SCHEMBL5899397

SCHEMBL5899397

O=C(C=C(O)c1nc[nH]n1)c1oc(-c2ccccc2)cc1CCc1ccccc1

nearest known ligand 0.36

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
FAAH O00519 7/20 0.36
CES1 P23141 1/20 0.34
ALDH1A1 P00352 3/20 0.33
POLB P06746 2/20 0.33
MAPT P10636 2/20 0.33
HSD17B10 Q99714 2/20 0.33
PKM P14618 1/20 0.33
HTT P42858 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
FFAR1 O14842 1/20 0.32
NR3C2 P08235 1/20 0.32
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
AURKA O14965 1/20 0.32
HPGD P15428 1/20 0.32
KDM5A P29375 1/20 0.32
KDM4E B2RXH2 1/20 0.32

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
SCHEMBL4675321 0.84 ALDH1A1 (0.39) FAAHCES1ALDH1A1POLBMAPT
SCHEMBL4670692 0.82 NR3C2 (0.33) FAAHCES1NR3C2NPC1RAB9A
SCHEMBL4674148 0.82 ABCB1 (0.35) NR3C2RAB9AKDM4E
SCHEMBL4674991 0.82 GSK3B (0.33) FAAHCES1ALDH1A1POLBMAPT
SCHEMBL4673697 0.82 DAO (0.35) CES1FFAR1NPC1RAB9A
SCHEMBL4672862 0.81 KDM4E (0.35) ALDH1A1NR3C2NPC1RAB9AKDM5A
SCHEMBL4672626 0.78 BRS3 (0.33) FAAHCES1NR3C2NPC1RAB9A
SCHEMBL4675307 0.78 HPGD (0.46) ALDH1A1POLBMAPTHSD17B10PKM
SCHEMBL4673309 0.78 CYP19A1 (0.35) ALDH1A1NR3C2RAB9AHPGDKDM4E
SCHEMBL4674795 0.78 DAO (0.35) CES1FFAR1NPC1RAB9A

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
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 FAAH 2547/4885CES1 445/4885ALDH1A1 980/4885

“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.