SCHEMBL4675650

SCHEMBL4675650

Cc1ccc(Cc2coc(CC(=O)C(=O)c3nn[nH]n3)c2)cc1

nearest known ligand 0.35

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 2/20 0.33
NPC1 O15118 1/20 0.33
CYP1A2 P05177 1/20 0.33
RECQL P46063 1/20 0.33
RAB9A P51151 1/20 0.33
PTGER4 P35408 2/20 0.32
SRD5A2 P31213 1/20 0.32
CES1 P23141 1/20 0.31
NCEH1 Q6PIU2 1/20 0.31
GAPDH P04406 1/20 0.30
PTGDR2 Q9Y5Y4 1/20 0.30
IDO1 P14902 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
SCHEMBL4674714 0.91 CYP2C19 (0.33) CYP2C19NPC1CYP1A2RECQLRAB9A
SCHEMBL4675871 0.89 KMT2A (0.40) CES1NCEH1
SCHEMBL4676898 0.89 CES1 (0.31) CES1NCEH1
SCHEMBL4679605 0.89 TDP1 (0.34) CES1NCEH1PTGDR2
SCHEMBL4676995 0.89 CES1 (0.42) CES1NCEH1PTGDR2
SCHEMBL4678112 0.88 MAPK8 (0.40) CYP2C19PTGDR2
SCHEMBL4675417 0.88 CES1 (0.32) NPC1RAB9ACES1NCEH1
SCHEMBL4673270 0.83 ALDH1A1 (0.39) CYP2C19NPC1RECQLRAB9ACES1
SCHEMBL4673321 0.82 NPC1 (0.35) CYP2C19NPC1CYP1A2RECQLRAB9A
SCHEMBL4675471 0.82 FFAR2 (0.40) CES1NCEH1PTGDR2

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 CYP2C19 53/4885NPC1 934/4885CYP1A2 61/4885

“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.