SCHEMBL4673095

SCHEMBL4673095

O=C(C=C(O)c1nc[nH]n1)c1occc1Oc1ccc(C(F)(F)F)cc1

nearest known ligand 0.34

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.34
THRB P10828 1/20 0.32
KDR P35968 1/20 0.32
FLT3 P36888 1/20 0.32
BRAF P15056 4/20 0.32
ICAM1 P05362 1/20 0.31
SELE P16581 1/20 0.31
IGFBP3 P17936 1/20 0.31
SCN9A Q15858 1/20 0.31
KDM4C Q9H3R0 1/20 0.31
FFAR1 O14842 2/20 0.31
RAB9A P51151 1/20 0.31
LTA4H P09960 1/20 0.31
EPHX2 P34913 1/20 0.31
PTPN1 P18031 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
SCHEMBL4671508 0.88 KDM4E (0.38) ALDH1A1THRBBRAFICAM1SELE
SCHEMBL4673610 0.87 MAPT (0.34) ALDH1A1RAB9A
SCHEMBL4675207 0.86 PARP10 (0.30)
SCHEMBL4673422 0.86 CDH1 (0.33) KDR
SCHEMBL4671915 0.86 KMT2A (0.36) ALDH1A1KDRRAB9A
SCHEMBL4670593 0.84 MAPT (0.37) ALDH1A1RAB9A
SCHEMBL4670849 0.84 KDM4C (0.35) ALDH1A1KDRFLT3BRAFKDM4C
SCHEMBL4670704 0.83 RXRA (0.33) THRB
SCHEMBL4674602 0.82 ALDH1A1 (0.34) ALDH1A1KDRFLT3ICAM1SELE
SCHEMBL4672110 0.81 HAO1 (0.32) ALDH1A1BRAFICAM1SELE

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 ALDH1A1 980/4885THRB 386/4885KDR 2342/4885

“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.