SCHEMBL4672014

SCHEMBL4672014

O=C(C=C(O)c1nc[nH]n1)c1coc(-c2ccc(F)cc2)c1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 1/20 0.37
MEN1 O00255 4/20 0.36
KMT2A Q03164 4/20 0.36
KDM4E B2RXH2 3/20 0.36
ALDH1A1 P00352 3/20 0.36
MAPT P10636 3/20 0.36
POLB P06746 1/20 0.36
PKM P14618 1/20 0.36
HDAC6 Q9UBN7 3/20 0.33
NQO2 P16083 1/20 0.33
LMNA P02545 2/20 0.33
CA12 O43570 1/20 0.33
ALPL P05186 1/20 0.33
RPA1 P27694 1/20 0.33
NPC1 O15118 6/20 0.32
RAB9A P51151 6/20 0.32
TDP1 Q9NUW8 1/20 0.32
TP53 P04637 2/20 0.32
HTT P42858 2/20 0.32
SMN1; SMN2 Q16637 2/20 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
SCHEMBL4676970 0.90 NR4A2 (0.36) NR4A2MEN1KMT2AKDM4EALDH1A1
SCHEMBL4671438 0.88 NR4A1 (0.40) NR4A2NQO2
SCHEMBL4678236 0.83 LMNA (0.34) NR4A2KDM4EALDH1A1POLBLMNA
SCHEMBL4676370 0.82 MEN1 (0.34) MEN1KMT2AKDM4EALDH1A1MAPT
SCHEMBL4671201 0.82 BRAF (0.30)
SCHEMBL4675030 0.82 CA12 (0.33) KMT2AALDH1A1MAPTCA12ALPL
SCHEMBL4674008 0.81 ALDH1A1 (0.43) NR4A2MEN1KMT2AKDM4EALDH1A1
SCHEMBL4673273 0.78 MAPK14 (0.34) KDM4EPOLBCA12ALPLRPA1
SCHEMBL4671509 0.77 MET (0.33) CA12ALPLRPA1
SCHEMBL4676082 0.77 MAPK14 (0.33) MEN1KMT2ACA12ALPLRPA1

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 NR4A2 454/4885MEN1 4663/4885KMT2A 597/4885

“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.