SCHEMBL4674141

SCHEMBL4674141

O=C(C=C(O)c1nc[nH]n1)c1ccoc1Oc1ccc(Cl)cc1

nearest known ligand 0.33

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CDH1 P12830 1/20 0.33
CTNNB1 P35222 1/20 0.33
TCF7L2 Q9NQB0 1/20 0.33
MEN1 O00255 1/20 0.32
LMNA P02545 1/20 0.32
RECQL P46063 1/20 0.32
KMT2A Q03164 1/20 0.32
RAB9A P51151 1/20 0.32
TDP1 Q9NUW8 1/20 0.31
CYP1A1 P04798 1/20 0.30
ABCB1 P08183 1/20 0.30
CYP1B1 Q16678 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
SCHEMBL4676663 0.90 CYP1A1 (0.36) MEN1LMNAKMT2ARAB9ACYP1A1
SCHEMBL4674086 0.89 CYP1A1 (0.36) MEN1LMNARECQLKMT2ARAB9A
SCHEMBL4679724 0.89 CYP1A1 (0.30) CYP1A1ABCB1CYP1B1
SCHEMBL4673044 0.88 KDM4C (0.36) LMNATDP1
SCHEMBL4676198 0.87 MAPT (0.37) LMNARAB9ACYP1A1ABCB1CYP1B1
SCHEMBL4670849 0.86 KDM4C (0.35) LMNARAB9A
SCHEMBL4675173 0.83 RAB9A (0.33) MEN1RECQLKMT2ARAB9ATDP1
SCHEMBL4673422 0.83 CDH1 (0.33) CDH1CTNNB1TCF7L2MEN1LMNA
SCHEMBL4677477 0.82 GAA (0.35) CDH1CTNNB1TCF7L2
SCHEMBL4674895 0.81 KDM4E (0.40) MEN1LMNAKMT2ARAB9ACYP1A1

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 5 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
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 CDH1 2472/4885CTNNB1 218/4885TCF7L2 2250/4885

“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.