SCHEMBL7044238

SCHEMBL7044238

COc1nn(-c2cccc(OCc3ccccc3)c2)c(=O)o1

nearest known ligand 0.81

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
BCHE P06276 1/20 0.81
LIPC P11150 1/20 0.81
ACHE P22303 1/20 0.81
LIPE Q05469 1/20 0.81
MGLL Q99685 8/20 0.72
FAAH O00519 6/20 0.70
ABHD16A O95870 2/20 0.56
MAOB P27338 1/20 0.51
GRM5 P41594 1/20 0.50

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
SCHEMBL6552559 0.89 BCHE (1.00) BCHELIPCACHELIPEMGLL
SCHEMBL6551894 0.89 ACHE (0.65) BCHELIPCACHELIPEMGLL
SCHEMBL2702372 0.85 BCHE (0.78) BCHELIPCACHELIPEMGLL
SCHEMBL6551376 0.84 MGLL (1.00) BCHELIPCACHELIPEMGLL
SCHEMBL11620781 0.80 FAAH (0.78) BCHELIPCACHELIPEMGLL
SCHEMBL7043150 0.80 MGLL (0.63) BCHELIPCACHELIPEMGLL
SCHEMBL6552790 0.80 MGLL (0.74) BCHELIPCACHELIPEMGLL
SCHEMBL2853749 0.80 BCHE (0.68) BCHELIPCACHELIPEMGLL
SCHEMBL7044409 0.79 MGLL (0.62) BCHELIPCACHELIPEMGLL
SCHEMBL7044272 0.77 MGLL (0.69) BCHELIPCACHELIPEMGLL

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
US-20030236288-A1 Use of substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadizol-2-ones for inhibiting pancreatic lipase AVENTIS PHARMA DEUTSCHLAND GMBH 2003-12-25 US claimed
US-20030236288-A1 Use of substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadizol-2-ones for inhibiting pancreatic lipase AVENTIS PHARMA DEUTSCHLAND GMBH 2003-12-25 US disclosed
EP-1214302-B1 SUBSTITUTED 3-PHENYL-5-ALKOXI-1,3,4-OXDIAZOL-2-ONES AND THEIR USE AS LIPASE INHIBITORS AVENTIS PHARMA GMBH (DE) 2003-10-29 EP disclosed
US-6596742-B1 Inhibitory effect on the hormone-sensitive lipase, HSL. insecticides, controlling metabolism and multistage synthesis AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2003-07-22 US disclosed
EP-1214302-A1 SUBSTITUTED 3-PHENYL-5-ALKOXI-1,3,4-OXDIAZOL-2-ONES AND THEIR USE AS LIPASE INHIBITORS Aventis Pharma Deutschland GmbH (DE) 2002-06-19 EP disclosed
WO-2001017981-A1 SUBSTITUTED 3-PHENYL-5-ALKOXI-1,3,4-OXDIAZOL-2-ONES AND THEIR USE AS LIPASE INHIBITORS AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2001-03-15 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 (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-20030236288-A1 Use of substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadizol-2-ones for inhibiting pancreatic lipase PNLIP, CEL, LIPE BCHE 626/4885LIPC 7/4885ACHE 649/4885

“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.