SCHEMBL994167

SCHEMBL994167

COc1ccc(CCc2ccccc2)c(O)c1

nearest known ligand 0.71

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 1/20 0.65
CYP19A1 P11511 1/20 0.65
ESR2 Q92731 1/20 0.65
POLB P06746 1/20 0.62
L3MBTL1 Q9Y468 2/20 0.56
TDP1 Q9NUW8 1/20 0.56
ABCB1 P08183 3/20 0.54
MAOB P27338 1/20 0.53
HTR1A P08908 1/20 0.51
DRD2 P14416 1/20 0.51
HSP90AA1 P07900 1/20 0.51
HSP90AB1 P08238 1/20 0.51
CALM1 P0DP23 1/20 0.50
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
TSHR P16473 1/20 0.50
ALDH1A1 P00352 1/20 0.49
MAPT P10636 1/20 0.49

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
SCHEMBL227115 0.90 ESR1 (0.73) ESR1CYP19A1ESR2POLBABCB1
SCHEMBL4736569 0.88 ESR1 (0.82) ESR1CYP19A1ESR2POLBCALM1
SCHEMBL8686118 0.87 TDP1 (0.56) ESR1CYP19A1ESR2POLBL3MBTL1
SCHEMBL30419864 0.85 ALOX5 (0.66) ESR1CYP19A1ESR2POLBMAOB
SCHEMBL6061390 0.83 LTA4H (0.50) ESR1CYP19A1ESR2POLBMAOB
SCHEMBL1847390 0.83 ESR1 (0.69) ESR1CYP19A1ESR2POLBCALM1
SCHEMBL29492427 0.83 ESR1 (0.69) ESR1CYP19A1ESR2POLBCALM1
SCHEMBL29492460 0.83 GABRA1 (0.59) ESR1CYP19A1ESR2POLBABCB1
SCHEMBL21830506 0.83 GABRA1 (0.59) ESR1CYP19A1ESR2POLBABCB1
SCHEMBL29350108 0.82 TDP1 (0.61) L3MBTL1TDP1ABCB1HTR1ADRD2

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-20110009447-A1 Substituted Benzoic Acid Amides and Use thereof for the Inhibition of Angiogenesis SCHERING AG (DE) 2011-01-13 US disclosed
EP-1280776-B1 SUBSTITUTED BENZOIC ACID AMIDES AND USE THEREOF FOR THE INHIBITION OF ANGIOGENESIS BAYER SCHERING PHARMA AG (DE) 2009-10-21 EP disclosed
EP-1280776-A1 SUBSTITUTED BENZOIC ACID AMIDES AND USE THEREOF FOR THE INHIBITION OF ANGIOGENESIS SCHERING AKTIENGESELLSCHAFT (DE) 2003-02-05 EP disclosed
WO-2001081311-A1 SUBSTITUTED BENZOIC ACID AMIDES AND USE THEREOF FOR THE INHIBITION OF ANGIOGENESIS SCHERING AKTIENGESELLSCHAFT (DE) 2001-11-01 WO disclosed
US-5843983-A Diphenylethane compounds containing a saturated heterocyclic group, their preparation, and their therapeutic use SANKYO COMPANY, LIMITED (JP) 1998-12-01 US disclosed
EP-0790235-A1 Diaryl alkane derivatives containing an alicyclic group, their preparation and their therapeutic and prophylactic uses SANKYO COMPANY LIMITED (JP) 1997-08-20 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-20110009447-A1 Substituted Benzoic Acid Amides and Use thereof for the Inhibition of Angiogenesis VEGFA, EGLN2, HIF1AN ESR1 526/4885CYP19A1 51/4885ESR2 182/4885

“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.