SCHEMBL15720571

SCHEMBL15720571

O=S(=O)(Oc1ccnc(C(F)(F)F)c1)C(F)(F)F

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LOXL2 Q9Y4K0 2/20 0.42
▸ LOX P28300 1/20 0.41
▸ CA1 P00915 1/20 0.40
▸ CA2 P00918 1/20 0.40
▸ KCNQ2 O43526 1/20 0.38
▸ SMARCA2 P51531 1/20 0.37
▸ SMARCA4 P51532 1/20 0.37
▸ ADAMTS4 O75173 1/20 0.37
▸ MMP13 P45452 1/20 0.37
▸ NOTUM Q6P988 1/20 0.36
▸ IDO1 P14902 1/20 0.36
▸ AR P10275 1/20 0.36
▸ HTR1A P08908 2/20 0.36
▸ HTR1D P28221 2/20 0.36
▸ HTR1B P28222 2/20 0.36
▸ HDAC4 P56524 1/20 0.36
▸ HSD11B1 P28845 1/20 0.35
▸ ALOX5AP P20292 1/20 0.35
▸ FEN1 P39748 1/20 0.35
▸ PDE4A P27815 1/20 0.34

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
SCHEMBL29211870 0.83 LOXL2 (0.40) LOXL2LOXCA2KCNQ2SMARCA2
SCHEMBL25318934 0.83 ADAMTS4 (0.43) LOXL2CA1CA2ADAMTS4MMP13
SCHEMBL28406146 0.82 LOXL2 (0.42) LOXL2LOXCA2KCNQ2SMARCA2
SCHEMBL17310149 0.79 CA1 (0.40) LOXL2LOXCA1CA2SMARCA2
SCHEMBL11945522 0.79 CA1 (0.40) CA1CA2HTR1AHTR1DHTR1B
SCHEMBL27894825 0.77 LOXL2 (0.50) LOXL2LOXCA2SMARCA2SMARCA4
SCHEMBL23674532 0.77 CA1 (0.39) CA1CA2HTR1AHTR1DHTR1B
SCHEMBL28741515 0.76 HTR1D (0.40) CA1CA2HTR1AHTR1DHTR1B
SCHEMBL28741615 0.76 RIPK2 (0.41) CA1CA2HTR1AHTR1DHTR1B
SCHEMBL30384914 0.74 PDE4A (0.41) CA1CA2HTR1AHTR1DHTR1B

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
EP-2920150-B1 PROCESS FOR THE PREPARATION OF 2-TRIFLUOROMETHYL ISONICOTINIC ACID AND ESTERS HOFFMANN LA ROCHE (CH) 2017-07-19 — — EP disclosed
US-9481650-B2 Process for the preparation of 2-trifluoromethyl isonicotinic acid and esters HOFFMANN LA ROCHE INC. (US) 2016-11-01 — — US disclosed
US-20150291530-A1 PROCESS FOR THE PREPARATION OF 2-TRIFLUOROMETHYL ISONICOTINIC ACID AND ESTERS HOFFMANN-LA ROCHE INC. (US) 2015-10-15 — — US disclosed
EP-2920150-A1 PROCESS FOR THE PREPARATION OF 2-TRIFLUOROMETHYL ISONICOTINIC ACID AND ESTERS F. Hoffmann-La Roche AG (CH) 2015-09-23 — — EP disclosed
WO-2014076127-A1 PROCESS FOR THE PREPARATION OF 2-TRIFLUOROMETHYL ISONICOTINIC ACID AND ESTERS F. HOFFMANN-LA ROCHE AG (CH) 2014-05-22 — — 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-20150291530-A1 PROCESS FOR THE PREPARATION OF 2-TRIFLUOROMETHYL ISONICOTINIC ACID AND ESTERS TAAR1, TAAR5, TSHR LOXL2 4769/4885LOX 2488/4885CA1 766/4885

“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.

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