SCHEMBL4674808

SCHEMBL4674808

O=C(C=C(O)c1nn[nH]n1)c1ccc(S(=O)(=O)c2ccc(F)cc2)o1

nearest known ligand 0.34

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CXCR3 P49682 1/20 0.34
PTGDR2 Q9Y5Y4 7/20 0.33
HTR2A P28223 4/20 0.32
KCNH2 Q12809 3/20 0.32
HTR2C P28335 1/20 0.32
CYP2C8 P10632 3/20 0.32
CYP2C19 P33261 3/20 0.32
CYP2C9 P11712 2/20 0.32
AKR1B1 P15121 1/20 0.31
MAPT P10636 1/20 0.31
MMEL1 Q495T6 1/20 0.30
CES1 P23141 1/20 0.30
NCEH1 Q6PIU2 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
SCHEMBL4676467 0.89 CXCR3 (0.36) CXCR3AKR1B1MMEL1CES1NCEH1
SCHEMBL4671017 0.83 HTR2A (0.34) HTR2AKCNH2HTR2CAKR1B1MAPT
SCHEMBL4671570 0.82 PTGDR2 (0.32) CXCR3PTGDR2CYP2C8CYP2C19CYP2C9
SCHEMBL4678118 0.81 PTGDR2 (0.32) CXCR3PTGDR2CYP2C8CYP2C19CYP2C9
SCHEMBL4671648 0.79 CES1 (0.34) CXCR3PTGDR2CYP2C19CYP2C9MAPT
SCHEMBL4672908 0.79 AKR1B1 (0.31) CXCR3AKR1B1
SCHEMBL4673134 0.78 MAPT (0.32) AKR1B1MAPT
SCHEMBL4671614 0.78 MAPT (0.32) AKR1B1MAPT
SCHEMBL4671903 0.77 PTGS2 (0.36) HTR2AKCNH2HTR2CMAPT
SCHEMBL4671905 0.77 PTGS2 (0.36) HTR2AKCNH2HTR2CMAPT

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 CXCR3 1130/4885PTGDR2 4591/4885HTR2A 441/4885

“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.