCHEMBL4673928 0.77 CES1 (0.41) CES1NCEH1
SCHEMBL4672817 0.77 CYSLTR2 (0.32) CES1NCEH1CYSLTR2CYSLTR1
SCHEMBL4678905 0.75 MAPT (0.33) CES1NCEH1CYSLTR2CYSLTR1

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 CES1 445/4885NCEH1 1046/4885XDH 112/4885

“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.