SCHEMBL3639751

SCHEMBL3639751

CN(Cc1cccc(F)c1)C(=O)C(C)(CCN1CCCN(S(C)(=O)=O)CC1)c1ccc(Cl)c(Cl)c1

nearest known ligand 0.54

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
TACR3 P29371 8/20 0.54
TACR1 P25103 6/20 0.54
TACR2 P21452 3/20 0.54
CCR2 P41597 5/20 0.42
RIPK1 Q13546 1/20 0.41
APAF1 O14727 1/20 0.41
UBE2N P61088 1/20 0.41
ALDH1A1 P00352 1/20 0.39
POLB P06746 1/20 0.39
GAA P10253 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39

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
SCHEMBL3864946 0.97 TACR3 (0.57) TACR3TACR1TACR2CCR2RIPK1
SCHEMBL3636715 0.92 TACR2 (0.52) TACR3TACR1TACR2CCR2RIPK1
SCHEMBL3666736 0.92 TACR3 (0.54) TACR3TACR1TACR2CCR2APAF1
SCHEMBL3675253 0.91 TACR3 (0.55) TACR3TACR1TACR2CCR2APAF1
SCHEMBL3864213 0.89 TACR3 (0.48) TACR3TACR1TACR2CCR2APAF1
SCHEMBL3856315 0.89 TACR3 (0.54) TACR3TACR1TACR2CCR2RIPK1
SCHEMBL3641840 0.88 TACR3 (0.56) TACR3TACR1TACR2APAF1UBE2N
SCHEMBL3672595 0.88 TACR3 (0.56) TACR3TACR1TACR2CCR2APAF1
SCHEMBL3641609 0.88 TACR3 (0.54) TACR3TACR1TACR2CCR2APAF1
SCHEMBL3638576 0.88 TACR3 (0.62) TACR3TACR1TACR2CCR2APAF1

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-2167509-A1 PIPERAZINE AND Ý1,4¨DIAZEPAN DERIVATIVES AS NK ANTAGONISTS F. Hoffmann-Roche AG (CH) 2010-03-31 EP claimed
US-7592345-B2 Piperazine and [1,4]diazepan derivatives as NK antagonists HOFFMANN-LA ROCHE INC. (US) 2009-09-22 US claimed
US-20080312216-A1 PIPERAZINE AND [1,4]DIAZEPAN DERIVATIVES AS NK ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2008-12-18 US claimed
WO-2008151969-A1 PIPERAZINE AND [1,4] DIAZEPAN DERIVATIVES AS NK ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2008-12-18 WO claimed
EP-2167509-A1 PIPERAZINE AND Ý1,4¨DIAZEPAN DERIVATIVES AS NK ANTAGONISTS F. Hoffmann-Roche AG (CH) 2010-03-31 EP disclosed
US-7592345-B2 Piperazine and [1,4]diazepan derivatives as NK antagonists HOFFMANN-LA ROCHE INC. (US) 2009-09-22 US disclosed
US-7592345-B2 Piperazine and [1,4]diazepan derivatives as NK antagonists HOFFMANN-LA ROCHE INC. (US) 2009-09-22 US disclosed
US-7592345-B2 Piperazine and [1,4]diazepan derivatives as NK antagonists HOFFMANN-LA ROCHE INC. (US) 2009-09-22 US disclosed
US-20080312216-A1 PIPERAZINE AND [1,4]DIAZEPAN DERIVATIVES AS NK ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2008-12-18 US disclosed
US-20080312216-A1 PIPERAZINE AND [1,4]DIAZEPAN DERIVATIVES AS NK ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2008-12-18 US disclosed
US-20080312216-A1 PIPERAZINE AND [1,4]DIAZEPAN DERIVATIVES AS NK ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2008-12-18 US disclosed
WO-2008151969-A1 PIPERAZINE AND [1,4] DIAZEPAN DERIVATIVES AS NK ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2008-12-18 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-20080312216-A1 PIPERAZINE AND [1,4]DIAZEPAN DERIVATIVES AS NK ANTAGONISTS DRD3, KCND3, GRIN3A TACR3 107/4885TACR1 21/4885TACR2 30/4885

“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.