SCHEMBL4672952

SCHEMBL4672952

O=C(C=C(O)c1nc[nH]n1)c1ccc(Cc2cccc(Cl)c2)o1

nearest known ligand 0.41

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 2/20 0.41
PTGER1 P34995 2/20 0.39
TP53 P04637 4/20 0.37
LMNA P02545 4/20 0.37
BRS3 P32247 1/20 0.36
THRB P10828 1/20 0.36
NPC1 O15118 1/20 0.35
POLB P06746 1/20 0.35
RAB9A P51151 1/20 0.35
MRGPRX4 Q96LA9 1/20 0.35
ATM Q13315 1/20 0.35
RXRA P19793 1/20 0.35
RXRB P28702 1/20 0.35
RXRG P48443 1/20 0.35
MAOB P27338 1/20 0.35
MAPT P10636 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
SCHEMBL4678961 0.89 PTGER1 (0.36) HCAR2PTGER1NPC1POLBRAB9A
SCHEMBL4671807 0.89 HCAR2 (0.40) HCAR2LMNABRS3THRBPOLB
SCHEMBL4678600 0.88 HSD17B10 (0.41) PTGER1LMNANPC1POLBRAB9A
SCHEMBL4671284 0.87 NR3C2 (0.40) TP53LMNABRS3NPC1POLB
SCHEMBL4677062 0.86 LMNA (0.41) LMNANPC1POLBRAB9AMAOB
SCHEMBL4676480 0.85 KDM5A (0.36) PTGER1NPC1POLBRAB9AMRGPRX4
SCHEMBL4673040 0.84 HCAR2 (0.40) HCAR2LMNABRS3RXRARXRB
SCHEMBL4679964 0.84 HCAR2 (0.39) HCAR2LMNARXRARXRBRXRG
SCHEMBL4672893 0.84 SMN1; SMN2 (0.34) PTGER1THRBNPC1POLBRAB9A
SCHEMBL4675323 0.83 PTGER1 (0.37) PTGER1TP53LMNABRS3POLB

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 276/4885PTGER1 4379/4885TP53 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.