SCHEMBL4677953

SCHEMBL4677953

O=C(C=C(O)c1nn[nH]n1)c1cc(CCc2ccccc2)cn1Cc1ccc(F)cc1

nearest known ligand 0.42

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.40
NCEH1 Q6PIU2 1/20 0.40
CA12 O43570 2/20 0.39
CA1 P00915 2/20 0.39
CA2 P00918 2/20 0.39
CA9 Q16790 2/20 0.39
L3MBTL1 Q9Y468 1/20 0.37
CNR2 P34972 1/20 0.36
POLB P06746 1/20 0.36
KMT2A Q03164 1/20 0.35
AGTR1 P30556 2/20 0.35
TP53 P04637 1/20 0.35
PIN1 Q13526 1/20 0.34
AGTR2 P50052 1/20 0.34

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
SCHEMBL4671888 0.94 CES1 (0.44) CES1NCEH1AGTR1AGTR2
SCHEMBL5899410 0.92 CES1 (0.39) CES1NCEH1L3MBTL1POLBKMT2A
SCHEMBL4671594 0.91 CES1 (0.40) CES1NCEH1AGTR1AGTR2
SCHEMBL4677334 0.91 CES1 (0.40) CES1NCEH1KMT2AAGTR1AGTR2
SCHEMBL4671002 0.90 CES1 (0.39) CES1NCEH1AGTR1AGTR2
SCHEMBL4671501 0.90 CCNC (0.41) CES1NCEH1CNR2POLBKMT2A
SCHEMBL4675583 0.89 P2RY14 (0.39) CA12CA1CA2CA9AGTR1
SCHEMBL4675890 0.88 LMNA (0.38) CES1NCEH1KMT2AAGTR1AGTR2
SCHEMBL4676205 0.88 CES1 (0.39) CES1NCEH1AGTR1AGTR2
SCHEMBL4675420 0.87 POLB (0.48) CA12CA1CA2CA9CNR2

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 1046/4885CA12 4245/4885

“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.