SCHEMBL4678041

SCHEMBL4678041

O=C(Cc1cc(Cc2ccccc2F)c[nH]1)C(=O)c1nn[nH]n1

nearest known ligand 0.35

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 1/20 0.35
PTGDR2 Q9Y5Y4 1/20 0.35
DAO P14920 2/20 0.35
CES1 P23141 1/20 0.34
NCEH1 Q6PIU2 1/20 0.34
CXCR3 P49682 4/20 0.33
MMEL1 Q495T6 1/20 0.32
SNCA P37840 2/20 0.32
MPO P05164 1/20 0.32
AR P10275 1/20 0.32
ALDH1A1 P00352 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
HCAR3 P49019 1/20 0.31
ERCC5 P28715 1/20 0.31
FEN1 P39748 1/20 0.31
LMNA P02545 1/20 0.31
MME P08473 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
SCHEMBL4674885 0.92 PTGDR2 (0.35) PTPN1PTGDR2DAOCES1NCEH1
SCHEMBL4676108 0.85 CES1 (0.43) PTGDR2CES1NCEH1MMEL1ERCC5
SCHEMBL4676035 0.84 TDP1 (0.34) PTGDR2DAOCES1NCEH1CXCR3
SCHEMBL4674287 0.83 HCAR2 (0.41) PTGDR2DAOCES1NCEH1SNCA
SCHEMBL4677682 0.83 SNCA (0.36) PTPN1DAOSNCAARALDH1A1
SCHEMBL4671973 0.82 ERCC5 (0.36) PTPN1PTGDR2DAOCES1NCEH1
SCHEMBL4677164 0.81 PTGDR2 (0.38) PTGDR2CES1NCEH1CXCR3MMEL1
SCHEMBL4675849 0.81 FFAR2 (0.35) DAOCES1NCEH1CXCR3L3MBTL1
SCHEMBL4674655 0.80 CES1 (0.32) CES1NCEH1
SCHEMBL4670705 0.80 PTPN1 (0.35) PTPN1PTGDR2CES1NCEH1CXCR3

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 PTPN1 2715/4885PTGDR2 4591/4885DAO 661/4885

“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.