SCHEMBL15539232

SCHEMBL15539232

CC(C)c1cc(C(O)C(F)(F)F)cc(Br)c1O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABRA1 P14867 5/20 0.44
GABRB1 P18505 4/20 0.44
GABRB2 P47870 3/20 0.42
CA1 P00915 2/20 0.38
CA2 P00918 2/20 0.38
THRA P10827 1/20 0.33
THRB P10828 1/20 0.33
GLRA1 P23415 1/20 0.33
CYP3A4 P08684 2/20 0.32
HPGD P15428 2/20 0.32
TSHR P16473 2/20 0.32
HIF1A Q16665 2/20 0.32
ALDH1A1 P00352 1/20 0.32
ALOX15 P16050 1/20 0.32
ALOX12 P18054 1/20 0.32
CASP1 P29466 1/20 0.32
RECQL P46063 1/20 0.32
HSD17B10 Q99714 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
ADRB2 P07550 2/20 0.32

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
SCHEMBL1795642 0.88 CA1 (0.50) GABRA1GABRB1GABRB2CA1CA2
SCHEMBL4775793 0.88 CA1 (0.50) GABRA1GABRB1GABRB2CA1CA2
SCHEMBL15538546 0.84 RORC (0.36) HPGDTSHRALDH1A1ALOX15HSD17B10
SCHEMBL16785950 0.80 GABRA1 (0.52) GABRA1GABRB1GABRB2CA1CA2
SCHEMBL6682827 0.80 GABRA1 (0.63) GABRA1GABRB1GABRB2CA1CA2
SCHEMBL15539638 0.80 CA2 (0.33) GABRA1GABRB1CA2THRATHRB
SCHEMBL16788662 0.79 CYP3A4 (0.34) CA1CA2CYP3A4HPGDTSHR
SCHEMBL21487350 0.76 ADRB2 (0.33) CYP3A4HPGDTSHRHIF1AALDH1A1
SCHEMBL16788668 0.75 CYP2C19 (0.35) GABRA1GABRB2CA1CA2CYP3A4
SCHEMBL15538671 0.73 HMGCR (0.33) CYP3A4HPGDTSHRHIF1AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9422248-B2 Phenyl- and pyridinyl-substituted 2,2,2-trifluoroethanols having anticonvulsant properties UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2016-08-23 US claimed
US-20150158821-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES UNIVERSITY OF IOWA RESEARCH FOUNDATION 2015-06-11 US claimed
WO-2013188716-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2013-12-19 WO claimed
US-9422248-B2 Phenyl- and pyridinyl-substituted 2,2,2-trifluoroethanols having anticonvulsant properties UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2016-08-23 US disclosed
US-9422248-B2 Phenyl- and pyridinyl-substituted 2,2,2-trifluoroethanols having anticonvulsant properties UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2016-08-23 US disclosed
US-20150158821-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES UNIVERSITY OF IOWA RESEARCH FOUNDATION 2015-06-11 US disclosed
US-20150158821-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES UNIVERSITY OF IOWA RESEARCH FOUNDATION 2015-06-11 US disclosed
WO-2013188716-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 2013-12-19 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-20150158821-A1 SUBSTITUTED PHENOLS HAVING ANTICONVULSANT PROPERTIES PNMT, COMT, GABRE GABRA1 75/4885GABRB1 37/4885GABRB2 22/4885

“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.