SCHEMBL4674264

SCHEMBL4674264

O=C(C=C(O)c1nc[nH]n1)c1ccc(Cc2cccc(F)c2)s1

nearest known ligand 0.39

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 3/20 0.39
GSK3B P49841 1/20 0.35
BACE1 P56817 1/20 0.35
LMNA P02545 1/20 0.34
POLB P06746 1/20 0.34
THRB P10828 1/20 0.34
NR4A2 P43354 2/20 0.34
NR3C2 P08235 1/20 0.34
SCD O00767 1/20 0.34
KDM5A P29375 2/20 0.33
KDM5B Q9UGL1 2/20 0.33
KDM4C Q9H3R0 1/20 0.33
SCD5 Q86SK9 1/20 0.33
FFAR1 O14842 1/20 0.32
PTGER1 P34995 1/20 0.32
BRS3 P32247 1/20 0.32

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
SCHEMBL4673367 0.88 PTGER1 (0.35) HCAR2LMNAPOLBPTGER1
SCHEMBL4671044 0.88 ABL1 (0.35) GSK3BBACE1LMNAFFAR1
SCHEMBL4676610 0.84 HCAR2 (0.39) HCAR2LMNAPOLBTHRBNR3C2
SCHEMBL4676758 0.84 HCAR2 (0.39) HCAR2GSK3BBACE1LMNAPOLB
SCHEMBL4678117 0.83 HCAR2 (0.39) HCAR2GSK3BBACE1LMNAPOLB
SCHEMBL4674814 0.82 TBXAS1 (0.32)
SCHEMBL4670932 0.82 ABL1 (0.37) LMNAPTGER1
SCHEMBL5899413 0.81 MAPT (0.35) LMNAPOLBTHRB
SCHEMBL4677831 0.81 TSHR (0.32)
SCHEMBL4675734 0.81 HCAR2 (0.40) HCAR2GSK3BBACE1LMNAPOLB

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 HCAR2 276/4885GSK3B 38/4885BACE1 140/4885

“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.