SCHEMBL4674115

SCHEMBL4674115

O=C(Cc1coc(Cc2ccccc2F)c1)C(=O)c1nc[nH]n1

nearest known ligand 0.33

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
AR P10275 1/20 0.33
PTPN1 P18031 1/20 0.33
TAAR1 Q96RJ0 1/20 0.32
LDHA P00338 1/20 0.32
HCAR3 P49019 1/20 0.31
MEN1 O00255 1/20 0.31
KMT2A Q03164 1/20 0.31
ALDH1A1 P00352 2/20 0.31
PTGER1 P34995 2/20 0.31
KDM4E B2RXH2 1/20 0.31
HDAC6 Q9UBN7 1/20 0.30
DAO P14920 1/20 0.30
PARP1 P09874 1/20 0.30
ACHE P22303 1/20 0.30

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
SCHEMBL4670908 0.92 PTPN1 (0.35) ARPTPN1TAAR1LDHAHCAR3
SCHEMBL4674478 0.88 AR (0.33) ARLDHAMEN1KMT2AALDH1A1
SCHEMBL4676340 0.87 AR (0.36) ARALDH1A1KDM4EHDAC6
SCHEMBL4672203 0.86 IDH1 (0.41) ARKMT2APTGER1DAOPARP1
SCHEMBL4679298 0.86 AR (0.37) ARTAAR1MEN1KMT2AKDM4E
SCHEMBL4678241 0.84 L3MBTL1 (0.32) PTGER1DAOPARP1
SCHEMBL4671425 0.83 HCAR2 (0.38) TAAR1MEN1KMT2APARP1ACHE
SCHEMBL4673700 0.83 PTGDR2 (0.35) ARPTPN1HCAR3ALDH1A1KDM4E
SCHEMBL4677055 0.83 AR (0.33) ARTAAR1HCAR3MEN1KMT2A
SCHEMBL5899365 0.82 TSHR (0.34) MEN1KMT2AALDH1A1KDM4EPARP1

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 AR 10/4885PTPN1 2715/4885TAAR1 847/4885

“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.