SCHEMBL4677157

SCHEMBL4677157

O=C(Cc1cscc1-c1ccccc1)C(=O)c1nc[nH]n1

nearest known ligand 0.33

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PTGS2 P35354 1/20 0.33
PTGDR2 Q9Y5Y4 7/20 0.33
FFAR4 Q5NUL3 2/20 0.33
TDP1 Q9NUW8 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
CYP2A6 P11509 1/20 0.32
CYP2B6 P20813 1/20 0.32
TGM2 P21980 1/20 0.32
ERCC5 P28715 1/20 0.31
FEN1 P39748 1/20 0.31
FFAR1 O14842 1/20 0.30
PDPK1 O15530 1/20 0.30
MAPT P10636 2/20 0.30
ALDH1A1 P00352 1/20 0.30
POLB P06746 1/20 0.30
USP2 O75604 1/20 0.30
LMNA P02545 1/20 0.30
MAPK1 P28482 1/20 0.30
HTT P42858 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
SCHEMBL4676445 0.83 SLC6A2 (0.33) L3MBTL1
SCHEMBL27575593 0.82 POLB (0.35) TDP1L3MBTL1MAPTALDH1A1POLB
SCHEMBL4675055 0.81 LMNA (0.32) TDP1L3MBTL1MAPTALDH1A1LMNA
SCHEMBL4675098 0.81 TDP1 (0.32) PTGDR2TDP1L3MBTL1
SCHEMBL4676518 0.81 HDAC3 (0.39) PTGS2L3MBTL1CYP2A6CYP2B6ERCC5
SCHEMBL4674765 0.79 MMP2 (0.36) PTGDR2MAPTALDH1A1
SCHEMBL4670874 0.78 ADORA2A (0.33)
SCHEMBL4675261 0.78 TP53 (0.50) PTGS2PTGDR2ERCC5FEN1MAPT
SCHEMBL4676076 0.78 AR (0.33) MAPTALDH1A1
SCHEMBL4673131 0.78 RAB9A (0.37) TDP1MAPTALDH1A1POLBLMNA

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 PTGS2 4586/4885PTGDR2 4591/4885FFAR4 1275/4885

“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.