SCHEMBL1713470

SCHEMBL1713470

O=C(C1CCCN(S(=O)(=O)c2ccc(F)cc2)C1)N1CCCC1c1ccccc1

nearest known ligand 0.66

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.66
LMNA P02545 5/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
KMT2A Q03164 3/20 0.57
DPP4 P27487 1/20 0.54
MEN1 O00255 1/20 0.53
TSHR P16473 2/20 0.53
KDM4E B2RXH2 1/20 0.53
HSD17B10 Q99714 1/20 0.53
GAA P10253 2/20 0.52
HTT P42858 2/20 0.52
AKR1C3 P42330 2/20 0.52
AKR1C1 Q04828 2/20 0.52
L3MBTL1 Q9Y468 1/20 0.51
CYP3A4 P08684 1/20 0.51
CYP2C19 P33261 1/20 0.51
TP53 P04637 1/20 0.51

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
SCHEMBL1713497 0.98 MAPT (0.64) MAPTLMNASMN1; SMN2KMT2ADPP4
SCHEMBL4094978 0.92 LMNA (0.67) MAPTLMNASMN1; SMN2TSHRGAA
SCHEMBL1712636 0.90 LMNA (0.67) MAPTLMNASMN1; SMN2TSHRHTT
SCHEMBL1712628 0.85 FAAH (0.51) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1712641 0.83 MAPT (0.54) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1712872 0.82 AKR1C3 (0.55) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1712968 0.82 MAPT (0.53) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1713030 0.82 CNR1 (0.56) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1713376 0.81 LMNA (0.55) MAPTLMNASMN1; SMN2KMT2AMEN1
SCHEMBL1712578 0.81 POLB (0.54) MAPTLMNASMN1; SMN2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8691846-B2 Piperidine sulphonamide derivatives HOFFMANN-LA ROCHE INC. (US) 2014-04-08 US disclosed
US-8691846-B2 Piperidine sulphonamide derivatives HOFFMANN-LA ROCHE INC. (US) 2014-04-08 US disclosed
US-20130217729-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2013-08-22 US disclosed
US-20130217729-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2013-08-22 US disclosed
US-20120238602-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES KNUST HENNER (DE) 2012-09-20 US disclosed
US-20120238602-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES KNUST HENNER (DE) 2012-09-20 US disclosed
US-8202888-B2 Piperidine sulphonamide derivatives HOFFMANN-LA ROCHE INC. (US) 2012-06-19 US disclosed
US-8202888-B2 Piperidine sulphonamide derivatives HOFFMANN-LA ROCHE INC. (US) 2012-06-19 US disclosed
EP-2252587-B1 PIPERIDINE SULFONAMIDE DERIVATIVES HOFFMANN LA ROCHE (CH) 2011-07-20 EP disclosed
US-20090203736-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2009-08-13 US disclosed
US-20090203736-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2009-08-13 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 (3 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-20090203736-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES HCRTR2, PER2, HCRTR1 MAPT 1778/4885LMNA 3629/4885SMN1; SMN2 514/4885
US-20120238602-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES HCRTR2, PER2, HCRTR1 MAPT 1778/4885LMNA 3629/4885SMN1; SMN2 514/4885
US-20130217729-A1 PIPERIDINE SULPHONAMIDE DERIVATIVES HCRTR2, PER2, HCRTR1 MAPT 1778/4885LMNA 3629/4885SMN1; SMN2 514/4885

“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.