SCHEMBL6151646

SCHEMBL6151646

CNC(=O)c1cc(S(N)(=O)=O)ccc1F

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CA2 P00918 13/20 0.56
CA1 P00915 11/20 0.51
CA9 Q16790 8/20 0.51
GAA P10253 2/20 0.50
EPHX2 P34913 1/20 0.46
NR1H4 Q96RI1 1/20 0.46
CA12 O43570 1/20 0.46
CA4 P22748 1/20 0.46
CA6 P23280 1/20 0.46
CA5A P35218 1/20 0.46
CA7 P43166 1/20 0.46
CA14 Q9ULX7 1/20 0.46
CA5B Q9Y2D0 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
KMT2A Q03164 1/20 0.45
MAOA P21397 1/20 0.44
SOS1 Q07889 1/20 0.44

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
SCHEMBL27565289 0.85 CA2 (0.49) CA2CA1CA9GAACA12
SCHEMBL7145771 0.81 CA2 (0.55) CA2CA1CA9GAACA12
SCHEMBL3362967 0.81 CA2 (0.58) CA2CA1CA9GAACA12
SCHEMBL283890 0.80 CYP3A4 (0.56) CA2CA1CA9GAACA12
SCHEMBL15076431 0.80 CA2 (0.52) CA2CA1CA9GAACA12
SCHEMBL15847661 0.79 MAPT (0.61) CA2CA1CA9CA12SOS1
SCHEMBL23677295 0.79 TP53 (0.56) CA2CA1CA9CA12SOS1
SCHEMBL3361559 0.79 CA2 (0.53) CA2CA1CA9EPHX2NR1H4
SCHEMBL13543311 0.77 CA2 (0.51) CA2CA1CA9EPHX2NR1H4
SCHEMBL13545187 0.77 CHRNA7 (0.49) CA2CA1CA9CA12CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1221524-C Diphenyl ether compounds for therapeutic use PFIZER LTD (US) 2005-10-05 CN disclosed
EP-1268396-B1 DIPHENYL ETHER COMPOUNDS USEFUL IN THERAPY PFIZER LTD (GB) 2005-07-20 EP disclosed
CN-1449380-A Phenoxybenzylamine derivatives as selective serotonin re-uptake inhibitors PFIZER LTD (US) 2003-10-15 CN disclosed
US-6610747-B2 Such as 4-(2,3-dihydro-1-benzothien-5-yloxy)-3-((methylamino) methyl)-benzenesulfonamide for use as serotonin re-uptake inhibitors (SSRIs) in treatment of depression, attention deficit hyperactivity disorder, obsessive-compulsive disorder PFIZER INC. 2003-08-26 US disclosed
CN-1419534-A Diphenyl ether compounds for therapeutic use PFIZER LTD (US) 2003-05-21 CN disclosed
US-6448293-B1 TREATMENT OR PREVENTION OF A DISORDER IN WHICH THE REGULATION OF MONOAMINE TRANSPORTER FUNCTION IS IMPLICATED, SUCH AS PREMATURE EJACULATION. PFIZER INC. 2002-09-10 US disclosed
US-20020052395-A1 Diphenyl ether compounds useful in therapy ANDREWS MARK DAVID (GB) 2002-05-02 US 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-20020052395-A1 Diphenyl ether compounds useful in therapy CBR1, OGFR, CBR3 CA2 1657/4885CA1 3037/4885CA9 892/4885

“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.