SCHEMBL4670978

SCHEMBL4670978

CCc1cn(Cc2ccc(OC)cc2)cc1C(=O)C=C(O)c1nn[nH]n1

nearest known ligand 0.39

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CDK5 Q00535 1/20 0.35
CDK5R1 Q15078 1/20 0.35
CYP19A1 P11511 1/20 0.35
PTGDR2 Q9Y5Y4 3/20 0.34
MAPK8 P45983 1/20 0.34
MAPK10 P53779 1/20 0.34
TAS2R14 Q9NYV8 1/20 0.34
HSP90AA1 P07900 1/20 0.34
MEN1 O00255 1/20 0.34
NPC1 O15118 1/20 0.34
RAB9A P51151 1/20 0.34
KMT2A Q03164 1/20 0.34
CXCR3 P49682 1/20 0.34
PDE8B O95263 1/20 0.33
TOP2A P11388 1/20 0.33

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
SCHEMBL4676235 0.90 CDK5 (0.38) CDK5CDK5R1TAS2R14MEN1NPC1
SCHEMBL4676225 0.89 AGTR1 (0.33) NPC1
SCHEMBL4675803 0.88 MAPT (0.33) PTGDR2RAB9A
SCHEMBL4694742 0.87 MEN1 (0.32) MEN1KMT2A
SCHEMBL4674474 0.85 CDK5 (0.38) CDK5CDK5R1CYP19A1HSP90AA1MEN1
SCHEMBL4674369 0.82 CYP19A1 (0.40) CDK5CDK5R1CYP19A1PTGDR2MAPK8
SCHEMBL4675325 0.81 PTGDR2 (0.37) PTGDR2
SCHEMBL4676460 0.80 CES1 (0.43)
SCHEMBL4675104 0.80 PTGDR2 (0.37) PTGDR2MAPK8MAPK10MEN1NPC1
SCHEMBL4677657 0.80 PTGDR2 (0.35) PTGDR2MEN1NPC1RAB9AKMT2A

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 CDK5 1442/4885CDK5R1 268/4885CYP19A1 96/4885

“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.