SCHEMBL4673049

SCHEMBL4673049

O=C(Cc1ccoc1Oc1cccc(Cl)c1)C(=O)c1nc[nH]n1

nearest known ligand 0.36

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.35
KDM4C Q9H3R0 1/20 0.35
FKBP1A P62942 1/20 0.34
POLB P06746 1/20 0.33
ABL1 P00519 1/20 0.33
NOTUM Q6P988 2/20 0.33
WDR5 P61964 1/20 0.33
PDE4B Q07343 1/20 0.32
MAOB P27338 1/20 0.32
AOC3 Q16853 1/20 0.32
RXRA P19793 1/20 0.32
RXRB P28702 1/20 0.32
RXRG P48443 1/20 0.32
KDM4E B2RXH2 2/20 0.32
S1PR1 P21453 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2C9 P11712 1/20 0.31
CYP2C19 P33261 1/20 0.31
TDP1 Q9NUW8 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
SCHEMBL4674896 0.88 LMNA (0.38) POLBKDM4E
SCHEMBL4674144 0.87 MEN1 (0.32) KDM4E
SCHEMBL4676668 0.87 CES1 (0.33) KDM4ECYP1A2CYP2C9CYP2C19
SCHEMBL4672941 0.85 KDM4E (0.41) POLBMAOBAOC3KDM4E
SCHEMBL4672141 0.84 CYP3A4 (0.39) CYP3A4KDM4CFKBP1ANOTUMWDR5
SCHEMBL4672499 0.82 LMNA (0.35) CYP3A4FKBP1ANOTUMWDR5CYP1A2
SCHEMBL4674640 0.82 RXRA (0.34) CYP3A4KDM4CFKBP1APOLBNOTUM
SCHEMBL4675176 0.81 CXCL8 (0.38) POLBTDP1
SCHEMBL4674091 0.81 KMT2A (0.34) KDM4CPOLB
SCHEMBL4679728 0.81 PARP10 (0.31)

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 CYP3A4 4/4885KDM4C 785/4885FKBP1A 1142/4885

“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.