SCHEMBL296238

SCHEMBL296238

CN(Cc1ccc(Cl)c(Cl)c1)C(=O)C(C)(CCN1CCC(N(C)S(C)(=O)=O)CC1)c1ccc(Cl)c(Cl)c1

nearest known ligand 0.66

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TACR3 P29371 4/20 0.66
TACR2 P21452 3/20 0.66
TACR1 P25103 3/20 0.66
CCR2 P41597 6/20 0.42
CCR5 P51681 3/20 0.41
HRH3 Q9Y5N1 1/20 0.39
SIGMAR1 Q99720 1/20 0.38
KCNH2 Q12809 2/20 0.38
CACNA1I Q9P0X4 1/20 0.38
APAF1 O14727 1/20 0.38
UBE2N P61088 1/20 0.38
GPR119 Q8TDV5 1/20 0.38
MEN1 O00255 1/20 0.37
ALDH1A1 P00352 1/20 0.37
MAPT P10636 1/20 0.37
KMT2A Q03164 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
USP30 Q70CQ3 1/20 0.37

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
SCHEMBL296791 0.94 TACR3 (0.72) TACR3TACR2TACR1CCR2CCR5
SCHEMBL3271088 0.92 TACR3 (0.80) TACR3TACR2TACR1CCR2CCR5
SCHEMBL297231 0.92 TACR3 (0.65) TACR3TACR2TACR1CCR2CCR5
SCHEMBL296921 0.91 TACR3 (0.71) TACR3TACR2TACR1CCR2CCR5
SCHEMBL295923 0.91 TACR3 (0.81) TACR3TACR2TACR1CCR2CCR5
SCHEMBL295664 0.91 TACR3 (0.63) TACR3TACR2TACR1CCR5HRH3
SCHEMBL296042 0.89 TACR3 (0.56) TACR3TACR2TACR1CCR2CCR5
SCHEMBL296834 0.88 TACR3 (0.83) TACR3TACR2TACR1CCR5HRH3
SCHEMBL296958 0.87 TACR3 (0.60) TACR3TACR2TACR1CCR2CCR5
SCHEMBL296239 0.86 TACR3 (0.60) TACR3TACR2TACR1CCR5SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2200982-B1 PIPERIDINE DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS HOFFMANN LA ROCHE (CH) 2012-03-14 EP claimed
US-20110021565-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS KNUST HENNER 2011-01-27 US claimed
EP-2200982-A1 PIPERIDINE DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS F. Hoffmann-Roche AG (CH) 2010-06-30 EP claimed
WO-2009033995-A1 PIPERIDINE DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2009-03-19 WO claimed
US-20090076081-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2009-03-19 US claimed
EP-2200982-B1 PIPERIDINE DERIVATIVES AS NK3 RECEPTOR ANTAGONISTS HOFFMANN LA ROCHE (CH) 2012-03-14 EP disclosed
US-20110021565-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS KNUST HENNER 2011-01-27 US disclosed
US-20110021565-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS KNUST HENNER 2011-01-27 US disclosed
US-20110021565-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS KNUST HENNER 2011-01-27 US disclosed
US-20090076081-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2009-03-19 US disclosed
US-20090076081-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2009-03-19 US disclosed
US-20090076081-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2009-03-19 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 (2 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-20090076081-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS DRD2, DRD3, OPRL1 TACR3 95/4885TACR2 21/4885TACR1 26/4885
US-20110021565-A1 PIPERIDINE DERIVATIVES AS NK3 ANTAGONISTS DRD2, DRD3, OPRL1 TACR3 95/4885TACR2 21/4885TACR1 26/4885

“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.