SCHEMBL6437986

SCHEMBL6437986

CCOC(=O)c1ccc(Oc2ccc(C)c(C)c2)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 2/20 0.54
CA1 P00915 2/20 0.54
CA2 P00918 2/20 0.54
CA7 P43166 2/20 0.54
CA9 Q16790 2/20 0.54
CA14 Q9ULX7 2/20 0.54
ESR1 P03372 1/20 0.54
ESR2 Q92731 1/20 0.54
LMNA P02545 4/20 0.53
CYP1A2 P05177 1/20 0.53
CYP3A4 P08684 1/20 0.53
MAOA P21397 1/20 0.53
KMT2A Q03164 2/20 0.53
L3MBTL1 Q9Y468 2/20 0.53
GFER P55789 1/20 0.53
STS P08842 1/20 0.53
MAPT P10636 3/20 0.51
TSHR P16473 2/20 0.51
MEN1 O00255 1/20 0.50
TDP1 Q9NUW8 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
SCHEMBL8656770 0.88 CA12 (0.68) CA12CA1CA2CA7CA9
SCHEMBL27371998 0.86 CA12 (0.50) CA12CA1CA2CA7CA9
SCHEMBL4313106 0.83 CA12 (0.58) CA12CA1CA2CA7CA9
Ethylene Glycol SCHEMBL6701397 0.83 CA12 (0.61) CA12CA1CA2CA7CA9
SCHEMBL9923544 0.83 CA12 (0.61) CA12CA1CA2CA7CA9
SCHEMBL571193 0.83 CA12 (0.65) CA12CA1CA2CA7CA9
SCHEMBL31194402 0.83 CA12 (0.65) CA12CA1CA2CA7CA9
SCHEMBL8059469 0.81 CA1 (0.59) CA12CA1CA2CA7CA9
SCHEMBL5837526 0.81 MAPT (0.59) CA12CA1CA2CA7CA9
SCHEMBL21656957 0.81 CA12 (0.59) CA12CA1CA2CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050054882-A1 Diaryl ether condensation reactions NSF - DEITR 2005-03-10 US disclosed
US-6762329-B2 EFFECTS OF ACIDIC ACTIVATORS ON ULLMANN-TYPE COUPLINGS INVOLVING ELECTRON-POOR AND/OR RELATIVELY INSOLUBLE SUBSTRATES. MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2004-07-13 US disclosed
US-20030088128-A1 Diaryl ether condensation reactions NATIONAL SCIENCE FOUNDATION 2003-05-08 US disclosed
US-6395939-B1 CATALYTIC ETHERIFICATION AND CONDENSATION WITH COPPER CATALYSTS MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2002-05-28 US disclosed
WO-1999018057-A1 PREPARATION OF DIARYL ETHER BY CONDENSATION REACTIONS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1999-04-15 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 (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-20050054882-A1 Diaryl ether condensation reactions NSFL1C, DERL1, UBE2M CA12 829/4885CA1 1356/4885CA2 1884/4885
US-20030088128-A1 Diaryl ether condensation reactions NSFL1C, DERL1, UBE2M CA12 829/4885CA1 1356/4885CA2 1884/4885

“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.