SCHEMBL4674789

SCHEMBL4674789

O=C(C=C(O)c1nc[nH]n1)c1cc(S(=O)(=O)c2ccc(F)cc2)cs1

nearest known ligand 0.35

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.35
HTT P42858 2/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
CYP1A2 P05177 1/20 0.34
CYP3A4 P08684 1/20 0.34
CYP2D6 P10635 1/20 0.34
CYP2C9 P11712 1/20 0.34
CYP2C19 P33261 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
HTR2A P28223 3/20 0.32
KCNH2 Q12809 2/20 0.32
AKR1B1 P15121 1/20 0.30
ULK1 O75385 1/20 0.30
ALDH1A1 P00352 1/20 0.30
CA2 P00918 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
SCHEMBL4680017 0.90 ALDH1A1 (0.33) MAPTHTTMEN1KMT2ACYP3A4
SCHEMBL4677761 0.86 LMNA (0.35) HTR2AKCNH2AKR1B1ALDH1A1
SCHEMBL4680056 0.83 MAPT (0.35) MAPTHTTMEN1KMT2ACYP1A2
SCHEMBL4674438 0.82 HTR2A (0.31) HTR2AKCNH2AKR1B1
SCHEMBL4672156 0.80 HTR2A (0.36) MEN1KMT2AHTR2AKCNH2AKR1B1
SCHEMBL4677355 0.80 HTR2A (0.31) HTR2AKCNH2AKR1B1
SCHEMBL4673249 0.80 LMNA (0.35) MAPTALDH1A1
SCHEMBL4672012 0.79 IKBKB (0.32) MAPTHTR2AKCNH2AKR1B1
SCHEMBL4671743 0.79 MEN1 (0.32) MAPTHTTMEN1KMT2ASMN1; SMN2
SCHEMBL4674481 0.79 HTR2A (0.32) MAPTHTR2AKCNH2AKR1B1ALDH1A1

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 MAPT 205/4885HTT 1204/4885MEN1 4663/4885

“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.