SCHEMBL4676095

SCHEMBL4676095

O=C(Cc1cc(-c2ccccc2)cs1)C(=O)c1nc[nH]n1

nearest known ligand 0.36

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP11B1 P15538 1/20 0.36
CYP11B2 P19099 1/20 0.36
MMP12 P39900 3/20 0.36
HDAC6 Q9UBN7 1/20 0.35
NPC1 O15118 2/20 0.33
RAB9A P51151 2/20 0.33
CASP3 P42574 1/20 0.33
SENP7 Q9BQF6 1/20 0.33
S1PR1 P21453 2/20 0.33
PTGDR2 Q9Y5Y4 1/20 0.33
GAA P10253 2/20 0.32
TP53 P04637 1/20 0.32
KDM4E B2RXH2 2/20 0.32
ULK1 O75385 1/20 0.31
DGAT1 O75907 1/20 0.31

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
SCHEMBL4679302 0.83 SIRT2 (0.30)
SCHEMBL4671873 0.83 LTB4R (0.39) MMP12HDAC6CASP3SENP7
SCHEMBL27578577 0.82 PTGER1 (0.32) MMP12PTGDR2GAA
SCHEMBL4673473 0.81 LOX (0.39)
SCHEMBL4677961 0.81 HDAC6 (0.41) CYP11B1CYP11B2MMP12HDAC6NPC1
SCHEMBL27575661 0.80 DYRK1A (0.32) MMP12HDAC6TP53
SCHEMBL4673897 0.80 RPS6KB2 (0.40) MMP12PTGDR2GAATP53KDM4E
SCHEMBL4677544 0.79 CYP2E1 (0.40) CYP11B1CYP11B2RAB9A
SCHEMBL4673826 0.79 LTB4R (0.44) HDAC6NPC1RAB9ATP53KDM4E
SCHEMBL4672575 0.78 NOTUM (0.49) HDAC6NPC1RAB9AS1PR1GAA

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 CYP11B1 63/4885CYP11B2 129/4885MMP12 3456/4885

“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.