SCHEMBL4676965

SCHEMBL4676965

O=C(C=C(O)c1nc[nH]n1)c1occ(-c2ccccc2)c1CCc1ccccc1

nearest known ligand 0.34

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
GPR52 Q9Y2T5 4/20 0.34
ADORA3 P0DMS8 1/20 0.32
ADORA2A P29274 1/20 0.32
DAGLA Q9Y4D2 1/20 0.32
AURKA O14965 1/20 0.32
GSK3B P49841 1/20 0.31
BRS3 P32247 2/20 0.31
ALDH1A1 P00352 1/20 0.31
PPARG P37231 1/20 0.31
DHODH Q02127 1/20 0.30
CES1 P23141 2/20 0.30
FFAR1 O14842 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
SCHEMBL4678674 0.87 GPR52 (0.35) GPR52ADORA3ADORA2ADAGLAAURKA
SCHEMBL4673697 0.86 DAO (0.35) GPR52DAGLACES1FFAR1
SCHEMBL4675490 0.82 ALDH1A1 (0.31) ALDH1A1
SCHEMBL4671359 0.82 GPR52 (0.35) GPR52ALDH1A1CES1
SCHEMBL4675675 0.82 LMNA (0.35) BRS3ALDH1A1
SCHEMBL4672796 0.82 GPR52 (0.32) GPR52DAGLAALDH1A1PPARGCES1
SCHEMBL4674991 0.82 GSK3B (0.33) GPR52ADORA3ADORA2AGSK3BBRS3
SCHEMBL4672626 0.80 BRS3 (0.33) GPR52ADORA3ADORA2AGSK3BBRS3
SCHEMBL4672579 0.80 ABCB1 (0.35) GPR52
SCHEMBL4672261 0.80 GPR52 (0.32) GPR52DAGLAAURKAFFAR1

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 GPR52 2542/4885ADORA3 576/4885ADORA2A 1111/4885

“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.