SCHEMBL4474869

SCHEMBL4474869

CCO/N=C\C1CCNCC1

nearest known ligand 0.42

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
GNAI3 P08754 1/20 0.30
GNAO1 P09471 1/20 0.30
GNAI1 P63096 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
SCHEMBL4474871 1.00 GNAI3 (0.30) GNAI3GNAO1GNAI1
Hydrochloric Acid SCHEMBL4476787 0.98 GNAI3 (0.33) GNAI3GNAO1GNAI1
Hydrochloric Acid SCHEMBL4476786 0.98 GNAI3 (0.33) GNAI3GNAO1GNAI1
SCHEMBL13116715 0.87
SCHEMBL28210693 0.78
SCHEMBL14077938 0.76 CHRM2 (0.37)
SCHEMBL28021279 0.73
SCHEMBL18427101 0.70
SCHEMBL19544089 0.70
SCHEMBL17645614 0.68

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7524963-B2 Synthesis of (4-bromophenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION (US) 2009-04-28 US disclosed
US-7524963-B2 Synthesis of (4-bromophenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION (US) 2009-04-28 US disclosed
CN-1308308-C Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(z)-o-ethyloxime and salts SCHERING CORP (US) 2007-04-04 CN disclosed
US-20050171159-A1 Antiinflammatory agents; rheumatic diseases WONG GEORGE S (US) 2005-08-04 US disclosed
US-20050171159-A1 Antiinflammatory agents; rheumatic diseases WONG GEORGE S (US) 2005-08-04 US disclosed
US-6914142-B2 Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION (US) 2005-07-05 US disclosed
US-6914142-B2 Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION (US) 2005-07-05 US disclosed
CN-1571768-A Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(z)-o-ethyloxime and salts SCHERING CORP (US) 2005-01-26 CN disclosed
EP-1436262-A1 SYNTHESIS OF (4-BROMOPHENYL) (4-PIPERIDYL)METHANONE-(Z)-O-ETHYLOXIME AND SALTS Schering Corporation (US) 2004-07-14 EP disclosed
US-20030092731-A1 Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION 2003-05-15 US disclosed
US-20030092731-A1 Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts SCHERING CORPORATION 2003-05-15 US disclosed
WO-2003033465-A1 SYNTHESIS OF (4-BROMOPHENYL) (4-PIPERIDYL)METHANONE-(Z)-O-ETHYLOXIME AND SALTS SCHERING CORPORATION (US) 2003-04-24 WO 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 (2 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-20030092731-A1 Synthesis of (4-bromopnenyl)(4-piperidyl)methanone-(Z)-O-ethyloxime and salts PAM, PNMT, MSMO1 GNAI3 1246/4885GNAO1 344/4885GNAI1 2272/4885
US-20050171159-A1 Antiinflammatory agents; rheumatic diseases PTGES3, PTGES, PTGES2 GNAI3 919/4885GNAO1 759/4885GNAI1 1253/4885

“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.