SCHEMBL4676745

SCHEMBL4676745

O=C(Cc1coc(Cc2ccc(F)cc2)c1)C(=O)c1nn[nH]n1

nearest known ligand 0.34

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.34
PTGDR2 Q9Y5Y4 1/20 0.33
CXCR3 P49682 1/20 0.33
PIN1 Q13526 1/20 0.32
IDH1 O75874 1/20 0.32
MMEL1 Q495T6 2/20 0.32
CES1 P23141 1/20 0.31
NCEH1 Q6PIU2 1/20 0.31
TP53 P04637 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
ACHE P22303 1/20 0.30
LTB4R2 Q9NPC1 1/20 0.30
METAP2 P50579 1/20 0.30
MAPT P10636 1/20 0.30
MME P08473 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
SCHEMBL4679605 0.91 TDP1 (0.34) TDP1PTGDR2CXCR3PIN1MMEL1
SCHEMBL4672959 0.89 IDH1 (0.32) IDH1CES1NCEH1
SCHEMBL4674714 0.89 CYP2C19 (0.33) PTGDR2IDH1CES1NCEH1
SCHEMBL4675582 0.89 IDH1 (0.44) IDH1MMEL1CES1NCEH1MME
SCHEMBL4672624 0.88 FFAR2 (0.40) TDP1PTGDR2PIN1IDH1CES1
SCHEMBL4672335 0.88 CYP11B1 (0.33) IDH1CES1NCEH1
SCHEMBL4674378 0.87 XDH (0.39) IDH1CES1NCEH1
SCHEMBL4673593 0.86 MAPK8 (0.40) PTGDR2CXCR3TP53MAPT
SCHEMBL4673700 0.84 PTGDR2 (0.35) TDP1PTGDR2CXCR3IDH1MMEL1
SCHEMBL3228436 0.83 CXCR3 (0.34) TDP1PTGDR2CXCR3PIN1MMEL1

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 7 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
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 TDP1 306/4885PTGDR2 4591/4885CXCR3 1130/4885

“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.